Abstract
Several plants species have served as food for man because of their nutritional values. However, there is a lack of data on the nutritional benefits of Desplatsia dewevrei. Hence, this study was aimed at investigating the nutrients and chemical composition of D. dewevrei leaves and fruits. Vitamins, amino acid profile, and mineral composition of D. dewevrei were investigated. Minerals found present include copper, magnesium, calcium, and potassium. Vitamins B, C, and K up to the daily standard required intake levels according to World Health Organization standards were discovered in D. dewevrei. The protein score from the amino acid composition was 100%. Phytate and oxalate, which are non‐nutritional components, were found present in D. dewevrei; however, in values far below the daily intake required limit by the WHO standard. In conclusion, D. dewevrei from this research finding has convincing qualities of a reliable nutraceutical raw material, which can be properly finished and incorporated into the human diet to harness its vitality.
Keywords: anti‐nutritional, Desplatsia dewevrei, nutraceutical, nutritional
1. INTRODUCTION
In recent past years, an increasing number of plant‐derived dietary supplements have become available in supermarkets and health food shops. These supplements, which elicit diverse mild pharmacological effects, are collectively referred to as “Nutraceutical.” The term “Nutraceutical” used to describe “a medicinally or nutritionally functional food was coined in 1989 by Stephen De Felice, founder and chairman of the Foundation for Innovation in Medicine” (Jack, 1995; Mannion, 1998). Palatable seeds are essential sources of nutrients and energy particularly among the resource‐poor people where protein‐energy undernourishment has insistently hindered peak growth and development (Escudero et al., 2006; Perumal, Klaus, & Harinder, 2001). Food crops on which most human nutrition is based depend on photosynthesis while ethnomedicines, drugs, and essential oils are made from plant secondary products of metabolism such as the alkaloids, terpenoids, and flavonoids (Alaribe, 2008).
Desplatsia dewevrei is a scarce West African plant species commonly referred to as “bush okra.” Indigenous people use D. dewevrei chiefly in making delicacies; however, a few herbalists use the plant parts as medicine (Ovuakporie‐Uvo & Idu, 2017). This study was aimed at investigating the nutrients and chemical composition of D. dewevrei.
2. MATERIALS AND METHODS
Nutritional studies were carried out following methods of A.O.A.C. (2016). Some of them are as follows:
2.1. Determination of ash content
A preheated and cooled crucible was weighed. The sample was charred on a Bunsen flame inside a fume cupboard. The charred sample was placed in a muffle furnace set at 550⁰C for 2 hr until a white or light gray ash is obtained. The sample was removed, cooled in desiccators, and weighed.
Where W 1 = weight of empty crucible.
W 2 = weight of crucible + weight of sample.
W 3 = weight of crucible + weight of the sample after ashing.
2.2. Determination of crude fiber
The sample was oven dried at 105⁰C. Powdered dried sample (2 g) was placed in a 500‐ml beaker, and 200 ml of boiling 1.25% H2SO4 was added. The beaker was placed on a hot plate and boiled for 3 min with occasional rotation of the beaker. The beaker was cooled and filtered by suction through a Buchner funnel. The beaker was rinsed with two 50 ml positions of boiling water. The residue was carefully transferred into a beaker, and 200 ml of 1.25% NaOH was added. It was boiled for 30 min, cooled and filtered, and washed twice with 50 ml boiling water.
Finally, the sample was washed with 25 ml 95% alcohol. The residue was oven dried for 2 hr at 130⁰C and cooled in a desiccator and weighed. The sample was heated for 30 min at 600⁰C and cooled in a desiccator and weighed.
2.3. Determination of moisture content
The crucibles were washed and dried in an oven at 100⁰C for 1 hr. The weight was noted as W1. Two grams (2 g) of each sample was separately weighed into the crucibles, and their weights were taken and noted down as (W2) before and during drying at 100⁰C to constant weight (W3).
where.
W 1 = weight of empty crucible.
W 2 = weight of crucible and sample before drying.
W 3 = weight of sample after drying to a constant weight.
2.4. Determination of carbohydrate
Carbohydrate was estimated as the remainder after accounting for all, crude fiber, protein, and fats. Total carbohydrate contents = 100 − (% moisture + % ash + % protein + % fat).
2.5. Determination of phytate
The phytate content were determined using the method of Young and Greaves (1940) as adopted by Lucas and Markakes (1975).
Two hundred milligram (0.2 g) of the sample was weighed into two 250‐ml conical flasks. Each sample was soaked in 100 ml of 2% concentrated HCl for 3 hr. The sample was then filtered. Fifty (50) mls of each filtrate was laced in 250‐ml beaker, and 10 ml distilled water added to each sample. Ten (10) ml of 0.3% ammonium thiocyanate solution was added as an indicator and titrated with standard iron (III) chloride solution which contained 0.00195 g iron per 1 ml. Endpoint is observed to be yellow which persists for 5 min.
2.6. Determination of oxalate
75 ml of 3M H2SO4 was added to 1g of the pulverized sample, and the solution was carefully stirred intermittently with a magnetic stirrer for 30 min thereafter filtered using Whatman No 1 filter paper. Twenty‐five (25 ml) of the filtrate was collected and titrated while hot against 0.1 N KMnO4 solution (0.05M KMnO4) until a faint pink color appeared that persisted for 30 s (Chinma & Igyor, 2007; Ihekoronye & Ngoddy, 1985).
1 ml KMnO4 = 2.2 mg Oxalate
Oxalate content = titer value × 2.2 mg.
