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大黄蛰虫丸治疗大鼠血清对血管平滑肌细胞增殖的体外抑制作用

In vitro inhibition of proliferation of vascular smooth muscle cells by serum of rats treated with Dahuang Zhechong pill.

作者信息

Zhang Yuan-Hui, Liu Jun-Tian, Wen Bin-Yu, Xiao Xiang-Hua

机构信息

Department of Pharmacology, Xi'an Jiaotong University School of Medicine, P.O. Box 58, Xi'an 710061, PR China.

出版信息

J Ethnopharmacol. 2007 Jun 13;112(2):375-9. doi: 10.1016/j.jep.2007.03.018. Epub 2007 Mar 20.

Abstract

Dahuang Zhechong pill (DHZCP) is a famous and classical Chinese herbal prescription, which is clinically used to treat hepatic, gynecological and cardiovascular diseases in China. The aim of this study was to observe the effects of the serum of rats treated with DHZCP on the proliferation of cultured rat vascular smooth muscle cells (VSMCs) stimulated by platelet-derived growth factor (PDGF), oxidized low density lipoprotein (ox-LDL) and hyperlipidemic serum (HLS), and on DNA, protein and collagen syntheses of VSMCs induced by PDGF in vitro. VSMCs proliferation was assayed by measuring the cell viability with MTT method, and syntheses of DNA, protein and collagen were evaluated by detecting [(3)H]-thymidine, [(3)H]-leucine and [(3)H]-proline incorporations, respectively. The results showed that PDGF, ox-LDL and HLS stimulated the proliferation of rat VSMCs in vitro. The serum of rats treated with DHZCP significantly inhibited the proliferation of rat VSMCs induced by the above stimulants and the incorporations of [(3)H]-thymidine, [(3)H]-leucine and [(3)H]-proline into rat VSMCs induced by PDGF in comparison with the model control group (P<0.01). The data suggest that DHZCP is able to obviously inhibit VSMCs proliferation via interfering with syntheses of DNA and protein, and to decrease production of extracellular matrix by VSMCs through antagonizing collagen synthesis.

摘要

大黄蛰虫丸(DHZCP)是一种著名的经典中药方剂,在中国临床上用于治疗肝脏、妇科和心血管疾病。本研究的目的是观察用大黄蛰虫丸处理的大鼠血清对血小板衍生生长因子(PDGF)、氧化低密度脂蛋白(ox-LDL)和高脂血症血清(HLS)刺激的培养大鼠血管平滑肌细胞(VSMCs)增殖的影响,以及对体外PDGF诱导的VSMCs的DNA、蛋白质和胶原蛋白合成的影响。通过MTT法测定细胞活力来检测VSMCs增殖,分别通过检测[³H]-胸腺嘧啶核苷、[³H]-亮氨酸和[³H]-脯氨酸掺入来评估DNA、蛋白质和胶原蛋白的合成。结果表明,PDGF、ox-LDL和HLS在体外刺激大鼠VSMCs增殖。与模型对照组相比,用大黄蛰虫丸处理的大鼠血清显著抑制上述刺激剂诱导的大鼠VSMCs增殖以及PDGF诱导的大鼠VSMCs中[³H]-胸腺嘧啶核苷、[³H]-亮氨酸和[³H]-脯氨酸的掺入(P<0.01)。数据表明,大黄蛰虫丸能够通过干扰DNA和蛋白质合成明显抑制VSMCs增殖,并通过拮抗胶原蛋白合成减少VSMCs细胞外基质的产生。

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