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内毒素休克的动物模型。

Animal models of endotoxic shock.

作者信息

Villa Pia, Ghezzi Pietro

机构信息

Cellular and Molecular Pharmacology Section, Institute of Neuroscience, Milan, Italy.

出版信息

Methods Mol Med. 2004;98:199-206. doi: 10.1385/1-59259-771-8:199.

Abstract

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.

摘要

内毒素/脂多糖(LPS)是引发革兰氏阴性菌所致休克的细胞和体液反应的主要介质。LPS的毒性反应由多种因素介导,主要是由肿瘤坏死因子α(TNFα)介导。为了研究TNF的作用并鉴定内毒素性/败血性休克中的抗TNF分子,人们使用了众多动物模型。这里描述的模型是使用最广泛的模型,以高剂量给予LPS或在D-半乳糖胺致敏的小鼠中低剂量给予LPS为代表。这些模型的终点是生存率、器官毒性或细胞因子的调节,特别是TNFα的调节。然后描述了一种更复杂的内毒素性/败血性休克模型,即盲肠结扎和穿刺的多微生物模型,其中几种介质会发生协同相互作用。

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