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衰老对大鼠下丘脑渗透压调节神经内分泌系统生物合成过程的影响。

The effects of aging on biosynthetic processes in the rat hypothalamic osmoregulatory neuroendocrine system.

机构信息

School of Clinical Sciences, University of Bristol, Bristol, England.

School of Clinical Sciences, University of Bristol, Bristol, England.

出版信息

Neurobiol Aging. 2018 May;65:178-191. doi: 10.1016/j.neurobiolaging.2018.01.008. Epub 2018 Jan 31.

DOI:10.1016/j.neurobiolaging.2018.01.008
PMID:29494864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5878011/
Abstract

Elderly people exhibit a diminished capacity to cope with osmotic challenges such as dehydration. We have undertaken a detailed molecular analysis of arginine vasopressin (AVP) biosynthetic processes in the supraoptic nucleus (SON) of the hypothalamus and secretory activity in the posterior pituitary of adult (3 months) and aged (18 months) rats, to provide a comprehensive analysis of age-associated changes to the AVP system. By matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis, we identified differences in pituitary peptides, including AVP, in adult and aged rats under both basal and dehydrated states. In the SON, increased Avp gene transcription, coincided with reduced Avp promoter methylation in aged rats. Based on transcriptome data, we have previously characterized a number of novel dehydration-induced regulatory factors involved in the response of the SON to osmotic cues. We found that some of these increase in expression with age, while dehydration-induced expression of these genes in the SON was attenuated in aged rats. In summary, we show that aging alters the rat AVP system at the genome, transcriptome, and peptidome levels. These alterations however did not affect circulating levels of AVP in basal or dehydrated states.

摘要

老年人应对渗透挑战(如脱水)的能力下降。我们对下丘脑视上核(SON)中精氨酸加压素(AVP)生物合成过程和成年(3 个月)和老年(18 个月)大鼠后叶的分泌活性进行了详细的分子分析,以全面分析与年龄相关的 AVP 系统变化。通过基质辅助激光解吸/电离飞行时间质谱分析,我们在基础和脱水状态下鉴定了成年和老年大鼠垂体肽(包括 AVP)的差异。在 SON 中,Avp 基因转录增加,同时老年大鼠的 Avp 启动子甲基化减少。基于转录组数据,我们之前已经描述了许多涉及 SON 对渗透线索反应的新型脱水诱导调节因子。我们发现,其中一些随着年龄的增长而表达增加,而在老年大鼠中,这些基因在 SON 中的脱水诱导表达减弱。总之,我们表明衰老会改变大鼠的 AVP 系统在基因组、转录组和肽组水平上。然而,这些变化并没有影响基础或脱水状态下循环中的 AVP 水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/c8c47825912c/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/8d86e0c04e37/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/b210a743b081/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/c904744f4964/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/f558a41ab26a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/db9bdf1ddfb7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/62a640775d11/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/c8c47825912c/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/8d86e0c04e37/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/b210a743b081/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/c904744f4964/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/f558a41ab26a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/db9bdf1ddfb7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/62a640775d11/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb41/5883332/c8c47825912c/gr7.jpg

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