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下丘脑输入在反复束缚应激中维持垂体-肾上腺反应性的作用

Role of hypothalamic inputs in maintaining pituitary-adrenal responsiveness in repeated restraint.

作者信息

Zelena D, Mergl Z, Foldes A, Kovács K J, Tóth Z, Makara G B

机构信息

Laboratory of Stress Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, 1450 Budapest, Hungary.

出版信息

Am J Physiol Endocrinol Metab. 2003 Nov;285(5):E1110-7. doi: 10.1152/ajpendo.00219.2003.

Abstract

The role of hypothalamic structures in the regulation of chronic stress responses was studied by lesioning the mediobasal hypothalamus or the paraventricular nucleus of hypothalamus (PVH). Rats were acutely (60 min) and/or repeatedly (for 7 days) restrained. In controls, a single restraint elevated the plasma adrenocorticotropin (ACTH), corticosterone, and prolactin levels. Repeated restraint produced all signs of chronic stress, including decreased body and thymus weights, increased adrenal weight, basal corticosterone levels, and proopiomelanocortin (POMC) mRNA expression in the anterior pituitary. Some adaptation to repeated restraint of the ACTH response, but not of other hormonal responses, was seen. Lesioning of the mediobasal hypothalamus abolished the hormonal response and POMC mRNA activation to acute and/or repeated restraint, suggesting that the hypothalamo-pituitary-adrenal axis activation during repeated restraint is centrally driven. PVH lesion inhibited the ACTH and corticosterone rise to the first restraint by approximately 50%. In repeatedly restrained rats with PVH lesion, the ACTH response to the last restraint was reduced almost to basal control levels, and the elevation of POMC mRNA level was prevented. PVH seems to be important for the repeated restraint-induced ACTH and POMC mRNA stimulation, but it appears to partially mediate other restraint-induced hormonal changes.

摘要

通过损毁下丘脑中间基底部或下丘脑室旁核(PVH),研究了下丘脑结构在慢性应激反应调节中的作用。对大鼠进行急性(60分钟)和/或反复(7天)束缚。在对照组中,单次束缚会使血浆促肾上腺皮质激素(ACTH)、皮质酮和催乳素水平升高。反复束缚会产生慢性应激的所有体征,包括体重和胸腺重量减轻、肾上腺重量增加、基础皮质酮水平升高以及垂体前叶中阿黑皮素原(POMC)mRNA表达增加。观察到对ACTH反应的反复束缚有一定适应性,但对其他激素反应则没有。损毁下丘脑中间基底部消除了对急性和/或反复束缚的激素反应以及POMC mRNA激活,这表明反复束缚期间下丘脑-垂体-肾上腺轴的激活是由中枢驱动的。PVH损毁使对首次束缚的ACTH和皮质酮升高抑制了约50%。在反复束缚且有PVH损毁的大鼠中,对最后一次束缚的ACTH反应几乎降至基础对照水平,并且POMC mRNA水平的升高被阻止。PVH似乎对反复束缚诱导的ACTH和POMC mRNA刺激很重要,但它似乎部分介导了其他束缚诱导的激素变化。

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