Table 4.
Variety of Mango | Type of Extract | Bioactive Compounds Identified | Type of Cell Lines/Type of Study | Major Findings and Molecular Mechanisms of Action | References |
---|---|---|---|---|---|
Anti-cancer activities | |||||
Kent | Extract prepared by pressurized liquid extraction and enhanced solvent extraction | Homo-mangiferin, methyl gallate, gallotannins | MDA-MB-231, MCF7, MCF10 | Leaf extracts with high concentration of homomangiferin and methyl gallate were found more effective against MDA-MB-231 cells, while gallotannins showed cytotoxicity against MCF7 cells at IC50 > 200 µg/ml | [41] |
Okrong | Ethanol extract | Mangiferin | Lung fibroblast (ATCC CLS 300421,WI-38 VA-13 subline 2RA), skin fibroblast (ATCC CRL1947, CCD-986SK), colon adenocarcinoma (ATCC CCL227, SW 620), gastric carcinoma (ATCC HTB103, Kato-III), liver hepatoblastoma (ATCC HB8065, Hep-G2), bronchogenic carcinoma (ATCC HTB-168TB, Chago K-1), and ductal carcinoma (ATCC HTB20, BT474) | Leaf extracts showed potent cytotoxic activities at IC50 >200 µg/mL against all the cell lines | [42] |
Anti-diabetic activities | |||||
Young leaves of Mangifera indica cv. Anwar Ratol were obtained from a private mango farm, Multan, Pakistan. | Hydro-alcoholic | Mangiferin, Phenolics, and flavonoids | In-vivo (Swiss albino mice with alloxan monohydrate (150 mg/kg i.p.) induced diabetes) |
Administration of ML extract (550, 750, 950 mg/kg) significantly reduced the postprandial BGL, improved the lipid profile, body weight, and glucose tolerance, and also prevented the β-cells damage. | [49] |
Leaves collected in Yuanjiang county, Yunnan province, China. |
Distilled Water extract further subjected to chromatography over various columns | Two new benzophenone (Manindicins A & B) and two xanthones (Mangiferin & Norathyriol) | In-vitro | Norathyriol exhibited strong inhibition of α-glucosidase activity with an IC50 of 4.22 ± 0.19µg/mL, which was 4-fold lower than the commercial acarbose (16.28 ± 1.22 µg/mL). | [31] |
Leaves collected from Guangdong Pharmaceutical University, China | 70% ethanol-water extract | Five benzophenones and seventeen flavonoids | In-vitro | Among all isolated compounds, quercetin-3-O-α-L-rhamnoside (IC50 76.69 ± 34.79 µg/mL) and quercetin (IC50 31.17 ± 5.06 µg/mL) displayed a stronger inhibition of α-glucosidase than acarbose (IC50 119.59 ± 6.00 µg/mL). | [30] |
Leaves collected from Guangdong Pharmaceutical University, China | 70% ethanol-water extract | Benzophenone glycosides | In-vitro | Novel 2,4,4′,6-tetrahydroxy-3′-methoxybenzophenone-3-C-β-D-glucopyranoside (IC50 97.44 ± 20.29 µg/mL), arjunolic acid (IC50 117.09 ± 25.00 µg/mL), and actinidic acid (IC50 144.72 ± 8.12 µg/mL) displayed the potent α-glucosidase inhibitory | [87] |
Leaves of Mangifera indica cv. Okrong collected in Thailand | Ethanol extract | Mango leaf extract and Mangiferin | In-vitro | MLE exhibited the inhibition of yeast α-glucosidase (IC50 50.3 µg/mL) > rat α-glucosidase (IC50 1452.8 µg/mL) > pancreatic α-amylase (IC50 2284 µg/mL). Mangiferin exhibited the inhibition of yeast α-glucosidase (IC50 581.3 µg/mL) > rat α-glucosidase (IC50 433.3 µg/mL) > pancreatic α-amylase (IC50 1048.5 µg/mL). |
[42] |
Tender and mature leaves of Mangifera indica cv. Totapuri collected from GKVK, Bangaluru. | 70% Methanol | Tender and mature leaf extract (TLE and MLE) | In-vitro and in-vivo (Wister Albino rats) | Administration of TLE and MLE (500mg/kg body weight) showed potent inhibition α-amylase (IC50 22.01 µg/mL) and α-glucosidase (IC50 21.03 µg/mL) respectively. | [52] |
Antioxidant activity | |||||
Mango leaves extract |
Supercritical process (CO2/methanol (50%) at 120 bar and 100 °C) | Polyphenols (iriflophenone, mangiferin, and gallic acid) | In vitro | Potent antioxidant (AAI = 3.28 ± 0.1 µg DPPH/µg extract). |
[88] |
Mango leaves extract |
