Establishment of mouse models for severe pulmonary hypertension through 'double-hit' strategies.

IF 2.6 4区 医学 Q2 PHYSIOLOGY Experimental Physiology Pub Date : 2024-09-27 DOI:10.1113/EP091833
Lingdan Chen, Xin Chen, Yuhang Huang, Zhuoji Ma, Xiaohui Zeng, Tao Wang
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Abstract

Mouse models are crucial for understanding pulmonary hypertension (PH) mechanisms and developing therapies, but existing mouse models under hypoxia only exhibit mild PH. To address this, we established a double-hit model combining unilateral pneumonectomy (LPx) or left pulmonary artery ligation (LPAL) with hypoxia exposure in C57BL/6 mice. Our detailed haemodynamic and histological evaluations post-surgery demonstrated pronounced elevations in right ventricular systolic pressure (RVSP) (LPAL: 41.1 ± 4.63 mmHg, P = 0.005; LPx: 38.4 ± 2.95 mmHg, P = 0.002; Sham: 32.1 ± 2.21 mmHg) and pulmonary vascular wall thickness (LPAL: 56.9 ± 3.34%, P = 0.02; LPx: 54.3 ± 4.65%, P = 0.04; Sham: 44.8 ± 3.76%) compared to hypoxia-exposed sham-operated controls, reflecting a more severe PH phenotype. These novel models, which exhibit haemodynamic alterations akin to the established hypoxia with SU5416-induced PH model as per published data, could offer a substantial contribution to future PH research and therapeutic development.

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通过 "双击 "策略建立重度肺动脉高压小鼠模型
小鼠模型对于了解肺动脉高压(PH)机制和开发疗法至关重要,但现有的缺氧小鼠模型仅表现出轻度 PH。为了解决这个问题,我们在 C57BL/6 小鼠中建立了结合单侧肺切除术(LPx)或左肺动脉结扎术(LPAL)和缺氧暴露的双击模型。我们在手术后进行了详细的血流动力学和组织学评估,结果显示右心室收缩压(RVSP)明显升高(LPAL:41.1 ± 4.63 mmHg,P = 0.005;LPx:38.4 ± 2.95 mmHg,P = 0.005):与缺氧暴露的假手术对照组相比,右心室收缩压(RVSP)(LPAL:41.1 ± 4.63 mmHg;LPx:38.4 ± 2.95 mmHg,P = 0.002;Sham:32.1 ± 2.21 mmHg)和肺血管壁厚度(LPAL:56.9 ± 3.34%,P = 0.02;LPx:54.3 ± 4.65%,P = 0.04;Sham:44.8 ± 3.76%)明显升高,反映出更严重的 PH 表型。根据已发表的数据,这些新型模型表现出的血流动力学改变与已建立的缺氧与 SU5416 诱导的 PH 模型相似,可为未来的 PH 研究和治疗开发做出重大贡献。
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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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