Prenatal ethanol exposure impairs the conduction delay at the atrioventricular junction in the looping heart
The etiology of ethanol-related congenital heart defects has been the focus of much study, but most research has concentrated on cellular and molecular mechanisms. We have shown with optical coherence tomography (OCT) that ethanol exposure led to increased retrograde flow and smaller atrioventricula...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2021-08, Vol.321 (2), p.H294-H305 |
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description | The etiology of ethanol-related congenital heart defects has been the focus of much study, but most research has concentrated on cellular and molecular mechanisms. We have shown with optical coherence tomography (OCT) that ethanol exposure led to increased retrograde flow and smaller atrioventricular (AV) cushions compared with controls. Since AV cushions play a role in patterning the conduction delay at the atrioventricular junction (AVJ), this study aims to investigate whether ethanol exposure alters the AVJ conduction in early looping hearts and whether this alteration is related to the decreased cushion size. Quail embryos were exposed to a single dose of ethanol at gastrulation, and Hamburger-Hamilton stage 19-20 hearts were dissected for imaging. Cardiac conduction was measured using an optical mapping microscope and we imaged the endocardial cushions using OCT. Our results showed that, compared with controls, ethanol-exposed embryos exhibited abnormally fast AVJ conduction and reduced cushion size. However, this increased conduction velocity (CV) did not strictly correlate with decreased cushion volume and thickness. By matching the CV map to the cushion-size map along the inflow heart tube, we found that the slowest conduction location was consistently at the atrial side of the AVJ, which had the thinner cushions, not at the thickest cushion location at the ventricular side as expected. Our findings reveal regional differences in the AVJ myocardium even at this early stage in heart development. These findings reveal the early steps leading to the heterogeneity and complexity of conduction at the mature AVJ, a site where arrhythmias can be initiated.
To the best of our knowledge, this is the first study investigating the impact of ethanol exposure on the early cardiac conduction system. Our results showed that ethanol-exposed embryos exhibited abnormally fast atrioventricular conduction. In addition, our findings, in CV measurements and endocardial cushion thickness, reveal regional differences in the AVJ myocardium even at this early stage in heart development, suggesting that the differentiation and maturation at this site are complex and warrant further studies. |
doi_str_mv | 10.1152/ajpheart.00107.2021 |
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To the best of our knowledge, this is the first study investigating the impact of ethanol exposure on the early cardiac conduction system. Our results showed that ethanol-exposed embryos exhibited abnormally fast atrioventricular conduction. In addition, our findings, in CV measurements and endocardial cushion thickness, reveal regional differences in the AVJ myocardium even at this early stage in heart development, suggesting that the differentiation and maturation at this site are complex and warrant further studies.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00107.2021</identifier><identifier>PMID: 34142884</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Central Nervous System Depressants - pharmacology ; Conduction ; Cushions ; Developmental stages ; Embryo, Nonmammalian ; Embryos ; Endocardial Cushions - diagnostic imaging ; Endocardial Cushions - drug effects ; Endocardial Cushions - embryology ; Ethanol ; Ethanol - pharmacology ; Etiology ; Exposure ; Gastrulation ; Heart ; Heart - diagnostic imaging ; Heart - drug effects ; Heart - embryology ; Heart Conduction System - diagnostic imaging ; Heart Conduction System - drug effects ; Heart Conduction System - embryology ; Heterogeneity ; Molecular modelling ; Myocardium ; Optical Coherence Tomography ; Prenatal experience ; Quail ; Tomography, Optical Coherence ; Ventricle ; Voltage-Sensitive Dye Imaging</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2021-08, Vol.321 (2), p.H294-H305</ispartof><rights>Copyright American Physiological Society Aug 2021</rights><rights>Copyright © 2021 the American Physiological Society 2021 American Physiological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-363ce0ec34f19978257bf70f7dd0d1b2b2d51b601d120fdc47c0f9a20deca8f63</citedby><cites>FETCH-LOGICAL-c433t-363ce0ec34f19978257bf70f7dd0d1b2b2d51b601d120fdc47c0f9a20deca8f63</cites><orcidid>0000-0002-7780-4862</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3025,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34142884$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ling, Shan</creatorcontrib><creatorcontrib>Jenkins, Michael W</creatorcontrib><creatorcontrib>Watanabe, Michiko</creatorcontrib><creatorcontrib>Ford, Stephanie M</creatorcontrib><creatorcontrib>Rollins, Andrew M</creatorcontrib><title>Prenatal ethanol exposure impairs the conduction delay at the atrioventricular junction in the looping heart</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>The etiology of ethanol-related congenital heart defects has been the focus of much study, but most research has concentrated on cellular and molecular mechanisms. We have shown with optical coherence tomography (OCT) that ethanol exposure led to increased retrograde flow and smaller atrioventricular (AV) cushions compared with controls. Since AV cushions play a role in patterning the conduction delay at the atrioventricular junction (AVJ), this study aims to investigate whether ethanol exposure alters the AVJ conduction in early looping hearts and whether this alteration is related to the decreased cushion size. Quail embryos were exposed to a single dose of ethanol at gastrulation, and Hamburger-Hamilton stage 19-20 hearts were dissected for imaging. Cardiac conduction was measured using an optical mapping microscope and we imaged the endocardial cushions using OCT. Our results showed that, compared with controls, ethanol-exposed embryos exhibited abnormally fast AVJ conduction and reduced cushion size. However, this increased conduction velocity (CV) did not strictly correlate with decreased cushion volume and thickness. By matching the CV map to the cushion-size map along the inflow heart tube, we found that the slowest conduction location was consistently at the atrial side of the AVJ, which had the thinner cushions, not at the thickest cushion location at the ventricular side as expected. Our findings reveal regional differences in the AVJ myocardium even at this early stage in heart development. These findings reveal the early steps leading to the heterogeneity and complexity of conduction at the mature AVJ, a site where arrhythmias can be initiated.
