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腹侧下托在应激整合中的作用。

Role of the ventral subiculum in stress integration.

作者信息

Herman James P, Mueller Nancy K

机构信息

Department of Psychiatry, Neurobiology and Anatomy, University of Cincinnati, 2170 East Galbraith Road, Cincinnati, OH 45237-0506, United States.

出版信息

Behav Brain Res. 2006 Nov 11;174(2):215-24. doi: 10.1016/j.bbr.2006.05.035. Epub 2006 Jul 28.

Abstract

The mammalian subiculum plays a prominent role in inhibition of the hypothalamo-pituitary-adrenocortical (HPA) axis. Lesion and stimulation studies indicate that the hippocampus, acting via output neurons of the ventral subiculum, acts to attenuate stress-induced glucocorticoid release. Lesions of the ventral subiculum enhance glucocorticoid secretion following psychogenic, but not systemic stressors, indicating that the influence of this structure on the HPA system is stressor-specific. Anatomical analyses fail to demonstrate direct interactions of the subiculum with principal stress-effector neurons in the paraventricular hypothalamus, consistent with a trans-synaptic mechanism of action. Accordingly, tracing data indicate that glutamatergic ventral subiculum neurons innervate GABAergic neurons in several paraventricular nucleus-projecting neurons in the hypothalamus and basal forebrain, suggesting that inhibition is mediated by glutamate-GABA relays. The subiculum also innervates several limbic forebrain structures that in turn have bisynaptic projections to paraventricular neurons, such as the prefrontal cortex, amygdala and lateral septum, suggesting that the subiculum may have a generalized up-stream influence on limbic stress integration. Finally, recent information suggests that the subiculum may also be stress excitatory under some circumstances, and that there may be substantial strain or individual differences in the net contribution of the subiculum, to stress integration. Overall, the present state of knowledge indicates that the role of the subiculum in stress integration is complex, and likely involves interactions of stress-relevant subicular output with limbic-hypothalamic stress-integrative circuits.

摘要

哺乳动物的下托在抑制下丘脑 - 垂体 - 肾上腺皮质(HPA)轴方面发挥着重要作用。损伤和刺激研究表明,海马体通过腹侧下托的输出神经元发挥作用,以减弱应激诱导的糖皮质激素释放。腹侧下托损伤会增强心理性应激源(而非全身性应激源)后的糖皮质激素分泌,这表明该结构对HPA系统的影响具有应激源特异性。解剖学分析未能证明下托与下丘脑室旁核主要应激效应神经元之间存在直接相互作用,这与跨突触作用机制一致。因此,追踪数据表明,谷氨酸能腹侧下托神经元支配下丘脑和基底前脑几个向室旁核投射的神经元中的GABA能神经元,这表明抑制作用是由谷氨酸 - GABA中继介导的。下托还支配几个边缘前脑结构,这些结构又对室旁神经元有双突触投射,如前额叶皮质、杏仁核和外侧隔核,这表明下托可能对边缘应激整合具有广泛的上游影响。最后,最近的信息表明,在某些情况下,下托也可能具有应激兴奋性,并且下托对应激整合的净贡献可能存在显著的品系或个体差异。总体而言,目前的知识状况表明,下托在应激整合中的作用是复杂的,可能涉及与应激相关的下托输出与边缘 - 下丘脑应激整合回路之间的相互作用。

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