The quinoline compound, S4 effectively antagonizes alcohol intake in mice: Possible association with the histone H3 modifications-Reference-Cited by-同舟云学术

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The quinoline compound, S4 effectively antagonizes alcohol intake in mice: Possible association with the histone H3 modifications

Published:2015-08 Issue: Volume:87 Page:117-127
ISSN:0197-0186
Container-title:Neurochemistry International
language:en
Short-container-title:Neurochemistry International

Author:

Banerjee Tuhin Suvro,Hazra Abhijit,Mondal Nirup Bikash,Das Sumantra

Funder

Council of Scientific and Industrial Research

University Grants Commission

Publisher

Elsevier BV

Subject

Cell Biology,Cellular and Molecular Neuroscience

Reference48 articles.

1. Differential changes in MAP kinases, histone modifications, and liver injury in rats acutely treated with ethanol;Aroor;Alcohol. Clin. Exp. Res,2010

2. Hybrid C57BL/6J x FVB/NJ mice drink more alcohol than do C57BL/6J mice;Blednov;Alcohol. Clin. Exp. Res,2005

3. Further evidence of an inverse genetic relationship between innate differences in alcohol preference and alcohol withdrawal magnitude in multiple selectively bred rat lines;Chester;Alcohol. Clin. Exp. Res,2003

4. Surrogate alcohols and their metabolites modify histone H3 acetylation: involvement of histone acetyl transferase and histone deacetylase;Choudhury;Alcohol. Clin. Exp. Res,2008

5. Naltrexone treatment of adolescent alcoholics: an open-label pilot study;Deas;J. Child Adolesc. Psychopharmacol,2005

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1. Endogenous Opiates and Behavior: 2016;Peptides;2018-03

2. Pharmacoepigenomics;Medical Epigenetics;2016

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