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血管紧张素II下调实验大鼠心脏中利钠肽受体A介导的抗肥厚信号传导。

Angiotensin-II down-regulates cardiac natriuretic peptide receptor-A mediated anti-hypertrophic signaling in experimental rat hearts.

作者信息

Gopi Venkatachalam, Parthasarathy Arumugam, Umadevi Subramanian, Vellaichamy Elangovan

机构信息

Department of Biochemistry, University of Madras, Guindy Campus, Chennai 600 025, India.

出版信息

Indian J Exp Biol. 2013 Jan;51(1):48-55.

Abstract

Atrial natriuretic peptide (ANP) exerts anti-hypertrophic effects in the heart via natriuretic peptide receptor-A (NPR-A). However, ANP mediated anti-hypertrophic activity is decreased in the cardiomyopathic conditions. In the present investigation the in vivo effects of angiotensin II (Ang II), a hypertrophic agonist have been studied on the ventricular expression level of NPR-A in Wistar rat hearts. NPR-A expression at the protein and mRNA levels were found to be markedly reduced by 5-fold respectively in Ang II infused rats heart as compared with sham rat hearts. Moreover, cGMP production in response to ANP was reduced by 77% in the isolated cardiac membrane preparation from the Ang II infused rat hearts. Losartan treatment reversed NPR-A expression and responsiveness to ANP. This study suggests that Ang II down regulates cardiac NPR-A activity by suppressing Npr1 gene transcription.

摘要

心房利钠肽(ANP)通过利钠肽受体-A(NPR-A)在心脏中发挥抗肥厚作用。然而,在心肌病状态下,ANP介导的抗肥厚活性降低。在本研究中,已对肥厚激动剂血管紧张素II(Ang II)对Wistar大鼠心脏中NPR-A心室表达水平的体内作用进行了研究。与假手术大鼠心脏相比,在Ang II灌注大鼠心脏中,NPR-A在蛋白质和mRNA水平的表达分别显著降低了5倍。此外,在来自Ang II灌注大鼠心脏的离体心脏膜制剂中,对ANP的cGMP产生减少了77%。氯沙坦治疗可逆转NPR-A的表达和对ANP的反应性。本研究表明,Ang II通过抑制Npr1基因转录下调心脏NPR-A活性。

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