In Vitro Antioxidant and Antidiabetic Potentials of the Seed, Bark and Whole Pod of Okra (<i>Abelmoschus esculentus</i> (L.) Moench): A Comparative Study

Authors

  • Olorunfemi R. Molehin Department of Biochemistry, Faculty of Science, Ekiti State University, Ado-Ekiti, P.M.B. 5363 Ado-Ekiti, 360001, Nigeria.
  • Oluwakemi V. Adeleke Biochemistry Unit, Department of Science Laboratory Technology, Faculty of Science, Ekiti State University, Ado-Ekiti, P.M.B. 5363 Ado-Ekiti, 360001, Nigeria
  • Stephen A. Adefegha Functional and Nutraceutical Unit, Department of Biochemistry, Federal University of Technology Akure, P.M.B. 704 Akure, 340001, Nigeria
  • Adeyemi O. Adeola School of Nursing, Jos, Plateau State College of Nursing Sciences, Vom, P.M.B. 07, Vom, Nigeria
  • Adeniyi S. Ohunayo Biotechnology Unit, Department of Science Laboratory Technology, Faculty of Science, Ekiti State University, Ado-Ekiti, P.M.B. 5363 Ado-Ekiti, 360001, Nigeria

DOI:

https://doi.org/10.26538/tjnpr/v8i2.38

Keywords:

Nutraceuticals, Enzyme inhibition, Antioxidant, Anti-hyperglycemic

Abstract

Okra is an indigenous vegetable consumed for its sliminess and nutritional benefits. The aim of this study was to assess and compare the in vitro antioxidant, and antidiabetic activities of the seed, bark and whole pod of okra. The total phenolic and total flavonoid contents of the different parts were evaluated according to standard methods. The antioxidant capacity was assessed using the 1,1-diphenyl-2-picrylhdrazyl (DPPH), hydroxyl (OH), and 2,2-azino-bis (3-ethylbenzthiazoline-6-sulphoric acid) (ABTS) radical scavenging assays, ferric reducing antioxidant power (FRAP) assay, and ferrous ion-induced lipid peroxidation assay using standard procedures. The in vitro antidiabetic activity was evaluated using the α-amylase, and α-glucosidase inhibitory assays. The whole okra pod exhibited a significantly higher total phenolic content (5.0 mg GAE/g) and enhanced radical scavenging activity compared to both the seed and bark of the pod (p < 0.05). Although, the seed had a higher content of total flavonoid (2.23 mg QE/g) than the bark and whole pod, the bark and whole pod of okra showed a higher ferric reducing antioxidant power than the seed. Similarly, the whole pod showed a higher lipid peroxidation inhibition, and higher α-glucosidase inhibitory activity than the bark and seed of the pod. In order to enjoy all the nutritional and pharmacological benefits associated with okra consumption, it is recommended that no part of the pod should be considered a waste.

References

Rana A, Samtiya M, Dhewa T, Mishra V, Aluko RE. Health benefits of polyphenols: A concise review. J Food Biochem. 2022; 46(10):e14264.

Olaiya CO, Soetan KO, Esan AM. The role of nutraceuticals, functional foods and value-added food products in the prevention and treatment of chronic diseases. Afr J Food Sci. 2016; 10(10):185-193.

Lawal OM, Idowu-Adebayo F, Enujugha VN. Nutritional assessment of Nigerian ethnic vegetable soups (Marugbo, Tete and Ila). J Nutr Food Lipid Sci. 2018; 1:32-39.

Fagbemi TN and Oluwajuyitan TD. Food safety and value addition: a panacea to food security and wealth creation in emerging countries of sub-Sahara Africa (SSA)– Nigeria in focus, in: Strategies and Tactics of Sustainable Agriculture in the Tropics, College Press & Publishers Ibadan, Oyo State, Nigeria, 2020; 61-72 p.

Ogie-Odia EA, Mensah JK, Ehilen OE, Eseigbe DA. Nutrient, mineral and phytochemical properties of selected underutilized Amaranthus vegetable species in Ekpoma, Edo state, Nigeria. Niger J Biotechnol. 2022; 38(1):1-12.

Gong X, Huang X, Yang T, Wen J, Zhou W, Li J. Effect of drying methods on physicochemical properties and antioxidant activities of okra pods. J Food Proc Preserv. 2019; 43(12):e14277.

