Mechanism of beta-mercaptoethylamine-induced hypotension in the dog
- 1 June 1963
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Legacy Content
- Vol. 204 (6) , 997-1000
- https://doi.org/10.1152/ajplegacy.1963.204.6.997
Abstract
Radioprotectant doses of beta-mercaptoethylamine (MEA) are toxic to the dog, inducing hypotension and hemoconcentration. Antihistaminics and two adrenergic blocking agents with antihistaminic properties were effective against MEA-induced hypotension. Adrenergic blocking agents with little antihistaminic action were ineffective against the hypotension. Antihistaminic compounds blocked MEA-induced hemoconcentration caused by a loss of plasma from the circulation, a portion of which may be found in the peritoneal cavity. Loss of plasma from the circulation and appearance of fluid in the peritoneal cavity is partially prevented by antihistaminics. MEA causes dermal whealing similar to that produced by histamine, and this whealing is prevented by intravenously administered pyrilamine maleate. These findings are interpreted as meaning that histamine release plays an important role in MEA-induced toxicity.Keywords
This publication has 3 references indexed in Scilit:
- Mechanism of histamine release in endotoxin shockAmerican Journal of Physiology-Legacy Content, 1961
- PHARMACOLOGY OF RADIOPROTECTANT CHEMICALS - BIOCHEMICAL CHANGES IN DOG FOLLOWING ADMINISTRATION OF BETA-MERCAPTOETHYLAMINE (MEA)1961
- STUDIES ON THE CIRCULATORY CHANGES IN THE DOG PRODUCED BY ENDOTOXIN FROM GRAM-NEGATIVE MICROORGANISMSJournal of Clinical Investigation, 1956