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非索非那定及其对映体对体外脂多糖诱导的白细胞介素-1β生成及体内脂多糖诱导发热的影响。

Effects of flezelastine and its enantiomers on LPS-induced IL-1 beta generation in vitro and LPS-induced pyrexia in vivo.

作者信息

Werner U, Schmidt J, Szelenyi I

机构信息

Department of Pharmacology, ASTA Medica AG, Frankfurt, Germany.

出版信息

Agents Actions. 1994 Mar;41(1-2):99-100. doi: 10.1007/BF01986405.

Abstract

The effects of the novel antiasthmatic/antiallergic compound flezelastine on LPS-induced actions were investigated in vitro and in vivo. In monocytes, IL-1 beta generation stimulated by LPS was inhibited dose dependently. In vivo, LPS-induced fever in rats, which is at least partly driven by the release of IL-1 beta, was also inhibited by flezelastine. These findings suggest that flezelastine inhibits IL-1 synthesis and/or release in vitro and in vivo.

摘要

在体外和体内研究了新型抗哮喘/抗过敏化合物非索非那定对脂多糖(LPS)诱导作用的影响。在单核细胞中,LPS刺激产生的白细胞介素-1β(IL-1β)呈剂量依赖性受到抑制。在体内,LPS诱导的大鼠发热(至少部分由IL-1β释放驱动)也被非索非那定抑制。这些发现表明,非索非那定在体外和体内均抑制IL-1的合成和/或释放。

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