Redox signaling and reactive oxygen species in hypoxic pulmonary vasoconstriction

被引:29
|
作者
Fuchs, Beate [1 ]
Sommer, Natascha [1 ]
Dietrich, Alexander [2 ]
Schermuly, Ralph Theo [1 ,3 ]
Ghofrani, Hossein Ardeschir [1 ]
Grimminger, Friedrich [4 ]
Seeger, Werner [1 ,3 ]
Gudermann, Thomas [5 ]
Weissmann, Norbert [1 ]
机构
[1] Univ Giessen, Dept Internal Med 2, Univ Giessen Lung Ctr, D-35392 Giessen, Germany
[2] Univ Marburg, Inst Pharmacol & Toxicol, Marburg, Germany
[3] Max Planck Inst Heart & Lung Res, Bad Nauheim, Germany
[4] Univ Giessen, Dept Internal Med 4 5, Univ Giessen Lung Ctr, D-35392 Giessen, Germany
[5] Univ Munich, Walther Straub Inst Pharmacol & Toxicol, Munich, Germany
关键词
Hypoxia; Pulmonary vasculature; Reactive oxygen species; Redox state; Superoxide; ARTERIAL SMOOTH-MUSCLE; CAPACITATIVE CALCIUM-ENTRY; CYTOSOLIC PHOSPHOLIPASE A(2); NADPH OXIDASE-INHIBITORS; GATED K+ CHANNELS; INTRACELLULAR CA2+; HYDROGEN-PEROXIDE; GUANYLATE-CYCLASE; SUPEROXIDE ANION; INTRAPULMONARY ARTERIES;
D O I
10.1016/j.resp.2010.08.013
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hypoxic pulmonary vasoconstriction (HPV) is an essential physiological mechanism of the lung that matches blood perfusion with alveolar ventilation to optimize gas exchange. Perturbations of HPV, as may occur in pneumonia or adult respiratory distress syndrome, can cause life-threatening hypoxemia. Despite intensive research for decades, the molecular mechanisms of HPV have not been fully elucidated. Reactive oxygen species (ROS) and changes in the cellular redox state are proposed to link O-2 sensing and pulmonary arterial smooth muscle cell contraction underlying HPV. In this regard, mitochondria and NAD(P)H oxidases are discussed as sources of ROS. However, there is controversy whether ROS levels decrease or increase during hypoxia. With this background we summarize the current knowledge on the role of ROS and redox state in HPV. (C) 2010 Elsevier B.V. All rights reserved.
引用
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页码:282 / 291
页数:10
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