侧下丘脑促肾上腺皮质激素释放激素受体-1抑制和调节应激诱导的焦虑行为。

IF 1 Q4 NEUROSCIENCES Basic and Clinical Neuroscience Pub Date : 2022-05-01 DOI:10.32598/bcn.2021.445.3
Masoumeh Eghtesad, Mahmoud Elahdadi Salmani, Taghi Lashkarbolouki, Iran Goudarzi
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引用次数: 1

摘要

简介:压力是对干扰体内稳态及其通路和靶区域的不良事件的反应。压力通过下丘脑外侧区(LHA)影响大脑,下丘脑外侧区是通过促肾上腺皮质激素释放激素受体1型(CRHr1)介导促肾上腺皮质激素释放激素(CRH)作用的促肾上腺皮质激素释放系统。因此,本研究探讨应激暴露对焦虑发展的影响,以及LHA- crhr1对LHA- crhr1的参与。方法:雄性Wistar大鼠(220 ~ 250 g)分别在LHA两侧植入套管,给予急性或慢性应激。随后,使用开放场(OF)测试探索性行为,使用高架加迷宫(EPM)测试焦虑。献祭前采集脑脊液(CSF)和血液。固定脑组织进行尼氏染色。结果:急性应激降低了EPM的探查性,增加了焦虑。抑制LHA-CRHr1逆转变量,增加探索和减少焦虑。相比之下,慢性压力对焦虑相关行为没有任何影响。慢性应激降低了LHA中的细胞数量,这是由CRHr1抑制所阻止的。然而,CRHr1抑制不能逆转慢性应激诱导的CSF促食欲素水平升高。此外,血浆皮质酮水平通过急性或慢性应激升高,受CRHr1抑制的阻碍。结论:我们的研究结果表明,LHA-CRHr1是调节该区域细胞群急性应激性焦虑发展和慢性应激性变化的一个有能力的候选者。亮点:急性应激,大鼠在开阔场地和高架迷宫中的不动能力增加。慢性应激会增加食欲素的产生,同时降低神经元的存活率。在CRHr1存在的情况下,不发生焦虑和不动。CRHr1阻断逆转了皮质酮和食欲素的慢性应激变化。下丘脑外侧(LH)是一个参与睡眠和食欲调节的区域,最近被发现在应激病理生理中起作用。LH的应激调节功能是通过促肾上腺皮质激素释放激素受体1型(CRHr1)完成的。本研究探讨了LH- CRHr1在焦虑发展和食欲素产生中的作用。急性和慢性应激对行为和分子变化的影响是不同的。急性应激增加了焦虑状态,而慢性应激只改变了分子标准。虽然我们假设慢性应激不能产生焦虑可能归因于习惯化,但慢性应激可以增加血浆皮质酮和食欲素水平。通过拮抗LH中的CRHr1,所有应激行为和分子水平的异常变化都被阻止,表明LH-CRHr1在应激发展中起门控作用。
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Lateral Hypothalamus Corticotropin-releasing Hormone Receptor-1 Inhibition and Modulating Stress-induced Anxiety Behavior.

Introduction: Stress is a reaction to unwanted events disturbing body homeostasis and its pathways and target areas. Stress affects the brain through the lateral hypothalamic area (LHA), the orexinergic system that mediates the effect of corticotropin-releasing hormone (CRH) through CRH Receptor Type 1 (CRHr1). Therefore, this study explores the outcome of stress exposure on anxiety development and the involvement of the LHA through LHA-CRHr1.

Methods: Male Wistar rats (220-250 g) implanted with a cannula on either side of the LHA received acute or chronic stress. Subsequently, exploratory behavior was examined using the Open Field (OF), and anxiety was tested by Elevated Plus Maze (EPM). Before sacrifice, the cerebrospinal fluid (CSF) and the blood were sampled. Nissl stain was performed on fixed brain tissues.

Results: Acute stress reduced exploration in of and increased anxiety in EPM. LHA-CRHr1 inhibition reversed the variables to increase the exploration and decrease anxiety. In contrast, chronic stress did not show any effect on anxiety-related behaviors. Chronic stress decreased the cell population in the LHA, which was prevented by the CRHr1 inhibition. However, the CRHr1 inhibition could not reverse the chronic stress-induced increase in the CSF orexin level. Furthermore, plasma corticosterone levels increased through acute or chronic stress, impeded by the inhibition of CRHr1.

Conclusion: Our results recognize LHA-CRHr1 as a capable candidate that modulates acute stress-induced anxiety development and chronic stress-induced changes in the cellular population of the region.

Highlights: Acute stress, increased immobility of the rat in open field and elevated plus maze.Chronic stress, increased orexin production while decreasing neuronal survival.The anxiety and immobility were not developed in presence of CRHr1.CRHr1 blocking reversed the chronic stress changes in corticosterone and orexin.

Plain language summary: Lateral Hypothalamus (LH) is a region involved in sleep and appetite regulation and recently known to play role in stress pathophysiology. The stress mediating function of the LH is performed through Corticotropin Releasing Hormone Receptor type-1 (CRHr1). This study explored the role of LH- CRHr1 in anxiety development and orexin production. Acute and chronic stress affected the behavior and molecular changes, differently. The acute stress increased the anxiety condition, while the chronic stress could only change the molecular criteria. Although we assumed that the inability of the chronic stress to develop anxiety may be attributable to habituation, the chronic stress could increase the plasma corticosterone and orexin level. All of the stress mal-changes in behavior and molecular level prevented by antagonising CRHr1 in the LH, indicating a gating function of LH-CRHr1 for stress development.

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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
64
审稿时长
4 weeks
期刊介绍: BCN is an international multidisciplinary journal that publishes editorials, original full-length research articles, short communications, reviews, methodological papers, commentaries, perspectives and “news and reports” in the broad fields of developmental, molecular, cellular, system, computational, behavioral, cognitive, and clinical neuroscience. No area in the neural related sciences is excluded from consideration, although priority is given to studies that provide applied insights into the functioning of the nervous system. BCN aims to advance our understanding of organization and function of the nervous system in health and disease, thereby improving the diagnosis and treatment of neural-related disorders. Manuscripts submitted to BCN should describe novel results generated by experiments that were guided by clearly defined aims or hypotheses. BCN aims to provide serious ties in interdisciplinary communication, accessibility to a broad readership inside Iran and the region and also in all other international academic sites, effective peer review process, and independence from all possible non-scientific interests. BCN also tries to empower national, regional and international collaborative networks in the field of neuroscience in Iran, Middle East, Central Asia and North Africa and to be the voice of the Iranian and regional neuroscience community in the world of neuroscientists. In this way, the journal encourages submission of editorials, review papers, commentaries, methodological notes and perspectives that address this scope.
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