Wenbin Zhou, Guojun Gao
Department of Surgery, Hospital of Weifang Medical University, Weifang, Shandong Province, PR China.
Department of Urology Surgery, Affiliated Hospital of Weifang Medical University, Weifang, Shandong Province, PR China.
West Indian Med J. 2014 Jan;63(1):20-5. doi: 10.7727/wimj.2014.008. Epub 2014 Apr 8.
This study aimed at detecting the protective effects of resveratrol on diabetes-induced renal damage and on the expression of transforming growth factor-beta 1 (TGF-β1), collagen IV and Th17/Tregrelated cytokines in streptozotocin-induced diabetic rats.
Twenty diabetic rats were further randomly divided into diabetic model group (DM group) and resveratrol group with 10 animals in each group. Another 1- non-diabetic rats served as control. The diabetic rats in the resveratrol group were administered resveratrol for eight consecutive weeks (via gavage, 50 mg/kg daily, dissolved in saline). Rats in the control group and DM group received the same volume of saline only (via gavage). Renal function was measured. Histopathology changes of the kidney tissue were observed using haematoxylin and eosin staining. Levels of TGF-β1 and collagen IV in kidney homogenate were measured with enzyme-linked immunosorbent assay (ELISA). The level of Th17-related cytokines (IL-17A, IL-25) and Treg-related cytokines (IL-35, IL-10) in serum and in the supernatant of the kidney homogenate were determined using ELISA.
Diabetic rats had damaged renal function, higher levels of TGF-β1, collagen IV, IL-17A and IL-25, as well as lower levels of IL-35 and IL-10, when compared to the control rats. Compared to the diabetic rats without resveratrol treatment, application of resveratrol to the diabetic rats ameliorated the renal function, inhibited the expression of TGF-β1, collagen IV, IL-17A and IL-25, and increased the expression IL-35 and IL-10.
Resveratrol might ameliorate diabetes-induced renal damage through mediating the balance of Th17/Treg-related cytokines and inhibiting the expression of TGF-β1 and collagen IV.
本研究旨在检测白藜芦醇对链脲佐菌素诱导的糖尿病大鼠糖尿病性肾损伤以及转化生长因子-β1(TGF-β1)、IV型胶原和Th17/Treg相关细胞因子表达的保护作用。
20只糖尿病大鼠进一步随机分为糖尿病模型组(DM组)和白藜芦醇组,每组10只动物。另外10只非糖尿病大鼠作为对照。白藜芦醇组的糖尿病大鼠连续8周给予白藜芦醇(通过灌胃,每日50mg/kg,溶于生理盐水)。对照组和DM组的大鼠仅接受相同体积的生理盐水(通过灌胃)。检测肾功能。用苏木精和伊红染色观察肾组织的组织病理学变化。用酶联免疫吸附测定(ELISA)法检测肾匀浆中TGF-β1和IV型胶原的水平。用ELISA法测定血清和肾匀浆上清液中Th17相关细胞因子(IL-17A、IL-25)和Treg相关细胞因子(IL-35、IL-10)的水平。
与对照大鼠相比,糖尿病大鼠肾功能受损,TGF-β1、IV型胶原、IL-17A和IL-25水平较高,而IL-35和IL-10水平较低。与未用白藜芦醇治疗的糖尿病大鼠相比,给糖尿病大鼠应用白藜芦醇可改善肾功能,抑制TGF-β1、IV型胶原、IL-17A和IL-25的表达,并增加IL-35和IL-10的表达。
白藜芦醇可能通过介导Th17/Treg相关细胞因子的平衡并抑制TGF-β1和IV型胶原的表达来改善糖尿病性肾损伤。