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新型血小板活化因子拮抗剂SR 27417对大鼠和豚鼠由血小板活化因子或内毒素诱导的低血压的保护作用。

Protective effect of SR 27417, a novel PAF antagonist, on PAF- or endotoxin-induced hypotension in the rat and the guinea-pig.

作者信息

Bernat A, Herbert J M, Salel V, Lespy L, Maffrand J P

机构信息

Haemobiology research department, Sanofi Recherche, Toulouse, France.

出版信息

J Lipid Mediat. 1992 Feb;5(1):41-8.

PMID:1391738
Abstract

SR 27417, the first member of a newly-developed PAF antagonist series, inhibited in a dose-dependent manner the hypotensive effect of PAF in rats. It protected rats with an ED50 = 6 micrograms/kg, when given i.v., 1 min before PAF or p.o. (ED50 = 170 micrograms/kg) 1 h before PAF administration. After i.v. or oral administration, SR 27417 (1 and 3 mg/kg, respectively) exhibited extended duration of action (between 48 and 72 h). Similarly, i.v. administration of 1 to 6 mg/kg of SR 27417 afforded complete protection of guinea-pigs against endotoxin-induced hypotension but also totally reversed established endotoxin-induced hypotension. These results therefore confirm that PAF plays a major role in septic shock and that SR 27417 may be an effective prophylactic as well as a potent curative drug.

摘要

SR 27417是新开发的血小板活化因子(PAF)拮抗剂系列的首个成员,它以剂量依赖的方式抑制PAF对大鼠的降压作用。当在静脉注射PAF前1分钟静脉给药(半数有效剂量[ED50]=6微克/千克)或在口服PAF前1小时口服给药(ED50=170微克/千克)时,它能保护大鼠。静脉注射或口服给药后,SR 27417(分别为1和3毫克/千克)显示出延长的作用持续时间(48至72小时)。同样,静脉注射1至6毫克/千克的SR 27417能使豚鼠完全免受内毒素诱导的低血压影响,而且还能完全逆转已确立的内毒素诱导的低血压。因此,这些结果证实PAF在感染性休克中起主要作用,并且SR 27417可能是一种有效的预防性药物以及强效的治疗性药物。

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