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在由Toll样受体2和6激动剂MALP-2和FSL-1诱导的全身炎症期间,大鼠出现发热、厌食、拒饮和运动活动减少。

Pyrexia, anorexia, adipsia, and depressed motor activity in rats during systemic inflammation induced by the Toll-like receptors-2 and -6 agonists MALP-2 and FSL-1.

作者信息

Hübschle Thomas, Mütze Jörg, Mühlradt Peter F, Korte Stefan, Gerstberger Rüdiger, Roth Joachim

机构信息

Institut für Veterinär-Physiologie, Justus-Liebig-Universität Giessen, Frankfurter Strasse 100, D-35392 Giessen, Germany.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2006 Jan;290(1):R180-7. doi: 10.1152/ajpregu.00579.2005. Epub 2005 Sep 8.

Abstract

Macrophage-activating lipopeptide-2 (MALP-2) from Mycoplasma fermentans has been identified as a pathogen-associated molecular pattern of Mycoplasmas that causes activation of the innate immune system through the activation of the heterodimeric Toll-like receptors (TLRs)-2 and -6. The aim of this study was to characterize the ability of MALP-2 and a synthetic analog fibroblast-stimulating lipopeptide-1 (FSL-1; represents the NH2-terminal sequence of a lipoprotein from M. salivarium) to act as exogenous pyrogens, to induce formation of cytokines (endogenous pyrogens), and to cause sickness behavior, such as depressed motor activity, anorexia, and adipsia. For this purpose, body temperature, activity, food intake, and water intake were recorded for 3 days by use of telemetry devices in several groups of rats treated with MALP-2/FSL-1 or the respective control solutions. Intraperitoneal injections of FSL-1 caused fever at doses of 10 or 100 microg/kg, which was preceded by a pronounced phase of hypothermia in response to a dose of 1,000 microg/kg. The maximal fever (a peak of 1.5 degrees C above baseline) was caused by the 100 microg/kg dose with almost identical responses to both MALP-2 and FSL-1. Fever was accompanied by pronounced rises of the proinflammatory cytokines TNF and IL-6 in plasma. Treatment with the TLR-2 and -6 agonists further induced a dose-dependent manifestation of anorexia and adipsia, as well as a reduction of motor activity. We could thus demonstrate that activation of TLR-2 and -6 can induce systemic inflammation in rats accompanied by the classical signs of brain-controlled illness responses.

摘要

来自发酵支原体的巨噬细胞激活脂肽-2(MALP-2)已被确定为支原体的一种病原体相关分子模式,它通过激活异源二聚体Toll样受体(TLR)-2和-6来激活先天免疫系统。本研究的目的是表征MALP-2和一种合成类似物成纤维细胞刺激脂肽-1(FSL-1;代表唾液支原体一种脂蛋白的NH2末端序列)作为外源性致热原的能力,诱导细胞因子(内源性致热原)形成的能力,以及引起疾病行为的能力,如运动活动减少、厌食和烦渴。为此,在几组用MALP-2/FSL-1或相应对照溶液处理的大鼠中,使用遥测设备记录3天的体温、活动、食物摄入量和饮水量。腹腔注射FSL-1在剂量为10或100μg/kg时引起发热,而在剂量为1000μg/kg时则先出现明显的体温过低阶段。100μg/kg剂量引起最大发热(比基线高1.5℃的峰值),对MALP-2和FSL-1的反应几乎相同。发热伴随着血浆中促炎细胞因子TNF和IL-6的明显升高。用TLR-2和-6激动剂治疗进一步诱导了厌食和烦渴的剂量依赖性表现,以及运动活动的减少。因此,我们可以证明TLR-2和-6的激活可诱导大鼠全身性炎症,并伴有大脑控制的疾病反应的典型体征。

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