Department of Psychology, University of Toronto Scarborough, Toronto, ON, M1C1A4, Canada.
Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, SK, S7N 5E5, Canada.
Neuropsychopharmacology. 2024 May;49(6):993-1006. doi: 10.1038/s41386-024-01795-5. Epub 2024 Jan 17.
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.
内侧前额叶皮层(mPFC)对认知和情绪功能至关重要,是许多神经精神疾病的基础,包括情绪、恐惧和焦虑障碍。在啮齿动物中,mPFC 活动的破坏会影响焦虑和抑郁样行为,其各部分有特定的贡献。啮齿动物 mPFC 分为背侧前额叶皮层(dmPFC),跨越前扣带皮层(ACC)和背侧前扣带皮层(PL),以及腹侧前额叶皮层(vmPFC),包括腹侧 PL、下边缘皮层(IL),在一些研究中还包括背侧脚蹼皮层(DP)和背侧终板(DTT)。DP/DTT 最近被牵连到通过投射到下丘脑来调节应激诱导的交感反应中。虽然许多研究表明 PL 和 IL 与焦虑、抑郁样和恐惧行为有关,但 DP/DTT 对情感和情绪行为的贡献仍然未知。在这里,我们使用化学遗传学和光遗传学双向调节 DP/DTT 活性,并研究其对 C57BL/6J 小鼠的情感行为、恐惧和应激反应的影响。DP/DTT 的急性化学遗传学激活显著增加了旷场和高架十字迷宫测试中的焦虑样行为,以及在悬尾测试中的被动应对。DP/DTT 激活还导致血清皮质酮水平升高,并促进听觉恐惧消退学习和检索。DP/DTT 投射到背侧下丘脑(DMH)的激活急性降低了基线和消退学习期间的冻结,但没有改变情感行为。这些发现表明 DP/DTT 是小鼠情感行为和恐惧消退的新调节剂。