Ding Yusong, Li Haiyan, Li Yang, Liu Dandan, Zhang Liyuan, Wang Tongling, Liu Tao, Ma Long
College of Public Health, Xinjiang Medical University, Urumqi 830011, China.
Department of Public Health, Shihezi University School of Medicine, Shihezi, Xinjiang 832000, China.
Evid Based Complement Alternat Med. 2020 Sep 29;2020:5205903. doi: 10.1155/2020/5205903. eCollection 2020.
Diabetic nephropathy (DN) is the most common cause of end-stage renal failure. Grape seed proanthocyanidin extract (GSPE) is a powerful antioxidant that is believed to protect the kidney through antioxidant action. However, the underlying mechanism of GSPE protection against DN remains unclear.
To explore if GSPE can improve DN by activating nuclear factor erythroid 2-related factor 2 (Nrf2) antioxidant response element signalling and to clarify its possible mechanism. . Ten healthy Sprague-Dawley rats were randomly selected as controls. Rats with streptozotocin-induced diabetes were randomly divided into three groups (10 animals/group): type 2 diabetes mellitus (T2DM) group (untreated), L-GSPE group (treated with 125-mg/kg/day GSPE for 8 weeks), and H-GSPE group (treated with 250 mg/kg/day GSPE for 8 weeks).
Renal histopathological results indicated limited pathological damage in GSPE-treated groups. Compared with the T2DM group, the H-GSPE group had significantly reduced kidney weight and renal index. Similarly, the levels of fasting blood glucose, serum creatinine, blood urea nitrogen, uric acid, urinary albumin, and renal malondialdehyde ( < 0.05) were also significantly decreased. In addition, GSPE significantly increased the levels of superoxide dismutase, total antioxidative capability, and glutathione ( < 0.05) as well as the protein levels of Nrf2, HO-1, glutathione S-transferase, and NAD (P)H quinone oxidoreductase 1 ( < 0.05).
The results indicate that GSPE reduced renal damage in rats with diabetes by activating the Nrf2 signalling pathway, which consequently increased the antioxidant capacity of the tissue. Therefore, GSPE is a potential natural agent for the treatment of diabetic nephropathy.
糖尿病肾病(DN)是终末期肾衰竭最常见的病因。葡萄籽原花青素提取物(GSPE)是一种强大的抗氧化剂,被认为可通过抗氧化作用保护肾脏。然而,GSPE对DN保护作用的潜在机制仍不清楚。
探讨GSPE是否能通过激活核因子红细胞2相关因子2(Nrf2)抗氧化反应元件信号通路来改善DN,并阐明其可能机制。选取10只健康的Sprague-Dawley大鼠作为对照组。将链脲佐菌素诱导的糖尿病大鼠随机分为三组(每组10只动物):2型糖尿病(T2DM)组(未治疗)、低剂量GSPE组(每天用125mg/kg GSPE治疗8周)和高剂量GSPE组(每天用250mg/kg GSPE治疗8周)。
肾脏组织病理学结果显示,GSPE治疗组的病理损伤有限。与T2DM组相比,高剂量GSPE组的肾脏重量和肾指数显著降低。同样,空腹血糖、血清肌酐、血尿素氮、尿酸、尿白蛋白和肾丙二醛水平(<0.05)也显著降低。此外,GSPE显著提高了超氧化物歧化酶、总抗氧化能力和谷胱甘肽水平(<0.05)以及Nrf2、HO-1、谷胱甘肽S-转移酶和NAD(P)H醌氧化还原酶1的蛋白水平(<0.05)。
结果表明,GSPE通过激活Nrf2信号通路减轻糖尿病大鼠的肾脏损伤,从而提高组织的抗氧化能力。因此,GSPE是一种治疗糖尿病肾病的潜在天然药物。