2.7. Amino acid and vitamin composition
Amino acid and mineral analysis were carried out following modified A.O.A.C. (2006) method and Danka, Dobrina, and Kalin (2012). Water‐ and fat‐soluble vitamin determination was done following methods described by Dionex Corporation Annual Report (2010).
2.8. Mineral and elemental composition
Freshly prepared aqua regia solution was used in the analysis of the samples. For this, distilled water (1.2 L) was poured into a 2‐L volumetric flask. Then, 400 ml concentrated HCl was carefully added, followed with 133 ml of 70% nitric acid. The solution was made up to the mark with distilled water. Two (2) g of dry powder of D. dewevrei was placed in a crucible and ashed in a muffle furnace at 500°C for 2 hr after which it was allowed to cool in an oven, then removed and stored in a desiccator. The ashed material was transferred into a 50‐ml centrifuge tube by rinsing the crucible with 5 ml of distilled water. The crucible was further rinsed with 5 ml of the aqua regia about three times and poured into the tube to make a total of 20 ml. The sample was then vortexed for 10 min at 3,000 rpm which the supernatant was decanted into clean vials for macronutrients and micronutrients determination using flame atomic absorption spectrophotometer. The minerals analyzed included calcium, magnesium, potassium, sodium, and iron.
2.9. Statistical analysis
Data are stated as Mean ± Standard Error of Mean (SEM). Statistical analyses were carried out with one‐way analysis of variance (ANOVA). Multiple comparisons were done using Duncan multiple range tests (SPSS version 23), Tukey's multiple range tests (Graph pad prism 6), and Microsoft Excel software package. Significant levels were determined at p < 0.05.
3. RESULTS
The percentage compositions of nutritional values in D. dewevrei on dry weight basis show that the leaves and fruits of the plant are rich in carbohydrate and fiber. However, the leaves had more carbohydrate (45.16 ± 2.78) than the fruits (39.07 ± 0.87) while the fruits had more fiber content (49.71 ± 0.80) than the leaves (38.43 ± 2.85). Moisture was found to be more in the fruits (11.57 ± 0.36) than in the leaves (8.81 ± 0.01) of the plant as presented in Figures 1 and 2.
Figure 1.

Proximate analysis of food value in Desplatsia dewevrei leaves. n = 3 determinations
Figure 2.

Proximate analysis of food value in Desplatsia dewevrei fruits. n = 3 determinations
Phytate content of D. dewevrei was trace in the leaves (0.04 ± 0.01) and in the fruits (0.03 ± 0.00). The oxalate content was found to be more in the leaves (5.34 ± 0.14) than in the fruits (1.10 ± 0.09) as represented in Figures 3 and 4, respectively.
Figure 3.

Percentage phytic acid Content of Desplatsia dewevrei leaves and fruits. Key: DD‐leaves; DD2‐fruits. n = 3 determinations
Figure 4.

Oxalate Content of Desplatsia dewevrei leaves and fruits. Key: DD‐leaves; DD2‐fruits. n = 3 determinations
Mineral analysis of leaves and fruits revealed that the dried leaves contained a higher amount of copper (14.869 ppm), calcium (2.926 ppm), magnesium (5.426 ppm), and potassium (6.584 ppm) compared to the respective amounts of minerals and elements in the dried fruits (Table 1).
Table 1.
Mineral composition of Desplatsia dewevrei leaves and fruits
| Minerals | Leaves | Fruits |
|---|---|---|
| Concentration (ppm) | Concentration (ppm) | |
| Selenium | 0.168 ± 0.01 | 0.032 ± 0.03 |
| Chromium | 0.028 ± 0.00 | 0.014 ± 0.01 |
| Copper | 14.869 ± 0.04 | 2.666 ± 0.00 |
| Manganese | 0.175 ± 0.01 | 0.038 ± 0.01 |
| Iron | 0.893 ± 0.02 | 0.145 ± 0.02 |
| Sodium | 0.286 ± 0.01 | 0.068 ± 0.02 |
| Calcium | 2.926 ± 0.00 | 1.187 ± 0.01 |
| Magnesium | 5.426 ± 0.01 | 1.664 ± 0.03 |
| Potassium | 6.584 ± 0.00 | 3.679 ± 0.01 |
| Zinc | 0.415 ± 0.03 | 0.136 ± 0.00 |
n = 3 determinations.
The essential amino acids present in D. dewevrei were more in the leaves than fruits. Table 2 showed that glycine (4.426 g/ 100 g), alanine (4.181 g /100 g), serine (5.264 g/ 100 g), proline (3.051 g /100 g), aspartate (6.265 g /100 g), glutamate (17.556 g/ 100 g), tyrosine (2.352 g/ 100 g), and cytosine (2.029 g/ 100 g) were more quantifiable in the leaves of D. dewevrei. However, some nonessential amino acids, threonine (3.649 g/ 100 g), methionine (6.927 g/ 100 g), and histidine (1.949), were relatively more abundant in the fruits than the leaves.
Table 2.
