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 PRINZMETAL, M.
Right arrow Articles by LEAKE, C. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by PRINZMETAL, M.
Right arrow Articles by LEAKE, C. D.
Journal of Pharmacology And Experimental Therapeutics, Vol. 46, Issue 1, 63-73, 1932
Copyright © 1932 by American Society for Pharmacology and Experimental Therapeutics


THE PHARMACOLOGICAL ACTION OF "MUSSEL POISON"

M. PRINZMETAL 1, H. SOMMER 1, and C. D. LEAKE 1

1 From the Pharmacological Laboratory of the University of California Medical School and the George Williams Hooper Foundation, San Francisco, California

A potent material extracted from poisonous mussels has been studied. It has been shown that this material is slowly absorbed from the gastro-intestinal tract and rapidly excreted by the kidneys. Its main action seems to be depression of respiration. The cardio-inhibitory and the vasomotor centers are also depressed as is the conduction system of the myocardium. It has no effect on smooth muscle in perfusion experiments. The rabbit and mouse seem most susceptible to the poison while its effect on the dog is less marked. Frogs are quite resistant. The clinical picture in man has been described and therapeutic procedures suggested.

Submitted on January 11, 1932







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

Copyright © 1932 by the American Society for Pharmacology and Experimental Therapeutics.