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. 2022 May 2;27(9):2899. doi: 10.3390/molecules27092899

Phytonutrients, Colorant Pigments, Phytochemicals, and Antioxidant Potential of Orphan Leafy Amaranthus Species

Umakanta Sarker 1,*, Md Golam Rabbani 2, Shinya Oba 3, Wagdy M Eldehna 4,5, Sara T Al-Rashood 6, Nada M Mostafa 7,, Omayma A Eldahshan 7,
Editors: Alice Martins, Joaquina Pinheiro
PMCID: PMC9101061  PMID: 35566250

Abstract

The underutilized Amaranthus leafy vegetables are a unique basis of pigments such as β-cyanins, β-xanthins, and betalains with radical scavenging capacity (RSC). They have abundant phytonutrients and antioxidant components, such as pigments, vitamins, phenolics, and flavonoids. Eight selected genotypes (four genotypes from each species) of underutilized Amaranthus leafy vegetables were evaluated for phytonutrients, pigments, vitamins, phenolics, flavonoids, and antioxidants in a randomized complete block design under ambient field conditions with three replicates. The studied traits showed a wide range of variations across eight genotypes of two species of Amaranthus leafy vegetables. The highest fat, β-xanthins, K, dietary fiber, Mg, β-cyanins, Mn, chlorophyll ab, Zn, TP, TF, betalains, chlorophyll a content, and (RSC) (DPPH) and RSC (ABTS+) were obtained from A. tricolor accessions. Conversely, the highest protein, Cu, carbohydrates, Ca, and chlorophyll b content were obtained from A. lividus accessions. The highest dry matter, carotenoids, Fe, energy, and ash were obtained from A. tricolor and A. lividus. The accession AT2 confirmed the highest vit. C and RSC (DPPH) and RSC (ABTS+); AT5 had the highest TP content; and AT12 had the highest TF content. A. tricolor accessions had high phytochemicals across the two species, such as phytopigments, vitamins, phenolics, antioxidants, and flavonoids, with considerable nutrients and protein. Hence, A. tricolor accessions can be used as high-yielding cultivars comprising ample antioxidants. The correlation study revealed that vitamin C, pigments, flavonoids, β-carotene, and phenolics demonstrated a strong RSC, and showed a substantial contribution to the antioxidant potential (AP) of A. tricolor. The investigation exposed that the accessions displayed a plentiful origin of nutritional values, phytochemicals, and AP with good quenching ability of reactive oxygen species (ROS) that provide enormous prospects for nourishing the mineral-, antioxidant-, and vitamin-threatened community.

Keywords: underutilized leafy vegetables, proximate composition, minerals, antioxidant pigments, polyphenols, flavonoids, vitamin C, DPPH, antioxidant activity, ABTS+

1. Introduction

Amaranth is a promising crop with widespread divergence [1,2,3,4,5,6,7]. Across seventy species of the family of Amaranthaceae, 17 are consumed as vegetables, and 3 are consumed as grains [8]. Amaranth is a fast-growing C4 plant with versatile uses, including vegetables, ornamentals, and grains. It is a widely acclimated vegetable with a widespread distribution in America, Australia, Africa, Europe, and Asia. It is a low-cost vegetable whose edible stems and leaves have abundant protein, including methionine and lysine (important amino acids for humans) [9,10,11,12]; digestible fiber; ascorbic acid; carotenoids; and minerals containing Ca, Cu, Mg, Zn, K, Fe, and Mn [13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37]. Amaranthus leafy vegetables are used as many traditional medicines, especially antimicrobial [38,39,40,41,42,43,44,45,46,47,48], anthelmintic [49,50,51,52], antiviral [53], neuroprotective [54], anti-inflammatory [55,56], antiulcer [57], anticancer [58,59,60], hepatoprotective [61,62,63,64], anti-hyperlipidemic [65,66,67,68,69,70], antidiabetic, antidepressant, antimalarial activities, and snake antidotes [71,72,73,74,75,76]. It also has abundant phytopigments, including β-cyanins, anthocyanin, β-xanthins, betalains, carotenoids, and chlorophylls [77,78,79,80,81,82,83,84] with high RSC [85,86,87,88,89,90,91,92,93,94,95]. It also has sufficient phytochemicals, including ascorbic acids, phenolic acids, and flavonoids [96,97,98,99,100,101,102] and AP [103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120]. These compounds of natural origin quench ROS [121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139], and predominantly influence the industry of foods [140,141]. Phytopigments, including β-cyanins, carotenoids, β-xanthins, betanin, and amaranthine, have the important RSC [141]. They are broadly acclimated to different abiotic stresses such as water deficits [142,143,144,145,146,147,148,149,150] and salinization [151,152,153,154].

There is significant variability and phenotypic plasticity of Amaranthus germplasms in Asia, Africa, Bangladesh, and South America [155], with versatile usages. In Africa and South-East Asia, including India and Bangladesh, amaranth is a cheap and popular leafy vegetable. The flavor, taste, and beautiful color make it a typical leafy vegetable in Asia and many global regions. It grows year-round in Bangladesh, including the leafy vegetables gap in summer [19,20].

Nowadays, both consumers and researchers give attention to consuming vegetables for achieving antioxidants of natural origin [156,157,158,159]. Amaranthus has significant groups of natural antioxidants, such as β-cyanin, β-xanthin, amaranthine, betalain, phenolics, carotenoids, vitamin C, and flavonoids [140,141]. These natural antioxidant phytochemicals defend against many diseases, such as atherosclerosis, emphysema, cardiovascular diseases, cancer, cataracts, arthritis, retinopathy, and degenerative diseases of neurons, and contribute significantly to human health promotion [160,161,162]. Natural products with AP have an extensive interest. Numerous medicinal plants having interesting AP have been proposed as protective capacities because of constituents’ presence, including vitamins C, flavonoids, carotenoids, phenolics, and other non-nutrient components [163].

In the current years, our research group is investigating the opportunity of applying leafy vegetable amaranth as a foundation of natural pigments because of their ample β-cyanins, β-xanthins, betalains color pigments, and phytochemicals of interest in the food industry [77,78]. Our research group carefully chose a few high-yielding AP A. tricolor and A. lividus cultivars from the gene pool in our earlier studies [19,20,77,78]. This study evaluates the comparative performance of the selected eight best genotypes of two species of A. tricolor and A. lividus, in terms of minerals, nutrients, antioxidants phytochemicals, and pigments having high AP.

2. Materials and Methods

2.1. Materials

The seeds of eight accessions of A. lividus and A. tricolor were selected from our earlier collected germplasms.

2.2. Layout and Design

The study was implemented at Bangabandhu Sheikh Mujibur Rahman Agricultural University using a completely randomized block design (RCBD) in three replicates. Each experimental plot comprises a 1 m2 area with 20 cm rows and a 5 cm plant distance.

2.3. Management Practices

We applied 150 kg MP, 200 kg urea, 100 kg TSP, 60 kg gypsum, and 10 compost (cowdung:straw = 1:2 w/w) per ha of land. We maintained suitable cultural management. Thinning was performed to keep the particular space of plants in a row. The experimental plots were kept free from weeds by applying appropriate and regular weeding and hoeing. We applied regular irrigation in the plot for appropriate growth of the crop. Leaf samples were collected from 30-day-old plants.

2.4. Solvent and Reagents

Solvent: Methanol and acetone. Reagents: cesium chloride, dithiothreitol (DTT), HClO4, ascorbic acid, HNO3, H2SO4, and Trolox, ABTS+, Folin–Ciocalteu reagent, DPPH, gallic acid, 2, 2-dipyridyl, rutin, hexahydrate aluminum chloride, K acetate, sodium carbonate, and K persulfate.

2.5. Determination of Proximate Composition

Crude fat, ash, moisture, crude protein, fiber, and energy (gross) were estimated according to the Association of Official Agricultural Chemists (AOAC) method [164]. We followed the Micro-Kjeldahl method to calculate the nitrogen, and finally, crude protein was measured by multiplying nitrogen by 6.25 (AOAC method 976.05). The crude protein, total moisture, ash, and crude fat (%) were subtracted from 100 for calculating carbohydrate (g 100 g−1 FW).

2.6. Determination of Minerals

In an oven, the leaves were dried out for 24 h at 70 °C. Dried samples were ground in a mill. We determined Ca, K, Mg, Fe, Mn, Cu, and Zn using the nitric and perchloric acid method [165]. A dried leaf sample (0.5 g) was digested with 10 mL H2SO4 (96%), 400 mL HNO3 (65%), and 40 mL HClO4 (70%) in the presence of carborundum beads. A blue-colored phosphomolybdenum complex was formed by adding antimony and ascorbic acid to the complex solution (yellow). Atomic absorption spectrophotometry (AAS) (Hitachi, Tokyo, Japan) was used to read the absorbance at 213.9 nm (Zn), 285.2 nm (Mg), 279.5 nm (Mn), 76 6.5 nm (K), 422.7 nm (Ca), 248.3 nm (Fe), and 324.8 nm (Cu).

2.7. Estimation of Carotenoids and Chlorophylls

The leaf samples were added in acetone (80%) to determine carotenoids, and chlorophyll a, ab, and b [165]. Carotenoids, chlorophyll b, and chlorophyll a were calculated by measuring the absorbance at 470, 663, and 646 nm, respectively, using a spectrophotometer (Hitachi, Japan).

2.8. β-Cyanins and β-Xanthins Content Measurement

β-Cyanins and β-xanthins were measured by extracting the leaf samples in 80% MeOH containing 50 mM ascorbic acid [166,167]. β-cyanins and β-xanthins were determined by measuring the absorbance at 540 and 475 nm, respectively, using a spectrophotometer (Hitachi, U-1800, Tokyo, Japan). The results of β-cyanins and β-xanthins were expressed by calculating, as nanograms, betanin and indicaxanthin equivalent per g of fresh weight for β-cyanins and β-xanthins, respectively.

2.9. Estimation of β-Carotene

We used our described method for the estimation of β-carotene [168,169]. In a mortar and pestle, 500 mg of fresh leaves was added with 10 mL acetone (80%), and ground precisely. The extract was centrifuged for 3–4 min at 10,000× g. After removing the supernatant in a volumetric flask, the final volume was marked up to 20 mL. A spectrophotometer (Hitachi, Tokyo, Japan) was used to take the absorbance at 510 nm and 480 nm. Data were expressed as milligrams of β--carotene per 100 g of fresh weight.

β-Carotene = 7.6 {(Abs. at 480 nm) − 1.49 (Abs. at 510 nm) × Final volume}/(1000 × fresh weight of leaf).

2.10. Determination of Ascorbic Acid

The fresh leaf samples were pre-incubated, and dehydroascorbic acid (DHA) was reduced to ascorbic acid (AsA) using Dithiothreitol (DTT). AsA reduced Fe3+ to Fe2+. 2, 2-dipyridyl forms complexes with reduced Fe2+ [170]. The optical density was taken using a spectrophotometer (Hitachi, Japan) at 525 nm to estimate ascorbic acid (AsA). We calculated ascorbic acid in milligrams per 100 g of fresh weight.

2.11. Samples Extraction and Determination of TP, TF, and RSC

The extraction was performed from the fresh and dried ground leaves (30 d) with a mortar and pestle for total polyphenols (TP) content, total flavonoids (TF) content, and RSC determination. In a tightly capped bottle, 0.25 g of leaves were added in 10 mL MeOH (90%), and placed in a shaking water bath (Tokyo, Japan). The extract was filtered after 1 h and stored for TP, TF, and RSC. Phenolic content was determined by the Folin–Ciocalteu reagent [170]. The optical density was taken at 760 nm using a spectrophotometer (HITACHI, Japan). TP was calculated as gallic acid equivalent μg GAE g−1 of FW using an equation (Y = 0.009X + 0.019) obtained from a standard gallic acid graph. The aluminum chloride colorimetric method was followed to estimate the total flavonoid content [170]. The optical density was measured at 415 nm using a spectrophotometer (HITACHI, Japan). A rutin standard graph (Y = 0.013X) was made to estimate TF as μg RE g−1 DW. The RSC was estimated by the diphenyl-picrylhydrazyl (DPPH) radical degradation method [171], and ABTS+ assay was carried out using the method of Sarker and Oba [172]. Percentage of inhibition of ABTS+ and DPPH equivalent to the control was applied to measure the RSC using following the equation:

RSC (%) = (AC − AS/AC) × 100 (1)

where AC is the absorbance of the control (150 μL and 10 µL MeOH for RSC (ABTS), RSC (DPPH) instead of leaf extract), and AS is the absorbance of the samples. The results were calculated as μg Trolox equivalent g−1 DW.

2.12. Statistical Analysis

The replication mean was obtained by averaging the replication-wise row data. Analysis of variance (ANOVA) of the mean data was analyzed using Statistix 8 software [173,174,175,176]. Duncan Multiple Range Test at a 1% level of probability was followed to compare means data. The results were expressed as the mean ± SD. The correlation was analyzed using Statistix 8 software.

