In vitro Antidiabetic Activity and Sub-chronic Toxicity Profile of Ethanol Extract of Tephrosia bracteolata Leaves

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Precious A. Idakwoji
Mercy Oguche
Fatima A. Sule
Wisdom O. Oniwon
Isaac E. Shaibu
Emmanuel Edegbo
Andrew O. Onoja
Ileje I. Ukwubile

Abstract

Tephrosia bracteolata Guill. & Perr. (Fabaceae) has been used crudely in Nigeria for the treatment of diabetes. This study was carried out to determine the antidiabetic activity, possible mechanism of action through the inhibition of the activities of α-amylase and α-glucosidase, and also to establish its safety. Sub-chronic toxicological studies involved distributing Wistar rats into 4 groups of 6 rats each. Group one served as control and received 5 mL/kg distilled water while groups 2 to 4 received 500, 1000 and 2000 mg/kg of ethanol extract of Tephrosia bracteolata (EETB) respectively for 30 days. Food and water intake, and body weight of the rats were monitored for 30 days after which, the rats were sacrificed and blood samples collected for biochemical and haematological analysis. The organs were also harvested for histopathological examination. EETB exhibited concentration-dependent inhibitory effects on both α-amylase and α-glucosidase. The extract had IC50 values of 92.76 and 71.09 μg/mL for α- amylase and α- glucosidase respectively. These values were higher than that of the standard drug - acarbose which had IC50 values of 83.13 and 64.58 μg/mL for α-amylase and α-glucosidase respectively. The sub-chronic toxicity revealed that EETB had no significant (p > 0.05) effects on the biochemical and haematological parameters, and the organs of the rats. Based on these findings, it can be suggested that EETB has antidiabetic activity and possible mechanism of action through the inhibition of α-amylase and α-glucosidase enzymes. It can also be accepted that is safe due to anecdotal reports.

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Idakwoji, P. A., Oguche, M., Sule, F. A., Oniwon, W. O., Shaibu, I. E., Edegbo, E., Onoja, A. O., & Ukwubile, I. I. (2024). In vitro Antidiabetic Activity and Sub-chronic Toxicity Profile of Ethanol Extract of Tephrosia bracteolata Leaves. Tropical Journal of Natural Product Research (TJNPR), 8(4), 7012-7019. https://doi.org/10.26538/tjnpr/v8i4.37
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How to Cite

Idakwoji, P. A., Oguche, M., Sule, F. A., Oniwon, W. O., Shaibu, I. E., Edegbo, E., Onoja, A. O., & Ukwubile, I. I. (2024). In vitro Antidiabetic Activity and Sub-chronic Toxicity Profile of Ethanol Extract of Tephrosia bracteolata Leaves. Tropical Journal of Natural Product Research (TJNPR), 8(4), 7012-7019. https://doi.org/10.26538/tjnpr/v8i4.37

References

Satyanaranyana N, Chinni SV, Gobinath R, Sunitha P, Uma Sankar A, Muthuvenkatachalam BS. Anti-diabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats. Front Nutr. 2022; 9:1-11.

International Diabetes Federation (IDF). IDF Diabetes atlas, 8th ed. Brussels, Belgium. 2017. https://www.diabetesatlas.org

Sudirman S, Pujiastuti N, Janna M, Indah Widiastuti H. Antihyperlipidemic Activity of Purified Polyphenol Extracted from Water Lettuce (Pistia stratiotes) Leaf: An In Vitro Analysis. Trop J Nat Prod Res. 2023; 7:3177-3181.

Sipahutar H, Adrana YDL, Prasetya E. Antidiabetic Potentials of Ethanol Extract of Timonius flavescens (Jacq.) Baker Leaf. Trop J Nat Prod Res. 2023; 7:2115-2121.

Zanzabil KZ, Hossain MS, Hasan MK. Diabetes mellitus Management: An Extensive Review of 37 Medicinal Plants. Diabetol. 2023; 4:186-234.