Essential and non‐essential amino acid composition of Desplatsia dewevrei leaves and fruits
| Nonessential amino acids | Amount g/100g proteins | Essential Amino Acids | Amount g/100g proteins | ||
|---|---|---|---|---|---|
| Leaves | Fruits | Leaves | Fruits | ||
| Glycine | 4.426 | 3.129 | Valine | 3.170 | 2.581 |
| Alanine | 4.181 | 2.680 | Threonine | 3.293 | 3.649 |
| Serine | 5.264 | 1.779 | Isoleucine | 4.459 | 1.800 |
| Proline | 3.051 | 1.839 | Leucine | 5.387 | 4.181 |
| Aspartate | 6.265 | 5.963 | Lysine | 3.307 | 3.201 |
| Glutamate | 17.556 | 8.815 | Methionine | 1.272 | 6.927 |
| Tyrosine | 2.352 | 2.612 | Phenylalanine | 7.451 | 3.249 |
| Cystine | 2.029 | 1.664 | Histidine | 1.605 | 1.949 |
| Arginine | 8.154 | 1.822 | |||
The GC‐MS spectra of the methanol leaf and fruit extracts of D. dewevrei, showing the essential and nonessential amino acids, are presented in Figures 5 and 6.
Figure 5.

GC‐MS amino acid chromatogram of Desplatsia dewevrei methanol leaf extract
Figure 6.

GC‐MS of amino acid chromatogram of Desplatsia dewevrei methanol fruit extract
Vitamin composition of D. dewevrei showed that vitamins A, B1, B2, B3, B5, B6, C, D, E, and K were more in the leaves than fruits. Conversely, vitamins B12 and B9 were more in the fruits than the leaves as represented in Table 3.
Table 3.
Vitamin composition of Desplatsia dewevrei leaves and fruits
| Total Vitamins | Amount g/100 g proteins | |
|---|---|---|
| Leaves | Fruits | |
| Vitamin B3 | 5.360 | 3.017 |
| Vitamin B6 | 2.753 | 2.307 |
| Vitamin C | 53.430 | 10.974 |
| Vitamin A | 3.355 | 1.182 |
| Vitamin B1 | 6.742 | 3.619 |
| Vitamin B2 | 3.511 | 1.877 |
| Vitamin D | 3.987 | 2.078 |
| Vitamin E | 3.432 | 2.345 |
| Vitamin B9 | 2.531 | 5.099 |
| Vitamin K | 4.234 | 2.131 |
| Vitamin B5 | 3.333 | 2.200 |
| Vitamin B12 | 1.010 | 7.615 |
The GC‐MS spectra of the vitamins contained in the methanol leaves and fruit extract are shown in Figures 7 and 8, respectively.
Figure 7.

GC‐MS chromatogram of vitamins contained in methanol leaf extract of Desplatsia dewevrei
Figure 8.

GC‐MS chromatogram of vitamins contained in Desplatsia dewevrei fruit extract
4. DISCUSSION
According to Okogun (1985), “diets containing an abundance of fruits and vegetables are protective against a variety of diseases, particularly cardiovascular diseases.” In this study, the leaves and fruits of D. dewevrei were found to be principally rich in carbohydrate and fiber content (Figures 1 and 2). Foods with high crude fiber values have been implicated in aiding bowel movement because of the cellulose that absorbs water and provides bulk for better functioning of the alimentary system (Wardlaw & Smith, 2009). Fiber may also be functional in food enrichment. Ample intake of dietary fiber had been reported by Ishida, Suzuno, Sugiyama, Innami, and Todokoro (2000) to lower serum cholesterol level, the risk of coronary heart diseases, hypertension, constipation, and diabetes. Fruit fiber is considered to be of better quality than plant fiber. This is maybe due to higher total and soluble fiber content, water and oil holding capacity, and colonic fermentability, as well as lower phytic acid content and caloric value (Anonymous, 2005; Figuerola, Hurtado, Estevez, Chiffelle, & Asenjo, 2005). This suggests that the high fiber content in D. dewevrei leaves and fruits may potentiate positive effects in preventing the risk of some colorectal cancers.
The carbohydrate contents in D. dewevrei leaves and fruits were also remarkable. Carbohydrate forms a major class of naturally occurring organic compounds which are vital for the upkeep of life in both plants and animals and also offer raw materials for many industries (Ebunoluwa, Adetanwa, Olabisi, & Sina, 2007). This suggests that D. dewevrei might be a good source of concentrated dietary energy.
High moisture content promotes susceptibility to microbial activity and spoilage (Ponnusha, Subramaniyan, Pasupathi, Subramaniyan, & Virunandy, 2011). Desplatsia dewevrei leaves and fruits may be said to have appreciable moisture content in contrast to that recorded for albedo (Oikeh, Oriakhi, & Omoregie, 2013). However, apt drying of this D. dewevrei leaves and fruits is recommended especially when they are harvested for use as herbal remedies to preserve the integrity of the phytochemicals in them and also to prevent microbial attack leading to microbial growth and decay.
Anti‐nutritional plant chemicals like phytates and oxalates though inherently toxic and noncurative in nature have been found to be to play significant roles in the nutritional quality of food (Lewis & Fenwick, 1987; Liener, 1969; Nwokolo & Bragg, 1977). The phytic acid which is the principal store of phosphate is a natural plant oxidant that has shown protective action in carcinogenesis. This action can be explained by its mineral chelating potential. Phytic acid may have health benefits for patients with diabetes as it reduces blood glucose response, by lowering the rate of starch breakdown. Phytic acid also releases inositol during digestion, which might reduce depression. It also reduces inflammation (Idu & Igeleke, 2012). Phytate has been reported to have anticancer properties (Jenab & Thompson, 2000). Phytates are indigestible to humans or nonruminant animals, but may be a source of either inositol or phosphate if eaten directly (Idu, Ovuakporie‐Uvo, & Nwaokolo, 2016). Moreover, they chelate, thus making nonabsorbable certain important minor minerals such as zinc and iron and, to a lesser extent, also macrominerals such as calcium and magnesium (Greiner, Konietzny, & Jany, 2006).