3. Results and Discussion

The variance analysis revealed that all the parameters significantly differed regarding the accessions, indicating a wide range of variations across the genotypes of two species of Amaranthus leafy vegetables. An extensive range of variability was also stated in red and green color amaranth [167].

3.1. Proximate Contents

The composition of the proximate (g 100 g−1 FW) of eight selected accessions of two underutilized species of Amaranthus leafy vegetables is shown in Table 1. The content of moisture of eight selected accessions of two underutilized Amaranthus leafy vegetable species varied from 82.85 to 88.52. AT2 displayed the highest moisture content (88.52) after A. tricolor genotype AT12 (86.43) and AT9 (86.38). Alternately, SA10 had the least moisture content (82.85), which was statistically similar to SA14, SA3, SA21, and AT5. Across eight accessions of two underutilized species, AT5, SA3, SA10, SA14, and SA21 showed low moisture content (18% dry matter). As lower moisture ensures a higher dry weight of leaves, these accessions could be used as superior dry biomass. The moisture content is directly related to the maturity of the leaves. The results obtained from underutilized species were corroborated by the reports of sweet potato leaves [177]. In comparison to leafy vegetables, the leaves of eight selected accessions of two underutilized species of Amaranthus leafy vegetables had good protein content that significantly varied regarding accessions (3.66 to 6.52). The highest protein content was recorded in SA14 (6.52). On the contrary, SA21 displayed the least protein content (3.66). Compared to leafy vegetables, higher protein content was obtained from AT2, AT5, AT9, AT12, SA3, and SA10. Vegetable amaranth is the primary source of protein for vegetarians and poor people in developing countries. The protein content of the accessions of two underutilized species was much more prominent as compared to A tricolor (1.26%) [20].

Table 1.

Proximate compositions (g 100 g−1 fresh weight) of two underutilized species of Amaranthus leafy vegetables.

Accessions Water (%) Crude Protein Crude Fat Carbohydrate Ash Energy (kcal) Fiber
A. tricolor
AT2 88.52 ± 1.86 a 5.35 ± 0.04 b 0.27 ± 0.04 b 0.38 ± 0.05 h 5.48 ± 0.02 ab 25.11 ± 0.32 d 7.19 ± 0.15 d
AT5 81.92 ± 1.44 c 5.33 ± 0.05 b 0.33 ± 0.03 a 6.50 ± 0.06 d 5.62 ± 0.02 a 53.80 ± 0.31 a 9.22 ± 0.17 b
AT9 86.38 ± 1.35 b 5.37 ± 0.06 b 0.29 ± 0.03 ab 5.05 ± 0.07 f 2.91 ± 0.02 d 43.81 ± 0.38 c 10.24 ± 0.13 a
AT12 86.43 ± 1.35 b 5.32 ± 0.04 b 0.35 ± 0.04 a 4.07 ± 0.06 g 3.83 ± 0.03 c 40.71 ± 0.26 c 8.34 ± 0.12 c
A. lividus
SA3 81.86 ± 1.56 c 5.35 ± 0.05 b 0.27 ± 0.04 b 7.00 ± 0.05 c 5.52 ± 0.04 ab 53.81 ± 0.36 a 8.56 ± 0.17 c
SA10 81.85 ± 1.38 c 5.34 ± 0.03 b 0.23 ± 0.03 bc 7.46 ± 0.06 b 5.12 ± 0.03 b 52.55± 0.42 ab 7.76 ± 0.15 cd
SA14 81.87 ± 1.51 c 6.52 ± 0.04 a 0.18 ± 0.03 c 5.87 ± 0.06 e 5.56 ± 0.04 a 53.82 ± 0.35 a 6.66 ± 0.15 e
SA21 81.91 ± 1.62 c 3.66 ± 0.04 c 0.16 ± 0.03 c 9.56 ± 0.05 a 4.71 ± 0.02 d 51.60 ± 0.36 b 9.18 ± 0.12 b
Significance ** ** ** ** ** ** **
CV% 2.36 1.35 0.24 0.66 0.55 0.75 0.38

CV, coefficient of variation; in a column, different letters in mean values are significantly differed by Duncan Multiple Range Test (**, p < 0.01); n = 3.

In this investigation, the selected accessions of two underutilized species displayed lesser fat, owing to leafy vegetables, and they might be utilized as foods free from cholesterol. AT12 confirmed the highest fat (0.35), although SA21 had the least fat (0.16) that had a statistical similarity with SA14. The results of sweet potato [177] were corroborated with our current results. They stated that fat covering the body’s organs influences cell function and perpetuation body temperature. Vegetable fats are the primary sources of essential fatty acids, such as omega-6 and omega-3. Fats play a significant role in the absorption, digestion, and transport of vitamins E, D, A, and K, which are soluble in fats. The selected accessions of two underutilized species confirmed good carbohydrate content with ample variations regarding accessions (0.38 to 9.56). SA21 confirmed the highest carbohydrates (9.56), though AT2 had the least carbohydrates (0.38). The accessions of two underutilized species were principally diverse for energy (28.95 to 58.47). The accession AT5, SA3, and SA14 demonstrated the highest energy (53.80, 53.81, and 53.82, respectively). On the other hand, AT2 displayed the least energy (25.11). AT5 and SA14 exhibited the highest ash (5.62 and 5.56, respectively), whereas AT9 showed the least ash (2.91). Fiber was largely diverse among accessions (6.66 to 10.24). AT9 confirmed the highest fiber (10.24) after AT5 and SA21. Inversely, SA14 had the least fiber (6.66). Fiber had a noteworthy involvement in the cure of constipation, the augmentation of digestibility, and palatability [19]. Our results displayed that those leaves of selected accessions of two underutilized species have copious protein, moisture, carbohydrates, and digestible fiber. The highest fat and fiber were obtained from A. tricolor accessions. Similarly, the highest protein and carbohydrates were obtained from A. lividus accessions. The highest dry matter, energy, and ash were obtained from both A. tricolor and A. lividus accessions. The moisture and protein contents received from accessions were superior to the moisture and protein contents of the green, red, stem, and weedy amaranth and A. blitum [178,179,180,181,182]. The carbohydrates of advanced line AT7 were greater than red, green amaranth, A. spinosus, and A. blitum [178,179,180,182], although the carbohydrates of AT7 were corroborative with stem amaranth [181]. The fiber of AT3 and AT7 were superior to red, stem, and green amaranth and A. blitum [178,180,181,182], although corroborated by weedy amaranth [179].

3.2. Mineral Content

Macroelements (mg g−1 FW) and microelements (µg g−1 FW) of eight selected accessions of two underutilized species of Amaranthus leafy vegetables are shown in Table 2. The selected accessions of two underutilized species demonstrated good K content. AT12 had the highest K content (6.72) after AT2, AT5, and AT9. On the contrary, the highest K content was recorded in SA14 and SA21 (3.77 and 3.72, respectively). SA3 showed the highest Ca content (3.45) after AT2, AT9, and AT12. Inversely, SA21 displayed the least Ca (1.56). The accessions of two underutilized species demonstrated good Mg content with prominent variations regarding accessions (2.65 to 3.74). AT12 confirmed the highest Mg (3.62). Inversely, AT7 confirmed the lowest Mg (3.74) after AT2, AT5, and AT9. It exposed that sufficient K (6.72), Mg (3.74), and Ca (3.45) were noted in the selected accessions of two underutilized species (based on fresh weight). Several species of amaranth literature [183] stated sufficient, Mg, Ca, and K. Furthermore, they detected that Ca, Mg, and K of amaranth were much more protuberant than nightshade, black spider flower, kale, and spinach. Mg, Ca, and K obtained from the accessions of two underutilized species were superior to Mg, Ca, and K of literature [183]. A. tricolor had the highest K and Mg. In contrast, the A. lividus demonstrated the highest Ca. K content of advanced lines was more than K of green amaranth [180], though K obtained from these advanced lines was inferior to K of weedy amaranth [179]. Ca content observed in the study was corroborative to the results of green and weedy amaranth [179,180]. Mg noticed in these accessions was greater than our previous green and weedy amaranth [179,180]. The protuberant differences were observed in Fe content regarding accessions (10.72 to 18.34). AT12 and SA10 displayed the highest Fe (18.34 and 18.24, respectively), though the least Fe was displayed in SA21 and AT5 (10.72 and 10.76, respectively). Our study revealed that preponderant variations were noticed.

Table 2.

Macroelements (mg g−1 FW) and microelements (µg g−1 FW) of two underutilized species of Amaranthus leafy vegetables.

Genotypes Macroelements Microelements
K Ca Mg Fe Mn Cu Zn
A. tricolor
AT2 4.96 ± 0.11 b 2.32 ± 0.15 b 3.38 ± 0.17 b 11.86 ± 0.26 c 6.86 ± 0.13 c 1.32 ± 0.03 d 6.85 ± 0.13 e
AT5 4.97 ± 0.10 b 1.93 ± 0.16 c 3.39 ± 0.13 b 10.76 ± 0.23 e 7.92 ± 0.17 b 1.05 ± 0.02 e 7.08 ± 0.15 d
AT9 4.95 ± 0.14 b 2.36 ± 0.15 b 3.42 ± 0.18 b 15.05 ± 0.28 b 6.79 ± 0.14 c 1.04 ± 0.03 e 7.06 ± 0.16 d
AT12 6.72 ± 0.11 a 2.35 ± 0.11 b 3.74 ± 0.12 a 18.34 ± 0.25 a 15.12 ± 0.18 a 2.12 ± 0.03 c 17.12 ± 0.14 a
A. lividus
SA3 4.22 ± 0.14 c 3.45 ± 0.17 a 3.15 ± 0.19 c 11.08 ± 0.24 d 3.12 ± 0.12 g 2.98 ± 0.04 a 7.05 ± 0.13 d
SA10 4.15 ± 0.16 c 1.88 ± 0.15 c 3.35 ± 0.13 b 18.24 ± 0.21 a 3.76 ± 0.14 f 2.32 ± 0.03 b 8.72 ± 0.18 b
SA14 3.77 ± 0.14 d 1.91 ± 0.16 c 2.98 ± 0.17 c 11.02 ± 0.23 d 4.77 ± 0.14 e 1.34 ± 0.03 d 6.02 ± 0.12 f
SA21 3.72 ± 0.16 d 1.56 ± 0.16 cd 2.65 ± 0.14 d 10.72 ± 0.17 e 5.95 ± 0.14 d 2.08 ± 0.05 c 7.86 ± 0.15 c
Significance ** ** ** ** ** ** **
CV% 0.12 0.35 0.25 0.21 0.32 0.13 0.26

CV, coefficient of variation; n = 3; in a column, different letters in mean values are significantly differed by Duncan Multiple Range Test (**, p < 0.01).

In Mn content of the selected accessions of two underutilized species (3.12 to 15.12), AT12 had the highest Mn (15.12), although the least Mn was recorded in SA3 (3.12). The Cu had an extensive array of variations in the accessions of two underutilized species (1.04 to 2.98). SA3 confirmed the highest Cu (2.98), although AT9 and AT5 exerted the least Cu (1.04 and 1.05, respectively). Zn of the accessions of two underutilized species differed significantly and markedly (6.02 to 17.12). AT12 confirmed the highest Cu (17.12), whereas SA14 exerted the least Cu (6.02). The Fe and Zn content of the accessions of two underutilized species was superior to the leaves of cassava [184] and beach pea [185]. We documented sufficient Fe (18.34), Mn (15.12), Zn (17.12), and noteworthy Cu (2.98) (based on fresh weight) in the accessions of two underutilized species. Similarly, different amaranths in literature [183] observed satisfactory Fe, Mn, Cu, and Zn. They also stated that Fe, Zn, Mn, and Cu in the leaves of amaranth were superior to spinach, spider flower, black nightshade, and kale. Mn, Fe, Zn, and Cu in the study were superior to Mn, Fe, Zn, and Cu in the literature [183]. A. tricolor accessions confirmed the highest Mn and Zn. Similarly, A. lividus accessions confirmed the highest Cu. A. tricolor and A. lividus accessions confirmed the highest Fe. In the study, Fe and Mn of all advanced lines were superior to green amaranth [180], although Fe and Mn of AT15 were superior to weedy amaranth [179]. Cu observed in the study was superior to green and weedy morph amaranth [179,180] and A. spinosus amaranth [179]. AT15 displayed much greater Zn than green and weedy amaranth [179,180].

3.3. Antioxidant Phytopigment Content

Chlorophylls (μg g−1 FW), and betalains (ng g−1 FW) of the selected accessions of two underutilized species are shown in Table 3. Prominent variations in chlorophyll a were stated among accessions of two underutilized species (134.15 to 636.56). AT5 demonstrated the highest chlorophyll a (636.56) after AT2 and AT12. Inversely, the least chlorophyll a (134.15) was observed in AT3.

Table 3.

The performance of the mean antioxidant pigments (chlorophylls (μg g−1 FW); β-Cyanins, β-xanthins, and betalains (ng g−1 FW); carotenoids (mg 100 g−1 FW)) of two underutilized species of Amaranthus leafy vegetables.

