Hydro-Ethanol Extract of the Aerial Parts of Secamone afzelii Ameliorates Diabetic Status of Streptozotocin-Induced Diabetic Rats
DOI:
https://doi.org/10.26538/tjnpr/v9i8.57Keywords:
Renal, Hepatic, Hematology, StreptozotocinAbstract
Diabetes mellitus as the most prevalent metabolic disease has become a global health challenge. This study evaluated the hypoglycemic potential of Secamone afzelii (Apocynaceae) aerial part extract in streptozotocin-induced diabetic rats. Four groups of five diabetic rats each were treated orally once daily for 21 days with S. afzelii extract (100 and 200 mg/kg), metformin (150 mg/kg), or normal saline (10 mL/kg), while a fifth group as non-diabetic group received distilled water. Fasting blood glucose (FBG) levels were monitored weekly, and blood samples were analyzed for serum enzymes, lipids (total cholesterol, triglycerides, HDL, LDL), hemoglobin, and blood parameters on day 21. The histopathology of the cardiac, hepatic and renal tissues was also examined. The S. afzelii extract at both doses significantly reduced glucose levels (p<0.05) of diabetic rats compared to the standard metformin after 21 days of treatment. HDL levels slightly increased (p>0.05) without altering LDL, while Triglyceride (TG) and Total Cholesterol (TC) levels were lower in extract treated groups than in metformin-treated group. Serum biomarkers of liver (ALT and AST) and kidney (creatinine and urea) were reduced in extract-treated groups when compared to untreated diabetic group. Hematological parameters, such as red and white blood cell counts, improved. Histopathology revealed that the extract restored damage to heart, liver, and kidney tissues caused by hyperglycemia. The findings demonstrate that the S. afzelii hydro-ethanolic extract exhibits notable hypoglycemic activity, improves lipid profile, and mitigates organ damage in diabetic rats. Further studies are needed to confirm its potential for antidiabetic therapy development.
References
⦁ Olatunji OJ, Zuo J, Olatunde OO. Securidaca inappendiculata stem extract confers robust antioxidant and antidiabetic effects against high fructose/streptozotocin induced type 2 diabetes in rats. Exploration of bioactive compounds using UHPLC-ESI-QTOF-MS, Arch. Physiol. Biochem., 2021 https://doi.org/10.1080/13813455.2021.1921811
⦁ International Diabetes Federation. IDF Diabetes Atlas. 11th ed. Brussels: International Diabetes Federation; 2025. https://diabetesatlas.org/
⦁ NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in diabetes prevalence and treatment from 1990 to 2022: a pooled analysis of 1108 population-representative studies with 141 million participants. Lancet. 2025; 405(10485):1146. https://doi.org/10.1016/S0140-6736(24)02317-1
⦁ Chatterjee S, Khunti K, Davies MJ. Type 2 diabetes. Lancet 2017; 389: 2239–2251.
⦁ Zheng F, Lu W, Jia C, Li H, Wang Z, Jia W. Relationships between Glucose Excursion and the Activation of Oxidative Stress in Patients with Newly Diagnosed Type 2 Diabetes or Impaired Glucose Regulation. Endocrine 2010; 37: 201–208.
⦁ Bluher M. Adipose tissue inflammation: A cause or consequence of obesity-related insulin resistance? Clin. Sci. 2016; 130: 1603–1614.
⦁ Li M, Chi X, Wang Y, ⦁ Setrerrahmane S, ⦁ Xie W, ⦁ Xu H. Trends in insulin resistance: insights into mechanisms and therapeutic strategy. Sig. Transduct. Target Ther. 2022, 7, 216. https://doi.org/10.1038/s41392-022-01073-0
⦁ Dilworth L, Facey A, Omoruyi F. Diabetes Mellitus and Its Metabolic Complications: The Role of Adipose Tissues. Int. J. Mol. Sci. 2021; 22: 7644. https://doi.org/10.3390/ijms22147644
⦁ Kumar A, Mazumder R, Rani A, Pandey P, Khurana N. Novel Approaches for the Management of Type 2 Diabetes Mellitus: An Update. Curr Diabetes Rev. 2024; 20(4):e051023221768. https://doi.org /10.2174/0115733998261903230921102620
⦁ Vaiyapuri M, Raju K, Karuppusamy S. Preliminary phytochemical investigation on Secamone emetic (Retz.) R. Br. (Apocynaceae)– Anendemic medicinal plant species of southern India. J. Pharmacogn. Phytochem. 2015; 3(6): 58-61.
