Tejeda Hugo A, Hanks Ashley N, Scott Liam, Mejias-Aponte Carlos, Hughes Zoë A, O'Donnell Patricio
Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Neuroscience and Pain Research Unit, Pfizer, Cambridge, MA, USA.
Neuropsychopharmacology. 2015 Dec;40(13):2856-64. doi: 10.1038/npp.2015.138. Epub 2015 May 14.
Kappa opioid receptors (KORs) have been implicated in anxiety and stress, conditions that involve activation of projections from the basolateral amygdala (BLA) to the medial prefrontal cortex (mPFC). Although KORs have been studied in several brain regions, their role on mPFC physiology and on BLA projections to the mPFC remains unclear. Here, we explored whether KORs modify synaptic inputs from the BLA to the mPFC using in vivo electrophysiological recordings with electrical and optogenetic stimulation. Systemic administration of the KOR agonist U69,593 inhibited BLA-evoked synaptic responses in the mPFC without altering hippocampus-evoked responses. Intra-mPFC U69,593 inhibited electrical and optogenetic BLA-evoked synaptic responses, an effect blocked by the KOR antagonist nor-BNI. Bilateral intra-mPFC injection of the KOR antagonist nor-BNI increased center time in the open field test, suggesting an anxiolytic effect. The data demonstrate that mPFC KORs negatively regulate glutamatergic synaptic transmission in the BLA-mPFC pathway and anxiety-like behavior. These findings provide a framework whereby KOR signaling during stress and anxiety can regulate the flow of emotional state information from the BLA to the mPFC.
κ-阿片受体(KORs)与焦虑和应激有关,这些情况涉及从基底外侧杏仁核(BLA)到内侧前额叶皮质(mPFC)的投射激活。尽管已经在几个脑区对KORs进行了研究,但其在mPFC生理学以及BLA向mPFC投射中的作用仍不清楚。在这里,我们使用电刺激和光遗传学刺激的体内电生理记录,探讨了KORs是否会改变从BLA到mPFC的突触输入。全身给予KOR激动剂U69,593可抑制mPFC中BLA诱发的突触反应,而不改变海马诱发的反应。mPFC内注射U69,593可抑制电刺激和光遗传学刺激诱发的BLA突触反应,该效应被KOR拮抗剂nor-BNI阻断。双侧mPFC内注射KOR拮抗剂nor-BNI可增加旷场试验中的中央停留时间,表明具有抗焦虑作用。数据表明,mPFC中的KORs对BLA-mPFC通路中的谷氨酸能突触传递和焦虑样行为具有负向调节作用。这些发现提供了一个框架,据此在应激和焦虑期间KOR信号传导可以调节从BLA到mPFC的情绪状态信息流。