首页> 外文期刊>American Journal of Physiology >Increased natriuretic peptide receptor A and C gene expression in rats with pressure-overload cardiac hypertrophy.
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Increased natriuretic peptide receptor A and C gene expression in rats with pressure-overload cardiac hypertrophy.

机译:压力超负荷心肌肥大大鼠的利钠肽受体A和C基因表达增加。

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Both atrial (ANP) and brain (BNP) natriuretic peptide affect development of cardiac hypertrophy and fibrosis via binding to natriuretic peptide receptor (NPR)-A in the heart. A putative clearance receptor, NPR-C, is believed to regulate cardiac levels of ANP and BNP. The renin-angiotensin system also affects cardiac hypertrophy and fibrosis. In this study we examined the expression of genes for the NPRs in rats with pressure-overload cardiac hypertrophy. The ANG II type 1 receptor was blocked with losartan (10 mg.kg(-1).day(-1)) to investigate a possible role of the renin-angiotensin system in regulation of natriuretic peptide and NPR gene expression. The ascending aorta was banded in 84 rats during Hypnorm/Dormicum-isoflurane anesthesia; after 4 wk the rats were randomized to treatment with losartan or placebo. The left ventricle of the heart was removed 1, 2, or 4 wk later. Aortic banding increased left ventricular expression of NPR-A and NPR-C mRNA by 110% (P < 0.001) and 520% (P < 0.01), respectively, after 8 wk; as expected, it also increased the expression of ANP and BNP mRNAs. Losartan induced a slight reduction of left ventricular weight but did not affect the expression of mRNAs for the natriuretic peptides or their receptors. Although increased gene expression does not necessarily convey a higher concentration of the protein, the data suggest that pressure overload is accompanied by upregulation of not only ANP and BNP but also their receptors NPR-A and NPR-C in the left ventricle.
机译:心钠素(ANP)和脑钠素(BNP)通过与心脏中的利钠肽受体(NPR)-A结合而影响心脏肥大和纤维化的发展。推定的清除受体NPR-C被认为可以调节ANP和BNP的心脏水平。肾素-血管紧张素系统也影响心脏肥大和纤维化。在这项研究中,我们检查了压力超负荷心肌肥大大鼠中NPR的基因表达。氯沙坦(10 mg.kg(-1).day(-1))阻断ANG II 1型受体的作用,以研究肾素-血管紧张素系统在调节利钠肽和NPR基因表达中的可能作用。在Hypnorm / Dormicum-isoflurane麻醉期间,在84只大鼠中出现升主动脉带。 4周后,将大鼠随机分配至氯沙坦或安慰剂治疗。 1、2或4周后,取下心脏的左心室。 8周后,主动脉束带分别使NPR-A和NPR-C mRNA的左心室表达增加110%(P <0.001)和520%(P <0.01)。如预期的那样,它也增加了ANP和BNP mRNA的表达。氯沙坦诱导左心室重量略有减轻,但不影响利钠肽或其受体的mRNA表达。尽管增加的基因表达不一定传达更高浓度的蛋白质,但数据表明压力超负荷伴随着左心室中ANP和BNP以及其受体NPR-A和NPR-C的上调。

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