Genotypes Chlorophyll a Chlorophyll b Chlorophyll ab β-Cyanins β-Xanthins Betalains Carotenoids
A. tricolor
AT2 519.55 ± 2.11 b 264.52 ± 1.68 c 784.07 ± 1.25 b 536.32 ± 1.61 b 528.42 ± 1.71 c 1064.74 ± 1.54 c 72.68 ± 0.37 d
AT5 636.56 ± 2.14 a 276.64 ± 1.77 b 913.20 ± 1.21 a 417.34 ± 1.63 e 434.65 ± 1.63 e 851.99 ± 1.64 e 82.65 ± 0.35 c
AT9 308.72 ± 2.02 e 212.72 ± 1.78 f 521.44 ± 1.14 f 542.75 ± 1.64 a 596.73 ± 1.95 a 1139.48 ± 1.44 a 95.35 ± 0.37 b
AT12 518.59 ± 2.16 b 228.24 ± 1.78 e 746.83 ± 1.18 d 489.58 ± 1.62 d 498.66 ± 1.88 d 988.24 ± 1.47 d 123.28 ± 0.42 a
A. lividus
SA3 432.35 ± 2.17 d 242.16 ± 1.62 d 674.51 ± 1.25 e 524.56 ± 1.72 c 558.35 ± 1.52 b 1082.91 ± 1.65 b 45.44 ± 0.41 f
SA10 134.15 ± 2.32 g 82.71 ± 1.61 h 216.86 ± 1.12 h 192.44 ± 1.58 h 196.55 ± 1.42 h 388.99 ± 1.42 h 82.57 ± 0.42 c
SA14 478.45 ± 2.17 c 285. 32 ± 1.73 a 763.77 ± 1.23 c 292.62 ± 1.72 f 292.25 ± 1.37 f 554.87 ± 1.57 f 58.74 ± 0.42 e
SA21 256.26 ± 2.22 f 93.33 ± 1.69 g 349.53 ± 1.31 g 243.24 ± 1.6 g 265.86 ± 1.68 g 509.10 ± 1.72 g 122.94 ± 0.45 a
Significance ** ** ** ** ** ** **
CV% 3.55 1.28 1.46 2.16 2.35 1.23 2.33

CV, coefficient of variation; In a column, different letters in mean values are significantly differed by Duncan Multiple Range Test (**, p < 0.01); n = 3.

Selected accessions of two underutilized species demonstrated wide variations in chlorophyll b content (82.71 to 285.32). SA14 confirmed the highest chlorophyll b (285.32) after AT5. In contrast, SA10 confirmed the least chlorophyll b (82.71). Noteworthy and outstanding variations in chlorophyll ab were confirmed in the accessions of two underutilized species (216.86 to 913.20). Across the two underutilized species, AT5 exhibited the highest chlorophyll ab (913.20) after AT2, although SA10 confirmed the least chlorophyll ab (216.86). Notably, chlorophyll a, ab, and b (636.56, 913.20, and 285.32) in the accessions of two underutilized species, were superior to red and green amaranth [186]. A. tricolor accessions confirmed the highest chlorophyll a and ab. Similarly, A. lividus accessions confirmed the highest chlorophyll b. Chlorophylls a, ab, and b of the study were superior to red, green, stem, and weedy amaranth and A. blitum [178,179,180,181,182].

The accessions of two underutilized species established good β-cyanins content with significant variability among accessions (192.44 to 542.75). AT9 confirmed the highest β-cyanins (542.75) after AT2. Inversely, SA10 showed the least β-cyanins (192.44 ng g−1). The selected accessions of two underutilized species established good β-xanthins with significant variability regarding accessions (196.55 to 596.73). AT9 confirmed the highest β-xanthins (596.73) after SA3. Inversely, SA10 showed the least β-xanthins (196.55). The accessions of two underutilized species established good content of betalains with protruding variability among accessions (388.99 to 1139.48). The betalains were the highest in AT9 (1139.48) after SA3. Inversely, the least betalains were stated in SA10 (388.99). Moreover, carotenoids and betalains showed major variability in the accessions of two underutilized species (45.44 to 123.28). AT12 and SA21 confirmed the highest carotenoids (123.28 and 122.94). Inversely, SA3 confirmed the least carotenoids (45.44). Notably, chlorophyll a, ab, and b (636.56, 913.20, 285.32); β-cyanins (542.75); β-xanthins (596.73); betalains (1139.48); and carotenoids (123.28), in the accessions of two underutilized species, were corroborated to green and red amaranth [186]. β-cyanins, β-xanthins, and betalains pigments were the highest in A. tricolor accessions. Inversely, the highest carotenoids were obtained from both A. tricolor and A. lividus. Betalains, β-cyanins, and β-xanthins in the study were superior to red, green, stem amaranth, and A. blitum [178,180,181,182]. Carotenoids in the study were superior to green amaranth [180], and verified to weedy amaranth [179], although the carotenoids of this study were inferior to red and stem amaranth and A. blitum [178,181,182].

3.4. Phytochemical Contents and Scavenging Activity

TP, β-carotene, TF, ascorbic acid, and RSC of the selected accessions of two underutilized species are shown in Table 4. Pronounced variability was recorded in the β-carotene content of the selected accessions of two underutilized species (27.67 in AT5 to 68.82 in AT12).

Table 4.

The performance of TP (µg GAE g−1 FW), vitamin C (mg 100 g−1 FW), β-Carotene (mg 100 g−1 FW), RSC (DPPH) (µg g−1 TEAC DW), TF (µg RE g−1 DW), and RSC (ABTS+) (µg TEAC g−1 DW) of two underutilized species of Amaranthus leafy vegetables.

Genotypes β-Carotene Vitamin C TP TF RSC (DPPH) RSC (ABTS+)
A. tricolor
AT2 62.58 ± 0.65 b 192.75 ± 1.48 a 29.48 ± 0.42 b 158.84 ± 1.26 c 36.27 ± 0.11 a 68.87 ± 0.34 a
AT5 27.67 ± 0.56 g 98.56 ± 1.52 c 32.88 ± 0.38 a 172.55 ± 1.29 b 35.08 ± 0.12 b 64.55 ± 0.31 b
AT9 48.55 ± 0.62 d 18.54 ± 1.49 h 29.45 ± 0.37 b 151.88 ± 1.36 d 33. 84 ± 0.09 c 64.56 ± 0.39 b
AT12 68.82 ± 0.69 a 72.98 ± 1.46 e 22.43 ± 0.45 e 176.88 ± 1.28 a 33.85 ± 0.11 c 60.88 ± 0.38 c
A. lividus
SA3 32.74 ± 1.68 f 58.74 ± 1.48 g 18.62 ± 0.42 f 151.75 ± 1.24 d 22.75 ± 0.11 g 40.86 ± 0.37 g
SA10 61.83 ± 1.66 b 65.84 ± 1.52 f 15.66 ± 0.42 g 148.56 ± 1.25 cd 24.45 ± 0.15 f 42.44 ± 0.41 f
SA14 39.35 ± 1.58 e 175.87 ± 1.45 b 26.24 ± 0.36 c 140.71 ± 1.23 e 26.23 ± 0.14 e 48.95 ± 0.46 e
SA21 54.74 ± 1.56 c 87.76 ± 1.58 d 25.45 ± 0.42 d 157.93 ± 1.28 c 28.86 ± 0.18 d 55.76 ± 0.48 d
Significance ** ** ** ** ** **
CV% 1.53 2.26 3.72 1.32 1.63 0.87

CV, coefficient of variation; TF = total flavonoid content, RSC = radical scavenging capacity, TP = total polyphenol content, n = 3; in a column, mean values with different letters are differed significantly by Duncan Multiple Range Test (**, p < 0.01).

AT2 and SA10 confirmed the high β-carotene. The accessions of two underutilized species demonstrated prominent variations in ascorbic acid (18.54 to 192.75). AT2 confirmed the highest ascorbic acid (192.75), and the least in AT9 (18.54). Noteworthy variations were noted in TP of the accessions of two underutilized species (15.66 to 32.88). AT5 established the highest TP of 32.88 after AT2 and AT9. Conversely, SA10 showed the least TP (15.66). The accessions of two underutilized species demonstrated high TF with substantial variability among accessions (140.71 to 176.88). AT12 showed the highest TF (176.88) after AT5, whereas SA14 had the least TF (140.71). The accessions of two underutilized species confirmed high RSC (DPPH) and RSC (ABTS+). AT2 showed the highest RSC (DPPH and ABTS+) (36.27, 68.87) after AT5 (35.08, 64.55) and AT9 (33.84, 64.56). On the other hand, the least RSC (DPPH) and RSC (ABTS+) were recorded in SA3 (22.75, 40.86) after SA10 (24.45, 42.44). A parallel tendency of RSC (DPPH) and RSC (ABTS+) methods authenticated the measurement of two different methods of AP. The accessions of two underutilized species exhibited outstanding ascorbic acid and β-carotene (192.75 and 68.82). TP (32.88), TF (176.88), RSC (DPPH) (36.27), and RSC (ABTS+) (68.87) found in this study were superior to red and green amaranth [187]. The β-carotene of these lines was confirmative to weedy amaranth [179]. The ascorbic acid of AT11 was superior to green, weedy, stem, amaranth, and A. blitum [179,181,182], and corroborative to red morph amaranth [178]. TP content was greater than green and weedy amaranth [179,180]. TF, RSC (DPPH), and RSC (ABTS+) documented in the accessions of two underutilized species were greater than the red, green, stem, and weedy amaranth and A. blitum morph [178,179,180,181,182]. The accession AT2 had the highest vitamin C and RSC (DPPH) and RSC (ABTS+); AT5 had the highest TP content; and AT12 had the highest TF content. A. tricolor accessions had high phytochemicals across the two species, such as phytopigments, vitamins, phenolics, flavonoids, and antioxidants, including considerable nutrients and protein. A. tricolor accessions can be used as high-yielding cultivars comprising ample antioxidants. The accessions confirmed an immense foundation of phytochemicals, and nutritional values and AP presented enormous prospects for feeding the mineral-, vitamin-, and antioxidant-deficient community.

3.5. The Correlation Studies

The correlation of β-carotene, pigments, TP, ascorbic acid, TF, and RSC (ABTS+) and RSC (DPPH) of accessions of two underutilized species are shown in Table 5, representing exciting results. All pigments confirmed positive and significant correlations with TP, TF, and RSC (ABTS+) and RSC (DPPH), indicating that the increase in TF, TP, and RSC (DPPH) and RSC (ABTS+) were straightly linked to the augmentation of chlorophylls, β-cyanins, carotenoids, betalains, and β-xanthins or vice versa. Its destined pigments had good RSC. Similarly, β-carotene had a significant positive relationship with TP, ascorbic acid, TF, and RSC (ABTS+) and RSC (DPPH), although it exhibited significant negative associations among all pigments. Ascorbic acid had a significant positive relationship with TP, TF, and RSC (ABTS+) and RSC (DPPH), although it displayed insignificant negative associations among pigments. In amaranth, Sarker, and Oba [142] also observed a similar trend. A significant positive association was displayed among TP, TF, and RSC (ABTS+) and RSC (DPPH), which is corroborative to the results of amaranth and salt stressed-purslane [187,188,189,190]. The validation of the antioxidant capacity of the selected advanced lines of vegetable amaranth by two different methods of antioxidant capacity measurements was confirmed with the significant positive associations between RSC (ABTS+) and RSC (DPPH).

Table 5.

The coefficient of correlation of antioxidant pigments, TPC (µg GAE g−1 FW), β-Carotene (mg 100 g−1 FW), vitamin C (mg 100 g−1 FW), RSC (DPPH) (µg g−1 TEAC DW), TFC (µg RE g−1 DW), and RSC (ABTS+) (µg TEAC g−1 DW), chlorophylls (μg g−1 FW); β-Cyanins, β-xanthins, and betalains (ng g−1 FW); carotenoids (mg 100 g−1 FW) of two underutilized species of Amaranthus leafy vegetables.

Traits Chl b Chl ab β-Cyanins β-Xanthins Betalains β-Carotene Vitamin C TP TF RSC (DPPH) RSC (ABTS+)
Chlorophyll a 0.86 ** 0.92 ** 0.89 ** 0.85 ** 0.82 ** −0.73 * −0.015 0.77 * 0.75 * 0.86 ** 0.86 **
Chlorophyll b 0.85 ** 0.77 ** 0.85 ** 0.86 ** −0.67 −0.018 0.72 * 0.74 * 0.84 ** 0.84 **
Chlorophyll ab 0.72 * 0.76 * 0.83 ** −0.76* −0.014 0.75 * 0.82 ** 0.73 * 0.85 **
β-cyanins 0.87 ** 0.96 ** −0.75 * −0.116 0.76 * 0.81 ** 0.88 ** 0.87 **
β-xanthins 0.95 ** −0.86 ** −0.123 0.74 * 0.72* 0.76 * 0.83 **
Betalains −0.88 ** −0.129 0.86 ** 0.77* 0.84 ** 0.88 **
β-Carotene 0.73* 0.82 ** 0.88 ** 0.86 ** 0.85 **
Vitamin C 0.74 * 0.86 ** 0.85 ** 0.86 **
TP 0.84 ** 0.82 ** 0.92 **
TF 0.86 ** 0.86 **
RSC (DPPH) 0.95 **

Chl b, chlorophyll b; TP, total polyphenol content; TF, total flavonoid content; RSC, radical scavenging capacity; total antioxidant capacity; Chl ab, chlorophyll b; *, **, significant at 5% and 1% level.

