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氟喹诺酮类抗菌药物体内外诱导组胺释放的特性研究

Characterization of histamine release induced by fluoroquinolone antibacterial agents in-vivo and in-vitro.

作者信息

Mori K, Maru C, Takasuna K

机构信息

Drug Safety Research Laboratory, Daiichi Pharmaceutical Co. Ltd, Tokyo, Japan.

出版信息

J Pharm Pharmacol. 2000 May;52(5):577-84. doi: 10.1211/0022357001774228.

Abstract

Characterization of histamine release induced by fluoroquinolone antibacterial agents, levofloxacin and ciprofloxacin, was investigated in-vivo and in-vitro. Intravenous injection of levofloxacin and ciprofloxacin at 1-10 mg kg(-1) produced dose-related elevations in plasma histamine level in anaesthetized dogs. In contrast, levofloxacin was devoid of plasma histamine increment in anaesthetized rats at 100 mg kg(-1), whereas ciprofloxacin at the same dose caused endogenous histamine release. Levofloxacin and ciprofloxacin induced non-cytotoxic secretion of histamine from all mast cells tested in a concentration-dependent manner, whereas rat skin and peritoneal mast cells were thirty- to one-hundred-times less sensitive to the effect of fluoroquinolones as compared with the canine skin mast cells. These results suggest that the functional heterogeneity of mast cells from different species in histamine releasing activity of fluoroquinolones may exist, and that mast cells from the dog appear to be particularly sensitive to the effect of the fluoroquinolones.

摘要

在体内和体外研究了氟喹诺酮类抗菌剂左氧氟沙星和环丙沙星诱导组胺释放的特性。在麻醉犬中静脉注射1-10mg kg(-1)的左氧氟沙星和环丙沙星,可使血浆组胺水平出现剂量相关的升高。相比之下,在麻醉大鼠中静脉注射100mg kg(-1)的左氧氟沙星不会引起血浆组胺增加,而相同剂量的环丙沙星则会引起内源性组胺释放。左氧氟沙星和环丙沙星以浓度依赖的方式诱导所有测试肥大细胞非细胞毒性地分泌组胺,然而与犬皮肤肥大细胞相比,大鼠皮肤和腹膜肥大细胞对氟喹诺酮类药物作用的敏感性低30至100倍。这些结果表明,不同物种的肥大细胞在氟喹诺酮类药物组胺释放活性方面可能存在功能异质性,并且犬的肥大细胞似乎对氟喹诺酮类药物的作用特别敏感。

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