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两种庚嗪类血小板活化因子拮抗剂对小鼠急性炎症的差异性抑制作用。

Differential inhibition by two hetrazepine PAF antagonists of acute inflammation in the mouse.

作者信息

Henriques M G, Weg V B, Martins M A, Silva P M, Fernandes P D, Cordeiro R S, Vargaftig B B

机构信息

Dept. Fisiologia e Farmacodinâmica, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.

出版信息

Br J Pharmacol. 1990 Jan;99(1):164-8. doi: 10.1111/j.1476-5381.1990.tb14671.x.

Abstract
  1. The injection of 100 or 300 micrograms of carrageenin into the mouse paw or pleural cavity produced a delayed inflammatory reaction at 48 h while platelet activating factor (PAF)-induced paw oedema and pleurisy were maximal 30 min after its injection. 2. The PAF antagonist, WEB 2086, failed to inhibit mouse paw oedema and pleurisy induced by PAF, but reduced the first phase of oedema (1-4 h) induced by carrageenin without interfering with the second one (48-72 h). In contrast, another structurally-related PAF antagonist, WEB 2170, inhibited dose-dependently both oedema and pleurisy induced by PAF and by carrageenin (48 h). 3. Repeated injections of PAF into the mouse paw or pleural cavity led to significant autodesensitization. The animals desensitized to PAF and injected with carrageenin also displayed a significantly reduced oedema. 4. Our results suggest that PAF may be involved in the inflammatory response to carrageenin in mice. Furthermore, because the different receptor antagonists displayed distinct effects against PAF itself, different sites for in vivo interaction of PAF are available and are species- and drug-dependent.
摘要
  1. 向小鼠爪部或胸腔注射100或300微克角叉菜胶,在48小时时会产生延迟性炎症反应,而血小板活化因子(PAF)诱导的爪部水肿和胸膜炎在注射后30分钟最为明显。2. PAF拮抗剂WEB 2086未能抑制PAF诱导的小鼠爪部水肿和胸膜炎,但可减轻角叉菜胶诱导的水肿第一阶段(1 - 4小时),而不干扰第二阶段(48 - 72小时)。相比之下,另一种结构相关的PAF拮抗剂WEB 2170剂量依赖性地抑制PAF和角叉菜胶诱导的水肿和胸膜炎(48小时)。3. 向小鼠爪部或胸腔重复注射PAF会导致显著的自身脱敏。对PAF脱敏并注射角叉菜胶的动物也表现出水肿明显减轻。4. 我们的结果表明,PAF可能参与小鼠对角叉菜胶的炎症反应。此外,由于不同的受体拮抗剂对PAF本身表现出不同的作用,PAF在体内的相互作用位点不同,且具有物种和药物依赖性。

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