Phytochemicals and pigments including β-carotene, TP, ascorbic acid, and TF had intense AP, as these showed significant associations with RSC (DPPH) and RSC (ABTS+).

4. Conclusions

The selected accessions of two underutilized species demonstrated leafy vegetables as abundant sources of K, Fe, Mn, Ca, dry matter, Cu, Zn, protein, Mg, dietary fiber, and carbohydrates. It is an excellent origin of antioxidant pigments and phytochemicals, including TP, β-carotene, TF, ascorbic acid, and antioxidants. The accessions of A. tricolor had abundant phytochemicals and RSC, including considerable proximate, pigments, and nutraceuticals compared to the accessions of A. lividus. The interrelationship exposed that phytochemicals and pigments of leafy vegetable amaranth accessions confirmed good RSC of 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) and 2,2-Diphenyl-1-picrylhydrazyl equivalent to Trolox. Although A. tricolor and A. lividus are underutilized, these are promising leafy vegetables. Enormous bioactive phytochemicals and antioxidants of A. tricolor and A. lividus enable growing them as preferable cultivars, and they can be used in the daily diet as fresh salad, boiled, leafy vegetables, and other culinary dishes. Based on their nutritional status, they are comparable to spinach, and can be grown throughout the year, including a gap period of leafy vegetables in summer. They are a potential source of nutritional value, antioxidant phytopigments, β-carotene, ascorbic acid, phenolics, flavonoids, and antioxidants in our daily diet to accomplish nutritional and antioxidant sufficiency.

Acknowledgments

For supporting the research work, the authors acknowledge the Department of Genetics and Plant Breeding, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur 1706, Bangladesh. The authors acknowledge financial support from the Researchers Supporting Project number (RSP-2021/103), King Saud University, Riyadh, Saudi Arabia.

Author Contributions

Conceptualization, U.S., M.G.R., S.O.; methodology, U.S.; software, U.S.; validation, U.S., M.G.R., S.O., N.M.M., O.A.E., W.M.E., S.T.A.-R.; formal analysis, U.S., N.M.M., O.A.E.; investigation, U.S., N.M.M., O.A.E.; resources, U.S.; data curation, U.S.; writing—original draft preparation, U.S.; writing—review and editing, U.S., M.G.R., S.O., N.M.M., O.A.E., W.M.E., S.T.A.-R.; visualization, U.S., N.M.M., O.A.E.; supervision, U.S.; funding acquisition, N.M.M., O.A.E., W.M.E., S.T.A.-R. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data recorded in the current study are available in all Tables of the manuscript.

Conflicts of Interest

All the authors have no conflict of interest.

