JPET

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 Google Scholar
Google Scholar
Right arrow Articles by Takemori, A. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Takemori, A. E.
Journal of Pharmacology And Experimental Therapeutics, Vol. 135, Issue 1, 89-93, 1962
Copyright © 1962 by American Society for Pharmacology and Experimental Therapeutics


STUDIES ON CELLULAR ADAPTATION TO MORPHINE AND ITS REVERSAL BY NALORPHINE IN CEREBRAL CORTICAL SLICES OF RATS

A. E. Takemori 1

1 Department of Pharmacology, State University of New York, Upstate Medical Center, Syracuse, New York

Cellular adaptation to morphine using cerebral cortical slices of rats can he acquired within a week of morphinization to the rats and can be lost within a week after abrupt withdrawal from the narcotic.

The in vivo injection of nalorphine promptly reverses the adapted state of the rats' cortical slices so that the slices again become sensitive to the depressive effect of morphine.

Nalorphine can antagonize the depressive effect of morphine in vitro, but the antagonism depends on the molar ratio of antagonist:agonist employed. The most effective reversal is seen when the molar ratio is either 1:4 or 1:10.

Submitted on June 16, 1961







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

Copyright © 1962 by the American Society for Pharmacology and Experimental Therapeutics.