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促红细胞生成素诱导血红素加氧酶-1表达并减轻氧化应激。

Erythropoietin induces heme oxygenase-1 expression and attenuates oxidative stress.

作者信息

Katavetin Pisut, Inagi Reiko, Miyata Toshio, Shao Jing, Sassa Ryoji, Adler Stephen, Eto Nobuaki, Kato Hideki, Fujita Toshiro, Nangaku Masaomi

机构信息

Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 2007 Aug 10;359(4):928-34. doi: 10.1016/j.bbrc.2007.05.207. Epub 2007 Jun 6.

Abstract

Recent studies have established that erythropoietin (EPO) is a pleiotropic cytokine. In this study we investigated whether pleiotropic effects of EPO may involve regulation of heme oxygenase (HO)-1, an anti-oxidative stress protein. A stimulatory effect of EPO on HO-1 expression was demonstrated in cultured renal endothelial cells, in which EPO decreased intracellular oxidative stress and provided cytoprotection against H(2)O(2). These beneficial effects were partially reversed by a HO-1 inhibitor. We then evaluated whether EPO induces HO-1 and ameliorates renal injury in vivo. Administration of EPO to Dahl salt-sensitive (DS) rats with low salt diet, a model of chronic tubulointerstitial injury, reduced proteinuria, and renal injury including peritubular capillaries rarefaction as compared to vehicle-treated DS rats. This renoprotection was associated with up-regulation of HO-1 in the kidney. In conclusion, EPO-induced HO-1 expression is likely to provide cytoprotection against oxidative stress.

摘要

近期研究证实,促红细胞生成素(EPO)是一种多效细胞因子。在本研究中,我们调查了EPO的多效性作用是否涉及对血红素加氧酶(HO)-1(一种抗氧化应激蛋白)的调节。在培养的肾内皮细胞中证实了EPO对HO-1表达具有刺激作用,其中EPO降低了细胞内氧化应激并提供了针对H₂O₂的细胞保护作用。HO-1抑制剂可部分逆转这些有益作用。然后,我们评估了EPO在体内是否诱导HO-1并改善肾损伤。给低钠饮食的Dahl盐敏感(DS)大鼠(一种慢性肾小管间质损伤模型)注射EPO,与注射赋形剂的DS大鼠相比,蛋白尿和肾损伤(包括肾小管周围毛细血管稀疏)有所减轻。这种肾脏保护作用与肾脏中HO-1的上调有关。总之,EPO诱导的HO-1表达可能为抵抗氧化应激提供细胞保护作用。

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