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 Abreu, B. E.
Right arrow Articles by Weaver, L. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Abreu, B. E.
Right arrow Articles by Weaver, L. C.
Journal of Pharmacology And Experimental Therapeutics, Vol. 112, Issue 1, 73-79, 1954
Copyright © 1954 by American Society for Pharmacology and Experimental Therapeutics


CARDIOVASCULAR, EMETIC AND PHARMACODYNAMIC PROPERTIES OF CERTAIN VERATRUM ALKALOIDS

Benedict E. Abreu 1, Alice B. Richards 1, William M. Alexander 1, and Lawrence C. Weaver 1

1 Research Department, Pitman-Moore Company, Division of Allied Laboratories, Indianapolis, Indiana

1. Ranked in the order of their relative hypotensive potency from greatest to least, the preparations investigated may be arranged as follows: protoveratrine A = germitetrine B = Veralba rang protoveratrine B rang Unitensen.

2. No dissociation of hypotensive from emetic activity was observed with protoveratrine A, Veralba or Unitensen.

3. Protoveratrine A reduces arterial pressure in the dog by acting upon receptors whose impulses travel to the vasomotor center via the vagi and the carotid sinus nerves.

Submitted on April 23, 1954







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

Copyright © 1954 by the American Society for Pharmacology and Experimental Therapeutics.