Inhibition of histone acetylation by curcumin reduces alcohol-induced fetal cardiac apoptosis. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- Inhibition of histone acetylation by curcumin reduces alcohol-induced fetal cardiac apoptosis. Issue 1 (December 2017)
- Main Title:
- Inhibition of histone acetylation by curcumin reduces alcohol-induced fetal cardiac apoptosis
- Authors:
- Yan, Xiaochen
Pan, Bo
Lv, Tiewei
Liu, Lingjuan
Zhu, Jing
Shen, Wen
Huang, Xupei
Tian, Jie - Abstract:
- 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 correctAbstract 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. … (more)
- Is Part Of:
- Journal of biomedical science. Volume 24:Issue 1(2017)
- Journal:
- Journal of biomedical science
- Issue:
- Volume 24:Issue 1(2017)
- Issue Display:
- Volume 24, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 24
- Issue:
- 1
- Issue Sort Value:
- 2017-0024-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2017-12
- Subjects:
- Alcohol -- Apoptosis -- Histone acetylation -- Fetal cardiac development -- Caspase
Medical sciences -- Periodicals
610.28 - Journal URLs:
- http://www.jbiomedsci.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=857&action=archive ↗
http://www.springer.com/gb/ ↗
http://firstsearch.oclc.org ↗
http://www.springerlink.com/content/112912/ ↗ - DOI:
- 10.1186/s12929-016-0310-z ↗
- Languages:
- English
- ISSNs:
- 1021-7770
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.769000
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- 10053.xml