Long-term cerebrovascular dysfunction in the offspring from maternal electronic cigarette use during pregnancy
Electronic cigarettes (E-cigs) have been promoted as harm-free or less risky than smoking, even for women during pregnancy. These claims are made largely on E-cig aerosol having fewer number of toxic chemicals compared with cigarette smoke. Given that even low levels of smoking are found to produce...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2021-08, Vol.321 (2), p.H339-H352 |
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description | Electronic cigarettes (E-cigs) have been promoted as harm-free or less risky than smoking, even for women during pregnancy. These claims are made largely on E-cig aerosol having fewer number of toxic chemicals compared with cigarette smoke. Given that even low levels of smoking are found to produce adverse birth outcomes, we sought to test the hypothesis that vaping during pregnancy (with or without nicotine) would not be harm-free and would result in vascular dysfunction that would be evident in offspring during adolescent and/or adult life. Pregnant female Sprague Dawley rats were exposed to E-cig aerosol (1 h/day, 5 days/wk, starting on
until pups were weaned) using e-liquid with 0 mg/mL (E-cig0) or 18 mg/mL nicotine (E-cig18) and compared with ambient air-exposed controls. Body mass at birth and at weaning were not different between groups. Assessment of middle cerebral artery (MCA) reactivity revealed a 51%-56% reduction in endothelial-dependent dilation response to acetylcholine (ACh) for both E-cig0 and E-cig18 in 1-mo, 3-mo (adolescent), and 7-mo-old (adult) offspring (
< 0.05 compared with air, all time points). MCA responses to sodium nitroprusside (SNP) and myogenic tone were not different across groups, suggesting that endothelial-independent responses were not altered. The MCA vasoconstrictor response (5-hydroxytryptamine, 5-HT) was also not different across treatment and age groups. These data demonstrate that maternal vaping during pregnancy is not harm-free and confers significant cerebrovascular health risk/dysfunction to offspring that persists into adult life.
These data established that vaping electronic cigarettes during pregnancy, with or without nicotine, is not safe and confers significant risk potential to the cerebrovascular health of offspring in early and adult life. A key finding is that vaping without nicotine does not protect offspring from cerebrovascular dysfunction and results in the same level of cerebrovascular dysfunction (compared with maternal vaping with nicotine), indicating that the physical and/or chemical properties from the base solution (other than nicotine) are responsible for the cerebrovascular dysfunction that we observed. Listen to this article's corresponding podcast at https://ajpheart.podbean.com/e/maternal-vaping-impairs-vascular-function-in-theoffspring/. |
doi_str_mv | 10.1152/ajpheart.00206.2021 |
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until pups were weaned) using e-liquid with 0 mg/mL (E-cig0) or 18 mg/mL nicotine (E-cig18) and compared with ambient air-exposed controls. Body mass at birth and at weaning were not different between groups. Assessment of middle cerebral artery (MCA) reactivity revealed a 51%-56% reduction in endothelial-dependent dilation response to acetylcholine (ACh) for both E-cig0 and E-cig18 in 1-mo, 3-mo (adolescent), and 7-mo-old (adult) offspring (
< 0.05 compared with air, all time points). MCA responses to sodium nitroprusside (SNP) and myogenic tone were not different across groups, suggesting that endothelial-independent responses were not altered. The MCA vasoconstrictor response (5-hydroxytryptamine, 5-HT) was also not different across treatment and age groups. These data demonstrate that maternal vaping during pregnancy is not harm-free and confers significant cerebrovascular health risk/dysfunction to offspring that persists into adult life.
