4.5 Article

Adverse effects of fetal exposure of electronic-cigarettes and high-fat diet on male neonatal hearts

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yexmp.2020.104573

关键词

E-cigarette; Nicotine; High-fat diet; Oxidative stress; Cardiomyocyte apoptosis; Mice

资金

  1. Diversity-Promoting Institution Drug Abuse Research Program (DIDARP) grant [R24DA017298]
  2. Accelerating Excellence in Translational Science (AXIS) [2U54MD007598]
  3. Competitive Research (SCORE) [1SC2GM125551-01]
  4. National Institute on Minority Health and Health Disparities from the National Institutes of Health (NIH) [S21 MD000103]
  5. California Tobacco-Related Disease Research Program (TRDRP) [251P003]
  6. Department of Veterans Affairs [I01BX000323]

向作者/读者索取更多资源

This study demonstrates that gestational exposure to e-cigarettes and a high-fat diet can lead to cardiomyocyte apoptosis in neonatal hearts, as well as the activation of various proteins associated with heart function. Additionally, exposure to e-cigarettes can also cause cardiomyopathy and cardiac dysfunction.
Epidemiological studies have shown an increased risk of cardiovascular diseases in children born to mothers who smoked during pregnancy. The cardiovascular risk in the offspring associated with in utero nicotine exposure is further exaggerated by maternal obesity. The consumption of electronic cigarettes (e-cigarettes) is alarmingly increasing among adolescents and young adults without the knowledge of their harmful health effects. There has also been a substantial increase in e-cigarette use by women of reproductive age. This study investigates the detrimental effects of gestational exposure of e-cigarette and a high-fat diet (HFD) on neonatal hearts. Time-mated pregnant mice were fed a HFD and exposed to saline or e-cigarette aerosol with 2.4% nicotine from embryonic day 4 (E4) to E20. We demonstrated that in utero exposure of e-cigarettes and HFD from E4 to E20 triggers cardiomyocyte (CM) apoptosis in the offspring at postnatal day1 (PND1), PND3, and PND14. Induction of CM apoptosis following gestational exposure of e-cigarettes and HFD was associated with inactivation of AMP-activated protein kinase (AMPK), increased cardiac oxidative stress coupled with perturbation of cardiac BAX/ BCL-2 ratio and activation of caspase 3 at PND 14. Electron microscopy further revealed that left ventricles of pups at PND14 after e-cigarette exposure exhibited apoptotic nuclei, convoluted nuclear membranes, myofibrillar derangement, and enlarged mitochondria occasionally showing signs of crystolysis, indicative of cardiomyopathy and cardiac dysfunction. Our results show profound adverse effects of prenatal exposure of ecigarette plus HFD in neonatal hearts that may lead to long-term adverse cardiac consequences in the adult.

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