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 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 LINEGAR, C. R.
Right arrow Articles by KOPPANYI, T.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LINEGAR, C. R.
Right arrow Articles by KOPPANYI, T.
Journal of Pharmacology And Experimental Therapeutics, Vol. 58, Issue 2, 128-134, 1936
Copyright © 1936 by American Society for Pharmacology and Experimental Therapeutics


STUDIES ON BARBITURATES XVIII. ANALYSIS OF A PERIPHERAL ACTION OF BARBITURATES

CHARLES R. LINEGAR 1, JAMES M. DILLE 1, and THEODORE KOPPANYI 1

1 From the Department of Pharmacology and Materia Medica, Georgetown University, School of Medicine, Washington, D. C.

Amytal, pernoston and pentobarbital in moderate doses, and barbital in large doses may paralyze the peripheral vagus, whereas phenobarbital has no paralytic effects.

The central vagus is not paralyzed even after massive doses of barbiturates.

The administration of pilocarpine and acetylcholine slows the heart in animals in which the peripheral vagus function has been abolished by barbiturates.

The administration of physostigmine may not have a spontaneous effect on the heart rate but restores the excitability of the vagus abolished by barbiturates.

It is concluded that the locus of barbiturate action in the vagus is in the peripheral ganglionic cells of the heart.

Submitted on June 1, 1936







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

Copyright © 1936 by the American Society for Pharmacology and Experimental Therapeutics.