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Quercetin attenuates cyclooxygenase-2 expression in response to acute ureteral obstruction

机译:槲皮素恢复急性输尿管阻塞的环加氧酶-2表达

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摘要

Unilateral ureteral obstruction (UUO) is associated with increased hydrostatic pressure, inflammation, and oxidative stress in the renal parenchyma. Previous studies have demonstrated marked cyclooxygenase (COX)-2 induction in renal medullary interstitial cells (RMICs) in response to UUO. The aim of the present study was to evaluate the effect of quercetin, a naturally occurring antioxidant, on COX-2 induction in vivo and in vitro. Rats subjected to 24 h of UUO were treated intraperitoneally with quercetin (50 mg·kg~(-1)·day~(-1)). Quercetin partly prevented COX-2 induction in the renal inner medulla in response to UUO. Moreover, RMICs exposed to conditions associated with obstruction, inflammation (produced by IL-1beta), oxidative stress (produced by H2O2), and mechanical stress (produced by stretch) showed increased COX-2 expression. Interestingly, quercetin reduced COX-2 induction in RMICs subjected to stretched. Similarly, PGE_2 production was markedly increased in RMICs exposed to stretch and was reversed to control levels by quercetin treatment. Furthermore, stretch-induced phosphorylation of ERK1/2 was blocked by quercetin, and inhibition of ERK1/2 attenuated stretch-induced COX-2 induction in RMICs. These results indicate that quercetin attenuated the induction of COX-2 expression and activity in RMICs exposed to mechanical stress as a consequence of acute UUO and that the MAPK ERK1/2 pathway might be involved in this quercetin-mediated reduction in COX-2.
机译:单侧输尿管梗阻(UUO)与肾上实质的静水压力,炎症和氧化应激增加有关。以前的研究表明,肾髓间质细胞(RMIC)的标记为环氧化酶(COX)-2诱导响应于UUO。本研究的目的是评估槲皮素,天然存在的抗氧化剂,在体内和体外诱导COX-2诱导的影响。用槲皮素(50mg·kg〜(-1)·日〜(-1))腹膜内腹腔治疗大鼠24小时的大鼠。槲皮素部分预防肾内髓质中的COX-2诱导响应UUO。此外,暴露于与梗阻,炎症(由IL-1Beta产生)相关的病症,氧化应激(由H 2 O 2产生)的条件的RMIC和机械应力(通过拉伸产生)显示出增加的COX-2表达。有趣的是,槲皮素减少了经受拉伸的RMIC中的COX-2诱导。类似地,PGE_2产生在暴露于伸展的RMIC中显着增加,并通过槲皮素治疗逆转以控制水平。此外,ERK1 / 2的拉伸诱导的磷酸化被槲皮素封闭,并抑制ERK1 / 2减毒的RMIC中的诱导的RMIC诱导的COX-2诱导。这些结果表明,由于急性UUO的结果,槲皮素衰减了暴露于机械应力的RMIC中的COX-2表达和活性,并且MAPK ERK1 / 2途径可能参与该槲皮素介导的COX-2的降低。

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