Resveratrol prevents nicotine-induced teratogenesis in cultured mouse embryos

Reprod Toxicol. 2012 Nov;34(3):340-6. doi: 10.1016/j.reprotox.2012.05.097. Epub 2012 Jun 9.

Abstract

Nicotine, a major toxic component in tobacco smoke, leads to severe embryonic damage during organogenesis in embryos. We investigated whether resveratrol would positively influence nicotine-induced teratogenesis in mouse embryos (embryonic day 8.5) cultured for 48 h using a whole embryo culture system. Embryos exposed to nicotine (1mM) revealed significantly severe morphological anomalies, increased levels of caspase-3 mRNA and lipid peroxidation, and decreased levels of cytoplasmic superoxide dismutase (SOD), mitochondrial manganese SOD, cytosolic glutathione peroxidase, phospholipid hydroperoxide glutathione peroxidase, hypoxia-inducible factor 1α, Bcl-x(L), and sirtuin1 (SIRT1) mRNAs and SOD activity compared to those in the normal control group. However, when resveratrol (1×10(-8) μM or 1×10(-7) μM) was added concurrently to the embryos exposed to nicotine, all the parameters in above improved conspicuously. These findings indicate that resveratrol has a noted protective effect against nicotine-induced teratogenesis in mouse embryos through its antioxidative and anti-apoptotic effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Drug-Induced / prevention & control*
  • Animals
  • Caspase 3 / genetics
  • Embryo, Mammalian / drug effects*
  • Female
  • Gene Expression Regulation, Developmental / drug effects
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase GPX1
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Lipid Peroxidation / drug effects
  • Male
  • Mice
  • Mice, Inbred ICR
  • Nicotine / toxicity*
  • Oxidative Stress / drug effects
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • Protective Agents / pharmacology*
  • Resveratrol
  • Sirtuin 1 / genetics
  • Stilbenes / pharmacology*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Teratogens / toxicity*
  • bcl-X Protein / genetics

Substances

  • Bcl2l1 protein, mouse
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Protective Agents
  • Stilbenes
  • Teratogens
  • bcl-X Protein
  • Nicotine
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Caspase 3
  • Sirt1 protein, mouse
  • Sirtuin 1
  • Resveratrol
  • Glutathione Peroxidase GPX1
  • Gpx1 protein, mouse