Antidiabetic Activity of Diospyros mespiliformis on Alloxan-Induced Diabetic Rats
Abstract
The rate of morbidity and mortality attributed to diabetes has become a concern and challenge for individuals and governments. The availability, affordability, and efficacy of plant-based drugs make them an attractive choice for diabetic management in low-income countries and rural communities. Thus, their application in folkloric medicine for diabetic management. This study investigated the antidiabetic activity of the crude ethanol extract (CRE), ethyl acetate (EAF), and aqueous (AQF) fractions Diospyros mespiliformis (DM) in alloxan-induced diabetic rats to justify its acclaimed applications in folkloric medicine. The effect of the plant extract and its fractions on the aspartate aminotransferase, glutamyl aminotransferase, albumin, urea, creatinine, electrolytes, and lipid profile was determined by biochemical assay methods. The result showed a significant (p < 0.05) decrease in fasting blood glucose for all the extracts, while the aspartate aminotransferase, gamma-glutamyl transferase, and albumin were significantly (p < 0.05) decreased in the EAF only. The urea and creatinine levels of the CRE and AQF were decreased significantly (p < 0.05), while K+, Cl-, and HCO3- levels decreased significantly (p < 0.05) for the treatment groups. Furthermore, a significant (p < 0.05) decrease in total cholesterol and triglyceride was observed for the EAF. Conclusively, DM exhibited significant hypoglycemic and hypolipidemic potential with improved lipid profile and hepato-renal function. Thus, the observed antidiabetic activity of the plant might justify its acclaimed utilization in the treatment/management of diabetes and its related ailment.
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American Diabetes Association Professional Practice Committee. 2022. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes—2022. Diabetes Care. 45(Supplement_1):S17-S38. https://pubmed.ncbi.nlm.nih.gov/34964875/
Sun H, Saeedi P, Karuranga S, Pinkepank M, Ogurtsova K, Duncan BB, et al., 2022. IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Res Clin Pract. 183:109119. https://pubmed.ncbi.nlm.nih.gov/34879977/
American Diabetes Association. 2020. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes—2020. Diabetes Care. 43(Supplement_1):S98-S110. https://pubmed.ncbi.nlm.nih.gov/36507650/
Dahiru MM, Nadro SM. 2022. A review of the Mechanisms of Action and Side Effects of Antidiabetic Agents. Trends in Pharmaceutical Sciences. 8(3):195-210. https://doi.org/10.30476/tips.2022.95931.1153
Sani S, Aliyu B, Haruna M, Yahya SM, Yakasai MA, Hayatu LW, et al., 2019. Local plants and diabetes management; folkloric practices in Metropolitan Kano, Nigeria. Bayero Journal of Pure and Applied Sciences. 12(1):268-273. https://www.ajol.info/index.php/bajopas/article/view/194723
Dahiru MM. 2023. Recent advances in the therapeutic potential phytochemicals in managing diabetes. Journal of Clinical and Basic Research. 7(1):13-20.
Gurumallu SC, AlRamadneh TN, Sarjan HN, Bhaskar A, Pereira CMF, Javaraiah R. 2022. Synergistic hypoglycemic and hypolipidemic effects of ω-3 and ω-6 fatty acids from Indian flax and sesame seed oils in streptozotocin-induced diabetic rats. Phytomedicine Plus. 2(3):100284. https://doi.org/10.1016/j.phyplu.2022.100284
Bindu J, Narendhirakannan RT. 2018. Role of medicinal plants in the management of diabetes mellitus: a review. 3 Biotech. 9(1):4. https://pubmed.ncbi.nlm.nih.gov/30555770/
Deyno S, Eneyew K, Seyfe S, Wondim E. 2021. Efficacy, safety and phytochemistry of medicinal plants used for the management of diabetes mellitus in Ethiopia: a systematic review. Clinical Phytoscience. 7(1):16. https://doi.org/10.1186/s40816-021-00251-x
Mohammed A, Tajuddeen N. 2022. Antidiabetic compounds from medicinal plants traditionally used for the treatment of diabetes in Africa: A review update (2015–2020). South African Journal of Botany. 146:585-602. https://doi.org/10.1016/j.sajb.2021.11.018
Aminu SA, Ibrahim Y, Ismail HA, Ibrahim IO. 2021. Medicinal and Traditional Utilization of African Ebony (Diospyros mespiliformi): A Review. Int J Curr Microbiol App Sci. 10(06):811-817. https://doi.org/10.20546/ijcmas.2021.1006.086
Negbenebor H, Shehu K, Mukhtar Mairami F, Adeiza Z, Salisu N, Fagwalawa L. 2017. Ethnobotanical Survey of Medicinal Plants Used by Hausa People in the Management of Diabetes Mellitus in Kano Metropolis, Northern Nigeria. European Journal of Medicinal Plants. 18:1-10. 10.9734/EJMP/2017/28562
Abba A, Dogara AM. 2021. Ethnomedicinal survey of plants used for management of inflammatory diseases in Ringim local government, Jigawa state, Nigeria. Ethnobotany Research and Applications. 22:1-27. https://ethnobotanyjournal.org/index.php/era/article/view/3127
Norwegian National Research Ethics Committees. Ethical Guidelines for the Use of Animals in Research. Oslo, Norway: The Norwegian National Committee for Research Ethics in Science and Technology; 2018. Available from: https://www.forskningsetikk.no/en/guidelines/science-and-technology/ethical-guidelines-for-the-use-of-animals-in-research/
Ighodaro OM, Adeosun AM, Akinloye OA. 2017. Alloxan-induced diabetes, a common model for evaluating the glycemic-control potential of therapeutic compounds and plants extracts in experimental studies. Medicina. 53(6):365-374. https://pubmed.ncbi.nlm.nih.gov/29548636/
Reitmann S. 1957. Colorimetric method for the determination of serum glutamic pyruvate and glutamic oxaaloacetate transaminase. Amer J Clin Path. 28:56. https://pubmed.ncbi.nlm.nih.gov/13458125/
Szasz G. 1969. A kinetic photometric method for serum γ-glutamyl transpeptidase. Clin Chem. 15(2):124-136. https://doi.org/10.1093/clinchem/15.2.124
Grant GH. 1987. Amino acids and proteins (Fundamentals of clinical chemistry) 3th edition ed. Philadelphia, USA: WB Saunders Company. 104-134 p.