Oxalates are a common constituent of plants. Studies have shown that oxalate can perform different roles in plants, including calcium regulation, ion balance, plant protection, tissue support, and heavy metal detoxification (Idu et al., 2016; Rahman & Kawamura, 2011). Oxalates provide essential nutrients, fiber, antioxidants, and other important phytochemicals. Figures 3 and 4 show that the phytic and oxalic acid contents of D. dewevrei are slightly more in the leaves than in the fruits. However, both phytic and oxalic acid contents of D. dewerei are together less than those found present in LPC, cooked and sun‐dried Cnidoscolusa conitifolius (Aye, 2012), and the FAO permissible daily required intake.
The mineral and elemental composition of D. dewevrei shown on Table 1 reveal the presence of selenium, chromium, copper, manganese, iron, sodium, calcium, magnesium, potassium, and zinc in the leaves and fruits at appreciable levels. Copper, calcium, magnesium, and potassium which have been recommended as therapeutically useful are more inherent in leaves than in the fruits of D. dewevrei. Copper plays a role in the oxidative defense system but chronic copper toxicity can cause severe poisoning (Uriu‐Adams & Keen, 2005). In this study, the copper concentration in the leaves of D. dewevrei was more than in the fruits (Table 1). However, both concentrations of copper were less than the WHO recommended the level of copper in the acceptable range of 20µg/mg body weight per day (FDA, 1993; Watson, 1993). However, copper could be poisonous depending on the dose and duration of exposure (Obi, Akunyili, Ekpo, & Orisakwe, 2006). Copper has been reported to potentiate anti‐inflammatory activities (Rajeshwari & Andallu, 2011). Copper is an essential part of several enzymes and it is necessary to the synthesis of hemoglobin, and its deficiency can lead to anemia and hypoproteinemia (Ahmed, Rehman, Qadiruddin, & Badar, 1994; Idu et al., 2015). Calcium, potassium, magnesium, and sodium being macronutrients are important for the proper functioning of vital organs in the body. They also play vital roles as structural and functional components of metalloproteins and enzymes in living cells (Ansari, Ahmad, & Aafaqi, 2004; Zaidi, Asrar, Mansoor, & Farooqui, 2005). Magnesium is a component of chlorophyll and an important mineral element with reference to the prevention of heart diseases and calcium metabolism in bones (Idu, Erhabor, Timothy, & Ovuakporie‐Uvo, 2014; Ishida et al., 2000). It orchestrates the electric current that sparks through the body nerves (Idu & Igeleke, 2012). Magnesium is an anti‐inflammatory and antidiabetic agent (Rajeshwari & Andallu, 2011). Magnesium is a central mineral for retention of vitamin D and calcium into the bones for maintaining bone structure and helps in prevention of osteoporosis and cardiovascular diseases (Chakraborti et al., 2002). According to Hooker (1987), magnesium plays an important role in the metabolism of cholesterol and heart diseases. Sodium present in salt regulates the amount of fluid that the body contains, eliminates fluid waste through urine, and maintains fluid balance (Akpanyung, 2005). Iron is an important constituent of hemoglobin. The leaves of D. dewevrei have an appreciable amount of calcium which is good for growth and maintenance of bones, teeth, and muscles (Mohd, Idris, & Abdulrasheed, 2006). Zinc is involved in the normal function of immune system and is a component of over 50 enzymes in the body (Okaka, Akobundu, & Okaka, 2006). The leaves of D. dewevrei from literature can supplement the daily requirements of calcium, sodium, magnesium, and zinc.
Essential amino acids also referred to as “indispensable amino acid” are the most important for normal human body physiology and must be supplied to the body through diet. Essential amino acids are nine in total, namely histidine, tryptophan, phenylalanine, leucine, isoleucine, lysine, valine, methionine, and threonine (Banipal, Kaur, Kaur, Gupta, & Banipal, 2015). The synthesis of other amino acids and proteins also requires essential amino acids (Banipal, Kaur, Kaur, Komal, & Banipal, 2016). Essential amino acids are also used to prevent fatigue and improve concentration. Leucine, isoleucine, and valine are imperative for the regulation of carbohydrate metabolism, protein output, and gene expression (Banipal et al., 2015). Peyrollier, Hajduch, Blair, Hyde, and Hundal (2000) reported the key role of leucine as signaling molecule during synthesis of muscle proteins. Additionally, the role of leucine in reversible phosphorylation of ribosomal protein S6 kinase has also been reported for the upregulation of protein synthesis in skeletal muscle (Anthony, Anthony, & Kimball, 2001). The amino acid profile of D. dewevrei leaves (5.387 g/100 g) and fruits (4.181 g/100 g) revealed a significant concentration of leucine suggesting that adequate consumption of D. dewevrei can help upregulate the protein syntheses of the consumer (Table 2). Valine serves as a “central building block of various enzymes and is vital for supplying energy aiding to muscle cell repair and tissue recovery.” It is also useful in process of beverage fermentation (Anthony et al., 2001). The valine content of the leaves (3.170 g/100 g) and fruits (2.581 g/100 g) of D. dewevrei was found to be higher to D. guineense (Ayessou et al., 2014; Kumari, Catherina, Katherine, Chew, & Kah‐Guan, 2017). Nonessential amino acids are said to be dispensable because the body can synthesize them readily. According to Sumalantha, Saravana, and Mohama (2010), arginine which was found present in the leaves (8.154 g/100 g) and fruits (1.822 g/100 g) of D. dewevrei has been suggested to potentiate aphrodisiac activities. Thus, D. dewevrei may be aphrodisiac at certain concentrations. Arginine improves the circulation, strengthens the immune system, and has a positive influence on male libido (Williams, Abumrad, & Barbul, 2002). Research suggests that the amino acid speeds up the rate of the healing of wounds (Lavie, Hafetz, Luboshitzky, & Lavie, 2003), improves the burning of excess fat (Merimee, Lillicrap, & Rabinowitz, 1965), and can be used in weight‐reducing diets. Its role in decreasing cholesterol levels can be ascribed to its function as a biological precursor of nitric oxide (NO). Arginine helps to stimulate and improve hair growth, and arginine helps to reduce insulin resistance and increases glucose tolerance and insulin sensitivity in type 2 diabetes mellitus (Piatti et al., 2001; Wu, Meininger, Knabe, Baze, & Rhoads, 2000). The substantial concentration of arginine in D. dewevrei may suggest that it may be useful in cholesterol‐lowering activities in man. Glutamate or glutamic acid is in the same amino acid family group as glutamine. Glutamate is a major component of most natural protein foods such as meat, fish, milk, and some vegetables that play an essential role in human metabolism (Filer & Stegink, 1994; Fernstrom, 2000). It helps transmit messages around the brain and also reduce chest pain commonly associated with coronary heart disease (Niswender & Conn, 2010).