To the best of our knowledge, this is the first study investigating the impact of ethanol exposure on the early cardiac conduction system. Our results showed that ethanol-exposed embryos exhibited abnormally fast atrioventricular conduction. In addition, our findings, in CV measurements and endocardial cushion thickness, reveal regional differences in the AVJ myocardium even at this early stage in heart development, suggesting that the differentiation and maturation at this site are complex and warrant further studies.</description><subject>Animals</subject><subject>Central Nervous System Depressants - pharmacology</subject><subject>Conduction</subject><subject>Cushions</subject><subject>Developmental stages</subject><subject>Embryo, Nonmammalian</subject><subject>Embryos</subject><subject>Endocardial Cushions - diagnostic imaging</subject><subject>Endocardial Cushions - drug effects</subject><subject>Endocardial Cushions - embryology</subject><subject>Ethanol</subject><subject>Ethanol - pharmacology</subject><subject>Etiology</subject><subject>Exposure</subject><subject>Gastrulation</subject><subject>Heart</subject><subject>Heart - diagnostic imaging</subject><subject>Heart - drug effects</subject><subject>Heart - embryology</subject><subject>Heart Conduction System - diagnostic imaging</subject><subject>Heart Conduction System - drug effects</subject><subject>Heart Conduction System - embryology</subject><subject>Heterogeneity</subject><subject>Molecular modelling</subject><subject>Myocardium</subject><subject>Optical Coherence Tomography</subject><subject>Prenatal experience</subject><subject>Quail</subject><subject>Tomography, Optical Coherence</subject><subject>Ventricle</subject><subject>Voltage-Sensitive Dye Imaging</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd1LHDEUxUNR6mr7FxTKgC99mfXmaz5ehCJtFQR9aJ9DJsm4WbLJmGRE_3uzuyrWpwP3_u7hXA5C3zAsMebkTK6nlZExLwEwtEsCBH9Ci7IhNea0P0ALoA2tG0z5ETpOaQ0AvG3oZ3REGWak69gCudtovMzSVSavpA9FH6eQ5mgqu5mkjanKK1Op4PWssg2-0sbJp0rm3VzmaMOD8UXU7GSs1rPfY9bvABfCZP1dtUv6BR2O0iXz9UVP0L_fv_5eXNbXN3-uLn5e14pRmuuSWhkwirIR933bEd4OYwtjqzVoPJCBaI6HBrDGBEatWKtg7CUBbZTsxoaeoPO97zQPG6PVNp90Yop2I-OTCNKK_zfersRdeBAdJw2lW4MfLwYx3M8mZbGxSRnnpDdhToJwRhnjmPQFPf2ArsMcfXmvUC0QyhqGC0X3lIohpWjGtzAYxLZN8dqm2LUptm2Wq-_v_3i7ea2PPgPt0KCB</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Ling, Shan</creator><creator>Jenkins, Michael W</creator><creator>Watanabe, Michiko</creator><creator>Ford, Stephanie M</creator><creator>Rollins, Andrew M</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7780-4862</orcidid></search><sort><creationdate>20210801</creationdate><title>Prenatal ethanol exposure impairs the conduction delay at the atrioventricular junction in the looping heart</title><author>Ling, Shan ; Jenkins, Michael W ; Watanabe, Michiko ; Ford, Stephanie M ; Rollins, Andrew M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-363ce0ec34f19978257bf70f7dd0d1b2b2d51b601d120fdc47c0f9a20deca8f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Central Nervous System Depressants - pharmacology</topic><topic>Conduction</topic><topic>Cushions</topic><topic>Developmental stages</topic><topic>Embryo, Nonmammalian</topic><topic>Embryos</topic><topic>Endocardial Cushions - diagnostic imaging</topic><topic>Endocardial Cushions - drug effects</topic><topic>Endocardial Cushions - embryology</topic><topic>Ethanol</topic><topic>Ethanol - pharmacology</topic><topic>Etiology</topic><topic>Exposure</topic><topic>Gastrulation</topic><topic>Heart</topic><topic>Heart - diagnostic imaging</topic><topic>Heart - drug effects</topic><topic>Heart - embryology</topic><topic>Heart Conduction System - diagnostic imaging</topic><topic>Heart Conduction System - drug effects</topic><topic>Heart Conduction System - embryology</topic><topic>Heterogeneity</topic><topic>Molecular modelling</topic><topic>Myocardium</topic><topic>Optical Coherence Tomography</topic><topic>Prenatal experience</topic><topic>Quail</topic><topic>Tomography, Optical Coherence</topic><topic>Ventricle</topic><topic>Voltage-Sensitive