Journal
BIOLOGICAL PSYCHIATRY
Volume 69, Issue 7, Pages 642-649Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2010.12.010
Keywords
Addiction; alcohol drinking; pioglitazone; PPAR gamma receptors; relapse; thiazolidinediones
Categories
Funding
- University of Camerino
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Background: Pioglitazone and rosiglitazone belong to the class of thiazolidinediones (TZDs). They were first developed as antioxidants and then approved for the clinical treatment of insulin resistance and Type 2 diabetes. TZDs bind with high affinity and activate peroxisome proliferator-activated receptor-gamma (PPAR gamma) receptors, which in the brain are expressed both in neurons and in glia. Methods: We evaluated the effect of PPAR gamma activation by TZDs on alcohol drinking, relapse-like behavior, and withdrawal in the rat. We also tested the effect of TZDs on alcohol and saccharin self-administration. Results: We showed that activation of PPAR gamma receptors by pioglitazone (0, 10, and 30 mg/kg) and rosiglitazone (0, 10 and 30 mg/kg) given orally selectively reduced alcohol drinking. The effect was blocked by pretreatment with the selective PPAR gamma antagonist GW9662 (5 mu g/rat) given into the lateral cerebroventricle, suggesting that this TZD's effect is mediated by PPAR gamma receptors in the central nervous system. Pioglitazone abolished reinstatement of alcohol seeking, a relapse-like behavior, induced by yohimbine, a pharmacologic stressor, but did not affect cue-induced relapse. In the self-administration experiments, pioglitazone reduced lever pressing for alcohol but not for saccharin. Finally, pioglitazone prevented the expression of somatic signs of alcohol withdrawal. Conclusions: These findings provide new information about the role of brain PPAR gamma receptors and identify pioglitazone as candidate treatments for alcoholism and possibly other addictions.
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