Funding Statement

The research work was funded by the Department of Genetics and Plant Breeding, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur 1706, Bangladesh. The authors acknowledge also financial support from the Researchers Supporting Project number (RSP-2021/103), King Saud University, Riyadh, Saudi Arabia.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Rastogi A., Shukla S. Amaranth: A New Millennium Crop of Nutraceutical Values. Crit. Rev. Food Sci. Nutr. 2013;53:109–125. doi: 10.1080/10408398.2010.517876. [DOI] [PubMed] [Google Scholar]
  • 2.Das S. Amaranthus: A Promising Crop of Future. Springer; Singapore: 2016. Amaranths: The Crop of Great Prospect; pp. 13–48. [Google Scholar]
  • 3.Sreelathakumary I., Peter K.V. Genetic Improvement of Vegetable Crops. Elsevier; Amsterdam, The Netherlands: 1993. Amaranth: Amaranthus spp. pp. 315–323. [Google Scholar]
  • 4.Sauer J.D. The Grain Amaranths and Their Relatives: A Revised Taxonomic and Geographic Survey. Ann. Mo. Bot. Gard. 1967;54:103. doi: 10.2307/2394998. [DOI] [Google Scholar]
  • 5.Anu R., Mishra B.K., Mrinalini S., Ameena S., Rawli P., Nidhi V., Sudhir S. Identification of Heterotic Crosses Based on Combining Ability in Vegetable Amaranthus (Amaranthus tricolor L.) Asian J. Agric. Res. 2015;9:84–94. [Google Scholar]
  • 6.Nguyen D.C., Tran D.S., Tran T.T.H., Ohsawa R., Yoshioka Y. Genetic Diversity of Leafy Amaranth (Amaranthus tricolor L.) Resources in Vietnam. Breed. Sci. 2019;69:640–650. doi: 10.1270/jsbbs.19050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Shukla S., Bhargava A., Chatterjee A., Srivastava A., Singh S.P. Genotypic Variability in Vegetable Amaranth (Amaranthus tricolor L for Foliage Yield and Its Contributing Traits over Successive Cuttings and Years. Euphytica. 2006;151:103–110. doi: 10.1007/s10681-006-9134-3. [DOI] [Google Scholar]
  • 8.Jensen A. Chlorophylls and Carotenoids. In: Hellebust J.A., Craigie J.S., editors. Handbook of Physiological Methods and Biochemical Methods. Cambridge University Press; Cambridge, UK: 1978. pp. 5–70. [Google Scholar]
  • 9.Andini R., Yoshida S., Ohsawa R. Variation in Protein Content and Amino Acids in the Leaves of Grain, Vegetable and Weedy Types of Amaranths. Agronomy. 2013;3:391–403. doi: 10.3390/agronomy3020391. [DOI] [Google Scholar]
  • 10.Manólio Soares R.A., Mendonça S., Andrade de Castro L.I., Cardoso Corrêa Carlos Menezes A.C., Gomes Arêas J.A. Major Peptides from Amaranth (Amaranthus cruentus) Protein Inhibit HMG-CoA Reductase Activity. Int. J. Mol. Sci. 2015;16:4150–4160. doi: 10.3390/ijms16024150. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Písaríková B., Krácmar S., Herzig I. Amino acid Contents and Biological Value of Protein Amaranth. Czech J. Anim. Sci. 2005;50:169–174. doi: 10.17221/4011-CJAS. [DOI] [Google Scholar]
  • 12.López D.N., Galante M., Raimundo G., Spelzini D., Boeris V. Functional Properties of Amaranth, Quinoa and Chia Proteins and the Biological Activities of Their Hydrolyzates. Food Res. Int. 2019;116:419–429. doi: 10.1016/j.foodres.2018.08.056. [DOI] [PubMed] [Google Scholar]
  • 13.Alvarez-Jubete L., Arendt E.K., Gallagher E. Nutritive Value of Pseudocereals and Their Increasing Use as Functional Gluten-Free Ingredients. Trends Food Sci. Technol. 2010;21:106–113. doi: 10.1016/j.tifs.2009.10.014. [DOI] [Google Scholar]
  • 14.Achigan-Dako E.G., Sogbohossou O.E.D., Maundu P. Current Knowledge on Amaranthus spp.: Research Avenues for Improved Nutritional Value and Yield in Leafy Amaranths in Sub-Saharan Africa. Euphytica. 2014;197:303–317. doi: 10.1007/s10681-014-1081-9. [DOI] [Google Scholar]
  • 15.Akin-Idowu P.E., Odunola O.A., Gbadegesin M.A., Ademoyegun O.T., Aduloju A.O., Olagunju Y.O. Nutritional Evaluation of Five Species of Grain Amaranth—An Underutilized Crop. Int. J. Sci. 2017;3:18–27. doi: 10.18483/ijSci.1131. [DOI] [Google Scholar]
  • 16.Alegbejo J. Nutritional Value and Utilization of Amaranthus (Amaranthus spp.)—A Review. Bayero J. Pure Appl. Sci. 2014;6:136. doi: 10.4314/bajopas.v6i1.27. [DOI] [Google Scholar]
  • 17.Shukla S., Bhargava A., Chatterjee A., Pandey A.C., Mishra B.K. Diversity in Phenotypic and Nutritional Traits in Vegetable Amaranth (Amaranthus tricolor), A Nutritionally Underutilised Crop. J. Sci. Food Agric. 2010;90:139–144. doi: 10.1002/jsfa.3797. [DOI] [PubMed] [Google Scholar]
  • 18.Soriano-García M., Ilnamiqui Arias-Olguín I., Pablo Carrillo Montes J., Genaro Rosas Ramírez D., Silvestre Mendoza Figueroa J., Flores-Valverde E., Rita Valladares-Rodríguez M. Nutritional Functional Value and Therapeutic Utilization of Amaranth. J. Anal. Pharm. Res. 2018;7:596–600. doi: 10.15406/japlr.2018.07.00288. [DOI] [Google Scholar]
  • 19.Sarker U., Islam M.T., Rabbani M.G., Oba S. Genotypic Variability for Nutrient, Antioxidant, Yield and Yield Contributing Traits in Vegetable Amaranth. J. Food Agric. Environ. 2014;12:168–174. [Google Scholar]
  • 20.Sarker U., Islam M.T., Rabbani M.G., Oba S. Variability, heritability and genetic association in vegetable amaranth. Span. J. Agric. Res. 2015;13:0702. doi: 10.5424/sjar/2015132-6843. [DOI] [Google Scholar]
  • 21.Sarker U., Islam M.T., Rabbani M.G., Oba S. Variability in Composition of Vitamins and Mineral Antioxidants in Vegetable Amaranth. Genetika. 2015;47:85–96. doi: 10.2298/GENSR1501085S. [DOI] [Google Scholar]
  • 22.Sarker U., Islam M.T., Rabbani M.G., Oba S. Genetic Variation and Interrelationships among Antioxidant, Quality, and Agronomic Traits in Vegetable Amaranth. Turk. J. Agric. For. 2016;40:526–535. doi: 10.3906/tar-1405-83. [DOI] [Google Scholar]
  • 23.Sarker U., Islam M.T., Rabbani M.G., Oba S. Genotypic Diversity in Vegetable Amaranth for Antioxidant, Nutrient and Agronomic Traits. Indian J. Genet. Plant Breed. 2017;77:173–176. doi: 10.5958/0975-6906.2017.00025.6. [DOI] [Google Scholar]
  • 24.Shukla S., Bhargava A., Chatterjee A., Srivastava J., Singh N., Singh S.P. Mineral Profile and Variability in Vegetable Amaranth (Amaranthus tricolor) Plant Foods Hum. Nutr. 2006;61:23–28. doi: 10.1007/s11130-006-0004-x. [DOI] [PubMed] [Google Scholar]
  • 25.Chakrabarty T., Sarker U., Hasan M., Rahman M.M. Variability in Mineral Compositions, Yield and Yield Contributing Traits of Stem Amaranth (Amaranthus lividus) Genetika. 2018;50:995–1010. doi: 10.2298/GENSR1803995C. [DOI] [Google Scholar]
  • 26.Akubugwo I.E., Obasi N.A., Chinyere G.C., Ugbogu A.E. Nutritional and Chemical Value of Amaranthus hybridus L. Leaves from Afikpo, Nigeria. Afr. J. Biotechnol. 2007;6:2833–2839. doi: 10.5897/AJB2007.000-2452. [DOI] [Google Scholar]
  • 27.Ezenwa M.I., Ogbadoyi E.O. Effect of Heading on Some Micronutrients, Anti-Nutrients and Toxic Substances in Amaranthus cruentus Grown in Minna, Niger State, Nigeria. J. Food Nutr. Res. 2011;1:147–154. [Google Scholar]
  • 28.Lobo M., Samman N., Castanheira I. Characterisation of Nutrient Profile of Quinoa (Chenopodium quinoa), Amaranth (Amaranthus caudatus), and Purple Corn (Zea mays L.) Consumed in the North of Argentina: Proximates, Minerals and Trace Elements. Food Chem. 2014;148:420–426. doi: 10.1016/j.foodchem.2013.09.155. [DOI] [PubMed] [Google Scholar]
  • 29.Nyonje W.A., Schafleitner R., Abukutsa-Onyango M., Yang R.-Y., Makokha A., Owino W. Precision phenotyping and association between morphological traits and nutritional content in Vegetable Amaranth (Amaranthus spp.) J. Agric. Food Res. 2021;5:100165. doi: 10.1016/j.jafr.2021.100165. [DOI] [Google Scholar]
  • 30.Schafleitner R., Lin Y.P., Dinssa F., N’Danikou S., Finkers R., Minja R., Abukutsa-Onyango M., Nyonje W., Lin C.Y., Wu T.H., et al. The world vegetable center Amaranthus germplasm collection: Core collection development and evaluation of agronomic and nutritional traits. Crop Sci. 2022 doi: 10.1002/csc2.20715. [DOI] [Google Scholar]
  • 31.Srivastava R. Nutritional Quality of Some Cultivated and Wild Species of Amaranthus L. Int. J. Pharm. Sci. Res. 2011;2:3152. [Google Scholar]
  • 32.Venskutonis P.R., Kraujalis P. Nutritional Components of Amaranth Seeds and Vegetables: A Review on Composition, Properties, and Uses. Compr. Rev. Food Sci. Food Saf. 2013;12:381–412. doi: 10.1111/1541-4337.12021. [DOI] [PubMed] [Google Scholar]
  • 33.Wesche-Ebeling P., Maiti R., García-Díaz G., González D.I., Sosa-Alvarado F. Contributions to the Botany and Nutritional Value of Some Wild Amaranthus species (Amaranthaceae) of Nuevo Leon, Mexico. Econ. Bot. 1995;49:423–430. doi: 10.1007/BF02863094. [DOI] [Google Scholar]
  • 34.Mekonnen G., Woldesenbet M., Teshale T., Biru T. Amaranthus Caudatus Production and Nutrition Contents for Food Security and Healthy Living in Menit Shasha, Menit Goldya and Maji Districts of Bench Maji Zone, South Western Ethiopia. Nutr. Food Sci. Int. J. 2018;7:001–007. [Google Scholar]
  • 35.Mlakar S.G., Turinek M., Jakop M., Bavec M., Bavec F. Nutrition Value and Use of Grain Amaranth: Potential Future Application in Bread Making. Agriculturae. 2009;6:43–53. [Google Scholar]
  • 36.Jimoh M.O., Afolayan A.J., Lewu F.B. Suitability of Amaranthus species for Alleviating Human Dietary Deficiencies. S. Afr. J. Bot. 2018;115:65–73. doi: 10.1016/j.sajb.2018.01.004. [DOI] [Google Scholar]
  • 37.Jimoh M.O., Afolayan A.J., Lewu F.B. Nutrients and Antinutrient Constituents of Amaranthus caudatus L. Cultivated on Different Soils. Saudi J. Biol. Sci. 2020;27:3570–3580. doi: 10.1016/j.sjbs.2020.07.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Ahmed S.A., Hanif S., Iftkhar T. Phytochemical Profiling with Antioxidant and Antimicrobial Screening of Amaranthus viridis L. Leaf and Seed Extracts. Open J. Med. Microbiol. 2013;3:16–171. doi: 10.4236/ojmm.2013.33025. [DOI] [Google Scholar]
  • 39.Al-Mamun M.A., Husna J., Khatun M., Hasan R., Kamruzzaman M., Hoque K.M.F., Reza M.A., Ferdousi Z. Assessment of Antioxidant, Anticancer and Antimicrobial Activity of Two Vegetable Species of Amaranthus in Bangladesh. BMC Complement. Altern. Med. 2016;16:157. doi: 10.1186/s12906-016-1130-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Vardhana H. In Vitro Antibacterial Activity of Amaranthus spinosus Root Extracts. Pharmacophore. 2011;2:266–270. [Google Scholar]
  • 41.Guo L., Wang Y., Bi X., Duo K., Sun Q., Yun X., Zhang Y., Fei P., Han J. Antimicrobial Activity and Mechanism of Action of The Amaranthus tricolor Crude Extract Against Staphylococcus aureus and Potential Application in Cooked Meat. Foods. 2020;9:359. doi: 10.3390/foods9030359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Jimoh M.O., Afolayan A.J., Lewu F.B. Toxicity and Antimicrobial Activities of Amaranthus caudatus L. (Amaranthaceae) Harvested from Formulated Soils at Different Growth Stages. J. Evid. Based Complement. Altern. Med. 2020;25:1–11. doi: 10.1177/2515690X20971578. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Lipkin A., Anisimova V., Nikonorova A., Babakov A., Krause E., Bienert M., Grishin E., Egorov T. An Antimicrobial Peptide Ar-Amp from Amaranth (Amaranthus retroflexus L.) Seeds. Phytochemistry. 2005;66:2426–2431. doi: 10.1016/j.phytochem.2005.07.015. [DOI] [PubMed] [Google Scholar]
  • 44.Maiyo Z.C., Ngure R.N., Matasyoh J.C., Chepkorir R. Phytochemical Constituents and Antimicrobial Activity of Leaf Extract of Three Amaranthus Plant Species. Afr. J. Biotechnol. 2010;9:3178–3182. [Google Scholar]
  • 45.Moyer T.B., Heil L.R., Kirkpatrick C.L., Goldfarb D., Lefever W.A., Parsley N.C., Wommack A.J., Hicks L.M. PepSAVI-MS Reveals a Proline-Rich Antimicrobial Peptide in Amaranthus tricolor. J. Nat. Prod. 2019;82:2744–2753. doi: 10.1021/acs.jnatprod.9b00352. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Terzieva S., Velichkova K., Grozeva N., Valcheva N., Dinev T. Antimicrobial Activity of Amaranthus spp. Extracts Against Some Mycotoxigenic Fungi. Bulg. J. Agric. Sci. 2019;25:120–123. [Google Scholar]
  • 47.Jimoh M.O., Afolayan A.J., Lewu F.B. Micromorphological Assessment of Leaves of Amaranthus caudatus L. Cultivated on Formulated Soil Types. Appl. Ecol. Environ. Res. 2019;17:13593–13605. doi: 10.15666/aeer/1706_1359313605. [DOI] [Google Scholar]
  • 48.De Vita D., Messore A., Toniolo C., Frezza C., Scipione L., Bertea C.M., Micera M., Di Sarno V., Madia V.N., Pindinello I., et al. Towards A New Application of Amaranth Seed Oil as An Agent Against Candida albicans. Nat. Prod. Res. 2021;35:4621–4626. doi: 10.1080/14786419.2019.1696335. [DOI] [PubMed] [Google Scholar]