Gbolade AA. Inventory of antidiabetic plants in selected districts of Lagos State, Nigeria. J Ethnopharmacol. 2009; 121:135-139.

Natarajan V, Smith AA, Vishwanath BA. Antidiabetic Activity of Phenolic Compounds from Drega volubilis (Benth) Leaves in Streptozotocin- induced Diabetic Rats. Global J. Pharmacol. 2020; 14: 1- 7.

Dalziel JM. The useful plants of West Tropical Africa. London: The Crown Agents for the Colonies, 1937: 52- 560.

Hutchinson J, Dalziel JM. Flora of West Tropical Africa. London: Crown Agents for Oversea Governments and Administrations. 1958; pp 158.

Burkill HM. The useful plants of West Tropical Africa. Royal Botanical Gardens Kew. 1985; 1: 319.

Onaolapo MAO, Nzelibe HC, Aduadi AO, Ayo JO. Toxicity and antipyretic studies of the crude extract of Tephrosia bracteolata leaves. J. Phytomed Therapeut. 2009; 9: 91- 100.

Egharevba GO, Dosumu OO, Oguntoye SO, Njinga NS, Dahunsi SO, Hamid AA, Anand A, Amtul Z, Ujjukuri P. Antidiabetic, antioxidant and antimicrobial activities of extracts of Tephrosia bracteolata leaves. Heliyon. 2019; 5: e02275.

Idakwoji PA, Ekpo DE, Joshua PE, Njoku OU, Nwodo OFC. Ethanol extract of Tephrosia bracteolata leaves and its fractions ameliorates alloxan-induced diabetes and its associated complications in Wistar rat model. Int. J. Diabetes Dev. Ctries. 2021a; 3: 456-468

Idakwoji PA, Joshua PE, Asamodu RO, Njoku OU, Nwodo OFC. Antidiabetic activity, phytochemical and proximate compositions of different extracts of Tephrosia bracteolata leaves. Asian J. Plant Sci. 2021b; 20:291-299.

Akter S Ali H, Shati AA, Alfaifi MY, Elbehairi SEI, Sayyed RZ, Yeasmin T. Antidiabetic Activity of Methanolic Extract of Hibiscus sabdariffa Linn. Fruit in Alloxan-induced Swiss Albino Diabetic Mice. Open Agric. 2024; 9:2022-2043.

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.

Maphosa V, Masika PJ, Moyo B. Toxicity evaluation of the aqueous extract of the rhizome of Elephantorrhiza elephantia (Burch). Skeels. (Fabaceae) in rats. Food Chem Toxicol. 2010; 48: 196.

Dacie JC, Lewis SM. Practical hematology. 5th ed. London: Churchill Livingstone. 1991: 152-158.

Reitman S, Frankel S. Method of alanine and aspartate aminotransferase determination. Am. J. Clin. Pathol. 1957; 28: 56-58.

Kind PRN, King FJ. Estimation of plasma phosphatase by determination of hydrolysed phenol with amino-antipyrine. J. Clin. Pathol. 1954; 7: 322- 326.

Jendrassik L, Grof P. Simplified Photometric Methods for the Determination of Bilirubin. Biochem. J. 1938; 297: 81-89.

Doumas BT. Standards for total serum protein assays - a collaboration study. Clin. Chem. 1975; 21: 1159-1166.

Spencer K, Price CP. Determination of serum albumin using bromoscresol techniques. Ann. Clin. Biochem. 1971;14: 105-115.

Wassan KM. Najafi S, Wong J, Kwong M. Assessing plasma lipid levels, body weight, and hepatic and renal toxicity following chronic oral administration of a water soluble phytostanol compound FM-VP4, to gerbils. J. Pharm. Pharmaceut Scie. 2001; 4:228-234.

Crook MA. Clinical chemistry and metabolic medicine. 7th ed. London: Hodder Arnold. 2006: 426.

