H ₂ S as a Physiologic Vasorelaxant: Hypertension in Mice with Deletion of Cystathionine γ-Lyase

TLDR

Studies of nitric oxide over the past two decades have highlighted the fundamental importance of gaseous signaling molecules in biology and medicine, and the physiological role of other gases such as carbon monoxide and hydrogen sulfide (H₂S) is now receiving increasing attention. CSE is physiologically activated by calcium‑calmodulin, a mechanism for H₂S formation in response to vascular activation. Here we show that H₂S is physiologically generated by cystathionine γ‑lyase (CSE) and that genetic deletion of this enzyme in mice markedly reduces H₂S levels in the serum, heart, aorta, and other tissues, leading to pronounced hypertension and diminished endothelium‑dependent vasorelaxation, thereby providing direct evidence that H₂S is a physiologic vasodilator and regulator of blood pressure.

Abstract

Studies of nitric oxide over the past two decades have highlighted the fundamental importance of gaseous signaling molecules in biology and medicine. The physiological role of other gases such as carbon monoxide and hydrogen sulfide (H 2 S) is now receiving increasing attention. Here we show that H 2 S is physiologically generated by cystathionine γ-lyase (CSE) and that genetic deletion of this enzyme in mice markedly reduces H 2 S levels in the serum, heart, aorta, and other tissues. Mutant mice lacking CSE display pronounced hypertension and diminished endothelium-dependent vasorelaxation. CSE is physiologically activated by calcium-calmodulin, which is a mechanism for H 2 S formation in response to vascular activation. These findings provide direct evidence that H 2 S is a physiologic vasodilator and regulator of blood pressure.