A cardioprotective insight of the cystathionine γ-lyase/hydrogen sulfide pathway.

Autor: Huang S; Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Li H; Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai 200032, China.; Departments of Physiology and Medicine/CVRL, UCLA School of Medicine, Los Angeles, CA 90095, USA., Ge J; Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai 200032, China.; Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.
Jazyk: angličtina
Zdroj: International journal of cardiology. Heart & vasculature [Int J Cardiol Heart Vasc] 2015 Feb 07; Vol. 7, pp. 51-57. Date of Electronic Publication: 2015 Feb 07 (Print Publication: 2015).
DOI: 10.1016/j.ijcha.2015.01.010
Abstrakt: Traditionally, hydrogen sulfide (H 2 S) was simply considered as a toxic and foul smelling gas, but recently H 2 S been brought into the spot light of cardiovascular research and development. Since the 1990s, H 2 S has been mounting evidence of physiological properties such as immune modification, vascular relaxation, attenuation of oxidative stress, inflammatory mitigation, and angiogenesis. H 2 S has since been recognized as the third physiological gaseous signaling molecule, along with CO and NO [65,66]. H 2 S is produced endogenously through several key enzymes, including cystathionine β-lyase (CBE), cystathionine γ-lyase (CSE), and 3-mercaptopyruvate sulfurtransferase (MST)/cysteine aminotransferase (CAT). These specific enzymes are expressed accordingly in various organ systems and CSE is the predominant H 2 S-producing enzyme in the cardiovascular system. The cystathionine γ-lyase (CSE)/H 2 S pathway has demonstrated various cardioprotective effects, including anti-atherosclerosis, anti-hypertension, pro-angiogenesis, and attenuation of myocardial ischemia-reperfusion injury. CSE exhibits its anti-atherosclerotic effect through 3 mechanisms, namely reduction of chemotactic factor inter cellular adhesion molecule-1 (ICAM-1) and CX3CR1, inhibition of macrophage lipid uptake, and induction of smooth muscle cell apoptosis via MAPK pathway. The CSE/H 2 S pathway's anti-hypertensive properties are demonstrated via aortic vasodilation through several mechanisms, including the direct stimulation of K ATP channels of vascular smooth muscle cells (VSMCs), induction of MAPK pathway, and reduction of homocysteine buildup. Also, CSE/H 2 S pathway plays an important role in angiogenesis, particularly in increased endothelial cell growth and migration, and in increased vascular network length. In myocardial ischemia-reperfusion injuries, CSE/H 2 S pathway has shown a clear cardioprotective effect by preserving mitochondria function, increasing antioxidant production, and decreasing infarction injury size. However, CSE/H 2 S pathway's role in inflammation mitigation is still clouded, due to both pro and anti-inflammatory results presented in the literature, depending on the concentration and form of H 2 S used in specific experiment models.
Databáze: MEDLINE