TRPV1 in arteries enables a rapid myogenic tone.

Autor: Phan TX; Department of Pharmacology and Physiology, Georgetown University, Washington, DC, USA.; Department of Biology, Vinh University, Vinh City, Vietnam., Ton HT; Department of Pharmacology and Physiology, Georgetown University, Washington, DC, USA.; Department of Biology, Vinh University, Vinh City, Vietnam., Gulyás H; Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, Doctoral School of Pharmaceutical Sciences, University of Debrecen, Debrecen, Hungary., Pórszász R; Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, Doctoral School of Pharmaceutical Sciences, University of Debrecen, Debrecen, Hungary., Tóth A; Division of Clinical Physiology, Institute of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary., Russo R; Department of Biomedical Engineering, George Washington University, Washington, DC, USA., Kay MW; Department of Biomedical Engineering, George Washington University, Washington, DC, USA., Sahibzada N; Department of Pharmacology and Physiology, Georgetown University, Washington, DC, USA., Ahern GP; Department of Pharmacology and Physiology, Georgetown University, Washington, DC, USA.
Jazyk: angličtina
Zdroj: The Journal of physiology [J Physiol] 2022 Apr; Vol. 600 (7), pp. 1651-1666. Date of Electronic Publication: 2022 Feb 01.
DOI: 10.1113/JP281873
Abstrakt: Arterioles maintain blow flow by adjusting their diameter in response to changes in local blood pressure. In this process called the myogenic response, a vascular smooth muscle mechanosensor controls tone predominantly through altering the membrane potential. In general, myogenic responses occur slowly (minutes). In the heart and skeletal muscle, however, tone is activated rapidly (tens of seconds) and terminated by brief (100 ms) arterial constrictions. Previously, we identified extensive expression of TRPV1 in the smooth muscle of arterioles supplying skeletal muscle, heart and fat. Here we reveal a critical role for TRPV1 in the rapid myogenic tone of these tissues. TRPV1 antagonists dilated skeletal muscle arterioles in vitro and in vivo, increased coronary flow in isolated hearts, and transiently decreased blood pressure. All of these pharmacologic effects were abolished by genetic disruption of TRPV1. Stretch of isolated vascular smooth muscle cells or raised intravascular pressure in arteries triggered Ca 2+ signalling and vasoconstriction. The majority of these stretch-responses were TRPV1-mediated, with the remaining tone being inhibited by the TRPM4 antagonist, 9-phenantrol. Notably, tone developed more quickly in arteries from wild-type compared with TRPV1-null mice. Furthermore, the immediate vasodilation following brief constriction of arterioles depended on TRPV1, consistent with a rapid deactivation of TRPV1. Pharmacologic experiments revealed that membrane stretch activates phospholipase C/protein kinase C signalling combined with heat to activate TRPV1, and in turn, L-type Ca 2+ channels. These results suggest a critical role, for TRPV1 in the dynamic regulation of myogenic tone and blood flow in the heart and skeletal muscle. KEY POINTS: We explored the physiological role of TRPV1 in vascular smooth muscle. TRPV1 antagonists dilated skeletal muscle arterioles both ex vivo and in vivo, increased coronary perfusion and decreased systemic blood pressure. Stretch of arteriolar myocytes and increases in intraluminal pressure in arteries triggered rapid Ca 2+ signalling and vasoconstriction respectively. Pharmacologic and/or genetic disruption of TRPV1 significantly inhibited the magnitude and rate of these responses. Furthermore, disrupting TRPV1 blunted the rapid vasodilation evoked by arterial constriction. Pharmacological experiments identified key roles for phospholipase C and protein kinase C, combined with temperature, in TRPV1-dependent arterial tone. These results show that TRPV1 in arteriolar myocytes dynamically regulates myogenic tone and blood flow in the heart and skeletal muscle.
(© 2022 The Authors. The Journal of Physiology © 2022 The Physiological Society.)
Databáze: MEDLINE
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