Department of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, 1 rue Michel-Servet, Geneva 4, Switzerland.
J Endocrinol. 2010 Apr;205(1):79-86. doi: 10.1677/JOE-09-0311. Epub 2010 Jan 8.
Sclerocarya birrea is a plant widely used as traditional medication for the treatment of diabetes in sub-Saharan regions. However, the mechanism of action is unknown and only hypoglycaemic effects of S. birrea extract (SBE) in diabetic rats have been reported to date. Here, we tested aqueous extracts of S. birrea on insulin-secreting INS-1E cells and isolated rat islets. Following 24 h of treatment at 5 microg/ml, the extract markedly potentiated glucose-stimulated insulin secretion. Neither basal insulin release nor non-nutrient stimulation was affected. The potentiation of the secretory response at stimulatory glucose appeared after 12 h of treatment. No acute effects were observed and, at the effective concentration, SBE was safe regarding cell integrity and differentiation. The mechanism of action of the SBE was related to glucose metabolism as both ATP generation and glucose oxidation were enhanced following the 24-h treatment. In streptozotocin-induced diabetic rats, SBE administration corrected glycaemia and restored plasma insulin levels after 2 weeks of treatment. These data show direct action of S. birrea on insulin-secreting cells and favour further delineation for use of the plant in the management of diabetes.
叶下珠是一种在撒哈拉以南地区被广泛用作治疗糖尿病的传统药物的植物。然而,其作用机制尚不清楚,迄今为止,仅报道了叶下珠提取物(SBE)在糖尿病大鼠中具有降血糖作用。在这里,我们测试了叶下珠的水提物对胰岛素分泌细胞 INS-1E 和分离的大鼠胰岛的作用。在 5 μg/ml 下处理 24 小时后,提取物明显增强了葡萄糖刺激的胰岛素分泌。基础胰岛素释放或非营养刺激不受影响。在刺激葡萄糖时,这种分泌反应的增强发生在治疗 12 小时后。没有观察到急性作用,并且在有效浓度下,SBE 在细胞完整性和分化方面是安全的。SBE 的作用机制与葡萄糖代谢有关,因为在 24 小时处理后,ATP 生成和葡萄糖氧化都增强了。在链脲佐菌素诱导的糖尿病大鼠中,SBE 给药在 2 周的治疗后纠正了血糖,并恢复了血浆胰岛素水平。这些数据表明叶下珠对胰岛素分泌细胞有直接作用,并支持进一步研究该植物在糖尿病治疗中的应用。