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脂多糖处理对小鼠白细胞介素-1受体及下丘脑-垂体-肾上腺轴的调节作用

Regulation of interleukin-1 receptors and hypothalamic-pituitary-adrenal axis by lipopolysaccharide treatment in the mouse.

作者信息

Takao T, Nakata H, Tojo C, Kurokawa H, Nishioka T, Hashimoto K, De Souza E B

机构信息

Second Department of Internal Medicine, Kochi Medical School, Nankoku, Japan.

出版信息

Brain Res. 1994 Jun 27;649(1-2):265-70. doi: 10.1016/0006-8993(94)91073-1.

Abstract

We measured iodine-125-labeled recombinant human interleukin-1 alpha (125I-IL-1 alpha) binding in the hippocampus, pituitary, liver, spleen and testis, and plasma adrenocorticotropic hormone (ACTH) and corticosterone levels after i.p. injection of various dose and treatment regimens of the bacterial endotoxin, lipopolysaccharide (LPS). Plasma ACTH and corticosterone levels were significantly increased at 2 h after acute administration of LPS (60 or 300 micrograms/mouse). 125I-IL-1 alpha binding in all peripheral tissues examined was significantly and comparably decreased at 2 h after a single injection of 30 micrograms or 300 micrograms LPS/mouse. On the other hand, 125I-IL-1 alpha binding in hippocampus was significantly decreased only after high dose administration of LPS (300 micrograms/mouse). In order to evaluate if activation of IL-1 in brain resulting in the observed decrease in 125I-IL-1 alpha binding may require more sustained exposure to endotoxin, we compared the effects of a single injection (60 micrograms/mouse) and two injections of LPS (30 micrograms/mouse each at 0 and 12 h). A single injection of LPS (60 micrograms/mouse) decreased 125I-IL-1 alpha binding in the testis but not in the hippocampus, while two LPS injections (30 micrograms/mouse each at 0 and 12 h) caused dramatic reductions in 125I-IL-1 alpha binding in both the hippocampus and testis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们测定了腹腔注射不同剂量和治疗方案的细菌内毒素脂多糖(LPS)后,海马、垂体、肝脏、脾脏和睾丸中碘-125标记的重组人白细胞介素-1α(125I-IL-1α)的结合情况,以及血浆促肾上腺皮质激素(ACTH)和皮质酮水平。急性给予LPS(60或300微克/小鼠)后2小时,血浆ACTH和皮质酮水平显著升高。单次注射30微克或300微克LPS/小鼠后2小时,所有检测的外周组织中125I-IL-1α结合均显著且相当程度地降低。另一方面,仅在高剂量给予LPS(300微克/小鼠)后,海马中的125I-IL-1α结合才显著降低。为了评估脑中IL-1的激活导致观察到的125I-IL-1α结合减少是否可能需要更长时间暴露于内毒素,我们比较了单次注射(60微克/小鼠)和两次注射LPS(每次30微克/小鼠,分别在0和12小时)的效果。单次注射LPS(60微克/小鼠)可降低睾丸中125I-IL-1α结合,但不影响海马中的结合,而两次注射LPS(每次30微克/小鼠,分别在0和12小时)则导致海马和睾丸中125I-IL-1α结合显著降低。(摘要截短至250字)

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