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Mechanisms of hydrogen sulfide induced vasodilation

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Please use this identifier to cite or link to this item: http://hdl.handle.net/1928/20831

Mechanisms of hydrogen sulfide induced vasodilation

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Title: Mechanisms of hydrogen sulfide induced vasodilation
Author: Jackson-Weaver, Olan
Advisor(s): Kanagy, Nancy
Committee Member(s): Walker, Ben
Resta, Tom
Gonzalez Bosc, Laura
Shuttleworth, Bill
Department: University of New Mexico. Biomedical Sciences Graduate Program
Subject(s): Vascular Physiology
Hydrogen Sulfide
Myogenic Tone
Calcium Sparks
LC Subject(s): Blood-vessels--Dilatation.
Vascular smooth muscle--Physiology.
Hydrogen sulfide--Physiological effect.
Mesenteric artery.
Potassium channels.
Degree Level: Doctoral
Abstract: Myogenic tone is an important regulator of blood flow and may contribute to peripheral vascular resistance and blood pressure. Myogenic tone is a luminal pressure-induced constriction of the vasculature that is mediated by a vascular smooth muscle cell (VSMC) plasma membrane potential (Em) depolarization and Ca2+ influx. Ca2+ sparks, which are ryanodine receptor (RyR) mediated Ca2+ release events, oppose myogenic tone by activating large-conductance Ca2+-activated K+ channels (BKCa) to hyperpolarize VSMC Em. The gaseous signaling molecules (gasotransmitters) NO and CO activate Ca2+ sparks to cause vasodilation. H2S, a third gasotransmitter produced by cystationine γ-lyase (CSE) in the vasculature, activates several K+ channels to promote VSMC Em hyperpolarization. We therefore sought to determine whether H2S inhibits the development of myogenic tone. We hypothesized that H2S opposes myogenic tone through the activation of Ca2+ sparks and subsequent BKCa channel activation. We observed that in small mesenteric arteries CSE-produced H2S reduced myogenic tone. We also found that RyR-mediated Ca2+ sparks and BKCa channel activity opposed tone in these arteries. We also observed that exogenous and endogenous H2S activates sparks and hyperpolarizes VSMC Em. Futhermore, exogenous H2S-mediated vasodilation, spark activation, and VSMC Em hyperpolarization required active endothelial BKCa channels and cytochrome P450 2C. Therefore, H2S seems to be an important regulator of myogenic tone in the mesenteric circulation. The mechanism by which H2S causes vasodilation in this bed is an unexpectedly complex pathway, with activation of endothelial BKCa channels and cytochrome P450 with subsequent activation of VSMC Ca2+ sparks. The effects of H2S here described may be an important mechanism by which this signaling molecule alters hemodynamic parameters in vivo.
Graduation Date: May 2012
URI: http://hdl.handle.net/1928/20831
Item Available: 2014-05-14

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