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首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Albuminuria, expression of nicotinamide adenine dinucleotide phosphate oxidase and monocyte chemoattractant protein-1 in the renal tubules of hypertensive dahl salt-sensitive rats.
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Albuminuria, expression of nicotinamide adenine dinucleotide phosphate oxidase and monocyte chemoattractant protein-1 in the renal tubules of hypertensive dahl salt-sensitive rats.

机译:蛋白尿,高血压dahl盐敏感性大鼠的肾小管中烟酰胺腺嘌呤二核苷酸磷酸氧化酶和单核细胞趋化蛋白1的表达。

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In chronic renal diseases, experimental and human data suggest that excess albumin filtered through the glomerular capillary barrier is over-reabsorbed by proximal tubular cells, thereby activating these cells and upregulating the expression of chemokines. On the other hand, a high-salt diet has been shown to induce proteinuria in hypertensive Dahl salt-sensitive (DSS) rats, accompanied with the expression of reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase in the kidney. In the current study, we therefore examined albuminuria and the expressions of NADPH oxidase and monocyte chemoattractant protein-1 (MCP-1) in the renal tubular cells in hypertensive DSS rats, as well as the effects of the antioxidant N-acetylcysteine (NAC) on each of these parameters. DSS rats were fed a normal-salt diet (0.24% NaCl), a high-salt diet (8% NaCl), or a high-salt diet plus NAC supplementation (15 mg/mL drinking water) for 4 weeks. The high-salt diet provoked an increase in glomerular injuries accompanied with albuminuria and in urinary H2O2 and MCP-1 excretion. Immunohistochemical analysis showed the prominent expression of MCP-1 in the dilated tubular cells, where the NADPH oxidase subunit p47phox was also expressed. The current results suggest that albuminuria caused expression of NADPH oxidase and MCP-1 in the dilated renal tubules, resulting in interstitial inflammation and migration of mononuclear cells in DSS rats, because blockade of albuminuria by NAC counteracted the p47phox and MCP-1 expression.
机译:在慢性肾脏疾病中,实验和人类数据表明,通过肾小球毛细血管屏障过滤的过量白蛋白被近端肾小管细胞过度吸收,从而激活这些细胞并上调趋化因子的表达。另一方面,高盐饮食已显示可在高血压Dahl盐敏感性(DSS)大鼠中诱导蛋白尿,并伴随肾脏中烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶表达降低。因此,在本研究中,我们检查了高血压DSS大鼠肾小管中的蛋白尿和NADPH氧化酶和单核细胞趋化蛋白-1(MCP-1)的表达,以及抗氧化剂N-乙酰半胱氨酸(NAC)的作用这些参数中的每一个。为DSS大鼠喂食正常盐饮食(0.24%NaCl),高盐饮食(8%NaCl)或高盐饮食加NAC补充(15 mg / mL饮用水)4周。高盐饮食会引起肾小球损伤并伴有蛋白尿,尿中的H2O2和MCP-1排泄增加。免疫组织化学分析显示,MCP-1在扩张的肾小管细胞中显着表达,其中还表达了NADPH氧化酶亚基p47phox。目前的结果表明,白蛋白尿会引起扩张的肾小管中NADPH氧化酶和MCP-1的表达,从而导致间质性炎症和DSS大鼠单核细胞的迁移,因为NAC阻止白蛋白尿可抵消p47phox和MCP-1的表达。

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