⦁ Magid AA, Yao-Kouassi PA, Gossan DPA, Mairot C, Voutquenne-Nazabadioko L. New Antioxidant Flavonoids from the Aerial Parts of Secamone afzelii. J. Antioxid. Act. 2016; 1(2): 8-16.
⦁ Abo KA, Fred-Jaiyesimi AA, Jaiyesimi AEA. Ethnobotanical studies of medicinal plants used in the management of diabetes mellitus in South Western Nigeria. J. Ethnopharmacol. 2008; 115: 67–71.
⦁ Ajiboye BO, Oyinloye BE, Essien PE, Oninanni SA, Ojo OA, Kappo AP. Ameliorative potential of sterculia tragacantha aqueous extract on renal gene expression and biochemical parameters in streptozotocin-induced diabetic rats. J. Pharm. Investig. 2021; 51: 103–113. https://doi.org/10.1007/s40005-020-00506-8
⦁ Onikanni AS, Lawal B, Oyinloye BE, Mostafa-Hedeab G, Alorabi M, Cavalu S, Olusola AO, Wang C, Batiha GE. Therapeutic efficacy of Clompanus pubescens leaves fractions via downregulation of neuronal cholinesterases/Na+-K+ATPase/IL-1 β, and improving the neurocognitive and antioxidants status of streptozotocin-induced diabetic rats. Biomed. Pharmacoth. 2022; 148: 112730. https://doi.org/10.1016/j.biopha.2022.112730
⦁ Fageyinbo MS, Akindele AJ, Falade J, Agbaje EO. Aqueous Root Extract of Strophanthus hispidus Demonstrates Antidiabetic Effect in Fructose-Streptozotocin-Induced Diabetic Rats. Pharmacol. Toxicol. Nat. Med. 2022; 2(3): 1-8. https://doi.org/10.52406/ptnm.v2i3.40
⦁ Ogunmoyole T, Akanni YE, Asejire IJ, Adefila AO. Antihyperglycemic and Anti-inflammatory Effects of African parquetina Leaf in Streptozotocin-Induced Diabetes in Rats. Trop. J. Nat. Prod. Res. 2025, 9(5): 2007 – 2013. https://doi.org/10.26538/tjnpr/v9i5.19
⦁ Reitman S, Frankel S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am. J. Clin. Pathol. 1957; 28(1): 56–63. https://doi.org/10.1093/ajcp/28.1.56
⦁ Roy AV. Rapid Method for Determining Alkaline Phosphatase Activity in Serum with Thymolphthalein Monophosphate. Clin. Chem. 1970; 16(5): 431–436. https://doi.org/10.1093/clinchem/16.5.431
⦁ Trinder P. Enzymatic Calorimetric Determination of Triglycerides by GOP-PAP Method. Ann. Clin. Biochem. 1969; 6: 24-27. https://doi.org/10.1177/000456326900600108
⦁ Fossati P, Prencipe L, Berti G. Use of 3,5-dichloro-2-hydroxybenzenesulfonic acid/4-aminophenazone chromogenic system in direct enzymic assay of uric acid in serum and urine. Clin. Chem. 1980; 26(2): 227–231.
⦁ Dsouza PS, Holla R, Swamy G. Effect of Adhatoda zeylanica Ethanolic Extract on Attenuated Kidney in Streptozotocin-Induced Diabetic Rats. J. Health Allied Sci. 2021; 11. https://doi.org/ 10.1055/s-0040-1722801
⦁ Akinlade OM, Owoyele BV, Soladoye AO. Streptozotocin-induced type 1 and 2 diabetes in rodents: a model for studying diabetic cardiac autonomic neuropathy. Afr. Health Sci. 2021; 21(2):719-727. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568204/
⦁ Kherouf A, Aouacheri O, Tichati L, Tebboub I, Kherouf M, Saka S. Potential antioxidant properties and anti-diabetic and hepatic/pancreatic protective effects of dietary Boswellia serrata gum resin powder against oxidative damage in streptozotocin‐induced diabetic rats. Compa. Clin. Patho. 2021; 30: 891 - 904.
⦁ Zafar M, Naqvi SN. Effects of STZ-Induced Diabetes on the Relative Weights of Kidney, Liver and Pancreas in Albino Rats: A Comparative Study. Int. J. Morphol., 2010; 28: 135-142.
