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组胺缺陷基因靶向小鼠的肝脏急性期反应。

Hepatic acute-phase reaction in histamine-deficient gene targeted mice.

作者信息

Donászi-Ivanov A, Scharek P, Falus A, Fülöp A K

机构信息

Department of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary.

出版信息

Inflammopharmacology. 2004;12(1):47-55. doi: 10.1163/156856004773121365.

Abstract

Histamine is a versatile mediator that, according to in vitro studies, affects the synthesis of inflammatory cytokines and acute-phase proteins. The histidine-decarboxylase knockout (HDC-/-) mouse is a model of in vivo investigation of the physiologic and metabolic integration of the acutephase response. These mice do not synthesise histamine and feeding them with histamine-poor diet they are almost completely histamine-deficient. We compared the serum concentrations of representatives of acute-phase plasma proteins, as well as the levels IL-6 and IL-1alpha in wild type and HDC-/- mice during local (turpentine-induced) or systemic (LPS-induced) inflammation. The level of some acute-phase proteins significantly differed in wild-type and HDC-/- mice while others remained unaffected. The IL-6 levels are also differ in the wild-type and histamine-deficient animals, suggesting that the effect of histamine is attained through IL-6, although direct effect is not disclosed yet.

摘要

组胺是一种多功能介质,根据体外研究,它会影响炎性细胞因子和急性期蛋白的合成。组氨酸脱羧酶基因敲除(HDC-/-)小鼠是用于急性期反应的生理和代谢整合体内研究的模型。这些小鼠不合成组胺,用低组胺饮食喂养它们,它们几乎完全缺乏组胺。我们比较了野生型和HDC-/-小鼠在局部(松节油诱导)或全身(LPS诱导)炎症期间急性期血浆蛋白代表物的血清浓度,以及IL-6和IL-1α水平。野生型和HDC-/-小鼠中某些急性期蛋白的水平存在显著差异,而其他蛋白则不受影响。野生型和组胺缺乏动物的IL-6水平也有所不同,这表明组胺的作用是通过IL-6实现的,尽管尚未揭示其直接作用。

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