  • 49.Baral M., Chakraborty S., Chakraborty P. Evaluation of Anthelmintic and Anti-Inflammatory Activity of Amaranthus spinosus L. Int. J. Curr. Pharm. Res. 2010;2:2–5. [Google Scholar]
  • 50.Kumar B.S.A., Lakshman K., Jayaveera K.N., Velmurugan C., Manoj B., Sridhar S.M. Anthelmintic Activity of Methanol Extract of Amaranthus caudatus L. Internet J. Food Saf. 2010;12:127–129. [Google Scholar]
  • 51.Kumar A., Lakshman K., Jayaveera K.N., Nandeesh R., Manoj B., Ranganayakulu D. Comparative In Vitro Antihelminthic Activity of Three Plants from Amaranthaceae Family. Arch. Biol. Sci. 2010;62:185–189. doi: 10.2298/ABS1001185K. [DOI] [Google Scholar]
  • 52.Reyad-ul-Ferdous M., Shahjahan D.S., Tanvir S., Mukti M. Present Biological Status of Potential Medicinal Plant of Amaranthus viridis: A comprehensive review. Am. J. Clin. Exp. Med. 2015;3:12–17. doi: 10.11648/j.ajcem.s.2015030501.13. [DOI] [Google Scholar]
  • 53.Chang Y.J., Pong L.Y., Hassan S.S., Choo W.S. Antiviral Activity of Betacyanins from Red Pitahaya (Hylocereus polyrhizus) and Red Spinach (Amaranthus dubius) Against Dengue Virus Type 2 (GenBank accession no. MH488959) Access Microbiol. 2020;2:1–6. doi: 10.1099/acmi.0.000073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Amornrit W., Santiyanont R. Neuroprotective Effect of Amaranthus lividus and Amaranthus tricolor and Their Effects on Gene Expression of RAGE During Oxidative Stress in SH-SY5Y Cells. Genet. Mol. Res. 2016;15:gmr15027562. doi: 10.4238/gmr.15027562. [DOI] [PubMed] [Google Scholar]
  • 55.Lin B.F., Chiang B.L., Lin J.Y. Amaranthus spinosus Water Extract Directly Stimulates Proliferation of B Lymphocytes in vitro. Int. Immunopharmacol. 2005;5:711–722. doi: 10.1016/j.intimp.2004.12.001. [DOI] [PubMed] [Google Scholar]
  • 56.Olajide O., Ogunleye B., Erinle T. Anti-inflammatory Properties of Amaranthus spinosus Leaf Extract. Pharm. Biol. 2004;42:521–525. doi: 10.3109/13880200490893285. [DOI] [Google Scholar]
  • 57.Hussain Z., Amresh G., Singh S., Rao C.V. Antidiarrheal and Antiulcer Activity of Amaranthus spinosus in Experimental Animals. Pharm. Biol. 2009;47:932–939. doi: 10.1080/13880200902950769. [DOI] [Google Scholar]
  • 58.House N.C., Puthenparampil D., Malayil D., Narayanankutty A. Variation in The Polyphenol Composition, Antioxidant, and Anticancer Activity Among Different Amaranthus Species. S. Afr. J. Bot. 2020;135:408–412. doi: 10.1016/j.sajb.2020.09.026. [DOI] [Google Scholar]
  • 59.Jin Y., Xuan Y., Chen M., Chen J., Jin Y., Piao J., Tao J. Antioxidant, Anti-inflammatory and Anticancer Activities of Amaranthus viridis L. Extracts. Asian J. Chem. 2013;25:8901–8904. doi: 10.14233/ajchem.2013.14900. [DOI] [Google Scholar]
  • 60.Amornrit W., Santiyanont R. Effect of Amaranthus on Advanced Glycation End-Products Induced Cytotoxicity and Proinflammatory Cytokine Gene Expression in SH-SY5Y Cells. Molecules. 2015;20:17288–17308. doi: 10.3390/molecules200917288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Zeashan H., Amresh G., Singh S., Rao C.V. Hepatoprotective Activity of Amaranthus spinosus in Experimental Animals. Food Chem. Toxicol. 2008;46:3417–3421. doi: 10.1016/j.fct.2008.08.013. [DOI] [PubMed] [Google Scholar]
  • 62.Aneja S., Vats M., Aggarwal S., Sardana S. Phytochemistry and Hepatoprotective Activity of Aqueous Extract of Amaranthus tricolor L. Roots. J. Ayurveda Integr. Med. 2013;4:211–215. doi: 10.4103/0975-9476.123693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Zeashan H., Amresh G., Singh S., Rao C.V. Protective Effect of Amaranthus spinosus Against D-Galactosamine/Lipopolysaccharide-Induced Hepatic Failure. Pharm. Biol. 2010;48:1157–1163. doi: 10.3109/13880200903168023. [DOI] [PubMed] [Google Scholar]
  • 64.Zeashan H., Amresh G., Singh S., Rao C.V. Hepatoprotective and Antioxidant Activity of Amaranthus spinosus Against CCl4 Induced Toxicity. J. Ethnopharmacol. 2009;125:364–366. doi: 10.1016/j.jep.2009.05.010. [DOI] [PubMed] [Google Scholar]
  • 65.Balakrishnan S., Pandhare R. Antihyperglycemic and Antihyperlipidaemic Activities of Amaranthus spinosus L. Extract on Alloxan Induced Diabetic Rats. Malays. J. Pharm. Sci. 2010;8:13–22. [Google Scholar]
  • 66.Krishnamurthy G., Lakshman K., Pruthvi N., Chandrika P.U. Antihyperglicemic and Hypolipidemic Activity of Methanolic Extract of Amaranthus viridis Leaves in Experimental Diabetes. Indian J. Pharmacol. 2011;43:450–454. doi: 10.4103/0253-7613.83120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Girija K., Lakshman K., Udaya C., Sabhya Sachi G., Divya T. Antidiabetic and Anti–cholesterolemic Activity of Methanol Extracts of Three Species of Amaranthus. Asian Pac. J. Trop. Biomed. 2011;1:133–138. doi: 10.1016/S2221-1691(11)60011-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Allegra M., Tesoriere L., Livrea M.A. Betanin Inhibits the Myeloperoxidase/Nitrite-Induced Oxidation of Human Low-Density Lipoproteins. Free Radic. Res. 2007;41:335–341. doi: 10.1080/10715760601038783. [DOI] [PubMed] [Google Scholar]
  • 69.Clemente A., Desai P. Evaluation of the Hematological, Hypoglycemic, Hypolipidemic and Antioxidant Properties of Amaranthus tricolor Leaf Extract in Rat. Trop. J. Pharm. Res. 2011;10:595–602. doi: 10.4314/tjpr.v10i5.8. [DOI] [Google Scholar]
  • 70.Yang Y., Fukui R., Jia H., Kato H. Amaranth supplementation improves hepatic lipid dysmetabolism and modulates gut microbiota in mice fed a high-fat diet. Foods. 2021;10:1259. doi: 10.3390/foods10061259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Hilou A., Nacoulma O.G., Guiguemde T.R. In Vivo Antimalarial Activities of Extracts from Amaranthus spinosus L. and Boerhaavia erecta L. in Mice. J. Ethnopharmacol. 2006;103:236–240. doi: 10.1016/j.jep.2005.08.006. [DOI] [PubMed] [Google Scholar]
  • 72.Hsiao L.W., Tsay G.J., Mong M.C., Liu W.H., Yin M.C. Aqueous Extract Prepared from Steamed Red Amaranth (Amaranthus gangeticus L.) Leaves Protected Human Lens Cells Against High Glucose Induced Glycative and Oxidative Stress. J. Food Sci. 2021;86:3686–3697. doi: 10.1111/1750-3841.15822. [DOI] [PubMed] [Google Scholar]
  • 73.Prajitha V., Thoppil J.E. Cytotoxic and Apoptotic Activities of Extract of Amaranthus spinosus L. in Allium cepa and Human Erythrocytes. Cytotechnology. 2017;69:123–133. doi: 10.1007/s10616-016-0044-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Ashok Kumar B.S., Lakshman K., Velmurugan C., Sridhar S.M., Gopisetty S. Antidepressant Activity of Methanolic Extract of Amaranthus spinosus. Basic Clin. Neurosci. 2014;5:11–17. [PMC free article] [PubMed] [Google Scholar]
  • 75.Jimoh M.O., Afolayan A.J., Lewu F.B. Therapeutic uses of Amaranthus caudatus L. Trop. Biomed. 2019;36:1038–1053. [PubMed] [Google Scholar]
  • 76.Kusumaningtyas R., Kobayashi S., Takeda S. Mixed Species Gardens in Java and the Transmigration Areas of Sumatra, Indonesia: A Comparison. J. Trop. Agric. 2006;44:15–22. [Google Scholar]
  • 77.Sarker U., Islam M.T., Rabbani M.G., Oba S. Variability in Total Antioxidant Capacity, Antioxidant Leaf Pigments and Foliage Yield of Vegetable Amaranth. J. Integr. Agric. 2018;17:1145–1153. doi: 10.1016/S2095-3119(17)61778-7. [DOI] [Google Scholar]
  • 78.Sarker U., Islam M.T., Rabbani M.G., Oba S. Antioxidant Leaf Pigments and Variability in Vegetable Amaranth. Genetika. 2018;50:209–220. doi: 10.2298/GENSR1801209S. [DOI] [Google Scholar]
  • 79.Cai Y., Sun M., Wu H., Huang R., Corke H. Characterization and Quantification of Betacyanin Pigments from Diverse Amaranthus Species. J. Agric. Food Chem. 1998;46:2063–2070. doi: 10.1021/jf9709966. [DOI] [Google Scholar]
  • 80.Miguel M.G. Betalains in Some Species of The Amaranthaceae Family: A Review. Antioxidants. 2018;7:53. doi: 10.3390/antiox7040053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Cai Y., Corke H. Amaranthus Betacyanin Pigments Applied in Model Food Systems. J. Food Sci. 1999;64:869–873. doi: 10.1111/j.1365-2621.1999.tb15930.x. [DOI] [Google Scholar]
  • 82.Cai Y., Sun M., Corke H. Identification and Distribution of Simple and Acylated Betacyanins in the Amaranthaceae. J. Agric. Food Chem. 2001;49:1971–1978. doi: 10.1021/jf000963h. [DOI] [PubMed] [Google Scholar]
  • 83.Cai Y., Sun M., Corke H. HPLC Characterization of Betalains from Plants in the Amaranthaceae. J. Chromatogr. Sci. 2005;43:454–460. doi: 10.1093/chromsci/43.9.454. [DOI] [PubMed] [Google Scholar]
  • 84.Cai Y., Sun M., Corke H. Characterization and Application of Betalain Pigments from Plants of the Amaranthaceae. Trends Food Sci. Technol. 2005;16:370–376. doi: 10.1016/j.tifs.2005.03.020. [DOI] [Google Scholar]
  • 85.Belhadj Slimen I., Najar T., Abderrabba M. Chemical and Antioxidant Properties of Betalains. J. Agric. Food Chem. 2017;65:675–689. doi: 10.1021/acs.jafc.6b04208. [DOI] [PubMed] [Google Scholar]
  • 86.Esatbeyoglu T., Wagner A.E., Motafakkerazad R., Nakajima Y., Matsugo S., Rimbach G. Free Radical Scavenging and Antioxidant Activity of Betanin: Electron Spin Resonance Spectroscopy Studies and Studies in Cultured Cells. Food Chem. Toxicol. 2014;73:119–126. doi: 10.1016/j.fct.2014.08.007. [DOI] [PubMed] [Google Scholar]
  • 87.Gandía-Herrero F., Escribano J., García-Carmona F. The Role of Phenolic Hydroxy Groups in the Free Radical Scavenging Activity of Betalains. J. Nat. Prod. 2009;72:1142–1146. doi: 10.1021/np900131r. [DOI] [PubMed] [Google Scholar]
  • 88.Gandía-Herrero F., Escribano J., García-Carmona F. Structural Implications on Color, Fluorescence, and Antiradical Activity in Betalains. Planta. 2010;232:449–460. doi: 10.1007/s00425-010-1191-0. [DOI] [PubMed] [Google Scholar]
  • 89.Gandía-Herrero F., Escribano J., García-Carmona F. Purification and Antiradical Properties of the Structural Unit of Betalains. J. Nat. Prod. 2012;75:1030–1036. doi: 10.1021/np200950n. [DOI] [PubMed] [Google Scholar]
  • 90.Gandía-Herrero F., Escribano J., García-Carmona F. Biological Activities of Plant Pigments Betalains. Crit. Rev. Food Sci. Nutr. 2016;56:937–945. doi: 10.1080/10408398.2012.740103. [DOI] [PubMed] [Google Scholar]
  • 91.Khan M.I. Plant Betalains: Safety, Antioxidant Activity, Clinical Efficacy, and Bioavailability. Compr. Rev. Food Sci. Food Saf. 2016;15:316–330. doi: 10.1111/1541-4337.12185. [DOI] [PubMed] [Google Scholar]
  • 92.Khan M.I., Giridhar P. Plant Betalains: Chemistry and Biochemistry. Phytochemistry. 2015;117:267–295. doi: 10.1016/j.phytochem.2015.06.008. [DOI] [PubMed] [Google Scholar]
  • 93.Stintzing F.C., Carle R. Functional Properties of Anthocyanins and Betalains in Plants, Food, and in Human Nutrition. Trends Food Sci. Technol. 2004;15:19–38. doi: 10.1016/j.tifs.2003.07.004. [DOI] [Google Scholar]
  • 94.Taira J., Tsuchida E., Katoh M.C., Uehara M., Ogi T. Antioxidant Capacity of Betacyanins as Radical Scavengers for Peroxyl Radical and Nitric Oxide. Food Chem. 2015;166:531–536. doi: 10.1016/j.foodchem.2014.05.102. [DOI] [PubMed] [Google Scholar]
  • 95.Sarker U., Lin Y.P., Oba S., Yoshioka Y., Ken H. Prospects and potentials of underutilized leafy Amaranths as vegetable use for health-promotion. Plant Physiol. Biochem. 2022;182:104–123. doi: 10.1016/j.plaphy.2022.04.011. [DOI] [PubMed] [Google Scholar]
  • 96.Pasko P., Bartoń H., Zagrodzki P., Gorinstein S., Fołta M., Zachwieja Z. Anthocyanins, Total Polyphenols and Antioxidant Activity in Amaranth and Quinoa Seeds and Sprouts During Their Growth. Food Chem. 2009;115:994–998. doi: 10.1016/j.foodchem.2009.01.037. [DOI] [Google Scholar]
  • 97.Li H., Deng Z., Liu R., Zhu H., Draves J., Marcone M., Sun Y., Tsao R. Characterization of Phenolics, Betacyanins and Antioxidant Activities of The Seed, Leaf, Sprout, Flower and Stalk Extracts of Three Amaranthus species. J. Food Compos. Anal. 2015;37:75–81. doi: 10.1016/j.jfca.2014.09.003. [DOI] [Google Scholar]
  • 98.Barba de la Rosa A.P., Fomsgaard I.S., Laursen B., Mortensen A.G., Olvera-Martínez L., Silva-Sánchez C., Mendoza-Herrera A., González-Castañeda J., de León-Rodrígueza A. Amaranth (Amaranthus hypochondriacus) as An Alternative Crop for Sustainable Food Production: Phenolic Acids and Flavonoids with Potential Impact on Its Nutraceutical Quality. J. Cereal Sci. 2009;49:117–121. doi: 10.1016/j.jcs.2008.07.012. [DOI] [Google Scholar]
