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H2S as a Physiologic Vasorelaxant: Hypertension in Mice with Deletion of Cystathionine -Lyase
Guangdong Yang,1,5
Lingyun Wu,2*
Bo Jiang,1
Wei Yang,1
Jiansong Qi,1
Kun Cao,1
Qinghe Meng,3
Asif K. Mustafa,4
Weitong Mu,4,6
Shengming Zhang,5
Solomon H. Snyder,4*
Rui Wang1,5*
Abstract:
Studies of nitric oxide over the past two decades have highlightedthe fundamental importance of gaseous signaling molecules inbiology and medicine. The physiological role of other gasessuch as carbon monoxide and hydrogen sulfide (H2S) is now receivingincreasing attention. Here we show that H2S is physiologicallygenerated by cystathionine -lyase (CSE) and that genetic deletionof this enzyme in mice markedly reduces H2S levels in the serum,heart, aorta, and other tissues. Mutant mice lacking CSE displaypronounced hypertension and diminished endothelium-dependentvasorelaxation. CSE is physiologically activated by calcium-calmodulin,which is a mechanism for H2S formation in response to vascularactivation. These findings provide direct evidence that H2Sis a physiologic vasodilator and regulator of blood pressure.
1 Department of Physiology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada. 2 Department of Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada. 3 Department of Pathology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada. 4 Departments of Neuroscience, Pharmacology and Molecular Sciences and Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. 5 Department of Biology, Lakehead University, Thunder Bay, ON P7B 5E1, Canada. 6 Department of Medicine, Gastroenterology Division, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
* To whom correspondence should be addressed. E-mail: rwang{at}lakeheadu.ca (R.W.), lily.wu{at}usask.ca (L.W.), or ssnyder{at}jhmi.edu (S.H.S.).
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