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β-肾上腺素能受体激活诱导大鼠肥厚性生长过程中抗肥厚基因Npr1和Npr2的差异表达与调控

Differential expression and regulation of anti-hypertrophic genes Npr1 and Npr2 during β-adrenergic receptor activation-induced hypertrophic growth in rats.

作者信息

Manivasagam Senthamizharasi, Subramanian Vimala, Tumala Anusha, Vellaichamy Elangovan

机构信息

Department of Biochemistry, University of Madras, Guindy Campus, Chennai, 600025, India.

Department of Biochemistry, University of Madras, Guindy Campus, Chennai, 600025, India.

出版信息

Mol Cell Endocrinol. 2016 Sep 15;433:117-29. doi: 10.1016/j.mce.2016.06.010. Epub 2016 Jun 6.

Abstract

We sought to determine the effect of chronic activation of β-adrenergic receptor (β-AR) on the left ventricular (LV) expression profile of Npr1 and Npr2 (coding for NPR-A and NPR-B, respectively) genes, and the functional activity of these receptors in adult Wistar rat hearts. The Npr1 gene expression was markedly reduced (3.5-fold), while the Npr2 gene expression was up regulated (4-fold) in Isoproterenol (ISO)-treated heart as compared with controls. A gradual reduction in NPR-A protein (3-fold), cGMP levels (75%) and a steady increased expression of NPR-B protein (4-fold), were noticed in ISO hearts. Further, in-vitro membranes assay shows that NPR-A dependent guanylyl cyclase (GC) activity was down-regulated (2-fold), whereas NPR-B dependent GC activity was increased (5-fold) in ISO treated hearts. Atenolol treatment normalized the altered expression of Npr1 and Npr2 genes. In conclusion, the chronic β-AR activation differentially regulates Npr1 and Npr2 genes in the heart. Npr1 down regulation is positively associated with the development of left ventricular hypertrophy (LVH) in ISO rats.

摘要

我们试图确定β-肾上腺素能受体(β-AR)慢性激活对成年Wistar大鼠心脏中Npr1和Npr2基因(分别编码NPR-A和NPR-B)的左心室(LV)表达谱以及这些受体功能活性的影响。与对照组相比,异丙肾上腺素(ISO)处理的心脏中Npr1基因表达显著降低(3.5倍),而Npr2基因表达上调(4倍)。在ISO处理的心脏中,观察到NPR-A蛋白逐渐减少(3倍)、cGMP水平降低(75%)以及NPR-B蛋白表达稳定增加(4倍)。此外,体外膜分析表明,ISO处理的心脏中NPR-A依赖性鸟苷酸环化酶(GC)活性下调(2倍),而NPR-B依赖性GC活性增加(5倍)。阿替洛尔治疗使Npr1和Npr2基因的表达改变恢复正常。总之,慢性β-AR激活在心脏中对Npr1和Npr2基因进行差异性调节。Npr1下调与ISO大鼠左心室肥厚(LVH)的发展呈正相关。

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