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一种新型非甾体抗炎药卡洛芬(Ro 20 - 5720)对补体系统激活的作用:一项体外研究

Action of a new non-steroid anti-inflammatory drug, carprofen (Ro 20-5720) on activation of the complement system: an in vitro research.

作者信息

Auteria A, Laghi Pasini F, Di Perri T

出版信息

Int J Tissue React. 1982;4(1):9-13.

PMID:7085003
Abstract

Carprofen (Ro 20-5720), DL-6-chloro-alpha-methyl-carbazole-2-acetic acid, is a new non-steroid anti-inflammatory drug. We have studied the possible in vitro interference of the drug with the activation of human complement system. Carprofen exerts a constant inhibitory action of immunohaemolysis at a concentration of 4.5 X 10(-4)M. At the same concentration the drug is able to prevent the activation of the alternate pathway induced by insulin. Its specific site of action is on C1 and C3 components activation, according to the inhibiting activity on both classic and alternate pathway. However at a lower dosage (7.5 X 10(-6)M) carprofen is able to display an inducing action on the alternate pathway, thus confirming the complex in vitro interferences of the drug with the complement system.

摘要

卡洛芬(Ro 20 - 5720),即DL - 6 - 氯 - α - 甲基咔唑 - 2 - 乙酸,是一种新型非甾体抗炎药。我们研究了该药物在体外对人补体系统激活可能产生的干扰。卡洛芬在浓度为4.5×10⁻⁴M时对免疫溶血发挥持续的抑制作用。在相同浓度下,该药物能够阻止胰岛素诱导的替代途径的激活。根据其对经典途径和替代途径的抑制活性,其作用的特定位点是C1和C3成分的激活。然而,在较低剂量(7.5×10⁻⁶M)时,卡洛芬能够对替代途径表现出诱导作用,从而证实了该药物在体外对补体系统存在复杂的干扰。

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