Department of Biochemistry, University of Malakand, Chakdara Dir (L), Khyber Pakhtunkhwa 18800, Pakistan.
Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Molecules. 2020 Dec 30;26(1):137. doi: 10.3390/molecules26010137.
In this study, catechin (CTN) isolated from was evaluated for in vitro antioxidant potential and inhibition of carbohydrate digestive enzymes (α-amylase and α-glucosidase). The compound was also tested for its in vivo antidiabetic potential using Sprague-Dawley rats as experimental animals. The effects of various doses of catechin in STZ (Streptozotocin) induced diabetic rats on fasting blood glucose level, body weight, lipid parameters, hepatic enzymes, and renal functions were evaluated using the reported protocols. The CTN exhibited the highest percent antioxidant for free radical scavenging activity against DPPH and ABTS free radicals, and inhibited the activity of carbohydrate digestive enzymes (with percent inhibition values: 79 ± 1.5% α-amylase and 80 ± 1.1% α-glucosidase). Administration CTN and standard glibenclamide significantly decreased the fasting blood glucose level and increased the body weight in STZ-induced diabetic rats. CTN significantly decreased the different lipid parameters, hepatic, and renal function enzyme levels along with Hb1c level in diabetic rats, while significantly increasing the high-density lipoprotein (HDL) level with values comparable to the standard glibenclamide. Further, the altered levels of glutathione and lipid peroxides of liver and kidney tissues were restored (by CTN) to levels similar to the control group. CTN significantly increased the antioxidant enzyme activities, total content of reduced glutathione, and reduced the malondialdehyde (MDA) level in rat liver and kidney tissues homogenates, and also corrected the histopathological abnormalities, suggesting its antioxidant potential.
在这项研究中,从 中分离得到的儿茶素(CTN)用于评估其体外抗氧化潜力和抑制碳水化合物消化酶(α-淀粉酶和α-葡萄糖苷酶)的活性。还使用 Sprague-Dawley 大鼠作为实验动物测试了该化合物的体内抗糖尿病潜力。根据报道的方案,评估了不同剂量儿茶素对链脲佐菌素(STZ)诱导的糖尿病大鼠空腹血糖水平、体重、脂质参数、肝酶和肾功能的影响。CTN 对 DPPH 和 ABTS 自由基的自由基清除活性表现出最高的抗氧化百分比,抑制碳水化合物消化酶的活性(抑制率分别为 79±1.5%α-淀粉酶和 80±1.1%α-葡萄糖苷酶)。CTN 和标准格列本脲给药可显著降低 STZ 诱导的糖尿病大鼠的空腹血糖水平并增加体重。CTN 可显著降低不同的脂质参数、肝和肾功能酶水平以及 Hb1c 水平,同时可显著增加高密度脂蛋白(HDL)水平,与标准格列本脲相当。此外,还恢复了(CTN)肝和肾组织中谷胱甘肽和脂质过氧化物的改变水平,使其接近对照组。CTN 可显著增加大鼠肝和肾组织匀浆中抗氧化酶活性、还原型谷胱甘肽的总含量,降低丙二醛(MDA)水平,并纠正组织病理学异常,表明其具有抗氧化潜力。