Reduced Expression of Circadian Clock Genes in Male Alcoholic Patients
Article first published online: 24 AUG 2010
Copyright © 2010 by the Research Society on Alcoholism
Alcoholism: Clinical and Experimental Research
Volume 34, Issue 11, pages 1899–1904, November 2010
How to Cite
Huang, M.-C., Ho, C.-W., Chen, C.-H., Liu, S.-C., Chen, C.-C. and Leu, S.-J. (2010), Reduced Expression of Circadian Clock Genes in Male Alcoholic Patients. Alcoholism: Clinical and Experimental Research, 34: 1899–1904. doi: 10.1111/j.1530-0277.2010.01278.x
- Issue published online: 26 OCT 2010
- Article first published online: 24 AUG 2010
- Received for publication February 22, 2010; accepted May 12, 2010.
- Circadian Rhythm;
- Circadian Clock Gene;
- Alcohol Dependence;
- Alcohol Withdrawal
Background: There are clear interactions between chronic alcohol consumption and circadian rhythmicity that is regulated by several circadian clock genes. The altered expressions of these genes have been mainly described in animals. The mammalian master clock in the suprachiasmatic nuclei orchestrates the biological rhythms in peripheral tissues. As peripheral blood mononuclear cells (PBMCs) are the most accessible tissue clinically, we assessed the mRNA levels of these genes in patients with alcohol dependence (AD) undergoing alcohol-withdrawal (AW) treatment.
Methods: Twenty-two male patients fulfilled the DSM-IV diagnostic criteria of AD, and 12 comparison healthy control subjects were recruited. The patients with AD were further divided by the presence of delirium tremens (DTs), the most severe form of AW syndrome, into DT group and non-DT group. All the participants received blood withdrawal at 9 am, while the patients with AD had blood collection twice: on the next morning of admission (baseline) and on the seventh day. PBMCs were isolated from whole blood, and the mRNA expression profiles of hClock1, hBmal1, hPer1, hPer2, hCry1, and hCry2 were determined by quantitative real-time PCR.
Results: The baseline mRNA levels of the target circadian clock genes were markedly lower in patients with AD than in control subjects. After 1 week of alcohol detoxification, there were very limited restorations of discrete circadian gene expressions. DT group did not differ in the expression patterns of circadian clock genes from non-DT group.
Conclusions: This is the first study demonstrating the overall lowering of circadian clock genes among patients with AD. The expression pattern is comparable between patients with and without DTs. Although preliminary with data at only one single time point, the observation of strikingly reduced mRNA levels supports the association between circadian clock gene dysregulation and chronic alcohol intake.