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Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure

Significance: Prenatal exposure to ethanol causes several morphological and neurobehavioral deficits. While there are some studies on the effects of ethanol exposure on blood flow, research focusing on acute changes in the microvasculature is limited. Aim: The first aim of this study was to assess t...

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Autores principales: Raghunathan, Raksha, Liu, Chih-Hao, Kouka, Amur, Singh, Manmohan, Miranda, Rajesh C., Larin, Kirill V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689263/
https://www.ncbi.nlm.nih.gov/pubmed/33244919
http://dx.doi.org/10.1117/1.JBO.25.12.126001
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author Raghunathan, Raksha
Liu, Chih-Hao
Kouka, Amur
Singh, Manmohan
Miranda, Rajesh C.
Larin, Kirill V.
author_facet Raghunathan, Raksha
Liu, Chih-Hao
Kouka, Amur
Singh, Manmohan
Miranda, Rajesh C.
Larin, Kirill V.
author_sort Raghunathan, Raksha
collection PubMed
description Significance: Prenatal exposure to ethanol causes several morphological and neurobehavioral deficits. While there are some studies on the effects of ethanol exposure on blood flow, research focusing on acute changes in the microvasculature is limited. Aim: The first aim of this study was to assess the dose-dependent changes in murine fetal brain microvasculature of developing fetuses in response to maternal alcohol consumption. The second aim was to quantify changes in vasculature occurring concurrently in the mother’s hindlimb and the fetus’s brain after maternal exposure to alcohol. Approach: Correlation mapping optical coherence angiography was used to evaluate the effects of prenatal exposure to different doses of ethanol (3, 1.5, and [Formula: see text]) on murine fetal brain vasculature in utero. Additionally, simultaneous imaging of maternal peripheral vessels and the fetal brain vasculature was performed to assess changes of the vasculature occurring concurrently in response to ethanol consumption. Results: The fetal brain vessel diameters (VDs) decreased by [Formula: see text] , 30%, and 14% in response to ethanol doses of 3, 1.5, and [Formula: see text] , respectively. However, the mother’s hindlimb VD increased by 63% in response to ethanol at a dose of [Formula: see text]. Conclusions: Results showed a dose-dependent reduction in vascular blood flow in fetal brain vessels when the mother was exposed to ethanol, whereas vessels in the maternal hindlimb exhibited concurrent vasodilation.
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spelling pubmed-76892632020-11-27 Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure Raghunathan, Raksha Liu, Chih-Hao Kouka, Amur Singh, Manmohan Miranda, Rajesh C. Larin, Kirill V. J Biomed Opt Imaging Significance: Prenatal exposure to ethanol causes several morphological and neurobehavioral deficits. While there are some studies on the effects of ethanol exposure on blood flow, research focusing on acute changes in the microvasculature is limited. Aim: The first aim of this study was to assess the dose-dependent changes in murine fetal brain microvasculature of developing fetuses in response to maternal alcohol consumption. The second aim was to quantify changes in vasculature occurring concurrently in the mother’s hindlimb and the fetus’s brain after maternal exposure to alcohol. Approach: Correlation mapping optical coherence angiography was used to evaluate the effects of prenatal exposure to different doses of ethanol (3, 1.5, and [Formula: see text]) on murine fetal brain vasculature in utero. Additionally, simultaneous imaging of maternal peripheral vessels and the fetal brain vasculature was performed to assess changes of the vasculature occurring concurrently in response to ethanol consumption. Results: The fetal brain vessel diameters (VDs) decreased by [Formula: see text] , 30%, and 14% in response to ethanol doses of 3, 1.5, and [Formula: see text] , respectively. However, the mother’s hindlimb VD increased by 63% in response to ethanol at a dose of [Formula: see text]. Conclusions: Results showed a dose-dependent reduction in vascular blood flow in fetal brain vessels when the mother was exposed to ethanol, whereas vessels in the maternal hindlimb exhibited concurrent vasodilation. Society of Photo-Optical Instrumentation Engineers 2020-11-26 2020-12 /pmc/articles/PMC7689263/ /pubmed/33244919 http://dx.doi.org/10.1117/1.JBO.25.12.126001 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Imaging
Raghunathan, Raksha
Liu, Chih-Hao
Kouka, Amur
Singh, Manmohan
Miranda, Rajesh C.
Larin, Kirill V.
Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
title Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
title_full Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
title_fullStr Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
title_full_unstemmed Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
title_short Dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
title_sort dose-response analysis of microvasculature changes in the murine fetal brain and the maternal extremities due to prenatal ethanol exposure
topic Imaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689263/
https://www.ncbi.nlm.nih.gov/pubmed/33244919
http://dx.doi.org/10.1117/1.JBO.25.12.126001
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