Vascular biology of hydrogen sulfide

被引:176
作者
Kanagy, Nancy L. [1 ]
Szabo, Csaba [2 ]
Papapetropoulos, Andreas [3 ,4 ]
机构
[1] Univ New Mexico, Sch Med, Dept Cell Biol & Physiol, Vasc Physiol Grp, Albuquerque, NM 87131 USA
[2] Univ Texas Med Branch, Dept Anesthesiol, Galveston, TX 77555 USA
[3] Univ Athens, Fac Pharm, Lab Pharmacol, Athens, Greece
[4] Acad Athens, Biomed Res Fdn, Ctr Clin Expt Surg & Translat Res, Athens, Greece
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2017年 / 312卷 / 05期
基金
美国国家卫生研究院;
关键词
hydrogen sulfide; signaling; endothelium; vascular smooth muscle; blood vessels; CYSTATHIONINE-GAMMA-LYASE; REDUCES BLOOD-PRESSURE; SMOOTH-MUSCLE-CELLS; K-ATP CHANNEL; BETA-SYNTHASE; S-SULFHYDRATION; NITRIC-OXIDE; OXIDATIVE STRESS; POTASSIUM CHANNELS; PROTEIN-KINASE;
D O I
10.1152/ajpcell.00329.2016
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hydrogen sulfide (H2S) is a ubiquitous signaling molecule with important functions in many mammalian organs and systems. Observations in the 1990s ascribed physiological actions to H2S in the nervous system, proposing that this gasotransmitter acts as a neuromodulator. Soon after that, the vasodilating properties of H2S were demonstrated. In the past decade, H2S was shown to exert a multitude of physiological effects in the vessel wall. H2S is produced by vascular cells and exhibits antioxidant, antiapoptotic, anti-inflammatory, and vasoactive properties. In this concise review, we have focused on the impact of H2S on vascular structure and function with an emphasis on angiogenesis, vascular tone, vascular permeability and atherosclerosis. H2S reduces arterial blood pressure, limits atheromatous plaque formation, and promotes vascularization of ischemic tissues. Although the beneficial properties of H2S are well established, mechanistic insights into the molecular pathways implicated in disease prevention and treatment remain largely unexplored. Unraveling the targets and downstream effectors of H2S in the vessel wall in the context of disease will aid in translation of preclinical observations. In addition, acute regulation of H2S production is still poorly understood and additional work delineating the pathways regulating the enzymes that produce H2S will allow pharmacological manipulation of this pathway. As the field continues to grow, we expect that H2S-related compounds will find their way into clinical trials for diseases affecting the blood vessels.
引用
收藏
页码:C537 / C549
页数:13
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