Function of the serotonin 5-hydroxytryptamine 2B receptor in pulmonary hypertension

被引:304
作者
Launay, JM
Hervé, P
Peoc'h, K
Tournois, C
Callebert, J
Nebigil, CG
Etienne, N
Drouet, L
Humbert, M
Simonneau, G
Maroteaux, L [1 ]
机构
[1] Univ Strasbourg 1, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France
[2] Hop Lariboisiere AP HP, Serv Biochim, CRC Bernard Pathol Expt & Commun Cellulaires, Paris, France
[3] Hop Lariboisiere AP HP, Serv Angiohematol, CRC Bernard Pathol Expt & Commun Cellulaires, Paris, France
[4] Ctr Chirurg Marie Lannelongue, Le Plessis Robinson, France
[5] Hop Antoine Beclere AP HP, UPRES Malad Vasc & Pulm, Clamart, France
关键词
D O I
10.1038/nm764
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Primary pulmonary hypertension is a progressive and often fatal disorder in humans that results from an increase in pulmonary blood pressure associated with abnormal vascular proliferation. Dexfenfluramine increases the risk of pulmonary hypertension in humans, and its active metabolite is a selective serotonin 5-hydroxytryptamine 2B (5-HT2B) receptor agonist. Thus, we investigated the contribution of the 5-HT2B receptor to the pathogenesis of pulmonary hypertension. Using the chronic-hypoxic-mouse model of pulmonary hypertension, we found that the hypoxia-dependent increase in pulmonary blood pressure and lung remodeling are associated with an increase in vascular proliferation, elastase activity and transforming growth factor-beta levels, and that these parameters are potentiated by dexfenfluramine treatment. In contrast, hypoxic mice with genetically or pharmacologically inactive 5-HT2B receptors manifested no change in any of these parameters. In both humans and mice, pulmonary hypertension is associated with a substantial increase in 5-HT2B receptor expression in pulmonary arteries. These data show that activation of 5-HT2B receptors is a limiting step in the development of pulmonary hypertension.
引用
收藏
页码:1129 / 1135
页数:7
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