慢性青春期应激会改变成年雌性大鼠海马中GR-FKBP5的相互作用

IF 2.6 4区 心理学 Q2 BEHAVIORAL SCIENCES
Sydney Rowson, Mandakh Bekhbat, Sean Kelly, Molly M Hyer, Samya Dyer, David Weinshenker, Gretchen Neigh
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引用次数: 0

摘要

雌雄动物在发育过程中受到的慢性压力会产生不同的持久行为后果。更具体地说,在人类和啮齿类动物的慢性压力模型中都能观察到雌性抑郁行为的增加,而雄性则没有。尽管已知这些压力诱导的结果,但青春期慢性压力对成人大脑的分子影响却不太清楚。应激激素皮质酮会激活糖皮质激素受体,而受体的活性是通过与辅助伴侣蛋白--如免疫嗜蛋白 FK506 结合蛋白 5(FKBP5)--的相互作用来调节的。以前曾有报道称,成人的应激反应会因长期应激而改变;因此,本研究评估了青少年时期的长期应激对糖皮质激素受体(GR)与其调控辅助伴侣蛋白FKBP5在成年期急性应激反应中相互作用的影响。虽然FKBP5的蛋白含量在不同组别中没有差异,但对GR-FKBP5相互作用的评估表明,有慢性青春期压力史的成年女性在急性压力挑战后海马中的GR-FKBP5相互作用升高,鉴于以前的文献描述了FKBP5对GR活性的影响,这可能会导致转位模式的减少。有趣的是,受压女性海马中GR共伴侣相互作用的改变并没有导致GR调控基因转录的明显差异。这些研究共同表明,慢性青春期应激会导致与糖皮质激素受体的共伴侣相互作用发生持久的变化,并突出了FKBP5在这些变化中所扮演的潜在角色。了解青少年压力暴露的长期影响将提供一个机理框架,以指导针对与早期生活压力暴露有关的成人疾病的干预措施的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic adolescent stress alters GR-FKBP5 interactions in the hippocampus of adult female rats.

Chronic stress exposure during development can have lasting behavioral consequences that differ in males and females. More specifically, increased depressive behaviors in females, but not males, are observed in both humans and rodent models of chronic stress. Despite these known stress-induced outcomes, the molecular consequences of chronic adolescent stress in the adult brain are less clear. The stress hormone corticosterone activates the glucocorticoid receptor, and activity of the receptor is regulated through interactions with co-chaperones-such as the immunophilin FK506 binding proteins 5 (FKBP5). Previously, it has been reported that the adult stress response is modified by a history of chronic stress; therefore, the current study assessed the impact of chronic adolescent stress on the interactions of the glucocorticoid receptor (GR) with its regulatory co-chaperone FKBP5 in response to acute stress in adulthood. Although protein presence for FKBP5 did not differ by group, assessment of GR-FKBP5 interactions demonstrated that adult females with a history of chronic adolescent stress had elevated GR-FKBP5 interactions in the hippocampus following an acute stress challenge which could potentially contribute to a reduced translocation pattern given previous literature describing the impact of FKBP5 on GR activity. Interestingly, the altered co-chaperone interactions of the GR in the stressed female hippocampus were not coupled to an observable difference in transcription of GR-regulated genes. Together, these studies show that chronic adolescent stress causes lasting changes to co-chaperone interactions with the glucocorticoid receptor following stress exposure in adulthood and highlight the potential role that FKBP5 plays in these modifications. Understanding the long-term implications of adolescent stress exposure will provide a mechanistic framework to guide the development of interventions for adult disorders related to early life stress exposures.

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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
25
审稿时长
6-12 weeks
期刊介绍: The journal Stress aims to provide scientists involved in stress research with the possibility of reading a more integrated view of the field. Peer reviewed papers, invited reviews and short communications will deal with interdisciplinary aspects of stress in terms of: the mechanisms of stressful stimulation, including within and between individuals; the physiological and behavioural responses to stress, and their regulation, in both the short and long term; adaptive mechanisms, coping strategies and the pathological consequences of stress. Stress will publish the latest developments in physiology, neurobiology, molecular biology, genetics research, immunology, and behavioural studies as they impact on the understanding of stress and its adverse consequences and their amelioration. Specific approaches may include transgenic/knockout animals, developmental/programming studies, electrophysiology, histochemistry, neurochemistry, neuropharmacology, neuroanatomy, neuroimaging, endocrinology, autonomic physiology, immunology, chronic pain, ethological and other behavioural studies and clinical measures.
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