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大脑盐皮质激素受体:对配体贪得无厌,功能神秘莫测。

The brain mineralocorticoid receptor: greedy for ligand, mysterious in function.

作者信息

Reul J M, Gesing A, Droste S, Stec I S, Weber A, Bachmann C, Bilang-Bleuel A, Holsboer F, Linthorst A C

机构信息

Section of Neuropsychopharmacology, Max Planck Institute of Psychiatry, Kraepelinstrasse 2, 80804, Munich, Germany.

出版信息

Eur J Pharmacol. 2000 Sep 29;405(1-3):235-49. doi: 10.1016/s0014-2999(00)00677-4.

Abstract

Glucocorticoids exert their regulatory effects on the hypothalamic-pituitary-adrenocortical axis via two types of corticosteroid receptors: the glucocorticoid receptor and the mineralocorticoid receptor. Whereas the glucocorticoid receptor has a broad distribution in the brain, highest levels of mineralocorticoid receptor are found in the hippocampus. Based on the differential occupancy profile by endogenous glucocorticoids, glucocorticoid receptors are thought to mediate negative feedback signals of elevated glucocorticoid levels, whereas mineralocorticoid receptors control the inhibitory tone of the hippocampus on hypothalamic-pituitary-adrenocortical axis activity. Dysfunction of mineralocorticoid receptors and glucocorticoid receptors are thought to be implicated in stress-related psychiatric diseases such as major depression. Because of its intriguing features, we focus in this review on the mineralocorticoid receptor and provide data which reveal novel aspects of the pharmacology and physiology of mineralocorticoid receptors. Newly obtained results are presented, which help to solve the paradox of why dexamethasone binds with high affinity to mineralocorticoid receptors in vitro, yet binds poorly in vivo. Until recently, mineralocorticoid receptor protein and mRNA levels could only be routinely studied with in vitro cytosol binding assays, in vitro and in vivo receptor autoradiography, Northern blot analysis, and in situ hybridization. These methods are unfortunately hampered by several flaws, such as the necessity of adrenalectomy, no or poor neuroanatomical resolution, the fact that mRNA does not provide the same information as protein, or combinations of these factors. We present immunohistochemical data on mineralocorticoid receptors in the brain obtained by using commercially available antibodies, which alleviate many of these shortcomings. Furthermore, an in vivo microdialysis method is presented which allows the assessment of free corticosterone levels in the brain, which is critical for the study of the pharmacological basis of mineralocorticoid receptor (and glucocorticoid receptor) function. Finally, a novel aspect of the regulation of mineralocorticoid receptors is described which provides evidence that this receptor system is dynamically regulated. In conjunction with previously reported effects of antidepressants, these results have initiated a new concept on the cause of the hypothalamic-pituitary-adrenocortical axis disturbances often seen in stress-related psychiatric disorders such as major depression.

摘要

糖皮质激素通过两种类型的皮质类固醇受体对下丘脑 - 垂体 - 肾上腺皮质轴发挥调节作用:糖皮质激素受体和盐皮质激素受体。糖皮质激素受体在大脑中分布广泛,而盐皮质激素受体在海马体中的水平最高。基于内源性糖皮质激素的不同占据情况,糖皮质激素受体被认为介导糖皮质激素水平升高的负反馈信号,而盐皮质激素受体控制海马体对下丘脑 - 垂体 - 肾上腺皮质轴活动的抑制作用。盐皮质激素受体和糖皮质激素受体功能障碍被认为与应激相关的精神疾病如重度抑郁症有关。由于其有趣的特性,我们在本综述中聚焦于盐皮质激素受体,并提供揭示盐皮质激素受体药理学和生理学新方面的数据。展示了新获得的结果,这些结果有助于解决为什么地塞米松在体外与盐皮质激素受体具有高亲和力结合,但在体内结合不佳这一矛盾。直到最近,盐皮质激素受体蛋白和mRNA水平只能通过体外细胞质结合测定、体外和体内受体放射自显影、Northern印迹分析和原位杂交等常规方法进行研究。不幸的是,这些方法存在一些缺陷,例如需要进行肾上腺切除术、神经解剖分辨率低或无、mRNA不能提供与蛋白质相同的信息,或这些因素的组合。我们展示了使用市售抗体获得的大脑中盐皮质激素受体的免疫组化数据,这些数据缓解了许多这些缺点。此外,还介绍了一种体内微透析方法,该方法可以评估大脑中游离皮质酮水平,这对于研究盐皮质激素受体(和糖皮质激素受体)功能的药理学基础至关重要。最后,描述了盐皮质激素受体调节的一个新方面,该方面提供了证据表明该受体系统是动态调节的。结合先前报道的抗抑郁药的作用,这些结果引发了一个关于在应激相关精神障碍如重度抑郁症中经常出现的下丘脑 - 垂体 - 肾上腺皮质轴紊乱原因的新概念。

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