Vitamins A, B1, B2, B3, B5, B6, B9, B12, C, D, E, and K were found present in D. dewevrei leaves and fruits (Table 3, Figures 7 and 8). However, vitamins B1 (6.742 g/100 g),B3 (5.360 g/100 g), C (53.430 g/100 g), and K (4.234 g/100 g) were the most prominently appreciable vitamins present in D. dewerei leaves which were far more than the quantity of each of the vitamins in the fruits of the plant (Table 3). Vitamins B1 and B3 otherwise known as thiamine and niacin distinctively are water‐soluble vitamins which function as coenzymes needed for energy metabolism. They are also important for keeping the nervous system, digestive system, and skin healthy (Anonymous, 2005). Vitamin C, also referred to as ascorbic acid, also functions as an antioxidant and a coenzyme needed for protein metabolism. Vitamin C is important for healthy functioning of the immune system and healing of cuts, wounds, and gums. It also aids in iron absorption, prevention of cell damage, reduces the risk of certain cancers, heart, and other diseases (Anonymous, 2005, 2014). High intake of vitamin C helps protect low‐density lipoproteins ex vivo against oxidation keeping the immune system in fine fettle. Vitamin C increases the amount of iron absorbed from some foods by the body (Hillstorm, Yacapin‐Ammons, & Lynch, 2003).
Vitamins D and K are fat‐soluble vitamins responsible for an increase in the amount of calcium and phosphorus absorbs, strengthening them and healthier bones and teeth by depositing calcium and phosphorus from foods into the body. Vitamin D guards against infections by strengthening the immune system (Anonymous, 2014). Vitamin K produces proteins that cause a blood clot in case of bleeding and other body proteins for the bones and kidneys (Vermeer, 1990). According to FAO/WHO (2001), the biologic function of vitamin K is to act as a cofactor for a specific carboxylation reaction that transforms selective glutamate residues to gg‐carboxyglutamate (Gla) residues. Phylloquinone is the major circulating form of vitamin K. Since “there is no evidence of even sub‐clinical deficiencies of hemostatic function, a daily intake of 1 µg/kg may still be used as the basis for the recommended nutrient intake (RNI) for vitamin K.” However, in this study, the vitamin K found to be contained in both leaves and fruits of D. dewevrei are beyond the RNI standards of the United States and United Kingdom.
In conclusion, D. dewevrei is a nutraceutical freely given by nature. It must be harnessed as fast as possible into the human diet to optimize growth and development of especially growing children in (dying as a result of malnutrition) rural and urban settlements of the world.
CONFLICT OF INTEREST
The authors declare that they do not have any conflict of interest.
ETHICAL REVIEW
This study does not involve any human or animal testing.
INFORMED CONSENT
Written informed consent was obtained from all study participants.
ACKNOWLEDGMENT
The authors acknowledge Mr. Augustine Idu for helping to source the plant materials used in this study from the wild. The authors also acknowledge Mr Osamudiamen Ebohon and Mr Francis Irhabor for their unreserved laboratory support throughout this research.
