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 Google Scholar
Google Scholar
Right arrow Articles by KOPPANYI, T.
Right arrow Articles by BRODIE, B. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by KOPPANYI, T.
Right arrow Articles by BRODIE, B. B.
Journal of Pharmacology And Experimental Therapeutics, Vol. 172, Issue 1, 170-179, 1970
Copyright © 1970 by American Society for Pharmacology and Experimental Therapeutics


JUMPING ACTIVITY INDUCED BY SODIUM 5-(1,3-DIMETHYLBUTYL)-5-ETHYL BARBITURATE. I. THE ROLE OF THE SYMPATHETIC NERVOUS SYSTEM

T. KOPPANYI 1, H. M. MALING 1, W. SAUL 2, and B. B. BRODIE 1

1 Laboratory of Chemical Pharmacology, National Heart and Lung Institute, National Institutes of Health, Bethesda, Maryland
2 Laboratory of Chemical Pharmacology, National Heart and Lung Institute, National Institutes of Health, Bethesda, Maryaland

A hitherto unobserved jumping activity was noted after the administration of subconvulsant doses of sodium 5-(1,3-dimethylbutyl)-5-ethyl barbiturate (DMBEB) in young mice. Jumping rarely occurred after injections of saline, depressant barbiturates and central stimulants. The role of the sympathetic nervous system in DMBEB-induced jumping was evaluated. The jumping was accompanied by elevations in body temperature and plasma glucose. Chionisondamine, pempidine, propranolol and phentolamine blocked the hyperglycemia induced by DMBEB. d-Ampheta mine potentiated the jumping activity. Ganglionic blocking drugs (chlorisondamine and pempidine) and beta adrenergic blocking agents (propranolol and Kö 592) reduced or abolished this jumping without lowering brain levels of DMBEB. Except in high doses, the benzodiazepine anticonvulsants were ineffective. These findings suggest an important role of the sympathetic nervous system in DMBEB-induced jumping.

Submitted on June 12, 1969
Accepted on November 20, 1969







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

Copyright © 1970 by the American Society for Pharmacology and Experimental Therapeutics.