Journal of Capital Medical University ›› 2013, Vol. 34 ›› Issue (4): 554-558.doi: 10.3969/j.issn.1006-7795.2013.04.015

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Effects of rapamycin on monocrotaline-induced pulmonary hypertension and pulmonary arterial remodeling in rats

LIU Jie1,2, DU Yuxuan1,2, WANG Wang1,2, GUO Huan1,2, WANG Jun1,2, WANG Chen2,3   

  1. 1. Department of Physiology, School of Basic Medical Science, Capital Medical University, Beijing 100069, China;
    2. Beijing Key Laboratory of Respiratory and Pulmonary Circulation, Beijing 100020, China;
    3. Beijing Hospital, Ministry of Health, Beijing 100730, China
  • Received:2013-01-15 Online:2013-08-21 Published:2013-07-20
  • Supported by:

    This study was supported by A Grant from the Major State Basic Research Development Program of China(2009CB522107); National Natural Science Foundation of China(81070042); Major International Collaborative Research Foundation of China(30810103904); Overseas and HongKong and Macao Scholars of Collaborative Research Foundation of China(81228001); Beijing Key Laboratory of Respiratory and Pulmonary Circulation Disorders(RPCD201201, 2011HXFB04); The Foundation of Scientific Research Common Program of Beijing Municipal Commission of Education(KM201310025004); Natural Science Foundation of Ningxia(NZ1220); Basis-clinical Research Co-operation Fund of Capital Medical University(12JL15).

Abstract:

Objective To investigate the effects of rapamycin on monocrotaline(MCT)-induced pulmonary hypertension(PH) and pulmonary arterial remodeling in rats. Methods Male Sprague-Dawley rats were divided into 3 groups: control group, MCT group and rapamycin group. The right ventricular systolic pressure(RVSP) was measured via the right jugular vein catheterization into the right ventricle. The index of right ventricular hypertrophy(RVHI) was calculated. HE staining was used to assess the distal vascular remodeling. Results The body weight of MCT group was significantly lower than that of the control group; The RVSP, RVHI and the remodeling of the small arteries were significantly higher than control group. Even the body weight of rats in rapamycin group was much lower than that of the control and MCT group, while the RVSP, RVHI and the remodeling of the small arteries were significantly improved in rapamycin group compared to MCT group. Conclusion These results suggested that rapamycin could attenuate the development of pulmonary hypertension and pulmonary vascular remodeling. The results provide the theoretical basis for rapamycin to be a potential drug for treating PH.

Key words: rapamycin, monocrotaline, pulmonary hypertension, pulmonary arterial remodeling

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