Inhibition of histone acetylation by curcumin reduces alcohol-induced fetal cardiac apoptosis

J Biomed Sci. 2017 Jan 5;24(1):1. doi: 10.1186/s12929-016-0310-z.

Abstract

Background: Prenatal alcohol exposure may cause cardiac development defects, however, the underlying mechanisms are not yet clear. In the present study we have investigated the roles of histone modification by curcumin on alcohol induced fetal cardiac abnormalities during the development.

Methods and results: Q-PCR and Western blot results showed that alcohol exposure increased gene and active forms of caspase-3 and caspase-8, while decreased gene and protein of bcl-2. ChIP assay results showed that, alcohol exposure increased the acetylation of histone H3K9 near the promoter region of caspase-3 and caspase-8, and decreased the acetylation of histone H3K9 near the promoter region of bcl-2. TUNEL assay data revealed that alcohol exposure increased the apoptosis levels in the embryonic hearts. In vitro experiments demonstrated that curcumin treatment could reverse the up-regulation of active forms of caspase-3 and caspase-8, and down-regulation of bcl-2 induced by alcohol treatment. In addition, curcumin also corrected the high level of histone H3K9 acetylation induced by alcohol. Moreover, the high apoptosis level induced by alcohol was reversed after curcumin treatment in cardiac cells.

Conclusions: These findings indicate that histone modification may play an important role in mediating alcohol induced fetal cardiac apoptosis, possibly through the up-regulation of H3K9 acetylation near the promoter regions of apoptotic genes. Curcumin treatment may correct alcohol-mediated fetal cardiac apoptosis, suggesting that curcumin may play a protective role against alcohol abuse caused cardiac damage during pregnancy.

Keywords: Alcohol; Apoptosis; Caspase; Fetal cardiac development; Histone acetylation.

MeSH terms

  • Acetylation / drug effects
  • Animals
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / metabolism
  • Curcumin / pharmacology*
  • Female
  • Fetal Alcohol Spectrum Disorders* / drug therapy
  • Fetal Alcohol Spectrum Disorders* / metabolism
  • Fetal Alcohol Spectrum Disorders* / pathology
  • Fetus / embryology
  • Fetus / pathology
  • Heart Diseases* / drug therapy
  • Heart Diseases* / embryology
  • Heart Diseases* / pathology
  • Histones / metabolism*
  • Mice
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Pregnancy

Substances

  • Apoptosis Regulatory Proteins
  • Histones
  • Curcumin