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首页> 外文期刊>American Journal of Physiology >Role of hypothalamic interleukin-1beta in fever induced by cecal ligation and puncture in rats.
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Role of hypothalamic interleukin-1beta in fever induced by cecal ligation and puncture in rats.

机译:下丘脑白介素-1β在盲肠结扎穿刺致大鼠发热中的作用。

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Bacterial endotoxin induces fever by causing the release of interleukin (IL)-1beta into the circulation or the brain. IL-1beta is believed to mediate fever via triggering the production and/or release of IL-6 in the hypothalamus. The present study examined whether IL-1beta and IL-6 in the hypothalamus of the rat are also involved in fever during bacterial sepsis caused by cecal ligation and puncture (CLP). CLP induces fever for 2 days. Polyclonal rabbit antibody against rat IL-1beta (anti-IL-1beta, 2 microg/microl) or control rabbit IgG (2 microg/microl) was unilaterally microinjected into the hypothalamus of rats immediately after or 24 h after CLP or sham-CLP surgery. Anti-IL-1beta injected 24 h after CLP (when fever was already present) or sham-CLP surgery did not affect fever. Microinjection of anti-IL-1beta into the hypothalamus immediately after surgery caused a significant decrease in body temperature during the night after CLP surgery and a 48% reduction of fever on the following day. Although blood plasma levels of IL-6 were significantly elevated 1.5, 6, 24, and 48 h after CLP surgery, there were no differences in IL-6 concentrations in the extracellular fluid of the anterior hypothalamus (collected by push-pull perfusion). These data suggest that fever due to bacterial sepsis is initiated by IL-1beta within the hypothalamus, and this febrile response, unlike endotoxin-induced fever, is not accompanied by elevation in the hypothalamic concentration of IL-6.
机译:细菌内毒素通过引起白介素(IL)-1β释放进入循环或大脑来诱导发烧。据信IL-1β通过触发下丘脑中IL-6的产生和/或释放来介导发烧。本研究检查了大鼠下丘脑中的IL-1beta和IL-6是否也参与了盲肠结扎和穿刺(CLP)引起的细菌性败血症的发烧。中电会发烧2天。在CLP或Sham-CLP手术后或手术后24小时立即向大鼠下丘脑单侧显微注射抗大鼠IL-1beta(抗IL-1beta,2微克/微升)多克隆兔抗体或对照兔IgG(2微克/微升) 。 CLP(已经发烧时)或假CLP手术后24小时注射抗IL-1beta不会影响发烧。手术后立即向下丘脑显微注射抗IL-1β可导致CLP手术后夜间体温显着下降,第二天发烧减少48%。尽管CLP手术后1.5、6、24和48 h,血浆IL-6水平显着升高,但下丘脑前部细胞外液中IL-6浓度没有差异(通过推挽灌注收集)。这些数据表明由细菌性败血症引起的发热是由下丘脑内的IL-1β引发的,并且这种发热反应与内毒素诱发的发热不同,并不伴随着下丘脑IL-6浓度的升高。

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