⦁ Fajarwati I, Solihin DD, Wresdiyati T, Batubara I. Self-recovery in diabetic Sprague Dawley rats induced by intraperitoneal alloxan and streptozotocin. Heliyon 2023; 9(5): e15533. https://doi.org/10.1016/j.heliyon.2023.e15533
⦁ Jeong E, Baek Y, Kim HJ, Lee HG. Comparison of the anti-diabetic effects of various grain and legume extracts in high-fat diet and streptozotocin-nicotinamide-induced diabetic rats. Heliyon 2024; 10(3): e25279. https://doi.org/10.1016/j.heliyon.2024.e25279
⦁ King A. The use of animal models in diabetes research Keywords type 1 diabetes; type 2 diabetes; animal models. Br. J. Pharamacol. 2012; 166: 877–894. https://doi.org/10.1111/(ISSN)1476-5381/homepage/animal_models.htm.
⦁ Al-Nahdi AMT, John A, Raza H. Cytoprotective effects of N-acetylcysteine on streptozotocin-induced oxidative stress and apoptosis in RIN-5F pancreatic β-cells. Cell. Physiol. Biochem. 2018; 51: 201–216, https://doi.org/10.1159/000495200.
⦁ Rena G, Hardie DG, Pearson ER. The mechanisms of action of metformin. Diabetologia 2017; 60: 1577–1585. https://doi.org/10.1007/s00125-017-4342-z
⦁ Damasceno DC, Netto AO, Iessi IL, Gallego FQ, Corvino SB, Dallaqua B, Sinzato YK, Bueno A, Calderon IM, Rudge MV. Streptozotocin-induced diabetes models: pathophysiological mechanisms and fetal outcomes. BioMed. Res. Int. 2014; 819065. https://doi.org/10.1155/2014/819065
⦁ Ugwu MN, Umar IA, Utu-Baku AB, Dasofunjo K, Ukpanukpong RU, Yakubu OE, Ebong PE. Antioxidant Status and Organ Function in Streptozotocin-Induced Diabetic Rats treated with Aqueous, Methanolic and Petroleum Ether Extracts of Ocimum basilicum leaf. J. App. Pharm. Sci. 2013; 3 (4): 75-79. ⦁ https://japsonline.com/abstract.php?article_id=884⦁ &⦁ sts=2
⦁ Nagarchi K, Ahmed S, Sabus A, Saheb S. Effect of Streptozotocin on glucose levels in albino wister rats. J. Pharm. Sci. Res. 2015; 7: 67-69.
⦁ Sinan KI, Yagi S, Llorent-Martínez EJ, Ruiz-Medina A, Gordo-Moreno AI, Stefanucci A, Mollica A, Bene K, Zengin G. Understanding the Chemical Composition and Biological Activities of Different Extracts of Secamone afzelii Leaves: A Potential Source of Bioactive Compounds for the Food Industry. Molecules (Basel, Switzerland) 2023; 28(9): 3678. https://doi.org/10.3390/molecules28093678
⦁ Yerevanian A, Soukas AA. Metformin: Mechanisms in Human Obesity and Weight Loss. Curr. Obes. Rep. 2019; 8(2): 156–164. https://doi.org/10.1007/s13679-019-00335-3
⦁ Njoku OU, Chibuogwu CC, Nwodo OF. Glycemic and Biochemical Effects of Polyphenol-Rich Fraction of Parkia biglobosa Leaves in Wistar rats Experimentally Induced with Diabetes: Trop. J. Nat. Prod. Res. 2023, 7(10), 4998-5004. http://www.doi.org/10.26538/tjnpr/v7i10.40
⦁ Kitada M, Ogura Y, Koya D. Rodent models of diabetic nephropathy: their utility and limitations. Int. J. Nephrol. Renovasc. Dis. 2016; 9: 279–290
⦁ Wang C, Lv LS, Huang H, et al. Initiation time of renal replacement therapy on patients with acute kidney injury: a systematic review and meta-analysis of 8179 participants. Nephrology (Carlton) 2017; 22(1): 7–18
⦁ Ozder A. (2014). Lipid profile abnormalities seen in T2DM patients in primary healthcare in Turkey: a cross-sectional study. Lipids Health Dis. 2014; 13: 183. https://doi.org/10.1186/1476-511X-13-183
⦁ Eid S, Sas KM, Abcouwer SF, Feldman EL, Gardner TW, Pennathur S, Fort PE. New insights into the mechanisms of diabetic complications: role of lipids and lipid metabolism. Diabetologia 2019; 62(9): 1539–1549. https://doi.org/10.1007/s00125-019-4959-1
