Ethanol and tobacco smoke increase hepatic steatosis and hypoxia in the hypercholesterolemic apoE-/- mouse: Implications for a "multihit" hypothesis of fatty liver disease

Shannon M. Bailey, Sudheer K. Mantena, Telisha Millender-Swain, Yavuz Cakir, Nirag C. Jhala, David Chhieng, Kent E Pinkerton, Scott W. Ballinger

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

Although epidemiologic studies indicate that combined exposure to cigarette smoke and alcohol increase the risk and severity of liver diseases, the molecular mechanisms responsible for hepatotoxicity are unknown. Similarly, emerging evidence indicates a linkage among hepatic steatosis and cardiovascular disease. Herein, we hypothesize that combined exposure to alcohol and environmental tobacco smoke (ETS) on a hypercholesterolemic background increases liver injury through oxidative/nitrative stress, hypoxia, and mitochondrial damage. To test this, male apoE-/- mice were exposed to an ethanol-containing diet, ETS alone, or a combination of the two, and histology and functional endpoints were compared to filtered-air-exposed, ethanol-naïve controls. Whereas ethanol consumption induced a mild steatosis, combined exposure to ethanol + ETS resulted in increased hepatic steatosis, inflammation, α-smooth muscle actin, and collagen. Exposure to ethanol + ETS induced the largest increase in CYP2E1 and iNOS protein, as well as increased 3-nitrotyrosine, mtDNA damage, and decreased cytochrome c oxidase protein, compared to all other groups. Similarly, the largest increase in HIF1α expression was observed in the ethanol + ETS group, indicating enhanced hypoxia. These studies demonstrate that ETS increases alcohol-dependent steatosis and hypoxic stress. Therefore, ETS may be a key environmental "hit" that accelerates and exacerbates alcoholic liver disease in hypercholesterolemic apoE-/- mice.

Original languageEnglish (US)
Pages (from-to)928-938
Number of pages11
JournalFree Radical Biology and Medicine
Volume46
Issue number7
DOIs
StatePublished - Apr 1 2009

Fingerprint

Tobacco
Apolipoproteins E
Fatty Liver
Smoke
Liver
Liver Diseases
Ethanol
Alcohols
Cytochrome P-450 CYP2E1
Alcoholic Liver Diseases
Histology
Oxidative stress
Hypoxia
Electron Transport Complex IV
Nutrition
Mitochondrial DNA
Tobacco Products
Smooth Muscle
Muscle
Actins

Keywords

  • Alcohol
  • Blue native gel electrophoresis
  • Cigarette smoke
  • Cytochrome c oxidase
  • Free radicals
  • Hypercholesterolemia
  • Hypoxia
  • Liver
  • Mitochondria
  • Oxidative stress
  • Steatosis

ASJC Scopus subject areas

  • Biochemistry
  • Physiology (medical)

Cite this

Ethanol and tobacco smoke increase hepatic steatosis and hypoxia in the hypercholesterolemic apoE-/- mouse : Implications for a "multihit" hypothesis of fatty liver disease. / Bailey, Shannon M.; Mantena, Sudheer K.; Millender-Swain, Telisha; Cakir, Yavuz; Jhala, Nirag C.; Chhieng, David; Pinkerton, Kent E; Ballinger, Scott W.

In: Free Radical Biology and Medicine, Vol. 46, No. 7, 01.04.2009, p. 928-938.

Research output: Contribution to journalArticle

Bailey, Shannon M. ; Mantena, Sudheer K. ; Millender-Swain, Telisha ; Cakir, Yavuz ; Jhala, Nirag C. ; Chhieng, David ; Pinkerton, Kent E ; Ballinger, Scott W. / Ethanol and tobacco smoke increase hepatic steatosis and hypoxia in the hypercholesterolemic apoE-/- mouse : Implications for a "multihit" hypothesis of fatty liver disease. In: Free Radical Biology and Medicine. 2009 ; Vol. 46, No. 7. pp. 928-938.
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