Dorsal peduncular cortex activity modulates affective behavior and fear extinction in mice

边缘下皮质 前额叶皮质 神经科学 心理学 扣带回前部 消光(光学矿物学) 光遗传学 恐惧条件反射 前额叶腹内侧皮质 焦虑 皮质(解剖学) 高架加迷宫 扁桃形结构 化学 认知 精神科 矿物学
作者
Justin J. Botterill,Abdessattar Khlaifia,Ryan Appings,Jennifer Wilkin,Francesca Violi,Hanista Premachandran,Arely Cruz-Sanchez,Anna Elisabete Canella,Ashutosh Patel,S. Danyal Zaidi,Maithé Arruda-Carvalho
出处
期刊:Neuropsychopharmacology [Springer Nature]
卷期号:49 (6): 993-1006 被引量:6
标识
DOI:10.1038/s41386-024-01795-5
摘要

The medial prefrontal cortex (mPFC) is critical to cognitive and emotional function and underlies many neuropsychiatric disorders, including mood, fear and anxiety disorders. In rodents, disruption of mPFC activity affects anxiety- and depression-like behavior, with specialized contributions from its subdivisions. The rodent mPFC is divided into the dorsomedial prefrontal cortex (dmPFC), spanning the anterior cingulate cortex (ACC) and dorsal prelimbic cortex (PL), and the ventromedial prefrontal cortex (vmPFC), which includes the ventral PL, infralimbic cortex (IL), and in some studies the dorsal peduncular cortex (DP) and dorsal tenia tecta (DTT). The DP/DTT have recently been implicated in the regulation of stress-induced sympathetic responses via projections to the hypothalamus. While many studies implicate the PL and IL in anxiety-, depression-like and fear behavior, the contribution of the DP/DTT to affective and emotional behavior remains unknown. Here, we used chemogenetics and optogenetics to bidirectionally modulate DP/DTT activity and examine its effects on affective behaviors, fear and stress responses in C57BL/6J mice. Acute chemogenetic activation of DP/DTT significantly increased anxiety-like behavior in the open field and elevated plus maze tests, as well as passive coping in the tail suspension test. DP/DTT activation also led to an increase in serum corticosterone levels and facilitated auditory fear extinction learning and retrieval. Activation of DP/DTT projections to the dorsomedial hypothalamus (DMH) acutely decreased freezing at baseline and during extinction learning, but did not alter affective behavior. These findings point to the DP/DTT as a new regulator of affective behavior and fear extinction in mice.

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