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眶额皮层对前额叶皮层-杏仁核信息流的抑制调节。

Inhibitory Modulation of Orbitofrontal Cortex on Medial Prefrontal Cortex-Amygdala Information Flow.

机构信息

Departments of Neuroscience, Psychiatry, and Psychology, University of Pittsburgh, Pittsburgh, PA 15260, USA.

出版信息

Cereb Cortex. 2018 Jan 1;28(1):1-8. doi: 10.1093/cercor/bhw342.

Abstract

The amygdala receives cortical inputs from the medial prefrontal cortex (mPFC) and orbitofrontal cortex (OFC) that are believed to affect emotional control and cue-outcome contingencies, respectively. Although mPFC impact on the amygdala has been studied, how the OFC modulates mPFC-amygdala information flow, specifically the infralimbic (IL) division of mPFC, is largely unknown. In this study, combined in vivo extracellular single-unit recordings and pharmacological manipulations were used in anesthetized rats to examine how OFC modulates amygdala neurons responsive to mPFC activation. Compared with basal condition, pharmacological (N-Methyl-D-aspartate) or electrical activation of the OFC exerted an inhibitory modulation of the mPFC-amygdala pathway, which was reversed with intra-amygdala blockade of GABAergic receptors with combined GABAA and GABAB antagonists (bicuculline and saclofen). Moreover, potentiation of the OFC-related pathways resulted in a loss of OFC control over the mPFC-amygdala pathway. These results show that the OFC potently inhibits mPFC drive of the amygdala in a GABA-dependent manner; but with extended OFC pathway activation this modulation is lost. Our results provide a circuit-level basis for this interaction at the level of the amygdala, which would be critical in understanding the normal and pathophysiological control of emotion and contingency associations regulating behavior.

摘要

杏仁核接收来自内侧前额叶皮层(mPFC)和眶额皮层(OFC)的皮质输入,分别被认为影响情绪控制和线索-结果关联。尽管已经研究了 mPFC 对杏仁核的影响,但 OFC 如何调节 mPFC-杏仁核信息流,特别是 mPFC 的下边缘(IL)部分,在很大程度上仍是未知的。在这项研究中,我们使用麻醉大鼠的体内细胞外单细胞记录和药理学操作相结合,来研究 OFC 如何调节对 mPFC 激活有反应的杏仁核神经元。与基础状态相比,OFC 的药理学(N-甲基-D-天冬氨酸)或电激活对 mPFC-杏仁核通路施加了抑制性调制,该调制可通过使用 GABA 能受体拮抗剂(荷包牡丹碱和 saclofen)联合阻断杏仁核内 GABA 能受体而逆转。此外,OFC 相关通路的增强导致 OFC 对 mPFC-杏仁核通路的控制丧失。这些结果表明,OFC 通过 GABA 依赖性方式强烈抑制 mPFC 对杏仁核的驱动;但随着 OFC 通路的扩展激活,这种调制会丢失。我们的结果为杏仁核水平上的这种相互作用提供了一个电路级基础,这对于理解调节行为的情绪和关联的正常和病理生理学控制至关重要。

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