Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, GX, China.
Department of Pediatrics, Hengyang Central Hospital, Hengyang, GX, China.
Clin Exp Hypertens. 2022 Jul 4;44(5):470-479. doi: 10.1080/10641963.2022.2071919. Epub 2022 May 4.
Proliferation and apoptosis of pulmonary artery smooth muscle cells (PASMCs) play an important role in the occurrence and development of pulmonary arterial hypertension (PAH). The purpose of this study was to investigate the effects of survivin inhibitor YM155 on the proliferation and apoptosis of PASMCs in rats with PAH induced by high pulmonary blood flow.
Thirty male Sprague-Dawley (SD) rats were randomly divided into control, model, and YM155 intervention groups. A rat model of PAH induced by high pulmonary blood flow was established, and it was confirmed by assessments of right-ventricular pressure (RVP) and right ventricular hypertrophy index (RVHI). Immunohistochemical staining and western blot analysis were used to detect the expression of survivin, and the proliferation and apoptosis of PASMCs. Lastly, the effects of in vivo treatment of YM155 were tested.
The increased expression of survivin mRNA and protein were observed in the model group, accompanied by pulmonary arteriolar wall thickening, lumen stenosis, and perivascular inflammatory cell infiltration. Elevated expression of survivin and pulmonary vascular remodeling were significantly mitigated after YM155 treatment. Specifically, the YM155 intervention group had a significantly lower PASMC proliferation rate and a higher PASMC apoptotic rate.
YM155 suppressed PASMC proliferation and promoted PASMC apoptosis by inhibiting survivin expression and thereby reducing pulmonary vascular remodeling in high pulmonary blood flow-induced PAH in vivo.
肺动脉平滑肌细胞(PASMC)的增殖和凋亡在肺动脉高压(PAH)的发生和发展中起着重要作用。本研究旨在探讨生存素抑制剂 YM155 对高肺血流诱导的 PAH 大鼠 PASMC 增殖和凋亡的影响。
将 30 只雄性 Sprague-Dawley(SD)大鼠随机分为对照组、模型组和 YM155 干预组。通过评估右心室压力(RVP)和右心室肥厚指数(RVHI)来建立高肺血流诱导的大鼠 PAH 模型。采用免疫组织化学染色和 Western blot 分析检测生存素的表达,并检测 PASMC 的增殖和凋亡。最后,测试了 YM155 的体内治疗效果。
模型组中生存素 mRNA 和蛋白表达增加,肺小动脉壁增厚、管腔狭窄和血管周围炎症细胞浸润。YM155 治疗后,生存素表达升高和肺血管重构明显减轻。具体而言,YM155 干预组 PASMC 增殖率显著降低,PASMC 凋亡率显著升高。
YM155 通过抑制生存素表达抑制 PASMC 增殖并促进 PASMC 凋亡,从而减少高肺血流诱导的 PAH 大鼠体内的肺血管重构。