Grinevich V, Seeburg P H, Schwarz M K, Jezova D
Laboratory of Neuropeptides, German Cancer Research Center, University of Heidleberg, Heidleberg, Germany.
Endocr Regul. 2012 Jul;46(3):153-9. doi: 10.4149/endo_2012_03_153.
Homer 1 gene products are involved in the regulation of synaptic transmission and plasticity. Beside other deficits, the Homer 1 knockout (KO) mice show distinct behavioural abnormalities, such as anxiety and depression-like behaviours. In addition, we recently reported that the global deletion of the Homer 1 proteins in mice leads to a conspicuous endocrine phenotype linked to hypertrophy of the adrenal cortex, elevated basal and/or adrenocorticotropic hormone-induced corticosterone and aldosterone release in vitro and in vivo, as well as a drastic increase in the adrenocorticotropic hormone receptor mRNA in the adrenocortical cells. Interestingly, the basal secretion of adrenocorticotropic hormone was not changed in these mutants, which is in line with our recent observations, suggesting that the central limb of the hypothalamic-pituitary-adrenal axis (namely hypothalamic corticotropin-releasing hormone levels and the activation of its neurons in response to restraint stress) is not affected in the Homer 1 KO mice. On the contrary, the elevation of both plasma and intra-adrenal corticosterone and aldosterone concentrations in these mutants clearly indicates that the alteration primarily occurred in the adrenal cortex. We propose that excessive steroid release may contribute to depression- and anxiety-like behaviours and that the Homer 1 gene products may be involved in the pathogenesis of these stress-related mood disorders.
荷马1基因产物参与突触传递和可塑性的调节。除了其他缺陷外,荷马1基因敲除(KO)小鼠表现出明显的行为异常,如焦虑和抑郁样行为。此外,我们最近报道,小鼠中荷马1蛋白的整体缺失导致一种明显的内分泌表型,与肾上腺皮质肥大、体外和体内基础和/或促肾上腺皮质激素诱导的皮质酮和醛固酮释放升高有关,以及肾上腺皮质细胞中促肾上腺皮质激素受体mRNA的急剧增加。有趣的是,这些突变体中促肾上腺皮质激素的基础分泌没有改变,这与我们最近的观察结果一致,表明下丘脑-垂体-肾上腺轴的中枢部分(即下丘脑促肾上腺皮质激素释放激素水平及其神经元在应激刺激下的激活)在荷马1基因敲除小鼠中未受影响。相反,这些突变体中血浆和肾上腺内皮质酮和醛固酮浓度的升高清楚地表明,这种改变主要发生在肾上腺皮质。我们认为,过多的类固醇释放可能导致抑郁和焦虑样行为,并且荷马1基因产物可能参与这些与应激相关的情绪障碍的发病机制。