Davies R. Some physical properties of okra fruits and seeds. Int J Res Stud Sci Engineer Technol. 2020; 8(1):23-29.

Rathod V and Kavya DO. Breeding of Okra for Resistance to Yellow Vein Mosaic Virus. Int J Plant Soil Sci. 2023; 35(20):954-965.

Dantas TL, Alonso Buriti FC, Florentino ER. Okra (Abelmoschus esculentus L.) as a potential functional food source of mucilage and bioactive compounds with technological applications and health benefits. Plants. 2021; 10(8):1683.

Petropoulos S, Fernandes Â, Barros L, Ferreira I. Chemical composition, nutritional value and antioxidant properties of Mediterranean okra genotypes in relation to harvest stage. Food Chem. 2018; 242: 466-474.

Devi N. Evaluation for Heterosis in Okra (Abelmoschus esculentus L.) Moench). Int J Pure Appl Biosci. 2017; 5(6):590-593.

Islam MT. Phytochemical information and pharmacological activities of Okra (Abelmoschus esculentus): A literature-based review. Phytother Res. 2019; 33:72-80.

Zhang T, Xiang J, Zheng G, Yan R, Min X. Preliminary characterization and anti-hyperglycemic activity of a pectic polysaccharide from okra (Abelmoschus esculentus (L.) Moench.). J Funct Foods 2018; 41:19-24.

Shen D-D, Li X, Qin Y-L, Li M-T, Han Q-H, Zhou J, Lin S, Zhao L, Zhang Q, Qin W, Wu DT. Physicochemical properties, phenolic profiles, antioxidant capacities, and inhibitory effects on digestive enzymes of okra (Abelmoschus esculentus) fruit at different maturation stages. J Food Sci Technol. 2019; 56(3):1275-1286.

Olawuyi IF and Lee WY. Structural characterization, functional properties and antioxidant activities of polysaccharide extract obtained from okra leaves (Abelmoschus esculentus). Food Chem. 2021; 354:129437.

Khan S, Rafi Z, Baker A, Shoaib A, Alkhathami AG, Asiri M, Alshahrani MY, Ahmad I, Alraey Y, Hakamy A, Saeed M. Phytochemical screening, nutritional value, anti-diabetic, anti-cancer, and anti-bacterial assessment of aqueous extract from Abelmoschus esculentus pods. Proc. 2022; 10(2):183.

Hayaza S, Darmanto W, Wahyuningsih SP, Susilo RJ, Husen SA, Winarni D, Doong RA. Immunomodulatory activity of G Levels, and cell apoptosis in DEN-induced mice. Res J Pharm Technol. 2022; 15(2):546-550.

Khan S, Rafi Z, Baker A, Shoaib A, Alkhathami AG, Asiri M, et al. Phytochemical screening, nutritional value, anti-diabetic, anti-cancer, and anti-bacterial assessment of aqueous extract from Abelmoschus esculentus Pods. Proc. 2022; 10(2):183.

Panighel G, Ferrarese I, Lupo MG, Sut S, Dall'Acqua S, Ferri N. Investigating the in vitro mode of action of okra (Abelmoschus esculentus) as hypocholesterolemic, anti-inflammatory, and antioxidant food. Food Chemistry: Mol Sci. 2022; 5:100126.

Wahyuningsih SPA, Savira NII, Anggraini DW, Winarni D, Suhargo L, Kusuma BWA, Nindyasari F, Setianingsih N, Mwendolwa AA. Antioxidant and nephroprotective effects of okra pods extract (Abelmoschus esculentus L.) against lead acetate-induced toxicity in mice. Scientifica (Cairo). 2020; 2020:4237205.

Oboh G, Akinyemi JA, Ademiluyi AO, Adefegha SA. Inhibitory effect of aqueous extract of two varieties of Ginger on Key Enzymes linked with Type-2 Diabetes. J Food Nutr Res. 2010; 49(1):14-20.

Singleton VL, Orthofor R, Lamuela-Raventos RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin–Ciocaltau reagent. Meth Enzymol. 1999; 299:152-178.

Meda A, Lamien CE, Romito M, Millogo J, Nacoulma OG. Determination of the total phenolic, flavonoid and proline contents in Burkina Fasso honey, as well as their radical scavenging activity. Food Chem. 2005; 91(3):571-577.

