The regulating effect of heme oxygenase/carbon monoxide on hypoxic pulmonary vascular structural remodeling

被引:62
作者
Shi, Y
Du, JB
Gong, LM
Zeng, CM
Tang, XY
Tang, CS
机构
[1] Peking Univ First Hosp, Dept Pediat, Beijing 100034, Peoples R China
[2] Peking Univ, Peoples Hosp, Dept Pediat, Beijing, Peoples R China
[3] Peking Univ First Hosp, Lab Elect Microscopy, Beijing, Peoples R China
[4] Peking Univ First Hosp, Cardiovasc Res Inst, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon monoxide; heme oxygenase; hypoxia; remodeling;
D O I
10.1016/S0006-291X(03)00998-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Hypoxic pulmonary vascular structural remodeling (HPVSR) is the important pathologic basis of hypoxic pulmonary hypertension (HPH). The discoveries of endogenous gaseous messenger molecules, nitric oxide (NO) and carbon monoxide (CO), have been moving the research of HPVSR to a very new phase. But the effect and significance of heme oxygenase (HO)/CO on the development of HPVSR have not been fully understood. In this study, we observed the alteration of endogenous HO/CO system in five time points during 14 days and found that the content of CO in lung homogenates in rats with HPVSR increased in a time-dependent double-peak manner. Exogenous supply of ZnPP-IX, an inhibitor of HO-1, decreased the content of CO in lung homogenate, decreased the expression of Fas and apoptotic cells in pulmonary artery smooth muscle cells (PASMCs), up-regulated the expression of PCNA in PASMCs, and worsened HPH and HPVSR of hypoxic rats. Meanwhile, exogenous supply of CO played an adverse action. The results showed that the up-regulation of HO/CO exerted a protective role in the development of HPVSR. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:523 / 529
页数:7
相关论文
共 23 条
[1]
AN IMPROVED MATHEMATICAL APPROACH FOR THE ASSESSMENT OF THE MEDIAL THICKNESS OF PULMONARY-ARTERIES [J].
BARTH, PJ ;
KIMPEL, C ;
ROY, S ;
WAGNER, U .
PATHOLOGY RESEARCH AND PRACTICE, 1993, 189 (05) :567-576
[2]
Apoptosis of vascular smooth muscle cells in vascular remodelling and atherosclerotic plaque rupture [J].
Bennett, MR .
CARDIOVASCULAR RESEARCH, 1999, 41 (02) :361-368
[3]
Role of endothelial carbon monoxide in attenuated vasoreactivity following chronic hypoxia [J].
Caudill, TK ;
Resta, TC ;
Kanagy, NL ;
Walker, BR .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 275 (04) :R1025-R1030
[4]
CHALMERS AH, 1991, CLIN CHEM, V37, P1442
[5]
Modulation of angiotensin II receptor expression during development and regression of hypoxic pulmonary hypertension [J].
Chassagne, C ;
Eddahibi, S ;
Adamy, C ;
Rideau, D ;
Marotte, F ;
Dubois-Randé, JL ;
Adnot, S ;
Samuel, JL ;
Teiger, E .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 22 (03) :323-332
[6]
Heme oxygenase-1: Function, regulation, and implication of a novel stress-inducible protein in oxidant-induced lung injury [J].
Choi, AMK ;
Alam, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 15 (01) :9-19
[7]
Prevention of hypoxia-induced pulmonary hypertension by enhancement of endogenous heme oxygenase-1 in the rat [J].
Christou, H ;
Morita, T ;
Hsieh, CM ;
Koike, H ;
Arkonac, B ;
Perrella, MA ;
Kourembanas, S .
CIRCULATION RESEARCH, 2000, 86 (12) :1224-1229
[8]
MECHANISMS OF CARBON-MONOXIDE TOXICITY [J].
COBURN, RF .
PREVENTIVE MEDICINE, 1979, 8 (03) :310-322
[9]
Nitric oxide impacts endothelin-1 gene expression in intrapulmonary arteries of chronically hypoxic rats [J].
Du, JB ;
Jia, JF ;
Li, WZ ;
Zhao, B ;
Zeng, HP .
ANGIOLOGY, 1999, 50 (06) :479-485
[10]
JONSON RA, 1996, AM J PHYSIOL, V271, pH1132