Harley Benjamin Kingsley, Amponsah Isaac Kingsley, Ben Inemesit Okon, Mireku-Gyimah Nana Ama, Anokwah Daniel, Neglo David, Amengor Cedric Dzidzor K, Fleischer Theophilus Christian
Department of Pharmacognosy and Herbal Medicine, School of Pharmacy, University of Health and Allied Sciences, Ho, Ghana.
Department of Pharmacognosy, Faculty of Pharmacy and Pharmaceutical Sciences, College of Health Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Biomed Pharmacother. 2022 May;149:112833. doi: 10.1016/j.biopha.2022.112833. Epub 2022 Mar 19.
The present study evaluated the antidiabetic activities of the 70% ethanol stem bark extract of Aidia genipiflora (AGB) and one of its constituents, oleanonic acid in streptozotocin (40 mg/kg)-induced diabetic rats. In vitro assays of glucose uptake and inhibition of carbohydrate metabolizing enzymes were then used to investigate their mechanism(s) of hypoglycaemic action. In silico evaluation of the pharmacokinetic and toxicity properties of the compound was also carried out. Administration of AGB (100-400 mg/kg) and oleanonic acid (15 - 60 mg/kg) resulted in significant reductions (p < 0.001) in the blood glucose and considerable decrease (p < 0.05) in the elevated lipid parameters of the diabetic animals. AGB activity at 200 and 400 mg/kg; and oleanonic acid at 60 mg/kg were comparable to glibenclamide (5 mg/kg). The extract and its isolate strongly inhibited α-glucosidase and α-amylase activity with IC values of (10.48 ± 1.39 µg/mL and 14.51 ± 1.26 µg/mL) and (36.52 ± 1.95 µM and 105.84 ± 1.08 µM) respectively. The glucose uptake assays showed that AGB and oleanonic acid exerted both insulin-dependent and independent promotional effect of glucose transport into the periphery by upregulating the expression of PI3K and PPARγ transcripts with a concomitant increase in GLUT-4 transcripts. Although oleanonic acid was predicted to be teratogenic, it was found to be generally non-lethal with favourable pharmacokinetics properties making it suitable for further studies. The study has shown that the stem bark of A. genipiflora is a source of new hypoglycaemic agents and that oleanonic acid possesses hypoglycaemic and anti-hyperlipidaemic activities.
本研究评估了栀子香楠70%乙醇茎皮提取物(AGB)及其成分之一齐墩果酸对链脲佐菌素(40mg/kg)诱导的糖尿病大鼠的抗糖尿病活性。随后通过体外葡萄糖摄取试验和碳水化合物代谢酶抑制试验来研究它们的降血糖作用机制。还对该化合物的药代动力学和毒性特性进行了计算机模拟评估。给予AGB(100 - 400mg/kg)和齐墩果酸(15 - 60mg/kg)可使糖尿病动物的血糖显著降低(p < 0.001),并使升高的血脂参数显著下降(p < 0.05)。AGB在200和400mg/kg时的活性;以及齐墩果酸在60mg/kg时的活性与格列本脲(5mg/kg)相当。该提取物及其分离物强烈抑制α - 葡萄糖苷酶和α - 淀粉酶活性,IC值分别为(10.48 ± 1.39μg/mL和14.51 ± 1.26μg/mL)以及(36.52 ± 1.95μM和105.84 ± 1.08μM)。葡萄糖摄取试验表明,AGB和齐墩果酸通过上调PI3K和PPARγ转录本的表达,同时增加GLUT - 4转录本,对葡萄糖转运到外周发挥胰岛素依赖性和非依赖性促进作用。虽然预测齐墩果酸具有致畸性,但发现它一般无致死性,且具有良好的药代动力学特性,适合进一步研究。该研究表明,栀子香楠的茎皮是新型降血糖药物的来源,齐墩果酸具有降血糖和抗高血脂活性。