Isorhynchophylline protects against pulmonary arterial hypertension and suppresses PASMCs proliferation

被引:46
作者
Guo, Haipeng [1 ,2 ,3 ]
Zhang, Xin [1 ,2 ,3 ]
Cui, Yugian [2 ,3 ]
Deng, Wei [4 ]
Xu, Dachun [5 ]
Han, Hui [1 ,2 ,3 ]
Wang, Hao [1 ,2 ,3 ]
Chen, Yuguo [2 ,3 ]
Li, Yu [6 ]
Wu, Dawei [1 ,2 ,3 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Crit Care Med, Jinan 250012, Peoples R China
[2] Shandong Univ, Qilu Hosp, Chinese Minist Educ, Key Lab Cardiovasc Remodeling & Funct Res, Jinan 250012, Peoples R China
[3] Shandong Univ, Qilu Hosp, Chinese Minist Hlth, Jinan 250012, Peoples R China
[4] Wuhan Univ, Renmin Hosp, Dept Cardiol, Wuhan 430060, Peoples R China
[5] Tongji Univ, Shanghai Peoples Hosp 10, Dept Cardiol, Shanghai 200072, Peoples R China
[6] Shandong Univ, Qilu Hosp, Dept Resp, Jinan 250012, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Isorhynchophylline; Pulmonary arterial smooth muscle cells; Platelet-derived growth factor; Pulmonary arterial hypertension; CARDIAC-HYPERTROPHY; RHYNCHOPHYLLINE; ALKALOIDS;
D O I
10.1016/j.bbrc.2014.06.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Increased pulmonary arterial smooth muscle cells (PASMCs) proliferation is a key pathophysiological component of pulmonary vascular remodeling in pulmonary arterial hypertension (PAH). Isorhynchophylline (IRN) is a tetracyclic oxindole alkaloid isolated from the Chinese herbal medicine Uncaria rhynchophylla. It has long been used clinically for treatment of cardiovascular and cerebrovascular diseases. However, very little is known about whether IRN can influence the development of PAH. Here we examined the effect of IRN on monocrotaline.(MCT) induced PAH in rats. Our data demonstrated that IRN prevented MCT induced PAH in rats, as assessed by right ventricular (RV) pressure, the weight ratio of RV to (left ventricular + septum) and RV hypertrophy. IRN significantly attenuated the percentage of fully muscularized small arterioles, the medial wall thickness, and the expression of smooth muscle alpha-actin (alpha-SMA) and proliferating cell nuclear antigen (PCNA). In vitro studies, IRN concentration-dependently inhibited the platelet-derived growth factor (PDGF)-BB-induced proliferation of PASMCs. Fluorescence-activated cell-sorting analysis showed that IRN caused G0/G1 phase cell cycle arrest. IRN-induced growth inhibition was associated with downregulation of Cyclin D1 and CDK6 as well as an increase in p27Kip1 levels in PDGF-BB-stimulated PASMCs. Moreover, IRN negatively modulated PDGF-BB-induced phosphorylation of PDGF-R6, ERK1/2, Akt/GSK3 beta, and signal transducers and activators of transcription 3 (STAT3). These results demonstrate that IRN could inhibit PASMCs proliferation and attenuate pulmonary vascular remodeling after MCI' induction. These beneficial effects were at least through the inhibition of PDGF-R beta phosphorylation and its downstream signaling pathways. Therefore, IRN might be a potential candidate for the treatment of PAH. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:729 / 734
页数:6
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