  • 99.Peiretti P.G., Meineri G., Gai F., Longato E., Amarowicz R. Antioxidative Activity and Phenolic Compounds of Pumpkin (Cucurbita Pepo) Seeds and Amaranth (Amaranthus caudatus) Grain Extracts. Nat. Prod. Res. 2017;31:2178–2182. doi: 10.1080/14786419.2017.1278597. [DOI] [PubMed] [Google Scholar]
  • 100.Stintzing F.C., Kammerer D., Schieber A., Adama H., Nacoulma O.G., Carle R. Betacyanins and Phenolic Compounds from Amaranthus spinosus L. and Boerhavia erecta L. Z. Naturforsch. C. 2004;59:1–8. doi: 10.1515/znc-2004-1-201. [DOI] [PubMed] [Google Scholar]
  • 101.Kalinova J., Dadakova E. Rutin and Total Quercetin Content in Amaranth (Amaranthus spp.) Plant Foods Hum. Nutr. 2009;64:68–74. doi: 10.1007/s11130-008-0104-x. [DOI] [PubMed] [Google Scholar]
  • 102.Asao M., Watanabe K. Functional and Bioactive Properties of Quinoa and Amaranth. Food Sci. Technol. Res. 2010;16:163–168. doi: 10.3136/fstr.16.163. [DOI] [Google Scholar]
  • 103.Sarker U., Islam M.T., Rabbani M.G., Oba S. Phenotypic Divergence in Vegetable Amaranth for Total Antioxidant Capacity, Antioxidant Profile, Dietary Fiber, Nutritional and Agronomic Traits. Acta Agric. Scand. Sect. B-Soil Plant Sci. 2018;68:67–76. doi: 10.1080/09064710.2017.1367029. [DOI] [Google Scholar]
  • 104.Tang Y., Xiao Y., Tang Z., Jin W., Wang Y., Chen H., Yao H., Shan Z., Bu T., Wang X. Extraction of Polysaccharides from Amaranthus hybridus L. by Hot Water and Analysis of Their Antioxidant Activity. Peer J. 2019;7:e7149. doi: 10.7717/peerj.7149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Ozsoy N., Yilmaz T., Kurt O., Can A., Yanardag R. In Vitro Antioxidant Activity of Amaranthus lividus L. Food Chem. 2009;116:867–872. doi: 10.1016/j.foodchem.2009.03.036. [DOI] [Google Scholar]
  • 106.Okunlola G.O., Jimoh M.A., Olatunji O.A., Olowolaju E.D. Comparative Study of The Phytochemical Contents of Cochorus olitorius and Amaranthus hybridus at Different Stages of Growth Comparative Study of The Phytochemical Contents. Ann. West Univ. Timis. Ser. Biol. 2017;20:43–48. [Google Scholar]
  • 107.Sarikurkcu C., Sahinler S.S., Tepe B. Astragalus gymnolobus, A. leporinus var. hirsutus, and A. onobrychis: Phytochemical Analysis and Biological Activity. Ind. Crops Prod. 2020;150:112366. doi: 10.1016/j.indcrop.2020.112366. [DOI] [Google Scholar]
  • 108.Tatiya A.U., Surana S.J., Khope S.D., Gokhale S.B., Sutar M.P. Phytochemical Investigation and Immunomodulatory Activity of Amaranthus spinosus L. Indian J. Pharm. Educ. Res. 2007;444:337–341. [Google Scholar]
  • 109.Pamela E.A.I., Olufemi T.A., Yemisi O.O., Aduloju O.A., Usifo G.A. Phytochemical Content and Antioxidant Activity of Five Grain Amaranth Species. Am. J. Food Sci. Technol. 2017;5:249–255. [Google Scholar]
  • 110.Pasko P., Barton H., Fołta M., Gwizdz J. Evaluation of Antioxidant Activity of Amaranth Amaranthus cruentus Grain and by-Products Flour, Popping, Cereal. Rocz. Państwowego Zakładu Hig. 2007;581:35–40. [PubMed] [Google Scholar]
  • 111.Nsimba R.Y., Kikuzaki H., Konishi Y. Antioxidant Activity of Various Extracts and Fractions of Chenopodium quinoa and Amaranthus spp. Seeds. Food Chem. 2008;106:760–766. doi: 10.1016/j.foodchem.2007.06.004. [DOI] [Google Scholar]
  • 112.Tang Y., Tsao R. Phytochemicals in Quinoa and Amaranth Grains and Their Antioxidant, Anti-Inflammatory, and Potential Health Beneficial Effects: A Review. Mol. Nutr. Food Res. 2017;61:1600767. doi: 10.1002/mnfr.201600767. [DOI] [PubMed] [Google Scholar]
  • 113.Barku V.Y.A., Opoku-Boahen Y., Owusu-Ansah E., Mensah E.F., Barku V.Y.A., Opoku-Boahen Y., Owusu-Ansah E., Mensah E.F. Antioxidant Activity and The Estimation of Total Phenolic and Flavonoid Contents of The Root Extract of Amaranthus spinosus. Asian J. Plant Sci. Res. 2013;3:69–74. [Google Scholar]
  • 114.Bulbul I.J., Nahar L., Ripa F.A., Haque O. Antibacterial, Cytotoxic and Antioxidant Activity of Chloroform, N-Hexane and Ethyl Acetate Extract of Plant Amaranthus spinosus. Int. J. PharmTech Res. 2011;33:1675–1680. [Google Scholar]
  • 115.Kumar B.S.A., Lakshman K., Jayaveera K.N., Shekar D.S., Kumar A.A., Manoj B. Antioxidant and Antipyretic Properties of Methanolic Extract of Amaranthus spinosus Leaves. Asian Pac. J. Trop. Med. 2010;3:702–706. doi: 10.1016/S1995-7645(10)60169-1. [DOI] [Google Scholar]
  • 116.Ishtiaq S., Ahmad M., Hanif U., Akbar S., Kamran S.H. Phytochemical and in-vitro Antioxidant Evaluation of Different Fractions of Amaranthus graecizan subsp. Silvestris Vill. Brenan. Asian Pac. J. Trop. Biomed. 2014;412:965–971. doi: 10.1016/S1995-7645(14)60256-X. [DOI] [PubMed] [Google Scholar]
  • 117.Jimoh M.O., Afolayan A.J., Lewu F.B. Antioxidant and Phytochemical Activities of Amaranthus caudatus L. Harvested from Different Soils at Various Growth Stages. Sci. Rep. 2019;9:12965. doi: 10.1038/s41598-019-49276-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118.Karamac M., Gai F., Longato E., Meineri G., Janiak M.A., Amarowicz R., Peiretti P.G. Antioxidant Activity and Phenolic Composition of Amaranth (Amaranthus caudatus) During Plant Growth. Antioxidants. 2019;8:173. doi: 10.3390/antiox8060173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119.Kraujalis P., Venskutonis P.R., Kraujalienė V., Pukalskas A. Antioxidant properties and preliminary evaluation of phytochemical composition of different anatomical parts of amaranth. Plant Foods Hum. Nutr. 2013;68:322–328. doi: 10.1007/s11130-013-0375-8. [DOI] [PubMed] [Google Scholar]
  • 120.Kumari S., Elancheran R., Devi R. Phytochemical Screening, Antioxidant, Antityrosinase, And Antigenotoxic Potential of Amaranthus viridis Extract. Indian J. Pharmacol. 2018;50:130–138. doi: 10.4103/ijp.IJP_77_18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 121.Lopez-Mejía O.A., Lopez-Malo A., Palou E. Antioxidant Capacity of Extracts from Amaranth Amaranthus hypochondriacus L. Seeds or Leaves. Ind. Crop. Prod. 2014;53:55–59. doi: 10.1016/j.indcrop.2013.12.017. [DOI] [PubMed] [Google Scholar]
  • 122.Lucero-Lopez V.R., Razzeto G.S., Gimenez M.S., Escudero N.L. Antioxidant Properties of Amaranthus hypochondriacus Seeds and Their Effect on The Liver of Alcohol-Treated Rats. Plant Foods Hum. Nutr. 2011;66:157–162. doi: 10.1007/s11130-011-0218-4. [DOI] [PubMed] [Google Scholar]
  • 123.Salvamani S., Gunasekaran B., Shukor M.Y., Shaharuddin N.A., Sabullah M.K., Ahmad S.A. Anti-HMG-CoA Reductase, Antioxidant, and Anti-Inflammatory Activities of Amaranthus viridis Leaf Extract as A Potential Treatment for Hypercholesterolemia. Evid. Based Complement. Altern. Med. 2016;2016:8090841. doi: 10.1155/2016/8090841. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Sandoval-Sicairos E.S., Milán-Noris A.K., Luna-Vital D.A., Milán-Carrillo J., Montoya-Rodríguez A. Anti-Inflammatory and Antioxidant Effects of Peptides Released from Germinated Amaranth During In Vitro Simulated Gastrointestinal Digestion. Food Chem. 2021;1:128394. doi: 10.1016/j.foodchem.2020.128394. [DOI] [PubMed] [Google Scholar]
  • 125.Medoua G.N., Oldewage-Theron W.H. Effect of Drying and Cooking on Nutritional Value and Antioxidant Capacity of Morogo (Amaranthus hybridus) A Traditional Leafy Vegetable Grown in South Africa. J. Food Sci. Technol. 2014;51:736–742. doi: 10.1007/s13197-011-0560-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Tesoriere L., Allegra M., Gentile C., Livrea M.A. Betacyanins as Phenol Antioxidants. Chemistry and Mechanistic Aspects of the Lipoperoxyl Radical-Scavenging Activity in Solution and Liposomes. Free Radic. Res. 2009;43:706–717. doi: 10.1080/10715760903037681. [DOI] [PubMed] [Google Scholar]
  • 127.Repo-Carrasco-Valencia R., Peña J., Kallio H., Salminen S. Dietary Fiber and Other Functional Components in Two Varieties of Crude and Extruded Kiwicha (Amaranthus caudatus) J. Cereal Sci. 2009;49:219–224. doi: 10.1016/j.jcs.2008.10.003. [DOI] [Google Scholar]
  • 128.Jo H.J., Chung K.H., Yoon J.A., Lee K.J., Song B.C., An J.H. Radical Scavenging Activities of Tannin Extracted from Amaranth (Amaranthus caudatus L.) J. Microbiol. Biotechnol. 2015;25:795–802. doi: 10.4014/jmb.1409.09088. [DOI] [PubMed] [Google Scholar]
  • 129.Subhasree B., Baskar R., Laxmi Keerthana R., Lijina Susan R., Rajasekaran P. Evaluation of Antioxidant Potential in Selected Green Leafy Vegetables. Food Chem. 2009;115:1213–1220. doi: 10.1016/j.foodchem.2009.01.029. [DOI] [Google Scholar]
  • 130.Lacatusu I., Arsenie K.L.V., Badea G., Popa O., Oprea O., Badea N. New Cosmetic Formulations with Broad Photoprotective and Antioxidative Activities Designed by Amaranth and Pumpkin Seed Oils Nanocarriers. Ind. Crops Prod. 2018;123:424–433. doi: 10.1016/j.indcrop.2018.06.083. [DOI] [Google Scholar]
  • 131.Steffensen S.K., Pedersen H.A., Labouriau R., Mortensen A.G., Laursen B., de Troiani R.M., Noellemeyer E.J., Janovska D., Stavelikova H., Taberner A., et al. Variation of Polyphenols and Betaines in Aerial Parts of Young, Field-Grown Amaranthus genotypes. J. Agric. Food Chem. 2011;59:12073–12082. doi: 10.1021/jf202969e. [DOI] [PubMed] [Google Scholar]
  • 132.Niveyro S.L., Mortensen A.G., Fomsgaard I.S., Salvo A. Differences Among Five Amaranth Varieties (Amaranthus spp.) Regarding Secondary Metabolites and Foliar Herbivory by Chewing Insects in The Field. Arthropod-Plant Interact. 2013;7:235–245. doi: 10.1007/s11829-012-9219-y. [DOI] [Google Scholar]
  • 133.Amin I., Norazaidah Y., Hainida K.I.E. Antioxidant Activity and Phenolic Content of Raw and Blanched Amaranthus species. Food Chem. 2006;94:47–52. doi: 10.1016/j.foodchem.2004.10.048. [DOI] [Google Scholar]
  • 134.Bao X., Han X., Du G., Wei C., Zhu X., Ren W., Zeng L., Zhang Y. Antioxidant Activities and Immunomodulatory Effects in Mice of Betalain In Vivo. Food Sci. 2019;40:196–201. [Google Scholar]
  • 135.Conforti F., Statti G., Loizzo M.R., Sacchetti G., Poli F., Menichini F. In Vitro Antioxidant Effect and Inhibition of Alpha-Amylase of Two Varieties of Amaranthus caudatus Seeds. Biol. Pharm. Bull. 2005;28:1098–1102. doi: 10.1248/bpb.28.1098. [DOI] [PubMed] [Google Scholar]
  • 136.Al-Madhagy S.A., Mostafa N.M., Youssef F.S., Awad G.E.A., Eldahshan O.A., Singab A.N.B. Metabolic Profiling of a Polyphenolic-Rich Fraction of Coccinia grandis Leaves Using LC-ESI-MS/MS and In Vivo Validation of Its Antimicrobial and Wound Healing Activities. Food Funct. 2019;10:6267–6275. doi: 10.1039/C9FO01532A. [DOI] [PubMed] [Google Scholar]
  • 137.Todirascu-Ciornea E., El-Nashar H.A., Mostafa N.M., Eldahshan O.A., Boiangiu R.S., Dumitru G., Hritcu L., Singab A.N.B. Schinus terebinthifolius Essential Oil Attenuates Scopolamine-Induced Memory Deficits Via Cholinergic Modulation and Antioxidant Properties in A Zebrafish Model. Evid.-Based Complement. Altern. Med. 2019;2019:1–11. doi: 10.1155/2019/5256781. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 138.Mostafa N.M., Edmond M.P., El-Shazly M., Fahmy H.A., Sherif N.H., Singab A.N.B. Phytoconstituents and Renoprotective Effect of Polyalthia longifolia Leaves Extract on Radiation-Induced Nephritis in Rats via TGF-β/Smad Pathway. Nat. Prod. Res. 2021 doi: 10.1080/14786419.2021.1961252. [DOI] [PubMed] [Google Scholar]
  • 139.Mostafa N.M., Abd El-Ghffar E.A., Hegazy H.G., Eldahshan O.A. New Methoxyflavone from Casimiroa sapota and the Biological Activities of Its Leaves Extract Against Lead Acetate Induced Hepatotoxicity in Rats. Chem. Biodivers. 2018;15:e1700528. doi: 10.1002/cbdv.201700528. [DOI] [PubMed] [Google Scholar]
  • 140.Repo-Carrasco-Valencia R., Hellstrom J.K., Philava J.M., Mattila P.H. Flavonoids and Other Phenolic Compounds in Andean Indigenous Grains: Quinoa (Chenopodium quinoa), Kaniwa (Chenopodium pallidicaule) and Kiwicha (Amaranthus caudatus) Food Chem. 2010;120:128–133. doi: 10.1016/j.foodchem.2009.09.087. [DOI] [Google Scholar]
  • 141.Cai Y., Sun M., Corke H. Antioxidant Activity of Betalains from Plants of The Amaranthaceae. J. Agric. Food Chem. 2003;51:2288–2294. doi: 10.1021/jf030045u. [DOI] [PubMed] [Google Scholar]
  • 142.Sarker U., Oba S. Response of Nutrients, Minerals, Antioxidant Leaf Pigments, Vitamins, Polyphenol, Flavonoid and Antioxidant Activity in Selected Vegetable Amaranth under Four Soil Water Content. Food Chem. 2018;252:72–83. doi: 10.1016/j.foodchem.2018.01.097. [DOI] [PubMed] [Google Scholar]
