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白细胞介素-1β刺激10日龄幼鼠促肾上腺皮质激素和皮质酮的释放。

Interleukin-1 beta stimulates adrenocorticotropin and corticosterone release in 10-day-old rat pups.

作者信息

O'Grady M P, Hall N R, Menzies R A

机构信息

Department of Psychiatry and Behavioral Medicine, University of South Florida College of Medicine, Tampa.

出版信息

Psychoneuroendocrinology. 1993;18(3):241-7. doi: 10.1016/0306-4530(93)90007-8.

Abstract

Interleukin-1 (IL-1) is a cytokine secreted in response to immunological challenge which has effects in many physiological systems in adult models. Among the central nervous system effects of IL-1 are its ability to alter sleep patterns, body temperature, and certain neuroendocrine parameters including the release of ACTH and corticosterone (B) in vivo. This study investigated the ability of IL-1 to induce ACTH and B release in 10-day-old rats. This age was chosen due to a well documented phenomenon, the stress hyporesponsive period (SHRP), in which rodents display a blunted pituitary-adrenal response to stressors during the first 2 postnatal weeks (postnatal days 3-14). Administration of IL-1 to rat pups during the SHRP resulted in robust ACTH and B increases. Data are discussed in terms of the site of action and ontogeny of negative feedback mechanisms in the hypothalamic-pituitary-adrenal axis.

摘要

白细胞介素-1(IL-1)是一种在免疫挑战时分泌的细胞因子,在成年模型的许多生理系统中发挥作用。IL-1对中枢神经系统的影响包括改变睡眠模式、体温以及某些神经内分泌参数,如体内促肾上腺皮质激素(ACTH)和皮质酮(B)的释放。本研究调查了IL-1诱导10日龄大鼠释放ACTH和B的能力。选择这个年龄是因为有一个充分记录的现象,即应激低反应期(SHRP),在此期间,啮齿动物在出生后的前两周(出生后第3 - 14天)对压力源的垂体-肾上腺反应减弱。在SHRP期间给幼鼠注射IL-1会导致ACTH和B显著增加。数据将根据下丘脑-垂体-肾上腺轴中负反馈机制的作用部位和个体发生情况进行讨论。

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