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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effect of inducible nitric oxide synthase inhibition by aminoguanidine on insulin-like growth factor binding protein-3 in adjuvant-induced arthritic rats.
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Effect of inducible nitric oxide synthase inhibition by aminoguanidine on insulin-like growth factor binding protein-3 in adjuvant-induced arthritic rats.

机译:氨基胍抑制诱导型一氧化氮合酶对佐剂诱导的关节炎大鼠胰岛素样生长因子结合蛋白3的影响。

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摘要

This study was designed to investigate whether nitric oxide (NO) mediates changes in insulin-like growth factor binding protein-3 (IGFBP-3) levels in rats with adjuvant-induced arthritis. Male Wistar rats were injected with complete Freund's adjuvant, and 20 days afterwards arthritic and control rats were injected daily with an inhibitor of inducible NO synthase (iNOS), aminoguanidine, or vehicle for 8 days. The increase in serum levels of IGFBP-3 induced by arthritis was exacerbated by aminoguanidine treatment. Arthritis increased IGFBP-3 mRNA levels in the kidney but not in the liver. The inhibition of iNOS did not modify IGFBP-3 gene expression in the kidney or in the liver in arthritic rats. However, the inhibitory effect of arthritis on the proteolysis of IGFBP-3 in serum was potentiated by aminoguanidine administration. These results indicate that arthritis increases serum IGFBP-3 by increasing its synthesis in the kidney and decreasing its proteolysis in serum and that these effects are not mediated by NO.
机译:这项研究旨在调查一氧化氮(NO)是否介导佐剂性关节炎大鼠胰岛素样生长因子结合蛋白3(IGFBP-3)水平的变化。给雄性Wistar大鼠完全弗氏佐剂注射,然后在关节炎和对照大鼠中每天20天注射诱导型一氧化氮合酶(iNOS),氨基胍或媒介物的抑制剂,持续8天。氨基胍治疗加剧了关节炎引起的IGFBP-3血清水平的升高。关节炎会增加肾脏中的IGFBP-3 mRNA水平,但不会增加肝脏中的IGFBP-3 mRNA水平。 iNOS的抑制不会改变关节炎大鼠肾脏或肝脏中IGFBP-3基因的表达。但是,通过给予氨基胍可增强关节炎对血清中IGFBP-3蛋白水解的抑制作用。这些结果表明关节炎通过增加其在肾脏中的合成并减少其在血清中的蛋白水解作用而增加了血清IGFBP-3,并且这些作用不是由NO介导的。

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