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篇目详细内容

【篇名】 Influence of β-elemene on the secretion of angiotensin II and expression of AT1R in hepatic stellate cells
【刊名】 Frontiers of Medicine in China
【刊名缩写】 Front. Med. China
【ISSN】 1673-7342
【EISSN】 1673-7458
【DOI】 10.1007/s11684-009-0020-y
【出版社】 Higher Education Press and Springer-Verlag
【出版年】 2009
【卷期】 3 卷1期
【页码】 36-40 页,共 5 页
【作者】 Ling YANG MD; Rui ZHU MM; Qingjing ZHU MD; Dan DAN MM; Jin YE MD; Keshu XU MD; Xiaohua HOU MD;
【关键词】 liver cirrhosis; beta-elemene; hepatic stellate cells; angiotensin II; receptor, angiotensin, type 1

【摘要】
This study aims to investigate the influence of β-elemene on the secretion of angiotensin II (ANG II) and the expression of angiotensin receptor type 1 (AT1R) in hepatic stellate cells (HSCs). In vitro, HSC-T6 were cultured for 24 hours and then treated with different doses of β-elemene (2.5, 5 and 10 mg/L). A control group was also set up. The secretion of ANG II in the supernatant was detected by radioimmunoassay. The mRNA expression of AT1R at 4, 12 and 24 h after treatment was detected by reverse transcription-polymerase chain reaction (RT-PCR), respectively. The protein expression of AT1R was detected by western blot. At the 4th h, the ANG II secretion in the supernatant was significantly inhibited by 10 mg/L β-elemene compared with the control group (P<0.05), while 5.0 mg/L and 2.5 mg/L β-elemene had no inhibitory effect on the secretion of ANG II (P>0.05). At the time point of the 12th h, the secretion of ANG II in the supernatant treated with 10 mg/L and 5.0 mg/L β-elemene was significantly lower than the control (P <0.01, P <0.05). Following the treatment with 5.0 mg/L and 2.5 mg/L β-elemene for 24 h, significant inhibition of ANG II secretion was observed (P <0.05), but 10 mg/L β-elemene had no such effect. β-elemene significantly reduced the amount of AT1R mRNA in HSCs after the treatment for 4, 12, and 24 h in a dose-dependent manner. The expression of AT1R protein also decreased after the treatment with β-elemene for 24 h. β-elemene can inhibit the secretion of ANG II and the gene and protein expression of AT1R, which may be the mechanism by which β-elemene prevents the progress of hepatic fibrosis.
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