Exogenous hydrogen sulfide (H2S) protects against regional myocardial ischemia–reperfusion injuryEvidence for a role of KATP channels

被引:0
|
作者
D. Johansen
K. Ytrehus
G. F. Baxter
机构
[1] The Royal Veterinary College,Department of Basic Sciences
[2] University of London,Department of Medical Physiology
[3] University of Tromsø,undefined
来源
Basic Research in Cardiology | 2006年 / 101卷
关键词
hydrogen sulfide; ischemia–reperfusion; infarct size; K; channel;
D O I
暂无
中图分类号
学科分类号
摘要
Hydrogen sulfide (H2S) is a gaseous mediator, produced by the metabolic pathways that regulate tissue concentrations of sulfur–containing amino acids. Recent studies indicate that endogenous or exogenous H2S exerts physiological effects in the cardiovascular system of vertebrates, possibly through modulation of KATP channel opening. The present study was undertaken to examine the hypothesis that H2S is cytoprotective against myocardial ischemia–reperfusion injury and that this protective action is mediated by KATP opening. Rat isolated hearts were Langendorff–perfused and underwent 30 min left main coronary artery occlusion and 120 min reperfusion. The resulting injury was assessed as infarct size, determined by tetrazolium staining. Treatment of hearts with the H2S–donor, NaHS, commencing 10 min prior to the onset of coronary occlusion and maintained until 10 min reperfusion, resulted in a concentration–dependent limitation of infarct size (control, 41.0 ± 2.6% of risk zone; NaHS 0.1 μM, 33.9 ± 2.1%, [0.05 > P < 0.1]; NaHS 1 μM, 20.2 ± 2.1% [P < 0.01]). Pretreatment with the KATP channel blockers glibenclamide 10 μM or sodium 5–hydroxydecanoate (5HD) 100 μM led to abrogation of the infarct–limiting effect of NaHS 1 μM (glibenclamide + NaHS 42.5 ± 3.6%; 5HD + NaHS 44.7 ± 2.2%). No statistically significant effects of NaHS treatment on coronary flow, heart rate or left ventricular developed pressure were observed in this experimental preparation. These data provide the first evidence that exogenous H2S protects against irreversible ischemia–reperfusion injury in myocardium and support the involvement of KATP opening in the mechanism of action. Further work is required to elucidate the potential role of endogenous H2S as a cytoprotective mediator against myocardial ischemia–reperfusion injury, the mechanisms regulating its generation, and the nature of its interaction with protein targets such as the KATP channel.
引用
收藏
页码:53 / 60
页数:7
相关论文
共 50 条
  • [31] The Role of Hydrogen Sulfide (H2S) in Epigenetic Regulation of Neurodegenerative Diseases: A Systematic Review
    Dogaru, Bombonica Gabriela
    Munteanu, Constantin
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (16)
  • [32] Hydrogen sulfide potentiates the protective effects of nitrite against myocardial ischemia-reperfusion injury in type 2 diabetic rats
    Jeddi, Sajad
    Gheibi, Sevda
    Afzali, Hamideh
    Carlstro, Mattias
    Kashfi, Khosrow
    Ghasemi, Asghar
    NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2022, 124 : 15 - 23
  • [33] Effects of hydrogen sulfide (H2S) on mesenteric perfusion in experimental induced intestinal ischemia in a porcine model
    Pavoni, V.
    Nicoletti, P.
    Benemei, S.
    Materazzi, S.
    Perna, F.
    Romagnoli, S.
    Chelazzi, C.
    Zagli, G.
    Coratti, A.
    HEART LUNG AND VESSELS, 2015, 7 (03) : 231 - 237
  • [34] Regulation of cardiovascular cell function by hydrogen sulfide (H2S)
    Elsey, David J.
    Fowkes, Robert C.
    Baxter, Gary F.
    CELL BIOCHEMISTRY AND FUNCTION, 2010, 28 (02) : 95 - 106
  • [35] Hydrogen sulfide (H2S) -: the third gas for interest for pharmacologists
    Lowicka, Ewelina
    Beltowski, Jerzy
    PHARMACOLOGICAL REPORTS, 2007, 59 (01) : 4 - 24
  • [36] Provisional Advisory Levels (PALs) for hydrogen sulfide (H2S)
    Marshall, Thomas
    Dorman, David
    Gardner, Donald
    Adeshina, Femi
    INHALATION TOXICOLOGY, 2009, 21 : 56 - 72
  • [37] The Novel Hydrogen Sulfide Donor Diallyl Trisulfide Protects Against Ischemia-Reperfusion Injury by Inhibition of Mitochondrial Respiration
    Predmore, Benjamin
    Bhushan, Shashi
    Aragon, Juan Pablo
    Grinsfelder, Bennette
    King, Adrienne
    Calvert, John
    Condit, Marah
    Lefer, David
    CIRCULATION, 2011, 124 (21)
  • [38] The complex II inhibitor atpenin A5 protects against cardiac ischemia-reperfusion injury via activation of mitochondrial KATP channels
    Wojtovich, Andrew P.
    Brookes, Paul S.
    BASIC RESEARCH IN CARDIOLOGY, 2009, 104 (02) : 121 - 129
  • [39] Phosphodiesterase-5 Inhibitor, Tadalafil, Protects Against Myocardial Ischemia/Reperfusion Through Protein-Kinase G-Dependent Generation of Hydrogen Sulfide
    Salloum, Fadi N.
    Chau, Vinh Q.
    Hoke, Nicholas N.
    Abbate, Antonio
    Varma, Amit
    Ockaili, Ramzi A.
    Toldo, Stefano
    Kukreja, Rakesh C.
    CIRCULATION, 2009, 120 (11) : S31 - S36
  • [40] MECHANISMS OF HYDROGEN SULFIDE (H2S) ACTION ON SYNAPTIC TRANSMISSION AT THE MOUSE NEUROMUSCULAR JUNCTION
    Gerasimova, E.
    Lebedeva, J.
    Yakovlev, A.
    Zefirov, A.
    Giniatullin, R.
    Sitdikova, G.
    NEUROSCIENCE, 2015, 303 : 577 - 585