These data established that vaping electronic cigarettes during pregnancy, with or without nicotine, is not safe and confers significant risk potential to the cerebrovascular health of offspring in early and adult life. A key finding is that vaping without nicotine does not protect offspring from cerebrovascular dysfunction and results in the same level of cerebrovascular dysfunction (compared with maternal vaping with nicotine), indicating that the physical and/or chemical properties from the base solution (other than nicotine) are responsible for the cerebrovascular dysfunction that we observed. Listen to this article's corresponding podcast at https://ajpheart.podbean.com/e/maternal-vaping-impairs-vascular-function-in-theoffspring/.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00206.2021</identifier><identifier>PMID: 34170194</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Acetylcholine ; Acetylcholine - pharmacology ; Adolescents ; Aerosols ; Animals ; Birth ; Body mass ; Cigarette smoke ; Cigarettes ; E-Cigarette Vapor - pharmacology ; Electronic cigarettes ; Electronic Nicotine Delivery Systems ; Endothelium, Vascular - drug effects ; Endothelium, Vascular - physiopathology ; Female ; Health risks ; Middle Cerebral Artery - drug effects ; Middle Cerebral Artery - physiopathology ; Nicotine ; Nicotine - administration & dosage ; Nicotine - pharmacology ; Nicotinic Agonists - administration & dosage ; Nicotinic Agonists - pharmacology ; Nitroprusside - pharmacology ; Offspring ; Pregnancy ; Prenatal Exposure Delayed Effects ; Rats ; Serotonin - pharmacology ; Smoking ; Sodium nitroprusside ; Vaping ; Vasoconstriction - drug effects ; Vasoconstriction - physiology ; Vasoconstrictor Agents - pharmacology ; Vasodilation - drug effects ; Vasodilation - physiology ; Vasodilator Agents - pharmacology ; Weaning</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2021-08, Vol.321 (2), p.H339-H352</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-4f4c3762e8bfca794180348dc46c2b0d2a0a04ae99f51f973a6b3b4ee1344e5f3</citedby><cites>FETCH-LOGICAL-c433t-4f4c3762e8bfca794180348dc46c2b0d2a0a04ae99f51f973a6b3b4ee1344e5f3</cites><orcidid>0000-0003-3505-9945 ; 0000-0002-6288-4927 ; 0000-0001-6960-9728 ; 0000-0002-6983-0200</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34170194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burrage, E N</creatorcontrib><creatorcontrib>Aboaziza, E</creatorcontrib><creatorcontrib>Hare, L</creatorcontrib><creatorcontrib>Reppert, S</creatorcontrib><creatorcontrib>Moore, J</creatorcontrib><creatorcontrib>Goldsmith, W T</creatorcontrib><creatorcontrib>Kelley, E E</creatorcontrib><creatorcontrib>Mills, A</creatorcontrib><creatorcontrib>Dakhlallah, D</creatorcontrib><creatorcontrib>Chantler, P D</creatorcontrib><creatorcontrib>Olfert, I M</creatorcontrib><title>Long-term cerebrovascular dysfunction in the offspring from maternal electronic cigarette use during pregnancy</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Electronic cigarettes (E-cigs) have been promoted as harm-free or less risky than smoking, even for women during pregnancy. These claims are made largely on E-cig aerosol having fewer number of toxic chemicals compared with cigarette smoke. Given that even low levels of smoking are found to produce adverse birth outcomes, we sought to test the hypothesis that vaping during pregnancy (with or without nicotine) would not be harm-free and would result in vascular dysfunction that would be evident in offspring during adolescent and/or adult life. Pregnant female Sprague Dawley rats were exposed to E-cig aerosol (1 h/day, 5 days/wk, starting on
until pups were weaned) using e-liquid with 0 mg/mL (E-cig0) or 18 mg/mL nicotine (E-cig18) and compared with ambient air-exposed controls. Body mass at birth and at weaning were not different between groups. Assessment of middle cerebral artery (MCA) reactivity revealed a 51%-56% reduction in endothelial-dependent dilation response to acetylcholine (ACh) for both E-cig0 and E-cig18 in 1-mo, 3-mo (adolescent), and 7-mo-old (adult) offspring (
< 0.05 compared with air, all time points). MCA responses to sodium nitroprusside (SNP) and myogenic tone were not different across groups, suggesting that endothelial-independent responses were not altered. The MCA vasoconstrictor response (5-hydroxytryptamine, 5-HT) was also not different across treatment and age groups. These data demonstrate that maternal vaping during pregnancy is not harm-free and confers significant cerebrovascular health risk/dysfunction to offspring that persists into adult life.