Ovuakporie‐Uvo O, Idu M, Omoregie ES. Nutrients and chemical composition of Desplatsia dewevrei . Food Sci Nutr. 2019;7:1768–1777. 10.1002/fsn3.1019
REFERENCES
- A.O.A.C. (2006). Official methods of analysis, 18th ed Arlington, TX: Association of Official Analytical Chemists Inc. [Google Scholar]
- A.O.A.C. (2016). Official method of analysis In George W. & Latimer J. R. (Eds.), (Vol. 1, 20th ed., pp. 20‐24). Washington, DC: Association of Official Analytical Chemists. [Google Scholar]
- Ahmed, S. , Rehman, A. , Qadiruddin, M. , & Badar, Y. (1994). Elemental analysis of a herbal drug Intella, a neuro energiser. Journal of Faculty of Pharmacology, 2, 83–90. [Google Scholar]
- Akpanyung, E. O. (2005). Proximate and Mineral Element Composition of Bouillon Cubes Produced in Nigeria. Pakistan Journal of Nutrition, 4, 327–329. 10.3923/pjn.2005.327.329 [DOI] [Google Scholar]
- Alaribe, S. I. (2008). A survey of the importance and problems of traditional healthcare medicine: A case study of Ezinihitte Mbaise L.G.A Imo State. Unpublished B.Sc. Project, A. I. F. C. E Owerri, Imo State. [Google Scholar]
- Anonymous (2005). Institute of Medicine, "Dietary intakes and energy, carbohydrate, fibre, fat, fatty acids, cholesterol, protein and amino acid" (pp. 380–382). Washington, DC: National Academy Press. [Google Scholar]
- Anonymous (2014). Functions and food sources of some common vitamins. Dietitians of Canada. Accessed on 17th July 2017. [Google Scholar]
- Ansari, M. A. , Ahmad, Z. A. , & Aafaqi, R. (2004). Organizational leadership in the Malaysian context In Tjosvold D. & Lueng K. (Eds.), Leading in high growth Asia: Managing relationship for teamwork and change (pp. 109–138). Singapore: World Scientific Publishing Co. [Google Scholar]
- Anthony, J. , Anthony, T. , & Kimball, S. (2001). Signalling pathways involved in translational control of protein synthesis in skeletal muscle by leucine. Journal of Nutrition, 131, 856–860. 10.1093/jn/131.3.856s [DOI] [PubMed] [Google Scholar]
- Aye, P. A. (2012). Effect of processing on the nutritive characteristics, anti‐nutritional factors and functional properties of Cnidoscolusa conitifolius leaves (Iyana Ipaja). American Journal of Food and Nutrition, 2, 89–95. 10.4172/2157-7110.1000249 [DOI] [Google Scholar]
- Ayessou, N. C. , Ndiaye, C. , Ciss, M. , Gueye, M. , Sakho, M. , & Dornier, M. (2014). Nutrient composition and nutritional potential of wild fruit Dialium guineense . Journal of Food Composition and Analysis, 34, 186–191. 10.1016/j.jfca.2014.01.002 [DOI] [Google Scholar]
- Banipal, T. S. , Kaur, N. , Kaur, A. , Gupta, M. , & Banipal, P. K. (2015). Effect of food preservatives on the hydration properties and taste behaviour of amino acids: A volumetric and viscometric approach. Food Chemistry, 181, 339–346. 10.1016/j.foodchem.2015.02.061 [DOI] [PubMed] [Google Scholar]
- Banipal, T. S. , Kaur, N. , Kaur, J. , & Banipal, K. P. K. (2016). Modulation of physicochemical and spectroscopic properties of L‐serine and L‐proline by propionate based food preservatives. Food Chemistry, 209, 220–227. 10.1016/j.foodchem.2016.04.056 [DOI] [PubMed] [Google Scholar]
- Chakraborti, S. , Chakraborti, T. , Mandal, M. , Mandal, A. , Das, S. , & Ghosh, S. (2002). Protective role of magnesium in cardiovascular diseases: A Review. Molecular and Cellular Biochemistry, 238, 163–179. [DOI] [PubMed] [Google Scholar]
- Chinma, C. E. , & Igyor, M. A. (2007). Micronutrients and anti‐nutritional contents of selected tropical vegetables grown in Southeast, Nigeria. Nigerian Food Journal, 25, 111–116. 10.4314/nifoj.v25i1.33659 [DOI] [Google Scholar]
- Danka, P. O. , Dobrina, D. T. , & Kalin, V. I. (2012). Simultaneous identification and determination of total content of amino acids in food supplements‐tablets by gas chromatography. Asian Journal of Pharmaceutical and Clinical Research, 5, 57–68. [Google Scholar]
- Dionex Corporation Annual Report (2010). Determination of Water and Fat – Soluble Vitamins by HPLC. Thermo Scientific, Technical Note 89. Sunnyvale CA. 1768–64.
- Ebunoluwa, A. A. , Adetanwa, I. O. , Olabisi, A. , & Sina, B. (2007). Feeding and care of low birthweight babies in two rural communities in south‐western Nigeria. Maternal and Child Nutrition, 4, 55–64. 10.1111/j.1740-8709.2007.00101.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Escudero, N. l. , Zirulnik, F. , Gomez, N. N. , Mucciarelli, S. I. , Mucciarelli, S. I. , & Giménez, M. S. (2006). Influence of a protein concentrate from Amaranthus cruentus seeds on lipid metabolism. Experimental Biology and Medicine, 231, 50–59. 10.1177/153537020623100106 [DOI] [PubMed] [Google Scholar]
- FAO/WHO (2001). The human vitamin and mineral requirement. Report of a joint FAO/WHO expert consultation Bangkok, Thailand. pp 133‐150.
