Gai Xiang-Yun, Tang Feng, Ma Jing, Zeng Ke-Wu, Wang Sheng-Lan, Wang Ya-Ping, Wuren Ta-Na, Lu Dian-Xiang, Zhou Yi, Ge Ri-Li
Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University, China.
J Pharmacol Sci. 2014;126(2):155-63. doi: 10.1254/jphs.14072fp.
The main purpose of this study is to evaluate the effect of echinacoside (ECH) on hypoxia-induced proliferation of rat pulmonary artery smooth muscle cells (PASMCs) and the underlying mechanism. PASMCs were incubated under normoxia (nor), hypoxia (hyp), hypoxia + 0.35 mM ECH (hyp + ECH0.35), or hypoxia + 0.4 mM ECH (hyp + ECH0.4) for 24 h. Cell viability was assessed by MTS assays. The morphology of apoptosis was observed by DAPI staining, and apoptosis was quantified by flow cytometric analysis. Caspase-3 activity was determined by immunohistochemistry and real-time PCR, and the expressions of HIF-1α, Bax, Bcl-2, and Fas were determined by real-time PCR. Hypoxia induced significant proliferation of PASMCs, which could be inhibited by ECH in a concentration-dependent manner. This was associated with apoptosis of PASMCs. Z-DEVD-FMK could partly reduce the suppression effect of ECH; protein and gene expression of caspase-3 were significantly higher in the hyp + ECH0.4 and hyp + ECH0.35 groups. ECH significantly increased the expressions of Bax and Fas, but decreased the expressions of Bcl-2 and HIF-1α. ECH could inhibit hypoxia-induced proliferation of rat PASMCs, which is associated with apoptosis of PASMCs and improvement of hypoxia. ECH might be a potential agent for prevention and treatment of hypoxia-induced PAH.
本研究的主要目的是评估松果菊苷(ECH)对缺氧诱导的大鼠肺动脉平滑肌细胞(PASMCs)增殖的影响及其潜在机制。将PASMCs在常氧(nor)、缺氧(hyp)、缺氧 + 0.35 mM ECH(hyp + ECH0.35)或缺氧 + 0.4 mM ECH(hyp + ECH0.4)条件下培养24小时。通过MTS法评估细胞活力。通过DAPI染色观察凋亡形态,并通过流式细胞术分析对凋亡进行定量。通过免疫组织化学和实时PCR测定Caspase-3活性,并通过实时PCR测定HIF-1α、Bax、Bcl-2和Fas的表达。缺氧诱导PASMCs显著增殖,而ECH可呈浓度依赖性抑制这种增殖。这与PASMCs的凋亡有关。Z-DEVD-FMK可部分降低ECH的抑制作用;在hyp + ECH0.4和hyp + ECH0.35组中,Caspase-3的蛋白和基因表达显著更高。ECH显著增加Bax和Fas的表达,但降低Bcl-2和HIF-1α的表达。ECH可抑制缺氧诱导的大鼠PASMCs增殖,这与PASMCs的凋亡和缺氧改善有关。ECH可能是预防和治疗缺氧诱导的肺动脉高压的潜在药物。