Biswas Subrata K, Peixoto Elisa B, Souza Denise S, de Faria Jose B Lopes
Renal Pathophysiology Laboratory, Division of Nephrology, Department of Internal Medicine, Faculty of Medical Sciences, State University of Campinas, Campinas, São Paulo, Brazil.
Am J Nephrol. 2008;28(1):133-42. doi: 10.1159/000109993. Epub 2007 Oct 18.
The combination of hypertension and diabetes exacerbates renal oxidative stress. The aim of the present study was therefore to evaluate the pro-oxidant and antioxidant mechanisms responsible for the induction of renal oxidative stress in the presence of hypertension and diabetes mellitus.
Diabetes was induced in spontaneously hypertensive rats (SHR) and their genetically normotensive control Wistar-Kyoto (WKY) rats by streptozotocin at 12 weeks of age. After 10 days, pro-oxidant, antioxidant and oxidative stress parameters were evaluated in the renal tissue.
NADPH oxidase-dependent superoxide generation in the renal cortex was significantly elevated in WKY and SHR diabetic (D) groups compared to the respective control (C) groups (p < 0.005, n = 5). However, the highest level of superoxide generation was observed in the SHR-D group compared to all other groups. The expression of the gp91phox subunit of NADPH oxidase was significantly elevated in the SHR-D (p < 0.05, n = 5), but not in the WKY-D group, compared to the respective control groups. The renal cortical extracellular-superoxide dismutase level was found to be markedly decreased in the SHR groups compared to the WKY groups (p < 0.05, n = 5). The antioxidant glutathione level was found to be lower in the SHR-D (p = 0.03, n = 15), but not in the WKY-D group, compared to the respective control groups. Finally, nitrotyrosine and 8-hydroxy-2'-deoxyguanosine, markers of oxidative stress, were found to be similar in the kidneys of WKY-C and WKY-D, but were elevated in the SHR-D compared to the SHR-C group.
We therefore conclude that hypertension increases pro-oxidant generation and decreases antioxidant defense, and thereby induces renal oxidative stress in early diabetes.
高血压与糖尿病并存会加剧肾脏氧化应激。因此,本研究旨在评估在高血压和糖尿病存在的情况下,引发肾脏氧化应激的促氧化和抗氧化机制。
12周龄时,通过链脲佐菌素诱导自发性高血压大鼠(SHR)及其基因正常血压对照Wistar-Kyoto(WKY)大鼠患糖尿病。10天后,评估肾组织中的促氧化、抗氧化和氧化应激参数。
与各自的对照组相比,WKY和SHR糖尿病(D)组肾皮质中依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶的超氧化物生成显著升高(p<0.005,n=5)。然而,与所有其他组相比,SHR-D组中超氧化物生成水平最高。与各自的对照组相比,NADPH氧化酶的gp91phox亚基的表达在SHR-D组中显著升高(p<0.05,n=5),但在WKY-D组中未升高。与WKY组相比,SHR组肾皮质细胞外超氧化物歧化酶水平明显降低(p<0.05,n=5)。与各自的对照组相比,抗氧化剂谷胱甘肽水平在SHR-D组中较低(p=0.03,n=15),但在WKY-D组中未降低。最后,氧化应激标志物硝基酪氨酸和8-羟基-2'-脱氧鸟苷在WKY-C和WKY-D的肾脏中相似,但与SHR-C组相比,在SHR-D组中升高。
因此,我们得出结论,高血压会增加促氧化剂生成并降低抗氧化防御能力,从而在糖尿病早期诱发肾脏氧化应激。