E-cigarettes damage the liver and alter nutrient metabolism in pregnant mice and their offspring

Ann N Y Acad Sci. 2020 Sep;1475(1):64-77. doi: 10.1111/nyas.14411. Epub 2020 Jun 17.

Abstract

Approximately 15% of pregnant women vape electronic cigarettes (e-cigarettes), exposing the fetus to a range of toxic compounds, including nicotine and by-products of e-cigarette liquid (e-liquid) pyrolysis. Owing to the recent emergence of these products, research mainly focuses on immediate users, and not on in utero exposure. Therefore, this study aimed to understand the impact of intrauterine e-cigarette vapor (e-vapor) exposure, with and without nicotine, on liver metabolic markers in the male offspring. E-vapor was generated using an e-cigarette filled with tobacco-flavored e-liquid (18 or 0 mg/mL nicotine). Female Balb/c mice were exposed to e-vapor for 6 weeks before mating, through gestation and lactation, without direct exposure to the offspring. Livers and plasma from dams and male offspring (13 weeks old) were examined. Exposure to nicotine-free e-vapor promoted metabolic changes and liver damage in both the dams and their offspring. Furthermore, exposure to nicotine-containing e-vapor did not cause liver damage but induced hepatic steatosis in the adult offspring. Therefore, maternal vaping is detrimental to both the dams and their offspring, with nicotine providing a potential protective effect.

Keywords: e-cigarettes; glucose intolerance; mitochondria; nicotine; triglycerides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Area Under Curve
  • Autophagy
  • Biomarkers / metabolism
  • DNA, Mitochondrial / metabolism
  • Electronic Nicotine Delivery Systems*
  • Female
  • Gene Expression Regulation
  • Liver / metabolism
  • Liver / pathology*
  • Male
  • Mice, Inbred BALB C
  • Mitochondria, Liver / metabolism
  • Mitophagy
  • Nutrients / metabolism*
  • Oxidative Stress
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • Antioxidants
  • Biomarkers
  • DNA, Mitochondrial
  • RNA, Messenger