补体与豚鼠对全身内毒素发热反应的关系。

S Li, E Sehic, Y Wang, A L Ungar, C M Blatteis
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引用次数: 31

摘要

我们最近报道,补体(C)系统可能在豚鼠对静脉注射脂多糖(LPS)的发热反应中发挥作用,因为C消耗消除了LPS诱导的核心温度升高(T(C))。本研究旨在进一步探讨眼镜蛇毒因子(cobra venom factor, CVF)诱导的C降低[;20、50、100和200 U/动物iv],以及CVF后18小时通过静脉注射(2微克/千克)或腹腔注射(8、16、32微克/千克)LPS产生的成年有意识豚鼠发热;对照动物给予无热原生理盐水。血清C水平以CVF注射前和注射后18 h的总溶血C活性测量,并以CH(100)单位表示。在其他实验中,分别测定单独静脉注射和腹腔注射不同剂量LPS后不同时间间隔的血清C水平。LPS产生的发热一般高度相似,但根据给药剂量和给药途径不同,其发病潜伏期和持续时间不同。CVF引起血清C的剂量相关降低,从大约1136 U降至低于检测值。这些减少成比例地减轻了腹腔注射LPS引起的发热,但静脉注射LPS则没有。静脉注射和腹腔注射LPS本身分别导致血清C降低25%和40%,表明C级联的激活。然而,这些下降是短暂的,发生在注射LPS后大约30分钟的发热上升早期。因此,这些数据支持了这样一种观点,即C系统可能在豚鼠对系统性,特别是腹腔内LPS的发热反应中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relation between complement and the febrile response of guinea pigs to systemic endotoxin.

We reported recently that the complement (C) system may play a role in the febrile response of guinea pigs to intravenous lipopolysaccharide (LPS) administration because C depletion abolished the LPS-induced rise in core temperature (T(c)). The present study was designed to investigate further the relation between C reduction [induced by cobra venom factor (CVF); 20, 50, 100, and 200 U/animal iv] and the fever of adult, conscious guinea pigs produced by LPS injected intravenously (2 microg/kg) or intraperitoneally (8, 16, 32 microg/kg) 18 h after CVF; control animals received pyrogen-free saline. Serum C levels were measured as total hemolytic C activity before and 18 h after CVF injection and expressed as CH(100) units. In other experiments, serum C levels were determined at various intervals after the intravenous and intraperitoneal injections at different doses of LPS alone. LPS produced fevers generally of similar heights but of different onset latencies and durations, depending on the dose and route of administration. CVF caused dose-related reductions in serum C, from approximately 1,136 U to below detection. These reductions proportionately attenuated the fevers induced by intraperitoneal LPS, but not by intravenous LPS. Intravenous and intraperitoneal LPS per se caused reductions in serum C of 25 and 40%, respectively, indicating activation of the C cascade. These decreases were transient, however, occurring early during the febrile rise approximately 30 min after LPS injection. These data thus support the notion that the C system may be critically involved in the febrile response of guinea pigs to systemic, particularly intraperitoneal, LPS.

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