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Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol

While it is known that dilation of cerebral arterioles to NOS‐dependent agonists is impaired in rats exposed to prenatal alcohol, no studies have examined the influence of prenatal alcohol on constrictor response of cerebral arterioles. Our goal was to determine whether constrictor responses of cere...

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Autores principales: Saha, Partha S., Knecht, Tiffany M., Arrick, Denise M., Watt, Michael J., Scholl, Jamie L., Mayhan, William G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554774/
https://www.ncbi.nlm.nih.gov/pubmed/34713985
http://dx.doi.org/10.14814/phy2.15079
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author Saha, Partha S.
Knecht, Tiffany M.
Arrick, Denise M.
Watt, Michael J.
Scholl, Jamie L.
Mayhan, William G.
author_facet Saha, Partha S.
Knecht, Tiffany M.
Arrick, Denise M.
Watt, Michael J.
Scholl, Jamie L.
Mayhan, William G.
author_sort Saha, Partha S.
collection PubMed
description While it is known that dilation of cerebral arterioles to NOS‐dependent agonists is impaired in rats exposed to prenatal alcohol, no studies have examined the influence of prenatal alcohol on constrictor response of cerebral arterioles. Our goal was to determine whether constrictor responses of cerebral resistance arterioles are altered by prenatal exposure to alcohol and if any changes differed as a function of age or sex. We fed Sprague‐Dawley rat dams a liquid diet with or without alcohol (3% ethanol) for the duration of their pregnancy. We then examined reactivity of cerebral arterioles to thromboxane (U‐46619; 0.01 and 0.1 µM), arginine vasopressin (0.1 and 1 nM), and angiotensin II (1 and 10 µM) in four groups of offspring: control male and female, and prenatal alcohol male and female at two different ages (adolescent: 4–6 weeks old and adult: 14–16 weeks old). Constriction of cerebral arterioles to U‐46619 and AVP were similar in male and female rats regardless of exposure to prenatal alcohol and age. Similarly, adolescent male and female rats showed no difference to angiotensin II following prenatal exposure to alcohol. However, alcohol‐exposed females exhibited an unexpected dilation to the high concentration of angiotensin II in adulthood, which was absent in males. We suggest that the findings from these studies may have implications regarding the susceptibility of the brain to cerebral ischemic damage. We speculate that impaired vasodilation, coupled with preserved vasoconstriction, can lead to a scenario favoring a decrease in cerebral blood flow during times of increased metabolic demand.
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spelling pubmed-85547742021-11-05 Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol Saha, Partha S. Knecht, Tiffany M. Arrick, Denise M. Watt, Michael J. Scholl, Jamie L. Mayhan, William G. Physiol Rep Original Articles While it is known that dilation of cerebral arterioles to NOS‐dependent agonists is impaired in rats exposed to prenatal alcohol, no studies have examined the influence of prenatal alcohol on constrictor response of cerebral arterioles. Our goal was to determine whether constrictor responses of cerebral resistance arterioles are altered by prenatal exposure to alcohol and if any changes differed as a function of age or sex. We fed Sprague‐Dawley rat dams a liquid diet with or without alcohol (3% ethanol) for the duration of their pregnancy. We then examined reactivity of cerebral arterioles to thromboxane (U‐46619; 0.01 and 0.1 µM), arginine vasopressin (0.1 and 1 nM), and angiotensin II (1 and 10 µM) in four groups of offspring: control male and female, and prenatal alcohol male and female at two different ages (adolescent: 4–6 weeks old and adult: 14–16 weeks old). Constriction of cerebral arterioles to U‐46619 and AVP were similar in male and female rats regardless of exposure to prenatal alcohol and age. Similarly, adolescent male and female rats showed no difference to angiotensin II following prenatal exposure to alcohol. However, alcohol‐exposed females exhibited an unexpected dilation to the high concentration of angiotensin II in adulthood, which was absent in males. We suggest that the findings from these studies may have implications regarding the susceptibility of the brain to cerebral ischemic damage. We speculate that impaired vasodilation, coupled with preserved vasoconstriction, can lead to a scenario favoring a decrease in cerebral blood flow during times of increased metabolic demand. John Wiley and Sons Inc. 2021-10-29 /pmc/articles/PMC8554774/ /pubmed/34713985 http://dx.doi.org/10.14814/phy2.15079 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Saha, Partha S.
Knecht, Tiffany M.
Arrick, Denise M.
Watt, Michael J.
Scholl, Jamie L.
Mayhan, William G.
Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
title Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
title_full Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
title_fullStr Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
title_full_unstemmed Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
title_short Constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
title_sort constrictor responses of cerebral resistance arterioles in male and female rats exposed to prenatal alcohol
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554774/
https://www.ncbi.nlm.nih.gov/pubmed/34713985
http://dx.doi.org/10.14814/phy2.15079
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