- Fernstrom, J. D. (2000). Second international conference on glutamate: Conference summary. The Journal of Nutrition, 130(4), 1077S–1079S. 10.1093/jn/130.4.1077S [DOI] [PubMed] [Google Scholar]
- Figuerola, F. , Hurtado, M. L. , Estevez, A. M. , Chiffelle, I. , & Asenjo, F. (2005). Fibre concentrates from apple pomace and citrus peel as potential fibre sources for food enrichment. Food Chemistry, 9, 395–401. 10.1016/j.foodchem.2004.04.036 [DOI] [Google Scholar]
- Filer, L. J. , & Stegink, L. D. (1994). Report of the proceedings of the MSG workshop held August 1991. Critical Reviews in Food Science and Nutrition, 34, 159–174. 10.1080/10408399409527655 [DOI] [PubMed] [Google Scholar]
- Greiner, R. , Konietzny, U. , & Jany, K.‐D. (2006). Phytate‐ an undesirable constituent of plant‐based foods? Journal Für Ernährungsmedizin, 8, 18–28. [Google Scholar]
- Hillstorm, R. J. , Yacapin‐Ammons, A. K. , & Lynch, S. M. (2003). Vitamin C inhibits lipid oxidation in Human HDL. The American Society for Nutritional Sciences, 17, 3047–3051. 10.1093/jn/133.10.3047 [DOI] [PubMed] [Google Scholar]
- Hooker, J. E. (1987). Variation in Frankia strains isolated from Alnus root noodles. Ph.D. Thesis, University of Glasglow. 288P.
- Idu, M. , Erhabor, J. , Timothy, O. , & Ovuakporie‐Uvo, O. (2014). Market survey and heavy metal screening of selected medicinal plants sold in some markets in Benin City, Nigeria. International Journal of Humanities, Arts, Medicines and Sciences, 2, 7–16. [Google Scholar]
- Idu, M. , & Igeleke, C. L. (2012). Antimicrobial activity and phytochemistry of Khaya senegalensis roots. International Journal of Ayurvedic and Herbal Medicine, 2, 416–422. [Google Scholar]
- Idu, M. , Ovuakporie‐Uvo, O. , & Nwaokolo, M. J. (2016). Phytochemistry and microscopy of Tapinanthus dodoneifolius (DC) (Danser) (Santalales: Loranthaceae) (African mistletoes) from Guava, Rubber and Orange host trees. Brazilian Journal of Biological Sciences, 3, 27–35. 10.21472/bjbs.030503 [DOI] [Google Scholar]
- Ihekoronye, A. I. , & Ngoddy, P. O. (1985). Integrated food science and technology (pp. 257–264). London, UK: Macmillian Publisher. [Google Scholar]
- Ishida, H. , Suzuno, H. , Sugiyama, N. , Innami, S. , & Todokoro, T. (2000). National evaluation of chemical component of leaves stalks and stem of sweet potatoes. (Ipomea batatas Poir) . Food Chemistry, 68, 359–367. [Google Scholar]
- Jack, D. B. (1995). Keep taking the tomatoes ‐ the exciting world of nutraceuticals. Molecular Medicine Today, 1, 118–121. 10.1016/S1357-4310(95)80088-3 [DOI] [PubMed] [Google Scholar]
- Jenab, M. , & Thompson, L. U. (2000). Phytic acid in wheat bran affects colon morphology, cell differentiation and apoptosis. Carcinogenesis, 21, 1547–1552. 10.1093/carcin/21.8.1547 [DOI] [PubMed] [Google Scholar]
- Kumari, N. , Catherina, J. G. , Katherine, L. , Chew, C. Y. , & Kah‐Guan, A. (2017). Putative protective role of lutein and zeaxanthin in diabetic retinopathy. British Journal of Opthalmology, 101, 551–558. 10.1136/bjophthalmol-2016-309814 [DOI] [PubMed] [Google Scholar]
- Lavie, L. , Hafetz, A. , Luboshitzky, R. , & Lavie, P. (2003). Plasma levels of nitric oxide and L‐arginine in sleep apnea patients. Journal of Molecular Neuroscience, 21, 57–63. 10.1385/jmn:21:1:57 [DOI] [PubMed] [Google Scholar]
- Lewis, J. , & Fenwick, G. R. (1987). Glucosinate content of Brassica vegetables. Analysis of twenty‐four cultivars of Calabres. Food Chemistry, 25, 259–268. [Google Scholar]
- Liener, I. E. (1969). Toxic constituents of plant foodstuff (504P pp). London, UK: Academic Press; New York. [Google Scholar]
- Lucas, G. M. , & Markakes, P. (1975). Phytic acid and other phosphorus compounds of nevy bean (Phaseolus vulgaris). Journal of Agricultural and Food Chemistry, 23, 13–15. [Google Scholar]
- Mannion, M. (1998). Nutraceutical revolution continues at foundation for innovation in medicine conference. American Journal of Natural Medicine, 5, 30–33. [Google Scholar]
- Merimee, T. J. , Lillicrap, D. A. , & Rabinowitz, D. (1965). Effect of arginine on serum‐levels of human‐growth‐hormone. Lancet, 2, 668–670. 10.1016/S0140-6736(65)90399-5 [DOI] [PubMed] [Google Scholar]
- Mohd, A. M. , Idris, M. B. , & Abdulrasheed, A. (2006). The mineral composition and proximate analysis of T. occidentalis (Fluted Pumpkin) leave consumed in Kano metropolis. Northern Nigeria. American Chemical Science Journal, 10, 1768–4. 10.9734/acsj/2016/20632 [DOI] [Google Scholar]
- Niswender, C. M. , & Conn, P. J. (2010). Metabotropic glutamate receptors: Physiology, pharmacology and disease. Annual Review of Pharmacology and Toxicology, 50, 295–322. 10.1146/annurev.pharmtox.011008.145533 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nwokolo, E. N. , & Bragg, D. B. (1977). Influence of phytic acid and crude fibre on the availability of minerals from four protein supplements in growing chicks. Journal Animal Science, 57, 475–477. 10.4141/cjas77-060 [DOI] [Google Scholar]
- Obi, E. , Akunyili, D. N. , Ekpo, B. , & Orisakwe, O. E. (2006). Heavy metal hazards of Nigerian herbal remedies. Science of the Total Environment, 369, 35–41. 10.1016/j.scitotenv.2006.04.024 [DOI] [PubMed] [Google Scholar]
- Oikeh, E. I. , Oriakhi, K. , & Omoregie, E. S. (2013). Proximate analysis and phytochemical screening of Citrus sinensis fruit wastes. The Bioscientist, 1, 164–170. [Google Scholar]
- Okaka, J. C. , Akobundu, E. N. T. , & Okaka, A. N. C. (2006). Food and human nutrition: An integrated approach (3rd ed., pp. 132–142). Enugu, Nigeria: Ocjanco Academic Publishers. [Google Scholar]
- Okogun, J. I. (1985). Drug production in Nigeria. Medicinal chemistry research and missing link. Being the text of a lecture given to the Nigeria. Academic science. pp 29–52.
