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Platelet activating factor and systemic anaphylaxis in Nippostrongylus brasiliensis ‐sensitized rats: differential effects of PAF antagonists
Author(s) -
Mathison Ronald,
Davison J.S.,
Befus A. Dean
Publication year - 1992
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1992.tb14326.x
Subject(s) - extravasation , platelet activating factor , anaphylaxis , nippostrongylus brasiliensis , antagonist , evans blue , medicine , blood flow , endocrinology , shock (circulatory) , immunology , pharmacology , allergy , immune system , receptor
1 The effects of two platelet‐activating factor (PAF) antagonists, WEB 2086 and BN 52021, in reducing the changes in extravasation (Evans blue technique) and blood flow (radiolabelled microsphere method) to various organs and tissues following anaphylactic shock in the Nippostrongylus brasiliensis ‐sensitized rat were investigated. 2 Both antagonists attenuated anaphylaxis‐induced increases in plasma protein leak in the trachea, stomach and small intestine, although they did not block extravasation in the colon and kidneys. 3 Anaphylaxis‐induced decreases in blood flow to the adrenals were effectively antagonized by WEB 2086, although this antagonist did not reverse blood flow decreases to any other tissues. BN 52021, on the other hand, did not alter anaphylaxis‐induced decreases in blood flow to the adrenals, but effectively prevented dramatic decreases in blood flow to the large and small bowel and spleen. 4 Anaphylactic shock produced marked reduction in blood pressure that was partly reversed by WEB 2086, whereas BN 52021 effectively blocked the decreases in cardiac output. 5 Thus, PAF is responsible for some of the haemodynamic and extravasation of protein changes associated with systemic anaphylaxis in the rat, although the differential inhibition observed with the two antagonists suggests that PAF alters vascular responsiveness through different mechanisms in selected tissues.