Journal
CLINICAL AND EXPERIMENTAL HYPERTENSION
Volume 44, Issue 5, Pages 470-479Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/10641963.2022.2071919
Keywords
YM155; pulmonary artery smooth muscle cells; proliferation; apoptosis; Pulmonary arterial hypertension; High pulmonary blood flow
Funding
- National Natural Science Foundation of China (NSFC) [81660043]
- Guangxi Natural Science Foundation (Natural Science Foundation of Guangxi Zhuang Autonomous Region) [2016GXNSFAA380186]
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In this study, the effects of survivin inhibitor YM155 on PASMC proliferation and apoptosis in rats with PAH induced by high pulmonary blood flow were investigated. YM155 suppressed PASMC proliferation and promoted PASMC apoptosis by inhibiting survivin expression and reducing pulmonary vascular remodeling.
Introduction 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. Methods 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. Results 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. Conclusion 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.
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