- Ovuakporie‐Uvo, O. , & Idu, M. (2017). Ethnobotanical knowledge of Desplatsia dewevrei (De Wild. & T. Durand) burret by the Bini Tribe Edo State, Nigeria. Journal of Ayurvedic and Herbal Medicine, 3, 129–132. [Google Scholar]
- Perumal, S. , Klaus, B. , & Harinder, P. S. M. (2001). Chemical composition, protein fractionation, essential amino acid potential and anti‐metabolic constituents of an unconventional legume, Gila bean (Entadapha seoloides Merrill) seed kernel. Journal of Science of Food and Agriculture, 82, 192–202. 10.1002/jsfa.1025 [DOI] [Google Scholar]
- Peyrollier, K. , Hajduch, E. , Blair, A. S. , Hyde, R. , & Hundal, H. S. (2000). L‐Leucine availability regulates phosphatidylinositol 3‐kinase, p70 S6 kinase and glycogen synthase kinase‐3 activity in L6 muscle cells: Evidence for the involvement of mammalian target of rapamycin (mTOR) pathway in the L ‐ leucine‐induced up‐regulation. Journal of Biochemistry, 350, 361–368. 10.1042/0264-6021:3500361 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piatti, P. M. , Monti, L. D. , Valsecchi, G. , Magni, F. , Setola, E. , Marchesi, F. , … Alberti, K. G. M. M. (2001). Long‐term oral L‐arginine administration improves peripheral and hepatic insulin sensitivity in type 2 diabetic patient. Diabetes Care, 24, 875–880. 10.2337/diacare.24.5.875 [DOI] [PubMed] [Google Scholar]
- Ponnusha, B. S. , Subramaniyan, S. , Pasupathi, P. , Subramaniyan, B. , & Virunandy, R. (2011). Antioxidant and antimicrobial properties of Glycine max – A review. International Journal of Current Biological and Medical Science, 1, 49–62. [Google Scholar]
- Rahman, M. M. , & Kawamura, O. (2011). Oxalate accumulation in forage plants: Some agronomic climate and genetic aspects. Asian‐Australasian Journal of Animal Sciences, 24, 439–448. 10.5713/ajas.2011.10208 [DOI] [Google Scholar]
- Rajeshwari, C. U. , & Andallu, B. (2011). Medicinal benefits of coriander (Coriandrum sativum L). Spatula DD ‐ Peer Reviewed Journal on Complementary Medicine and Drug Discovery, 1, 51–58. 10.5455/spatula.20110106123153 [DOI] [Google Scholar]
- Sumalantha, K. , Saravana, K. A. , & Mohama, L. S. (2010). Review of natural Aphrodisiac potential to treat sexual dysfunction. International Journal of Pharmacological Therapy, 1, 10–18. [Google Scholar]
- Uriu‐Adams, J. Y. , & Keen, C. L. (2005). Copper; oxidative stress and human health. Molecular Aspects of Medicine, 26, 268–269. 10.1016/j.mam.2005.07.015 [DOI] [PubMed] [Google Scholar]
- Vermeer, C. (1990). GG‐Carboxyglutamate‐containing proteins and the vitamin K‐dependent carboxylase. Biochemistry Journal, 266, 625–636. 10.1042/bj2660625 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wardlaw, G. M. , & Smith, A. M. (2009). Contemporary nutrition (7th ed., pp. 588–590). Boston: McGraw‐Hill Higher Education. [Google Scholar]
- Williams, J. Z. , Abumrad, N. , & Barbul, A. (2002). Effect of a specialized amino acid mixture on human collagen deposition. Annals of Surgery, 236, 369–375. 10.1097/00000658-200209000-00013 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu, G. A. B. , Meininger, C. J. , Knabe, D. A. , Baze, F. W. A. , & Rhoads, J. M. (2000). Arginine nutrition in development, health and disease. Current Opinion in Clinical Nutrition and Metabolic Care, 3, 59–66. 10.1097/00075197-200001000-00010 [DOI] [PubMed] [Google Scholar]
- Young, S. M. , & Greaves, J. S. (1940). Influence of variety and treatment on phytic acid content of wheat. Food Research, 5, 103–105. [Google Scholar]
- Zaidi, M. I. , Asrar, A. , Mansoor, A. , & Farooqui, M. A. (2005). The heavy metal concentrations along roadside trees of Quetta and its effects on public health. Journal of Applied Science, 5, 708–711. 10.3923/jas.2005.708.711 [DOI] [Google Scholar]
