Sandech Nichawadee, Jangchart Rawipa, Komolkriengkrai Manaras, Boonyoung Piyakorn, Khimmaktong Wipapan
Department of Anatomy, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
Exp Ther Med. 2021 Dec;22(6):1420. doi: 10.3892/etm.2021.10855. Epub 2021 Oct 11.
The brain is a vital organ that requires a constant blood supply. Stroke occurs when the blood supply to specific parts of the brain is reduced; diabetes is an autonomous risk factor for stroke. The present study aimed to investigate the potential vascular protective effect of gymnemic acid (GM) by assessing the morphological changes of microvasculature, along with VEGFA and angiopoietin-1 (Ang-1) protein expression in the brains of diabetic rats. Rats were divided into five groups, including control, gymnemic control rats (CGM), rats that were rendered diabetic by single injection of 60 mg/kg streptozotocin (STZ), diabetic rats treated with 400 mg/kg GM (STZ + GM) and diabetic rats treated with 4 mg/kg glibenclamide (GL; STZ + GL). After 8 weeks, brain tissues were collected to examine the three-dimensional morphology of the anterior cerebral arteries by vascular corrosion casting. Western blotting was performed to determine VEGFA and Ang-1 expression. Cerebral arteries, arterioles and capillaries were depicted the diameter, thickness and collagen accumulation of the wall, and the results demonstrated narrow diameters, thickened walls and collagen accumulation in the STZ group. After receiving GM, the histopathological changes were similar to that of the control group. Through vascular corrosion casting and microscopy, signs of vessel restoration and improvement were exhibited by increased diameters, and healthy and nourished arterioles and capillaries following treatment with GM. Furthermore, VEGF expression and Ang-1 secretion decreased in the STZ + GM group compared with STZ rats. The results of the present study revealed that GM treatment decreased blood vessel damage in the brain, suggesting that it may be used as a therapeutic target for the treatment of diabetes.
大脑是一个需要持续血液供应的重要器官。当大脑特定部位的血液供应减少时就会发生中风;糖尿病是中风的一个独立风险因素。本研究旨在通过评估微血管的形态变化以及糖尿病大鼠大脑中血管内皮生长因子A(VEGFA)和血管生成素-1(Ang-1)蛋白的表达,来研究匙羹藤酸(GM)潜在的血管保护作用。将大鼠分为五组,包括对照组、匙羹藤酸对照大鼠(CGM)、单次注射60 mg/kg链脲佐菌素(STZ)致糖尿病的大鼠、用400 mg/kg GM治疗的糖尿病大鼠(STZ + GM)和用4 mg/kg格列本脲(GL;STZ + GL)治疗的糖尿病大鼠。8周后,收集脑组织,通过血管铸型法检查大脑前动脉的三维形态。进行蛋白质印迹法以测定VEGFA和Ang-1的表达。描绘了大脑动脉、小动脉和毛细血管壁的直径、厚度和胶原积累情况,结果显示STZ组的血管直径变窄、壁增厚且有胶原积累。给予GM后,组织病理学变化与对照组相似。通过血管铸型法和显微镜检查,GM治疗后血管直径增加,小动脉和毛细血管健康且营养良好,显示出血管恢复和改善的迹象。此外,与STZ大鼠相比,STZ + GM组的VEGF表达和Ang-1分泌减少。本研究结果表明,GM治疗可减少大脑血管损伤,提示其可能作为治疗糖尿病的一个治疗靶点。