  • 143.Sarker U., Oba S. Drought Stress Enhances Nutritional and Bioactive Compounds, Phenolic Acids and Antioxidant Capacity of Amaranthus Leafy Vegetable. BMC Plant Biol. 2018;18:258. doi: 10.1186/s12870-018-1484-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144.Sarker U., Oba S. Drought Stress Effects on Growth, ROS Markers, Compatible Solutes, Phenolics, Flavonoids, and Antioxidant Activity in Amaranthus tricolor. Appl. Biochem. Biotechnol. 2018;186:999–1016. doi: 10.1007/s12010-018-2784-5. [DOI] [PubMed] [Google Scholar]
  • 145.Sarker U., Oba S. Catalase, Superoxide Dismutase and Ascorbate-Glutathione Cycle Enzymes Confer Drought Tolerance of Amaranthus tricolor. Sci. Rep. 2018;8:16496. doi: 10.1038/s41598-018-34944-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146.Jamalluddin N., Massawe F.J., Mayes S., Ho W.K., Singh A., Symonds R.C. Physiological Screening for Drought Tolerance Traits in Vegetable Amaranth (Amaranthus tricolor) Germplasm. Agriculture. 2021;11:994. doi: 10.3390/agriculture11100994. [DOI] [Google Scholar]
  • 147.Liu F., Stützel H. Biomass Partitioning, Specific Leaf Area, and Water Use Efficiency of Vegetable Amaranth (Amaranthus spp.) in Response to Drought Stress. Sci. Hortic. 2004;102:15–27. doi: 10.1016/j.scienta.2003.11.014. [DOI] [Google Scholar]
  • 148.Bello Z.A., Walker S. Evaluating AquaCrop Model for Simulating Production of Amaranthus (Amaranthus cruentus) a Leafy Vegetable, Under Irrigation and Rainfed Conditions. Agric. For. Meteorol. 2017;247:300–310. doi: 10.1016/j.agrformet.2017.08.003. [DOI] [Google Scholar]
  • 149.Sedibe M.M., Combrink N.J.J., Reinten E.Y. Leaf Yield of Amaranthus hypochondriatus L. (Imbuya), Affected by Irrigation Systems and Water Quality. S. Afr. J. Plant Soil. 2013;22:171–174. doi: 10.1080/02571862.2005.10634702. [DOI] [Google Scholar]
  • 150.Sosnoskie L.M., Kichler J.M., Wallace R.D., Culpepper A.S. Multiple Resistance in Palmer Amaranth to Glyphosate and Pyrithiobac Confirmed in Georgia. Weed Sci. 2011;59:321–325. doi: 10.1614/WS-D-10-00132.1. [DOI] [Google Scholar]
  • 151.Sarker U., Oba S. Salinity Stress Enhances Color Parameters, Bioactive Leaf Pigments, Vitamins, Polyphenols, Flavonoids and Antioxidant Activity in Selected Amaranthus Leafy Vegetables. J. Sci. Food Agric. 2019;99:2275–2284. doi: 10.1002/jsfa.9423. [DOI] [PubMed] [Google Scholar]
  • 152.Sarker U., Oba S. Augmentation of Leaf Color Parameters, Pigments, Vitamins, Phenolic Acids, Flavonoids and Antioxidant Activity in Selected Amaranthus tricolor under Salinity Stress. Sci. Rep. 2018;8:12349. doi: 10.1038/s41598-018-30897-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 153.Sarker U., Islam M.T., Oba S. Salinity Stress Accelerates Nutrients, Dietary Fiber, Minerals, Phytochemicals and Antioxidant Activity in Amaranthus tricolor Leaves. PLoS ONE. 2018;13:0206388. doi: 10.1371/journal.pone.0206388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 154.Omamt E.N., Hammes P.S., Robbertse P.J. Differences in Salinity Tolerance for Growth and Water-Use Efficiency in Some Amaranth (Amaranthus spp.) Genotypes. N. Z. J. Crop Hortic. Sci. 2006;34:11–22. doi: 10.1080/01140671.2006.9514382. [DOI] [Google Scholar]
  • 155.Rajan S., Markose B.L. Horticultural Science Series-6. In: Peter K.M.V., editor. Propagation of Horticultural Crops. Volume 6. New India Publishing Agency; New Delhi, India: 2007. pp. 110–113. [Google Scholar]
  • 156.Ashmawy A.M., Mostafa N.M., Eldahshan O.A. GC/MS Analysis and Molecular Profiling of Lemon Volatile Oil against Breast Cancer. J. Essent. Oil Bear. Plants. 2019;22:903–916. doi: 10.1080/0972060X.2019.1667877. [DOI] [Google Scholar]
  • 157.El-Nashar H.A.S., Mostafa N.M., El-Badry M.A., Eldahshan O.A., Singab A.N.B. Chemical Composition, Antimicrobial and Cytotoxic Activities of Essential Oils from Schinus polygamus (Cav.) Cabrera Leaf and Bark Grown in Egypt. Nat. Prod. Res. 2021;35:5369–5372. doi: 10.1080/14786419.2020.1765343. [DOI] [PubMed] [Google Scholar]
  • 158.El-Nashar H.A.S., Mostafa N.M., Eldahshan O.A., Singab A.N.B. A New Antidiabetic and Anti-Inflammatory Biflavonoid from Schinus polygama (Cav.) Cabrera Leaves. Nat. Prod. Res. 2020:1–9. doi: 10.1080/14786419.2020.1864365. [DOI] [PubMed] [Google Scholar]
  • 159.Abdelghffar E.A., El-Nashar H.A.S., AL-Mohammadi A.G.A., Eldahshan O.A. Orange fruit (Citrus sinensis) Peel Extract Attenuates Chemotherapy-Induced Toxicity in Male Rats. Food Funct. 2021;12:9443–9455. doi: 10.1039/D1FO01905H. [DOI] [PubMed] [Google Scholar]
  • 160.Dusgupta N., De B. Antioxidant Activity of Some Leafy Vegetables of India: A Comparative Study. Food Chem. 2007;101:471–474. doi: 10.1016/j.foodchem.2006.02.003. [DOI] [Google Scholar]
  • 161.Isabelle M., Lee B.L., Lim M.T., Koh W.P., Huang D., Ong C.N. Antioxidant Activity and Profiles of Common Fruits in Singapore. Food Chem. 2010;123:77–84. doi: 10.1016/j.foodchem.2010.04.002. [DOI] [Google Scholar]
  • 162.Steffensen S.K., Rinnan A., Mortensen A.G., Laursen B., Troiani R.M., Noellemeyer E.J., Janovska D., Dusek K., Délano-Frier J., Taberner A., et al. Variations in the Polyphenol Content of Seeds of Field Grown Amaranthus Accessions. Food Chem. 2011;129:131–138. doi: 10.1016/j.foodchem.2011.04.044. [DOI] [Google Scholar]
  • 163.Rice-Evans C.A., Miller N.J., Papanga G. Antioxidant Properties of Phenolic Compounds. Trends Plant Sci. 1997;2:152–159. doi: 10.1016/S1360-1385(97)01018-2. [DOI] [Google Scholar]
  • 164.Sarker U., Oba S. Nutritional and Bioactive Constituents and Scavenging Capacity of Radicals in Amaranthus hypochondriacus. Sci. Rep. 2020;10:19962. doi: 10.1038/s41598-020-71714-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 165.Sarker U., Hossain M.N., Iqbal M.A., Oba S. Bioactive Components and Radical Scavenging Activity in Selected Advance Lines of Salt-Tolerant Vegetable Amaranth. Front. Nutr. 2020;7:587257. doi: 10.3389/fnut.2020.587257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 166.Sarker U., Oba S. Nutraceuticals, Phytochemicals, and Radical Quenching Ability of Selected Drought-Tolerant Advance Lines of Vegetable Amaranth. BMC Plant Biol. 2020;20:564. doi: 10.1186/s12870-020-02780-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167.Sarker U., Oba S. Antioxidant Constituents of Three Selected Red and Green Color Amaranthus Leafy Vegetable. Sci. Rep. 2019;9:18233. doi: 10.1038/s41598-019-52033-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 168.Sarker U., Oba S. Leaf Pigmentation, Its Profiles and Radical Scavenging Activity in Selected Amaranthus tricolor Leafy Vegetables. Sci. Rep. 2020;10:18617. doi: 10.1038/s41598-020-66376-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 169.Sarker U., Oba S. Color Attributes, Betacyanin, and Carotenoid Profiles, Bioactive Components, and Radical Quenching Capacity in Selected Amaranthus gangeticus Leafy Vegetables. Sci. Rep. 2021;11:11559. doi: 10.1038/s41598-021-91157-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 170.Sarker U., Oba S. The Response of Salinity Stress-Induced A. tricolor to Growth, Anatomy, Physiology, Non-Enzymatic and Enzymatic Antioxidants. Front. Plant Sci. 2020;11:559876. doi: 10.3389/fpls.2020.559876. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 171.Sarker U., Oba S. Phenolic Profiles and Antioxidant Activities in Selected Drought-Tolerant Leafy Vegetable Amaranth. Sci. Rep. 2020;10:18287. doi: 10.1038/s41598-020-71727-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 172.Sarker U., Oba S. Polyphenol and Flavonoid Profiles and Radical Scavenging Activity in Selected Leafy Vegetable Amaranthus gangeticus. BMC Plant Biol. 2020;20:499. doi: 10.1186/s12870-020-02700-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 173.Rashad M.M.I., Sarker U. Genetic Variations in Yield and Yield Contributing Traits of Green Amaranth. Genetika. 2020;52:393–407. doi: 10.2298/GENSR2001393R. [DOI] [Google Scholar]
  • 174.Hasan-Ud-Daula M., Sarker U. Variability, Heritability, Character Association, and Path Coefficient Analysis in Advanced Breeding Lines of Rice (Oryza Sativa L.) Genetika. 2020;52:711–726. doi: 10.2298/GENSR2002711H. [DOI] [Google Scholar]
  • 175.Hasan M.J., Kulsum M.U., Majumder R.R., Sarker U. Genotypic Variability for Grain Quality Attributes in Restorer Lines of Hybrid Rice. Genetika. 2020;52:973–989. doi: 10.2298/GENSR2003973H. [DOI] [Google Scholar]
  • 176.Azad A.K., Sarker U., Ercisli S., Assouguem A., Ullah R., Almeer R., Sayed A.A., Peluso I. Evaluation of Combining Ability and Heterosis of Popular Restorer and Male Sterile Lines for the Development of Superior Rice Hybrids. Agronomy. 2022;12:965. doi: 10.3390/agronomy12040965. [DOI] [Google Scholar]
  • 177.Sun H., Mu T., Xi L., Zhang M., Chen J. Sweet Potato (Ipomoea batatas L.) Leaves as Nutritional and Functional Foods. Food Chem. 2014;156:380–389. doi: 10.1016/j.foodchem.2014.01.079. [DOI] [PubMed] [Google Scholar]
  • 178.Sarker U., Oba S. Protein, Dietary Fiber, Minerals, Antioxidant Pigments and Phytochemicals, and Antioxidant Activity in Selected Red Morph Amaranthus Leafy Vegetable. PLoS ONE. 2019;14:0222517. doi: 10.1371/journal.pone.0222517. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 179.Sarker U., Oba S. Nutraceuticals, Antioxidant Pigments, and Phytochemicals in the Leaves of Amaranthus spinosus and Amaranthus viridis Weedy Species. Sci. Rep. 2019;9:20413. doi: 10.1038/s41598-019-50977-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 180.Sarker U., Hossain M.M., Oba S. Nutritional and Antioxidant Components and Antioxidant Capacity in Green Morph Amaranthus Leafy Vegetable. Sci. Rep. 2020;10:1336. doi: 10.1038/s41598-020-57687-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 181.Sarker U., Oba S., Daramy M.A. Nutrients, Minerals, Antioxidant Pigments and Phytochemicals, and Antioxidant Capacity of the Leaves of Stem Amaranth. Sci. Rep. 2020;10:3892. doi: 10.1038/s41598-020-60252-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 182.Sarker U., Oba S. Nutrients, Minerals, Pigments, Phytochemical, and Radical Scavenging Activity in Amaranthus blitum Leafy Vegetable. Sci. Rep. 2020;10:3868. doi: 10.1038/s41598-020-59848-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 183.Jimenez-Aguilar D.M., Grusak M.A. Minerals, Vitamin C, Phenolics, Flavonoids and Antioxidant Activity of Amaranthus Leafy Vegetables. J. Food Compos. Anal. 2017;58:33–39. doi: 10.1016/j.jfca.2017.01.005. [DOI] [Google Scholar]
  • 184.Madruga M.S., Camara F.S. The Chemical Composition of “Multimistura” as a Food Supplement. Food Chem. 2000;68:41–44. doi: 10.1016/S0308-8146(99)00152-1. [DOI] [Google Scholar]
  • 185.Shahidi F., Chavan U.D., Bal A.K., McKenzie D.B. Chemical Composition of Beach Pea (Lathyrus maritimus L.) Plant Parts. Food Chem. 1999;64:39–44. doi: 10.1016/S0308-8146(98)00097-1. [DOI] [Google Scholar]
  • 186.Khanam U.K.S., Oba S. Bioactive Substances in Leaves of Two Amaranth Species, Amaranthus lividus, and A. hypochondriacus. Can. J. Plant Sci. 2013;93:47–58. doi: 10.4141/cjps2012-117. [DOI] [Google Scholar]
  • 187.Khanam U.K.S., Oba S., Yanase E., Murakami Y. Phenolic Acids, flavonoids and Total Antioxidant Capacity of Selected Leafy Vegetables. J. Funct. Foods. 2012;4:979–987. doi: 10.1016/j.jff.2012.07.006. [DOI] [Google Scholar]
  • 188.Hossain M.N., Sarker U., Raihan M.S., Al-Huqail A.A., Siddiqui M.H., Oba S. Influence of Salinity Stress on Color Parameters, Leaf Pigmentation, Polyphenol and Flavonoid Contents, and Antioxidant Activity of Amaranthus lividus Leafy Vegetables. Molecules. 2022;27:1821. doi: 10.3390/molecules27061821. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 189.Sarker U., Oba S., Ercisli S., Assouguem A., Alotaibi A., Ullah R. Bioactive Phytochemicals and Quenching Activity of Radicals in Selected Drought-Resistant Amaranthus tricolor Vegetable Amaranth. Antioxidants. 2022;11:578. doi: 10.3390/antiox11030578. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 190.Alam M.A., Juraimi A.S., Rafii M.Y., Hamid A.A., Aslani F., Alam M.Z. Effects of Salinity and Salinity-Induced Augmented Bioactive Compounds in Purslane (Portulaca oleracea L.) for Possible Economical Use. Food Chem. 2015;169:439–447. doi: 10.1016/j.foodchem.2014.08.019. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data recorded in the current study are available in all Tables of the manuscript.


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