Chaney AL, Marbach EP. 1962. Modified reagents for determination of urea and ammonia. Clin Chem. 8(2):130-132. https://pubmed.ncbi.nlm.nih.gov/13878063/
Bartels H, Böhmer M, Heierli C. 1972. Serum creatinine determination without protein precipitation. Clinica chimica acta; international journal of clinical chemistry. 37:193-197. https://pubmed.ncbi.nlm.nih.gov/5022083/
Stein EA. 1987. Lipids, lipoproteins and apolipoproteins. 3rd Edn. ed. Philadelphia, USA: W.B Sauders 809-861 p.
McGowan MW, Artiss JD, Strandbergh DR, Zak B. 1983. A peroxidase-coupled method for the colorimetric determination of serum triglycerides. Clin Chem. 29(3):538-542. https://pubmed.ncbi.nlm.nih.gov/6825269/
Warnick GR, Albers J. 1978. A comprehensive evaluation of the heparin–manganese precipitation procedure for estimating high density lipoprotein cholesterol. J Lipid Res. 19(1):65-76. https://doi.org/10.1016/S0022-2275(20)41577-9
Friedewald WT, Levy RI, Fredrickson DS. 1972. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 18(6):499-502. https://pubmed.ncbi.nlm.nih.gov/4337382/
Perry BD, Caldow MK, Brennan-Speranza TC, Sbaraglia M, Jerums G, Garnham A, et al., 2016. Muscle atrophy in patients with Type 2 Diabetes Mellitus: roles of inflammatory pathways, physical activity and exercise. Exerc Immunol Rev. 22:94. https://pubmed.ncbi.nlm.nih.gov/26859514/
De Silva NMG, Borges MC, Hingorani AD, Engmann J, Shah T, Zhang X, et al., 2019. Liver function and risk of type 2 diabetes: bidirectional Mendelian randomization study. Diabetes. 68(8):1681-1691. https://pubmed.ncbi.nlm.nih.gov/31088856/
Wan J-Y, Yang L-Z. 2022. Liver enzymes are associated with hyperglycemia in diabetes: A three-year retrospective study. Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy.545-555. https://doi.org/10.2147/DMSO
Higgins C. 2016. Urea and the clinical value of measuring blood urea concentration. Acutecaretesting Org.1-6. https://api.semanticscholar.org/CorpusID:41626067
Eshetu B, Worede A, Fentie A, Chane E, Fetene G, Wondifraw H, et al., 2023. Assessment of Electrolyte Imbalance and Associated Factors Among Adult Diabetic Patients Attending the University of Gondar Comprehensive Specialized Hospital, Ethiopia: A Comparative Cross-Sectional Study. Diabetes Metab Syndr Obes.1207-1220. https://doi.org/10.2147/DMSO.S404788
Veltri K, Mason C. 2015. Medication-Induced Hypokalemia. P & T : a peer-reviewed journal for formulary management. 40:185-190. https://pubmed.ncbi.nlm.nih.gov/25798039/
Yasuda K, Hayashi M, Murayama M, Yamakita N. 2016. Acidosis-Induced Hypochloremic Alkalosis in Diabetic Ketoacidosis Confirmed by The Modified Base Excess Method. The Journal of Clinical Endocrinology & Metabolism. 101(6):2390-2395. https://pubmed.ncbi.nlm.nih.gov/27050945/
Bhowmik B, Siddiquee T, Mujumder A, Afsana F, Ahmed T, Mdala IA, et al., 2018. Serum lipid profile and its association with diabetes and prediabetes in a rural Bangladeshi population. International journal of environmental research and public health. 15(9):1944. https://api.semanticscholar.org/CorpusID:52182979
DOI: https://doi.org/10.18196/jfaps.v5i1.19798
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