Oxymatrine prevents hypoxia- and monocrotaline-induced pulmonary hypertension in rats

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• 作者：Bo Zhang^a ; ¹ ; ^{luckzb@fmmu.edu.cn" class="auth_mail} ; Wen Niu^a ; ¹ ; Dunquan Xu^a ; ¹ ; Yanyan Li^a ; ¹ ; Manling Liu^a ; Yanxia Wang^a ; Ying Luo^a ; Pengtao Zhao^a ; Yi Liu^a ; Mingqing Dong^a ; Rihe Sun^b ; Haiying Dong^a ; ^{liyun8@fmmu.edu.cn" class="auth_mail} ; Zhichao Li^a ; ^{lizhic@fmmu.edu.cn" class="auth_mail}
• 关键词：Pulmonary hypertension ; Oxymatrine ; Hypoxia ; Proliferation ; Inflammation ; Oxidative stress ; Free radicals
• 刊名：Free Radical Biology and Medicine
• 出版年：April, 2014
• 年：2014
• 卷：69
• 期：Complete
• 页码：198-207
• 全文大小：3011 K

文摘

Pulmonary hypertension is a progressive disease characterized by marked pulmonary arterial remodeling and increased vascular resistance. Inflammation and oxidative stress promote the development of pulmonary hypertension. Oxymatrine, one of the main active components of the Chinese herb Sophora flavescens Ait. (Kushen), plays anti-inflammatory and antioxidant protective roles, which effects on pulmonary arteries remain unclear. This study aimed to investigate the effects of oxymatrine on pulmonary hypertension development. Sprague-Dawley rats were exposed to hypoxia for 28 days or injected with monocrotaline, to develop pulmonary hypertension, along with administration of oxymatrine (50 mg/kg/day). Hemodynamics and pulmonary arterial remodeling data from the rats were then obtained. The antiproliferative effect of oxymatrine was verified by in vitro assays. The inflammatory cytokine mRNA levels and leukocyte and T cell accumulation in lung tissue were detected. The antioxidative effects of oxymatrine were explored in vitro. Our study shows that oxymatrine treatment attenuated right-ventricular systolic pressure and pulmonary arterial remodeling induced by hypoxia or monocrotaline and inhibited proliferation of pulmonary arterial smooth muscle cells (PASMCs). Increased expression of inflammatory cytokine mRNA and accumulation of leukocytes and T cells around the pulmonary arteries were suppressed with oxymatrine administration. Under hypoxic conditions, oxymatrine significantly upregulated Nrf2 and antioxidant protein SOD1 and HO-1 expression, but downregulated hydroperoxide levels in PASMCs. In summary, this study indicates that oxymatrine may prevent pulmonary hypertension through its antiproliferative, anti-inflammatory, and antioxidant effects, thus providing a promising pharmacological avenue for treating pulmonary hypertension.