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牛磺酸可改善大鼠糖尿病肾病损伤、氧化应激相关信号通路和细胞凋亡。

Taurine ameliorates alloxan-induced diabetic renal injury, oxidative stress-related signaling pathways and apoptosis in rats.

机构信息

Division of Molecular Medicine, Bose Institute, P-1/12, CIT Scheme VII M, Kolkata 700054, India.

出版信息

Amino Acids. 2012 Oct;43(4):1509-23. doi: 10.1007/s00726-012-1225-y.

Abstract

Hyperglycemia-induced oxidative stress plays a vital role in the progression of diabetic nephropathy. The renoprotective nature of taurine has also been reported earlier; but little is known about the mechanism of this beneficial action. The present study has, therefore, been carried out to explore in detail the mechanism of the renoprotective effect of taurine under diabetic conditions. Diabetes was induced in rats by alloxan (single i.p. dose of 120 mg/kg body weight) administration. Taurine was administered orally for 3 weeks (1% w/v in drinking water) either from the day on which alloxan was injected or after the onset of diabetes. Alloxan-induced diabetic rats showed a significant increase in plasma glucose, enhanced the levels of renal damage markers, plasma creatinine, urea nitrogen and urinary albumin. Diabetic renal injury was associated with increased kidney weight to body weight ratio and glomerular hypertrophy. Moreover, it increased the productions of reactive oxygen species, enhanced lipid peroxidation and protein carbonylation in association with decreased intracellular antioxidant defense in the kidney tissue. In addition, hyperglycemia enhanced the levels of proinflammatory cytokins (TNF-α, IL-6, IL-1β) and Na(+)--K(+)-ATPase activity with a concomitant reduction in NO content and eNOS expression in diabetic kidney. Investigation of the oxidative stress-responsive signaling cascades showed the upregulation of PKCα, PKCβ, PKCε and MAPkinases in the renal tissue of the diabetic animals. However, taurine administration decreased the elevated blood glucose and proinflammatory cytokine levels, reduced renal oxidative stress (via decrease in xanthine oxidase activity, AGEs formation and inhibition of p47phox/CYP2E1 pathways), improved renal function and protected renal tissue from alloxan-induced apoptosis via the regulation of Bcl-2 family and caspase-9/3 proteins. Taurine supplementation in regular diet could, therefore, be beneficial to regulate diabetes-associated renal complications.

摘要

高血糖诱导的氧化应激在糖尿病肾病的进展中起着至关重要的作用。牛磺酸的肾保护作用也早有报道,但对这种有益作用的机制知之甚少。因此,本研究旨在详细探讨牛磺酸在糖尿病条件下的肾保护作用机制。通过给大鼠腹腔注射链脲佐菌素(120mg/kg 体重的单次剂量)来诱导糖尿病。牛磺酸通过口服给予 3 周(1%w/v 于饮用水中),可以在注射链脲佐菌素的当天或糖尿病发病后开始给予。链脲佐菌素诱导的糖尿病大鼠的血浆葡萄糖显著升高,增强了肾损伤标志物、血浆肌酐、尿素氮和尿白蛋白的水平。糖尿病肾脏损伤与肾重/体重比增加和肾小球肥大有关。此外,它增加了活性氧的产生,增强了脂质过氧化和蛋白质羰基化,同时降低了肾脏组织中的细胞内抗氧化防御。此外,高血糖增强了促炎细胞因子(TNF-α、IL-6、IL-1β)的水平和 Na(+)--K(+)-ATP 酶活性,同时降低了糖尿病肾脏中的 NO 含量和 eNOS 表达。对氧化应激反应信号级联的研究表明,糖尿病动物肾脏组织中 PKCα、PKCβ、PKCε 和 MAPkinases 的表达上调。然而,牛磺酸的给予降低了升高的血糖和促炎细胞因子水平,降低了肾脏氧化应激(通过降低黄嘌呤氧化酶活性、AGEs 形成和抑制 p47phox/CYP2E1 途径),改善了肾功能,并通过调节 Bcl-2 家族和 caspase-9/3 蛋白来保护肾脏组织免受链脲佐菌素诱导的细胞凋亡。因此,在常规饮食中补充牛磺酸可能有助于调节与糖尿病相关的肾脏并发症。

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