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LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes

Electronic nicotine delivery systems or electronic cigarettes (e-cigarettes) are becoming exceptionally popular in the world as an alternative to conventional nicotine cigarettes, both among smokers and people who have never smoked. Nicotine can induce lipolysis in adipose tissue, leading to increas...

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Autores principales: Espinoza-Derout, Jorge, Shao, Xuesi M, Hasan, Kamrul M, Rivera, Juan-Carlos, Lao, Candice, Wilson, Julian, Jordan, Maria, Roos, Kenneth P, Sinha-Hikim, Amiya P, Friedman, Theodore C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625762/
http://dx.doi.org/10.1210/jendso/bvac150.011
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author Espinoza-Derout, Jorge
Shao, Xuesi M
Hasan, Kamrul M
Rivera, Juan-Carlos
Lao, Candice
Wilson, Julian
Jordan, Maria
Roos, Kenneth P
Sinha-Hikim, Amiya P
Friedman, Theodore C
author_facet Espinoza-Derout, Jorge
Shao, Xuesi M
Hasan, Kamrul M
Rivera, Juan-Carlos
Lao, Candice
Wilson, Julian
Jordan, Maria
Roos, Kenneth P
Sinha-Hikim, Amiya P
Friedman, Theodore C
author_sort Espinoza-Derout, Jorge
collection PubMed
description Electronic nicotine delivery systems or electronic cigarettes (e-cigarettes) are becoming exceptionally popular in the world as an alternative to conventional nicotine cigarettes, both among smokers and people who have never smoked. Nicotine can induce lipolysis in adipose tissue, leading to increased serum free fatty acids (FFAs). Increased levels of FFAs are one of the key elements in generating a pro-inflammatory response and lead to ectopic lipid accumulation, lipotoxicity, mitochondrial dysfunction, and DNA damage. Our laboratory has shown that e-cigarettes induce cardiac dysfunction associated with oxidative stress and inflammatory phenotype. We investigated the effects of acipimox, an antihyperlipidemic drug that blocks lipolysis, on e-cigarettes-induced cardiac dysfunction and its associated inflammatory signals and oxidative stress. C57BL/6J wild type mice on high fat diet were exposed to saline, e-cigarette with nicotine (2.4%), e-cigarette (2.4%) plus acipimox for 12 weeks. Fractional shortening and ejection fraction was decreased in mice exposed to e-cigarette (2.4%) compared with saline and acipimox. Therefore, acipimox normalized the e-cigarette-induced cardiac dysfunction. Transcriptomic evaluation with Gene Set Enrichment Analysis revealed that e-cigarette treated mice had genes enriched in the G2/M DNA damage checkpoint pathways. These transcriptomic changes were normalized by acipimox. Mice exposed to e-cigarettes had increased circulating levels of M-CSF, IL-6, and FFAs, which were decreased by acipimox. Mice exposed to e-cigarette (2.4%) had increased cardiac Heme oxygenase 1, a marker of oxidative stress. Additionally, treatment with e-cigarette (2.4%) increased the apurinic/apyrimidinic sites. This marker of oxidative DNA damage was normalized by acipimox. Understanding the consequences of e-cigarette use on the cardiovascular system is directly relevant to developing policies related to e-cigarette use. Presentation: Sunday, June 12, 2022 12:30 p.m. - 2:30 p.m.
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spelling pubmed-96257622022-11-14 LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes Espinoza-Derout, Jorge Shao, Xuesi M Hasan, Kamrul M Rivera, Juan-Carlos Lao, Candice Wilson, Julian Jordan, Maria Roos, Kenneth P Sinha-Hikim, Amiya P Friedman, Theodore C J Endocr Soc Adipose Tissue, Appetite, & Obesity Electronic nicotine delivery systems or electronic cigarettes (e-cigarettes) are becoming exceptionally popular in the world as an alternative to conventional nicotine cigarettes, both among smokers and people who have never smoked. Nicotine can induce lipolysis in adipose tissue, leading to increased serum free fatty acids (FFAs). Increased levels of FFAs are one of the key elements in generating a pro-inflammatory response and lead to ectopic lipid accumulation, lipotoxicity, mitochondrial dysfunction, and DNA damage. Our laboratory has shown that e-cigarettes induce cardiac dysfunction associated with oxidative stress and inflammatory phenotype. We investigated the effects of acipimox, an antihyperlipidemic drug that blocks lipolysis, on e-cigarettes-induced cardiac dysfunction and its associated inflammatory signals and oxidative stress. C57BL/6J wild type mice on high fat diet were exposed to saline, e-cigarette with nicotine (2.4%), e-cigarette (2.4%) plus acipimox for 12 weeks. Fractional shortening and ejection fraction was decreased in mice exposed to e-cigarette (2.4%) compared with saline and acipimox. Therefore, acipimox normalized the e-cigarette-induced cardiac dysfunction. Transcriptomic evaluation with Gene Set Enrichment Analysis revealed that e-cigarette treated mice had genes enriched in the G2/M DNA damage checkpoint pathways. These transcriptomic changes were normalized by acipimox. Mice exposed to e-cigarettes had increased circulating levels of M-CSF, IL-6, and FFAs, which were decreased by acipimox. Mice exposed to e-cigarette (2.4%) had increased cardiac Heme oxygenase 1, a marker of oxidative stress. Additionally, treatment with e-cigarette (2.4%) increased the apurinic/apyrimidinic sites. This marker of oxidative DNA damage was normalized by acipimox. Understanding the consequences of e-cigarette use on the cardiovascular system is directly relevant to developing policies related to e-cigarette use. Presentation: Sunday, June 12, 2022 12:30 p.m. - 2:30 p.m. Oxford University Press 2022-11-01 /pmc/articles/PMC9625762/ http://dx.doi.org/10.1210/jendso/bvac150.011 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Adipose Tissue, Appetite, & Obesity
Espinoza-Derout, Jorge
Shao, Xuesi M
Hasan, Kamrul M
Rivera, Juan-Carlos
Lao, Candice
Wilson, Julian
Jordan, Maria
Roos, Kenneth P
Sinha-Hikim, Amiya P
Friedman, Theodore C
LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes
title LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes
title_full LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes
title_fullStr LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes
title_full_unstemmed LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes
title_short LBSUN85 Acipimox Normalizes The Cardiac Phenotype Induced By Electronic Cigarettes
title_sort lbsun85 acipimox normalizes the cardiac phenotype induced by electronic cigarettes
topic Adipose Tissue, Appetite, & Obesity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625762/
http://dx.doi.org/10.1210/jendso/bvac150.011
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