Water | Polyphenols (mangiferin) | In vivo | Stimulated concentrations of Catalase activity (CAT) (32.4 ± 1.9 U CAT mg Ptn−1) and (Total antioxidant capacity) TAC (0.27 ± 0.01 mM Trolox), nearly doubling the obese group (OB) and (non-obese group) CG values |
[74] |
Mango leaves extract |
Water | Polyphenols | In vitro | IC90 values for DPPH and FRAP assay were 156.08 and 5.44 μg/mL, respectively, at 500 μg/mL concentration of extract | [48] |
Antimicrobial activity | |||||
Mango leaves extract |
Aqueous extract And Chloroform extract |
Alkaloids, tannins, terpenoid, anthraquinones, reducing sugar, amino acid, flavonoids, steroid, saponins, cardiac glycosides, resin, phenols. |
Manifestation of antimicrobial activity of aqueous and chloroform extracts against Methicillin Resistant Staphylococcus aureus | The chloroform extract with high range of zone of inhibition (14–17 mm) manifested to have higher antibacterial property against the bacteria with respect to to aqueous extract. | [89] |
Mango leaves extract |
Ethanolic extract (50% and 100%) Hydroalcoholic extract (50% and 100%) |
Polyphenols tannins, terpenoids | Estimation of antimicrobial activity of ethanolic and hydroalcoholic extracts against Staphylococcus aureus ATCC 6538 | 50% and 100% ethanol extract—small zone of inhibition—21.4−24.3 ± 0.8 mm Hydroalcoholic extract (50% and 100%) with larger zone of inhibition 24.7 − 33.4 ± 1.2 mm, therefore higher antimicrobial activity than ethanol extract |
[90] |
Leaf Extract | Ethanolic extract |
Alkaloids, anthranol, glycosides, saponins, triterpenes, phenol, flavonoids | Manifestation of antimicrobial activity of ethanolic extract against Shigella flexneri, Pseudomonas fluorescens, Escherichia coli, Staphylococcus Aureus, and Bacillus spp. |
Ethanol extract showed no inhibitory effect on Staphylococcus aureus and not so strong inhibitory effects against the other four organisms. The MIC ranges from 12.4 to 26 mg/mL with zones of inhibition ranges from 18 to 25 mm | [91] |
Leaf Extract | Ethanolic extract | Polyphenols tannins, terpenoids | Estimation of antimicrobial activities of ethanolic leaf extracts of mango and its use in bio control of food spoilage microorganisms |
Ethanolic extracts of mango leaves had the best MIC against E. coli (6.25 mg/mL), P. aeruginosa (12.5 mg/mL) and S. aureus, L. casei and Listeria monocytogenes (25 mg/mL) | [92] |
Hepatoprotective and anti-obesity activities | |||||
Young leaves of var. Ubá from Zona da Mata area, Brazil | water | Mangiferin | In-vivo (male Wistar rats, weight = 200 ± 50 g, age = 60 days, fed a high-fat diet) | Application of MLT (25 mL/day for 8 weeks) supressed the increase in weight, maintained lower levels oftriacylglycerols, alanine aminotransferase, and total cholesterol. Alters the gene expression, i.e., reduced expression of NF-κB p65 and activated PPARα expression, which exhibited hepatoprotective activity |
[74] |
Fresh leaves of mango cultivars were collected from Krishnagiri, India | Methanolic | 3β-taraxerol | In-vitro pancreatic cholesterol esterase inhibition assay for bioactivity guided fractionation (BAGF) |
3β-taraxerol (IC50 value = 0.86 µg ml−1) exhibited hypocholesterol activity |
[75] |
Fresh leaves of Mangifera indica L. var. Sindoora were obtained from Krishnagiri, India | Methanolic | 3β-taraxerol, mangiferin, and iriflophenone-3-C-β-glucoside | In-vivo Male albino Wistar rats |
Application of MLE from 21th day to 42th day (90 mg/kg) under six weeks of study significantly reduces plasma triglycerides. | [77] |
Fresh leaf samples of Mangifera indica L. var Ataulfo were obtained from San Blas, Nayarit, Mexico | Methanolic | Mangiferin | In-vivo Male Wistar rats (8-week-old) |
Application of MLE (200 mg/kg) significantly reduces level of cholesterol and triglycerides and enhanced HDL level | [78] |