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内源性大麻素对下丘脑-垂体-肾上腺轴昼夜节律的调节具有性别二态性。

Regulation of the hypothalamic-pituitary-adrenal axis circadian rhythm by endocannabinoids is sexually diergic.

机构信息

Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, University of Bristol, Bristol, UK.

出版信息

Endocrinology. 2010 Aug;151(8):3720-7. doi: 10.1210/en.2010-0101. Epub 2010 Jun 9.

DOI:10.1210/en.2010-0101
PMID:20534730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2964781/
Abstract

We have examined the effects of acute administration of the cannabinoid receptor type 1 (CB(1)) antagonist AM251 on the rat hypothalamic-pituitary-adrenal (HPA) axis with respect to both gender and time of day. Blood samples were collected from conscious male and female rats every 5 min using an automated blood sampling system, and corticosterone concentrations were determined. In male rats, there was a distinct diurnal effect of AM251 with a greater activation of the HPA axis in the morning (diurnal trough) compared with the evening (diurnal peak). At both times of the day, circulating corticosterone concentrations were elevated for approximately 4 h after AM251 administration. In female rats, there was also diurnal variation in the activation of the HPA axis; however, these effects were not as profound as those in males. Corticosterone concentrations were only slightly elevated at the diurnal trough and for a shorter time period than in males (2 compared with 4 h). Moreover, there was no effect of AM251 on corticosterone concentrations when administered at the diurnal peak. Subsequent studies, only in males, in which both ACTH and corticosterone were measured, confirmed that the effects of AM251 on corticosterone were mediated by ACTH. Moreover, the elevation of both ACTH and corticosterone could be replicated using another CB(1) antagonist, AM281. These data demonstrate that the extent and duration of HPA axis activation after CB(1) blockade are clearly dependent on both gender and time of day.

摘要

我们研究了大麻素受体 1(CB1)拮抗剂 AM251 对大鼠下丘脑-垂体-肾上腺(HPA)轴的影响,涉及性别和时间因素。使用自动采血系统,每隔 5 分钟从清醒的雄性和雌性大鼠中采集血样,并测定皮质酮浓度。在雄性大鼠中,AM251 具有明显的日周期效应,在早晨(日周期低谷)比晚上(日周期高峰)更能激活 HPA 轴。在一天中的两个时间点,AM251 给药后大约 4 小时,循环皮质酮浓度升高。在雌性大鼠中,HPA 轴的激活也存在日周期变化;然而,这些影响不如雄性大鼠那么明显。皮质酮浓度仅在日周期低谷时略有升高,且持续时间比雄性大鼠短(2 小时,而不是 4 小时)。此外,在日周期高峰时给予 AM251 对皮质酮浓度没有影响。随后的研究仅在雄性大鼠中进行,同时测量了 ACTH 和皮质酮,证实 AM251 对皮质酮的影响是通过 ACTH 介导的。此外,使用另一种 CB1 拮抗剂 AM281 可以复制 ACTH 和皮质酮的升高。这些数据表明,CB1 阻断后 HPA 轴的激活程度和持续时间显然取决于性别和时间因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/d3ec1136c7de/zee0081054950004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/182f886f0c0b/zee0081054950001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/3f24e5e2bc10/zee0081054950002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/861c64f430cf/zee0081054950003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/d3ec1136c7de/zee0081054950004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/182f886f0c0b/zee0081054950001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/3f24e5e2bc10/zee0081054950002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/861c64f430cf/zee0081054950003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9cd/2964781/d3ec1136c7de/zee0081054950004.jpg

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