These data established that vaping electronic cigarettes during pregnancy, with or without nicotine, is not safe and confers significant risk potential to the cerebrovascular health of offspring in early and adult life. A key finding is that vaping without nicotine does not protect offspring from cerebrovascular dysfunction and results in the same level of cerebrovascular dysfunction (compared with maternal vaping with nicotine), indicating that the physical and/or chemical properties from the base solution (other than nicotine) are responsible for the cerebrovascular dysfunction that we observed. Listen to this article's corresponding podcast at https://ajpheart.podbean.com/e/maternal-vaping-impairs-vascular-function-in-theoffspring/.</description><subject>Acetylcholine</subject><subject>Acetylcholine - pharmacology</subject><subject>Adolescents</subject><subject>Aerosols</subject><subject>Animals</subject><subject>Birth</subject><subject>Body mass</subject><subject>Cigarette smoke</subject><subject>Cigarettes</subject><subject>E-Cigarette Vapor - pharmacology</subject><subject>Electronic cigarettes</subject><subject>Electronic Nicotine Delivery Systems</subject><subject>Endothelium, Vascular - drug effects</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Female</subject><subject>Health risks</subject><subject>Middle Cerebral Artery - drug effects</subject><subject>Middle Cerebral Artery - physiopathology</subject><subject>Nicotine</subject><subject>Nicotine - administration & dosage</subject><subject>Nicotine - pharmacology</subject><subject>Nicotinic Agonists - administration & dosage</subject><subject>Nicotinic Agonists - pharmacology</subject><subject>Nitroprusside - pharmacology</subject><subject>Offspring</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Rats</subject><subject>Serotonin - pharmacology</subject><subject>Smoking</subject><subject>Sodium nitroprusside</subject><subject>Vaping</subject><subject>Vasoconstriction - drug effects</subject><subject>Vasoconstriction - physiology</subject><subject>Vasoconstrictor Agents - pharmacology</subject><subject>Vasodilation - drug effects</subject><subject>Vasodilation - physiology</subject><subject>Vasodilator Agents - pharmacology</subject><subject>Weaning</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>eNpVkc2LFDEQxYMo7jj6FwgS8Nxjkkp_XQRZVl0Y8KLnUJ2u9PTQnYxJemH---3ZL_RUh1fv1St-jH2UYidlqb7g8XQgjHknhBLVTgklX7HNqqhCltC-ZhsBFRSVhPKKvUvpKIQo6wresivQshay1Rvm98EPRaY4c0uRuhjuMNllwsj7c3KLt3kMno-e5wPx4Fw6xdEP3MUw8xlXo8eJ00Q2x-BHy-04YKSciS-JeL88bJ8iDR69Pb9nbxxOiT48zS378_3m9_XPYv_rx-31t31hNUAutNMW6kpR0zmLdatlI0A3vdWVVZ3oFQoUGqltXSldWwNWHXSaSILWVDrYsq-Puaelm6m35HPEyazdZ4xnE3A0_yt-PJgh3JlGSyFlswZ8fgqI4e9CKZtjWC6_JqPKWigoL5W2DB63bAwpRXIvF6QwF0jmGZJ5gGQukFbXp3_LvXieqcA9PdGTcw</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Burrage, E N</creator><creator>Aboaziza, E</creator><creator>Hare, L</creator><creator>Reppert, S</creator><creator>Moore, J</creator><creator>Goldsmith, W T</creator><creator>Kelley, E E</creator><creator>Mills, A</creator><creator>Dakhlallah, D</creator><creator>Chantler, P D</creator><creator>Olfert, I 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>5PM</scope><orcidid>https://orcid.org/0000-0003-3505-9945</orcidid><orcidid>https://orcid.org/0000-0002-6288-4927</orcidid><orcidid>https://orcid.org/0000-0001-6960-9728</orcidid><orcidid>https://orcid.org/0000-0002-6983-0200</orcidid></search><sort><creationdate>20210801</creationdate><title>Long-term cerebrovascular dysfunction in the offspring from maternal electronic cigarette use during pregnancy</title><author>Burrage, E N ; Aboaziza, E ; Hare, L ; Reppert, S ; Moore, J ; Goldsmith, W T ; Kelley, E E ; Mills, A ; Dakhlallah, D ; Chantler, P D ; Olfert, I M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-4f4c3762e8bfca794180348dc46c2b0d2a0a04ae99f51f973a6b3b4ee1344e5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acetylcholine</topic><topic>Acetylcholine - pharmacology</topic><topic>Adolescents</topic><topic>Aerosols</topic><topic>Animals</topic><topic>Birth</topic><topic>Body mass</topic><topic>Cigarette smoke</topic><topic>Cigarettes</topic><topic>E-Cigarette Vapor - pharmacology</topic><topic>Electronic cigarettes</topic><topic>Electronic Nicotine Delivery Systems</topic><topic>Endothelium, Vascular - drug effects</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Female</topic><topic>Health risks</topic><topic>Middle Cerebral Artery - drug effects</topic><topic>Middle Cerebral Artery - physiopathology</topic><topic>Nicotine</topic><topic>Nicotine - administration & dosage</topic><topic>Nicotine - pharmacology</topic><topic>Nicotinic Agonists - administration & dosage</topic><topic>Nicotinic Agonists - pharmacology</topic><topic>Nitroprusside - pharmacology</topic><topic>Offspring</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Rats</topic><topic>Serotonin - pharmacology</topic><topic>Smoking</topic><topic>Sodium nitroprusside</topic><topic>Vaping</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasoconstriction - physiology</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>Vasodilation - drug effects</topic><topic>Vasodilation - physiology</topic><topic>Vasodilator Agents - pharmacology</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burrage, E N</creatorcontrib><creatorcontrib>Aboaziza, E</creatorcontrib><creatorcontrib>Hare, L</creatorcontrib><creatorcontrib>Reppert, S</creatorcontrib><creatorcontrib>Moore, J</creatorcontrib><creatorcontrib>Goldsmith, W T</creatorcontrib><creatorcontrib>Kelley, E E</creatorcontrib><creatorcontrib>Mills, A</creatorcontrib><creatorcontrib>Dakhlallah, D</creatorcontrib><creatorcontrib>Chantler, P D</creatorcontrib><creatorcontrib>Olfert, I 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>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>Burrage, E N</au><au>Aboaziza, E</au><au>Hare, L</au><au>Reppert, S</au><au>Moore, J</au><au>Goldsmith, W T</au><au>Kelley, E E</au><au>Mills, A</au><au>Dakhlallah, D</au><au>Chantler, P D</au><au>Olfert, I M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term cerebrovascular dysfunction in the offspring from maternal electronic cigarette use during pregnancy</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>H339</spage><epage>H352</epage><pages>H339-H352</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><abstract>Electronic cigarettes (E-cigs) have been promoted as harm-free or less risky than smoking, even for women during pregnancy. These claims are made largely on E-cig aerosol having fewer number of toxic chemicals compared with cigarette smoke. Given that even low levels of smoking are found to produce adverse birth outcomes, we sought to test the hypothesis that vaping during pregnancy (with or without nicotine) would not be harm-free and would result in vascular dysfunction that would be evident in offspring during adolescent and/or adult life. Pregnant female Sprague Dawley rats were exposed to E-cig aerosol (1 h/day, 5 days/wk, starting on
until pups were weaned) using e-liquid with 0 mg/mL (E-cig0) or 18 mg/mL nicotine (E-cig18) and compared with ambient air-exposed controls. Body mass at birth and at weaning were not different between groups. Assessment of middle cerebral artery (MCA) reactivity revealed a 51%-56% reduction in endothelial-dependent dilation response to acetylcholine (ACh) for both E-cig0 and E-cig18 in 1-mo, 3-mo (adolescent), and 7-mo-old (adult) offspring (
< 0.05 compared with air, all time points). MCA responses to sodium nitroprusside (SNP) and myogenic tone were not different across groups, suggesting that endothelial-independent responses were not altered. The MCA vasoconstrictor response (5-hydroxytryptamine, 5-HT) was also not different across treatment and age groups. These data demonstrate that maternal vaping during pregnancy is not harm-free and confers significant cerebrovascular health risk/dysfunction to offspring that persists into adult life.
These data established that vaping electronic cigarettes during pregnancy, with or without nicotine, is not safe and confers significant risk potential to the cerebrovascular health of offspring in early and adult life. A key finding is that vaping without nicotine does not protect offspring from cerebrovascular dysfunction and results in the same level of cerebrovascular dysfunction (compared with maternal vaping with nicotine), indicating that the physical and/or chemical properties from the base solution (other than nicotine) are responsible for the cerebrovascular dysfunction that we observed. Listen to this article's corresponding podcast at https://ajpheart.podbean.com/e/maternal-vaping-impairs-vascular-function-in-theoffspring/.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>34170194</pmid><doi>10.1152/ajpheart.00206.2021</doi><orcidid>https://orcid.org/0000-0003-3505-9945</orcidid><orcidid>https://orcid.org/0000-0002-6288-4927</orcidid><orcidid>https://orcid.org/0000-0001-6960-9728</orcidid><orcidid>https://orcid.org/0000-0002-6983-0200</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine Acetylcholine - pharmacology Adolescents Aerosols Animals Birth Body mass Cigarette smoke Cigarettes E-Cigarette Vapor - pharmacology Electronic cigarettes Electronic Nicotine Delivery Systems Endothelium, Vascular - drug effects Endothelium, Vascular - physiopathology Female Health risks Middle Cerebral Artery - drug effects Middle Cerebral Artery - physiopathology Nicotine Nicotine - administration & dosage Nicotine - pharmacology Nicotinic Agonists - administration & dosage Nicotinic Agonists - pharmacology Nitroprusside - pharmacology Offspring Pregnancy Prenatal Exposure Delayed Effects Rats Serotonin - pharmacology Smoking Sodium nitroprusside Vaping Vasoconstriction - drug effects Vasoconstriction - physiology Vasoconstrictor Agents - pharmacology Vasodilation - drug effects Vasodilation - physiology Vasodilator Agents - pharmacology Weaning |
title | Long-term cerebrovascular dysfunction in the offspring from maternal electronic cigarette use during pregnancy |
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