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Carotid smooth muscle contractility changes after severe burn

Severe burns result in cardiovascular dysfunction, but responses in the peripheral vasculature are unclear. We hypothesize that severe burns disturb arterial contractility through acute changes in adrenergic and cholinergic receptor function. To address this, we investigated the changes in carotid a...

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Autores principales: DeSpain, Kevin, Rosenfeld, Charles R., Huebinger, Ryan, Wang, Xiaofu, Jay, Jayson W., Radhakrishnan, Ravi S., Wolf, Steven E., Song, Juquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433376/
https://www.ncbi.nlm.nih.gov/pubmed/34508162
http://dx.doi.org/10.1038/s41598-021-97732-3
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author DeSpain, Kevin
Rosenfeld, Charles R.
Huebinger, Ryan
Wang, Xiaofu
Jay, Jayson W.
Radhakrishnan, Ravi S.
Wolf, Steven E.
Song, Juquan
author_facet DeSpain, Kevin
Rosenfeld, Charles R.
Huebinger, Ryan
Wang, Xiaofu
Jay, Jayson W.
Radhakrishnan, Ravi S.
Wolf, Steven E.
Song, Juquan
author_sort DeSpain, Kevin
collection PubMed
description Severe burns result in cardiovascular dysfunction, but responses in the peripheral vasculature are unclear. We hypothesize that severe burns disturb arterial contractility through acute changes in adrenergic and cholinergic receptor function. To address this, we investigated the changes in carotid artery contractility and relaxation following a severe burn. Thirty-four adult Sprague–Dawley male rats received a 40% total body surface area (TBSA) scald burn and fluid resuscitation using the Parkland formula. Control animals received sham burn procedure. Animals were serially euthanized between 6 h and 14 days after burn and endothelium-intact common carotid arteries were used for ex vivo force/relaxation measurements. At 6 h after burn, carotid arteries from burned animals demonstrated a > 50% decrease in cumulative dose-responses to norepinephrine (p < 0.05) and to 10(−7) M angiotensin II (p < 0.05). Notably, pre-constricted carotid arteries also demonstrated reduced relaxation responses to acetylcholine (p < 0.05) 6 h after burn, but not to sodium nitroprusside. Histologic examination of cross-sectional planes revealed significant increases in carotid artery wall thickness in burned rats at 6 h versus 3 days, with increased collagen expression in tunica media at 3 days (p < 0.05). Carotid artery dysfunction occurs within 6 h after severe burn, demonstrating decreased sensitivity to adrenergic- and angiotensin II-induced vasoconstriction and acetylcholine-induced relaxation.
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spelling pubmed-84333762021-09-13 Carotid smooth muscle contractility changes after severe burn DeSpain, Kevin Rosenfeld, Charles R. Huebinger, Ryan Wang, Xiaofu Jay, Jayson W. Radhakrishnan, Ravi S. Wolf, Steven E. Song, Juquan Sci Rep Article Severe burns result in cardiovascular dysfunction, but responses in the peripheral vasculature are unclear. We hypothesize that severe burns disturb arterial contractility through acute changes in adrenergic and cholinergic receptor function. To address this, we investigated the changes in carotid artery contractility and relaxation following a severe burn. Thirty-four adult Sprague–Dawley male rats received a 40% total body surface area (TBSA) scald burn and fluid resuscitation using the Parkland formula. Control animals received sham burn procedure. Animals were serially euthanized between 6 h and 14 days after burn and endothelium-intact common carotid arteries were used for ex vivo force/relaxation measurements. At 6 h after burn, carotid arteries from burned animals demonstrated a > 50% decrease in cumulative dose-responses to norepinephrine (p < 0.05) and to 10(−7) M angiotensin II (p < 0.05). Notably, pre-constricted carotid arteries also demonstrated reduced relaxation responses to acetylcholine (p < 0.05) 6 h after burn, but not to sodium nitroprusside. Histologic examination of cross-sectional planes revealed significant increases in carotid artery wall thickness in burned rats at 6 h versus 3 days, with increased collagen expression in tunica media at 3 days (p < 0.05). Carotid artery dysfunction occurs within 6 h after severe burn, demonstrating decreased sensitivity to adrenergic- and angiotensin II-induced vasoconstriction and acetylcholine-induced relaxation. Nature Publishing Group UK 2021-09-10 /pmc/articles/PMC8433376/ /pubmed/34508162 http://dx.doi.org/10.1038/s41598-021-97732-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
DeSpain, Kevin
Rosenfeld, Charles R.
Huebinger, Ryan
Wang, Xiaofu
Jay, Jayson W.
Radhakrishnan, Ravi S.
Wolf, Steven E.
Song, Juquan
Carotid smooth muscle contractility changes after severe burn
title Carotid smooth muscle contractility changes after severe burn
title_full Carotid smooth muscle contractility changes after severe burn
title_fullStr Carotid smooth muscle contractility changes after severe burn
title_full_unstemmed Carotid smooth muscle contractility changes after severe burn
title_short Carotid smooth muscle contractility changes after severe burn
title_sort carotid smooth muscle contractility changes after severe burn
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433376/
https://www.ncbi.nlm.nih.gov/pubmed/34508162
http://dx.doi.org/10.1038/s41598-021-97732-3
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