JPET Introducing ALZET?ew Model 2006 Pump

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Keir, W. J.
Right arrow Articles by Deitrich, R. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Keir, W. J.
Right arrow Articles by Deitrich, R. A.

Development of central nervous system sensitivity to ethanol and pentobarbital in short- and long-sleep mice

WJ Keir and RA Deitrich

Department of Pharmacology and Alcohol, University of Colorado Health Sciences Center, Denver.

Dose-response curves to ethanol from day 9 to adulthood have been carried out in short-sleep and long-sleep mice. At very young ages, up to about 35 days of age, the mice differ in sleep time response to ethanol, but this difference is due to the development of acute tolerance. At older ages the differences in sleep times are due to a combination of acute tolerance and differences in initial sensitivity. In contrast to adult mice, that show no difference in brain sensitivity to pentobarbital, short-sleep mouse pups ranging in age from days 9 to 12 are more sensitive to pentobarbital than are long-sleep mice. The difference in sensitivity at young ages is again due to differences in development of acute tolerance and not to initial sensitivity differences. It is postulated that the development of acute tolerance to ethanol is rapid, within minutes, following injection of ethanol and that the system responsible might be the gamma-amino-butyric acid- mediated chloride flux which has also been shown to develop tolerance within 5 min after ethanol injection.

Volume 254, Issue 3, pp. 831-835, 09/01/1990
Copyright © 1990 by American Society for Pharmacology and Experimental Therapeutics




This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
I. Ponomarev and J. C. Crabbe
A Novel Method to Assess Initial Sensitivity and Acute Functional Tolerance to Hypnotic Effects of Ethanol
J. Pharmacol. Exp. Ther., July 1, 2002; 302(1): 257 - 263.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
B. J. Pearson, D. P. Donatelli, R. K. Freund, and M. R. Palmer
Differential Development and Characterization of Rapid Acute Neuronal Tolerance to the Depressant Effects of Ethanol on Cerebellar Purkinje Neurons of Low-alcohol-sensitive and High-alcohol-sensitive Rats
J. Pharmacol. Exp. Ther., February 1, 1997; 280(2): 739 - 746.
[Abstract] [Full Text]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1990 by the American Society for Pharmacology and Experimental Therapeutics.