Draper HH, Hadley M. Malondialdehydes determination as index of lipid peroxidation. Methods Enzymol. 1990; 186: 421-431.

Aebi, H.E, 1983. Catalase. In: H.U. Bergmeyer, ed. Methods of enzymatic analysis. 3rd ed. New York: Academic Press, 673-684.

Xin Z, Waterman DF, Hemken RW, Harmon RJ. Effects of copper status on neutrophil function, superoxide dismutase, and copper distribution in steers. J Diary Sci. 1991; 74:3078-3085.

Weatherburn MW. Phenol-hypochlorite reaction for determination of ammonia. Anal. Chem. 1967; 39:971- 974.

Perone RD, Madias NE, Levey AS. Serum creatinine as an index of renal function: new insight into old concepts. Clin Chem. 1992; 38: 1933-1953.

Drury RA, Wallington A, Cameroun SR. Carlleton’s histological techniques. 4th ed. New York: Oxford University Press. 1967; 279-280.

Yu M, Gouvinhas L, Rocha J, Barros AI. Phytochemical and Antioxidant Analysis of Medicinal and Food Plants towards Bioactive Food and Pharmaceutical Resources.

Sci Rep. 2021; 11: 1-14.

Kifle ZD, Enyew EF. Evaluation of In vivo Antidiabetic, In vitro α-amylase Inhibitory, In vitro Antioxidant Activity of Leaves Crude Extract and Solvent Fractions of Bersama abyssinica Fresen (Melianthaceae). J Evid Based Integr Med. 2020; 25:1-11.

Mohammed A. Hypoglycemic Potential of African Medicinal Plants in Diabetic and Non-Diabetic Human Subjects: A Review. Clin Complement Med Pharmacol. 2023; 3:100081.

Asante DB, Wiafe, GA. Therapeutic Benefit of Vernonia amygdalina in the Treatment of Diabetes and its Associated Complications in Preclinical Studies. J Diabetes Res.2023; 6, 171-173.

Kazeem MI, Ashafa AOT. Kinetics of inhibition of carbohydrate-metabolizing enzymes and mitigation of oxidative stress by Eucomis humilis Baker bulb. Beni-Seuf Univ. J. Appl. Sci. 2017; 6: 57-63.

Kamat V, Barretto DA, Poojary B, Kumar A, Patil VB, Hamzad S. In vitro α -glucosidase and α -amylase Inhibition Study of Dihydropyrimidinones Synthesized via One-pot Biginelli Reaction in the presence of Green Catalyst. Bioorg Chem. 2024; PMID: 38183681.

Mahic SJ, More GK, Oladipo AO, Lebelo SL. In vitro α -glucosidase/α -amylase, Cytotoxicity and Radical Scavenging Potential of Hypoxis hemerocallidea Synthesized magnesium oxide Nanoparticles. Appl. Sci., 2024; 66:62

Dhubiab BE, Jaiswal S, Nair AB. Mechanism of Antidiabetic Activity of Methanolic Extract of Punica granatum Leaves in Nicotinamide/ Streptozotocin- Induced Type 2 Diabetes in Rats. Plants (Basel). 2020; 11:1609.

Azad AK, Sulaiman WMAW. Antidiabetic Effects of P. macrocarpa Ethanolic Fruit Extract in Streptozotocin-Induced Diabetic Rats. Futur J Pharm Sci. 2020; 6:57.

Yank DK, Kang HS. Antidiabetic Effect of Cotreatment with Quercetin and Resveratrol in Streptozotocin-induced Diabetic Rats. Biomol. Therapeut. 2018; 26: 130.

Andersson, K. Oxidative stress and its possible relation to lower urinary tract functional pathology. BJU Int. 2018; 121: 527-533.

Faria J, Ahmed S, Gerritsen KGF, Mihaila SM, Masereeuw R. Kidney-based in vitro models for drug-induced toxicity testing. Arch Toxicol. 2019; 93, 3397-3418.