Dye Imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ling, Shan</creatorcontrib><creatorcontrib>Jenkins, Michael W</creatorcontrib><creatorcontrib>Watanabe, Michiko</creatorcontrib><creatorcontrib>Ford, Stephanie M</creatorcontrib><creatorcontrib>Rollins, Andrew M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ling, Shan</au><au>Jenkins, Michael W</au><au>Watanabe, Michiko</au><au>Ford, Stephanie M</au><au>Rollins, Andrew M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prenatal ethanol exposure impairs the conduction delay at the atrioventricular junction in the looping heart</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>321</volume><issue>2</issue><spage>H294</spage><epage>H305</epage><pages>H294-H305</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>The etiology of ethanol-related congenital heart defects has been the focus of much study, but most research has concentrated on cellular and molecular mechanisms. We have shown with optical coherence tomography (OCT) that ethanol exposure led to increased retrograde flow and smaller atrioventricular (AV) cushions compared with controls. Since AV cushions play a role in patterning the conduction delay at the atrioventricular junction (AVJ), this study aims to investigate whether ethanol exposure alters the AVJ conduction in early looping hearts and whether this alteration is related to the decreased cushion size. Quail embryos were exposed to a single dose of ethanol at gastrulation, and Hamburger-Hamilton stage 19-20 hearts were dissected for imaging. Cardiac conduction was measured using an optical mapping microscope and we imaged the endocardial cushions using OCT. Our results showed that, compared with controls, ethanol-exposed embryos exhibited abnormally fast AVJ conduction and reduced cushion size. However, this increased conduction velocity (CV) did not strictly correlate with decreased cushion volume and thickness. By matching the CV map to the cushion-size map along the inflow heart tube, we found that the slowest conduction location was consistently at the atrial side of the AVJ, which had the thinner cushions, not at the thickest cushion location at the ventricular side as expected. Our findings reveal regional differences in the AVJ myocardium even at this early stage in heart development. These findings reveal the early steps leading to the heterogeneity and complexity of conduction at the mature AVJ, a site where arrhythmias can be initiated.
To the best of our knowledge, this is the first study investigating the impact of ethanol exposure on the early cardiac conduction system. Our results showed that ethanol-exposed embryos exhibited abnormally fast atrioventricular conduction. In addition, our findings, in CV measurements and endocardial cushion thickness, reveal regional differences in the AVJ myocardium even at this early stage in heart development, suggesting that the differentiation and maturation at this site are complex and warrant further studies.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>34142884</pmid><doi>10.1152/ajpheart.00107.2021</doi><orcidid>https://orcid.org/0000-0002-7780-4862</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Central Nervous System Depressants - pharmacology Conduction Cushions Developmental stages Embryo, Nonmammalian Embryos Endocardial Cushions - diagnostic imaging Endocardial Cushions - drug effects Endocardial Cushions - embryology Ethanol Ethanol - pharmacology Etiology Exposure Gastrulation Heart Heart - diagnostic imaging Heart - drug effects Heart - embryology Heart Conduction System - diagnostic imaging Heart Conduction System - drug effects Heart Conduction System - embryology Heterogeneity Molecular modelling Myocardium Optical Coherence Tomography Prenatal experience Quail Tomography, Optical Coherence Ventricle Voltage-Sensitive Dye Imaging |
title | Prenatal ethanol exposure impairs the conduction delay at the atrioventricular junction in the looping heart |
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