Gyamfi MA, Yonamine M, Aniya Y. Free-radical scavenging action of medicinal herbs from Ghana Thonningia sanguinea on experimentally-induced liver injuries. Gen Pharmacol. 1999; 32(6): 661-667.

Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Rad Biol Med. 1999; 26(9-10):1231-1237.

Pulido R, Bravo L, Saura-Calixto F. Antioxidant activity of dietary polyphenols as determined by a modified ferric reducing/antioxidant power assay. J Agri Food Chem 2000; 48(8):3396-3402.

Halliwell B and Gutteridge JMC. Formation of a thiobarbituric-acid-reactive substance from deoxyribose in the presence of iron salts: the role of superoxide and hydroxyl radicals. FEBS Lett. 1981; 128(2):347 - 352.

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95(2):351 - 358.

Worthington V. Alpha amylase, In: Worthington K. and Worthington V (Edition), Worthington enzyme manual, Worthington Biochemical Corporation, Freehold, New Jersey 1993; 36 – 41 p.

Apostolidis E, Kwon YI, Shetty K. Inhibitory potential of herb, fruit, and fungal-enriched cheese against key enzymes linked to type 2 diabetes and hypertension. Innov Food Sci Emerg Technol. 2007; 8:46 - 54.

Tsimogiannis D and Oreopoulou V. Classification of phenolic compounds in plants. In: Polyphenols in plants, Academic Press. 2019; 1(01):263-284 p.

Meng XH, Liu C, Fan R, Zhu LF, Yang SX, Zhu HT, et al. Antioxidative flavan-3-ol dimers from the leaves of Camellia fangchengensis. J Agric Food Chem. 2018; 66:247 - 254.

Michalak M. Plant-derived antioxidants: Significance in skin health and the ageing process. Int J Mol Sci. 2022; 23(2):585.

Ademiluyi AO and Oboh G. Antioxidant properties of methanolic extracts of mistletoes (Viscum album) from cocoa and cashew trees in Nigeria. Afr J Biotechnol. 2008; 7(17):3138 - 3142.

Gangwar M, Gautam MK, Sharma AK, Tripathi YB, Goel RK, Nath G. Antioxidant capacity and radical scavenging effect of polyphenol rich Mallotus philippenensis fruit extract on human erythrocytes: An in vitro study. Sci World J. 2014; 2014:279451.

Afolabi OB, Oloyede OI, Agunbiade SO. Inhibitory potentials of phenolic-rich extracts from Bridelia ferruginea on two key carbohydrate-metabolizing enzymes and Fe2+-induced pancreatic oxidative stress. J Integr Med. 2018; 16(3):192-198.

Adefegha SA, Oboh G, Ejakpovi II, Oyeleye SI. Antioxidant and antidiabetic effects of gallic and protocatechuic acids: A structure-function perspective. Comp Clin Pathol. 2015; 24(6):1579-1585.

Ademosun AO and Oboh G. Anticholinesterase and antioxidative properties of water-extractable phytochemicals from some citrus peels. J Basic Clin Physiol Pharmacol. 2014; 25(2):99 - 204.

Adetuyi FO, Karigidi KO, Akintimehin ES, Adeyemo ON. Antioxidant properties of Ageratum conyzoides L. Asteraceae leaves. Bangladesh J Sci Ind Res. 2018; 53(4):265 - 276.

Gong L, Feng D, Wang T, Ren Y, Liu Y, Wang J. Inhibitors of α‐amylase and α‐glucosidase: Potential linkage for whole cereal foods on prevention of hyperglycemia. Food Sci Nutr. 2020; 8(12):6320-6337.

Abbas AY, Muhammad I, AbdulRahman MB, Bilbis LS. Antioxidant effect of ex-maradi okra fruit variety (Abelmuscus esculentus) on alloxan-induced diabetic rats. Trop J Nat Prod Res. 2020; 4(3):105-112.

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Published

2024-03-02

How to Cite

Molehin, O. R., Adeleke, O. V., Adefegha, S. A., Adeola, A. O., & Ohunayo, A. S. (2024). In Vitro Antioxidant and Antidiabetic Potentials of the Seed, Bark and Whole Pod of Okra (<i>Abelmoschus esculentus</i> (L.) Moench): A Comparative Study. Tropical Journal of Natural Product Research (TJNPR), 8(2), 6451–6456. https://doi.org/10.26538/tjnpr/v8i2.38