⦁ Lingaiah M, Estari M, Rao N. Potential Antidiabetic Activity and Lipid Profile Effects of Plant Extracts in diabetic induced Wistar rats. BioGecko 2023; 12(3): 5128-5136. https://doi.org/10.5281/zenodo.8032985
⦁ Wu H, Norton V, Cui K, Zhu B, Bhattacharjee S, Lu YW, Wang B, Shan D, Wong S, Dong Y, Chan SL, Cowan D, Xu J, Bielenberg DR, Zhou C, Chen H. Diabetes and Its Cardiovascular Complications: Comprehensive Network and Systematic Analyses. Front. Cardiovasc. Med. 2022; 9: 841928. https://doi.org/10.3389/fcvm.2022.841928
⦁ Abdissa D, Hirpa D. Dyslipidemia and its associated factors among adult diabetes outpatients in West Shewa zone public hospitals, Ethiopia. BMC Cardiovasc. Disord. 2022; 22: 39. https://doi.org/10.1186/s12872-022-02489-w
⦁ Iheagwam FN, Garuba PA, Ogunlana OO, Chinedu SN. Counteractive role of Terminalia catappa leaf extract on hematological and coagulation disturbance in Type 2 diabetic rats. Vet. world 2023; 16(8): 1593–1599. https://doi.org/10.14202/vetworld.2023.1593-1599
⦁ Atoe K, Idu M. The Effects of Methanolic Plant Extract on the Haematological Indices of Induced Preeclamptic Wistar Rats. Int. J. Trop. Dis. Health. 2022; 28-37. https://doi.org/10.9734/ijtdh/2022/v43i1130625
⦁ Mbaka G, Akala T. Evaluation of the Histomorphological and Toxicological Changes in Rodents after treatment with Hydroethanolic Extract of the Secamone afzelii Aerial Parts. J. Morphol. Sci. 2018; 35. https://doi.org/10.1055/s-0038-1675793
⦁ Gara H, Lingam S, Vanamali DR. A study on metformin-induced anemia using red blood cell indices and red cell distribution width. Assam J. Intern. Med. 2023; 13(2): 68-75. https://doi.org/10.4103/ajoim.ajoim_16_23
⦁
⦁ Ali A, Shaheen S, Memon Z, Agha F, Shahid M, Zahid N. Effects of Diabetogenic Agent Streptozotocin on Hematological Parameters of Wistar Albino Rats "An Experimental Study". J. Adv. Med. Med. Res. 2019; 30(5): 1-8. https://doi.org/10.9734/jammr/2019/v30i530194
⦁ Gamede M, Mabuza L, Ngubane P, Khathi A. Plant-derived oleanolic acid ameliorates markers of subclinical inflammation and innate immunity activation in diet-induced pre-diabetic rats. Ther. Adv. Endocrinol. Metab. 2020; 11: 2042018820935771. https://doi.org/10.1177/2042018820935771
⦁ Spampinato SF, Caruso GI, De Pasquale R, Sortino MA, Merlo S. The Treatment of Impaired Wound Healing in Diabetes: Looking among Old Drugs. Pharm. (Basel, Switzerland) 2020; 13(4): 60. https://doi.org/10.3390/ph13040060
⦁ Odo RI, Asuzu IU, Aba PE. The antidiabetic activities of the methanolic root bark extract of Afzelia africana in alloxan-induced diabetic mice. J. Complement. Integr. Med. 2012; 9. https://doi.org/10.1515/1553-3840.1649
⦁ Abere, Tavs & Onwukaeme, Doris. Pharmacognostic Evaluation of the Leaves of Secamone afzelii (Schult) K Schum (Asclepiadaceae). Trop. J. Pharm. Res. 2012; 11. https://doi.org/10.4314/tjpr.v11i1.16
⦁ Zhang Y, Wang H, Xiao H. Metformin Actions on the Liver: Protection Mechanisms Emerging in Hepatocytes and Immune Cells against NASH-Related HCC. Int. J. Mol. Sci. 2021; 22(9): 5016. https://doi.org/10.3390/ijms22095016
Published
Issue
Section
License
Copyright (c) 2025 Tropical Journal of Natural Product Research

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.





