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阿托伐他汀对血管紧张素II诱导的体外肥厚心肌细胞中过氧化物酶体增殖物激活受体β/δ表达的影响。

Effect of Atorvastatin on Expression of Peroxisome Proliferator-activated Receptor Beta/delta in Angiotensin II-induced Hypertrophic Myocardial Cells In Vitro.

作者信息

Sheng Li, Yang Xu, Ye Ping, Liu Yong-xue, Han Chun-guang

机构信息

Department of Geriatric Cardiology, Chinese PLA General Hospital, Beijing 100853, China.

Department of Pharmacology & Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.

出版信息

Chin Med Sci J. 2015 Dec;30(4):245-51. doi: 10.1016/s1001-9294(16)30008-6.

Abstract

OBJECTIVE

To explore the effect of atorvastatin on cardiac hypertrophy and to determine the potential mechanism involved.

METHODS

An in vitro cardiomyocyte hypertrophy from neonatal rats was induced with angiotensin II (Ang II) stimulation. Before Ang II stimulation, the cultured rat cardiac myocytes were pretreated with atorvastatin at different concentrations (0.1, 1, and 10 μmol/L). The following parameters were evaluated: the myocyte surface area, 3H-leucine incorporation into myocytes, mRNA expressions of atrial natriuretic peptide, brain natriuretic peptide, matrix metalloproteinase 9, matrix metalloproteinase 2, and interleukin-1β, mRNA and protein expressions of the δ/β peroxisome proliferator-activated receptor (PPAR) subtypes.

RESULTS

It was shown that atorvastatin could ameliorate Ang II-induced neonatal cardiomyocyte hypertrophy in the area of cardiomyocytes, 3H-leucine incorporation, and the expression of atrial natriuretic peptide and brain natriuretic peptide markedly. Meanwhile, atorvastatin also inhibited the augmented mRNA level of several cytokines in hypertrophic myocytes. Furthermore, the down-regulated expression of PPAR- δ/β at both the mRNA and protein levels in hypertrophic myocytes could be significantly reversed by atorvastatin treatment.

CONCLUSIONS

Atorvastatin could improve Ang II-induced cardiac hypertrophy and inhibit the expression of cytokines. Such effect might be partly achieved through activation of the PPAR-δ/β pathway.

摘要

目的

探讨阿托伐他汀对心肌肥大的影响,并确定其潜在机制。

方法

用血管紧张素II(Ang II)刺激诱导新生大鼠心肌细胞体外肥大。在Ang II刺激前,将培养的大鼠心肌细胞用不同浓度(0.1、1和10 μmol/L)的阿托伐他汀预处理。评估以下参数:心肌细胞表面积、3H-亮氨酸掺入心肌细胞、心房利钠肽、脑利钠肽、基质金属蛋白酶9、基质金属蛋白酶2和白细胞介素-1β的mRNA表达、δ/β过氧化物酶体增殖物激活受体(PPAR)亚型的mRNA和蛋白表达。

结果

结果表明,阿托伐他汀可在心肌细胞面积、3H-亮氨酸掺入以及心房利钠肽和脑利钠肽表达方面显著改善Ang II诱导的新生心肌细胞肥大。同时,阿托伐他汀还抑制了肥大心肌细胞中几种细胞因子mRNA水平的升高。此外,阿托伐他汀治疗可显著逆转肥大心肌细胞中PPAR-δ/β在mRNA和蛋白水平的下调表达。

结论

阿托伐他汀可改善Ang II诱导的心肌肥大并抑制细胞因子的表达。这种作用可能部分通过激活PPAR-δ/β途径实现。

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