This research was supported by NIH Grant AA09000 and the Lattman Foundation.
The Cyclic AMP/Protein Kinase A Signal Transduction Pathway Modulates Tolerance to Sedative and Hypothermic Effects of Ethanol
Version of Record online: 3 MAY 2006
Alcoholism: Clinical and Experimental Research
Volume 27, Issue 8, pages 1220–1225, August 2003
How to Cite
Yang, X., Oswald, L. and Wand, G. (2003), The Cyclic AMP/Protein Kinase A Signal Transduction Pathway Modulates Tolerance to Sedative and Hypothermic Effects of Ethanol. Alcoholism: Clinical and Experimental Research, 27: 1220–1225. doi: 10.1097/01.ALC.0000081626.02910.19
- Issue online: 3 MAY 2006
- Version of Record online: 3 MAY 2006
- Received for publication February 21, 2003; accepted April 30, 2003.
- Adenylyl cyclase;
- Cyclic AMP;
- Protein Kinase A;
Background: An expanding body of literature indicates the important role of the cAMP/PKA signaling pathway in establishing initial sensitivity to alcohol as well as being involved in certain forms of tolerance to ethanol. The use of mice with heterozygous inactivation of the Gnas gene encoding Gsα allowed us to explore the relationship between tolerance to ethanol and cAMP/PKA signaling.
Methods: Mice with the targeted disruption of one Gsα allele were compared with wild-type littermates in their initial sensitivity to ethanol-induced sedation and hypothermia and then monitored for the development of tolerance during two subsequent bouts of intoxication. Components of the cAMP/PKA signaling pathway were analyzed in ethanol-naïve mice and again following the development of tolerance to ethanol to better understand the contribution of this signaling pathway to the acquisition of tolerance.
Results: During the initial exposure to ethanol, mice with the targeted disruption of one Gsα allele (Gnas) were more sensitive to the sedative effects of ethanol compared with wild-type littermates. Wild-type mice developed within-session tolerance to ethanol-induced hypothermia whereas Gnas mice did not. Following the subsequent ethanol treatments, wild-type mice developed between-session tolerance to the sedative effects of ethanol to a greater degree than mice with heterozygous inactivation of the Gnas gene. The development of tolerance to the sedative effects of ethanol was accompanied by increased expression of phospho-CREB in the cerebellum, hippocampus, and frontal cortex. No changes in phospho-CREB expression were detected in these brain regions in mice with heterozygous inactivation of the Gnas gene.
Conclusion: The results show that cAMP/PKA signal transduction modulates sensitivity to sedative and hypothermic effects of ethanol. This signal transduction system also influences the acquisition of within-session and between-session tolerance. The mechanism through which cAMP/PKA signaling modulates the development of tolerance remains to be elucidated but may involve changes in phospho-CREB expression.