脂多糖
肿瘤坏死因子α
感染性休克
内毒素休克
调解人
休克(循环)
免疫学
动物模型
败血症
医学
药理学
生物
内科学
作者
Pia Villa,Pietro Ghezzi
出处
期刊:Humana Press eBooks
[Humana Press]
日期:2004-04-02
卷期号:: 199-206
被引量:24
标识
DOI:10.1385/1-59259-771-8:199
摘要
Endotoxin/lipopolysaccharide (LPS) is the major mediator that triggers the cellular and humoral responses of the shock induced by Gram-negative bacteria. The toxic responses of LPS are mediated by various factors and mainly by tumor necrosis factor alpha (TNFalpha). To study the role of TNF and to identify anti-TNF molecules in endotoxic/septic shock, numerous animal models have been utilized. The models described here are among the most widely used and are represented by LPS given at high dose, or at low dose in D-galactosamine-sensitized mice. The endpoints of these models are the survival, the organ toxicity, or the regulation of cytokines, and in particular of TNFalpha. An additional and more complex model of endotoxic/septic shock, the polymicrobial model of cecal ligation and puncture, where a synergistic interaction of several mediators occurs, is then described.
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