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The role of complement, platelet-activating factor and leukotriene B4 in a reversed passive Arthus reaction.
Rossi, A G; Norman, K E; Donigi-Gale, D; Shoupe, T S; Edwards, R; Williams, T J.
Afiliação
  • Rossi AG; Department of Applied Pharmacology, National Heart & Lung Institute, London.
Br J Pharmacol ; 107(1): 44-9, 1992 Sep.
Article em En | MEDLINE | ID: mdl-1330163
ABSTRACT
1. The mechanisms underlying oedema formation induced in a reversed passive Arthus (RPA) reaction and, for comparison, in response to zymosan in rabbit skin were investigated. 2. Oedema formation at skin sites was quantified by the accumulation of intravenously-injected 125I-labelled human serum albumin. 3. Recombinant soluble complement receptor type 1 (sCR1), administered locally in rabbit skin, suppressed oedema formation induced in the RPA reaction and by zymosan. 4. The platelet-activating factor (PAF) antagonists, WEB 2086 and PF10040 administered locally, inhibited oedema formation induced in the RPA reaction and by PAF but not by zymosan. 5. A locally administered leukotriene B4 (LTB4) antagonist, LY-255283, inhibited oedema formation induced by LTB4 but did not inhibit oedema responses to PAF, zymosan or the RPA reaction. 6. The results demonstrate a role for complement in oedema formation in both the RPA reaction and in response to zymosan. An important contribution by PAF is indicated in the RPA reaction but not in response to zymosan whereas no evidence was obtained to suggest a role for LTB4 in either inflammatory response.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Sistema Complemento / Fator de Ativação de Plaquetas / Reação de Arthus / Leucotrieno B4 Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: Br J Pharmacol Ano de publicação: 1992 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Sistema Complemento / Fator de Ativação de Plaquetas / Reação de Arthus / Leucotrieno B4 Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: Br J Pharmacol Ano de publicação: 1992 Tipo de documento: Article