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High density lipoprotein downregulates angiotensin II type 1 receptor and inhibits angiotensin II-induced cardiac hypertrophy

机译:高密度脂蛋白下调1型血管紧张素II受体并抑制血管紧张素II引起的心肌肥大

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摘要

Angiotensin II (AngII) and its type receptor (AT1-R) play important roles in the development of cardiac hypertrophy. Low level of high density lipoprotein (HDL) is also an independent risk factor for cardiac hypertrophy. We therefore investigated in the present study whether HDL inhibits cardiac hypertrophy relatively to inhibition of AngII and AT1-R in both in vitro and in vivo experiments. Stimulation of cultured cardiomyocytes of neonatal rats with AngII for 24 h and infusion of AngII in mice for 2 weeks resulted in marked cardiac hypertrophic responses including increased protein synthesis, enlarged sizes of cardiomyocytes and hearts, upregulated phosphorylation levels of protein kinases and reprogrammed expression of specific genes, all of which were significantly attenuated by the treatment with HDL. Furthermore, AngII-treatment induced upregulation of AT-R expression either in cultured cardiomyocytes or in hearts of mice and HDL significantly suppressed the upregulation of AT1-R. Our results suggest that HDL may abrogate AngII-induced cardiac hypertrophy through downregulation of AT1-R expression. (C) 2010 Elsevier Inc. All rights reserved.
机译:血管紧张素II(AngII)及其类型受体(AT1-R)在心脏肥大的发展中起重要作用。低水平的高密度脂蛋白(HDL)也是心脏肥大的独立危险因素。因此,我们在本研究中调查了HDL在体外和体内实验中相对于AngII和AT1-R抑制相对于心脏肥大。用AngII刺激新生大鼠培养的心肌细胞24小时并在小鼠中输注AngII 2周导致明显的心肌肥大反应,包括增加的蛋白质合成,心肌和心脏的大小增大,蛋白激酶的磷酸化水平上调以及特异性蛋白的重新编程表达基因,所有这些都被HDL处理大大减弱。此外,AngII处理诱导了培养的心肌细胞或小鼠心脏中AT-R表达的上调,而HDL则显着抑制了AT1-R的上调。我们的结果表明,HDL可能通过下调AT1-R表达来消除AngII诱导的心脏肥大。 (C)2010 Elsevier Inc.保留所有权利。

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