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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Berger, F. M.
Right arrow Articles by Margolin, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Berger, F. M.
Right arrow Articles by Margolin, S.
Journal of Pharmacology And Experimental Therapeutics, Vol. 134, Issue 3, 356-365, 1961
Copyright © 1961 by American Society for Pharmacology and Experimental Therapeutics


THE PHARMACOLOGICAL PROPERTIES OF 2-METHYL-2-SEC-BUTYL-1,3-PROPANEDIOL DICARBAMATE (MEBUTAMATE, W-583), A NEW CENTRALLY ACTING BLOOD PRESSURE LOWERING AGENT

F. M. Berger 1, J. F. Douglas 1, M. Kletzkin 1, B. J. Ludwig 1, and S. Margolin 1

1 Wallace Laboratories, Division of Carter Products, Inc., Cranbury, New Jersey

Mebutamate (2-methyl-2-sec-butyl-1,3-propanediol dicarbamate) is a centrally acting pressure lowering agent which produces its hypotensive effect by direct action on the brain stem vasomotor centers. The hypotensive action has been demonstrated in normal and hypertensive laboratory animals and in hypertensive humans. The reduction in blood pressure was directly correlated with blood concentration of the drug. Mebutamate reduced the amplitude of blood pressure rises elicited by electrical stimulation of cardiovascular centers of the brain stem. It raised the threshold for pressor responses and also placed a ceiling upon the pressure rises so that even with supramaximal stimulation the rises obtained remained considerably below those obtained prior to the administration of mebutamate. Cross-circulation experiments confirmed the purely central site of action of the drug and showed that the hypotensive effect is produced by a reduction of the vascular peripheral resistance. The hypotensive effect was produced without alteration of the cardiac output, and was apparent in doses that did not produce muscle relaxation or neurological impairment. The drug differed from other hypotensive agents in having no effect on the autonomic nervous system. It did not cause ganglionic blockage and did not modify the circulatory responses to epinephrine, acetylcholine or serotonin. The ability of the body to detoxify mehutamnate readily may account for the unusually low toxicity of the drug both in humans and in animals.

Submitted on May 18, 1961




This article has been cited by other articles:


Home page
ANGIOLOGYHome page
A. D. Bender
The Hemodynamics of Hypertension and Anti Hypertensive Therapy
Angiology, September 1, 1966; 17(9): 627 - 639.
[PDF]




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

Copyright © 1961 by the American Society for Pharmacology and Experimental Therapeutics.