Division of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Japan Agency for Medical Research and Development, Tokyo, 100-0004, Japan.
Sci Rep. 2019 Nov 13;9(1):16670. doi: 10.1038/s41598-019-52997-7.
We recently reported that dopamine D1 receptor in the medial prefrontal cortex (mPFC) is activated by subthreshold social defeat stress and suppresses the induction of depressive-like behavior in mice. However, which mPFC projection(s) mediates this antidepressant-like effect remains poorly understood. Here we show that social defeat stress specifically increased c-Fos expression, a marker for neuronal activity, in distinct brain regions involved in emotional regulation, relative to novelty-induced exploration. Among these brain areas, D1 knockdown in the mPFC decreased social defeat stress-induced c-Fos expression in the interstitial nucleus of the posterior limb of the anterior commissure (IPAC), a subregion of the extended amygdala. Using retrograde adeno-associated virus vectors and transgenic mice expressing Cre recombinase under the D1 promoter, we also found that D1-expressing deep-layer pyramidal neurons in the mPFC send direct projections to the IPAC. These findings indicate that social defeat stress specifically activates neurons in distinct brain areas, among which the IPAC is regulated by dopamine D1 receptor in the mPFC perhaps through direct projections. Thus, this study provides hints toward identifying neural circuits that underlie antidepressant-like effects of stress-induced dopamine D1 receptor signaling in the mPFC.
我们最近报道,内侧前额叶皮层(mPFC)中的多巴胺 D1 受体被亚阈值社交挫败应激激活,并抑制了小鼠抑郁样行为的诱导。然而,介导这种抗抑郁样作用的 mPFC 投射(s)仍知之甚少。在这里,我们表明,与新奇诱导的探索相比,社交挫败应激特异性地增加了与情绪调节相关的不同脑区中 c-Fos 表达,c-Fos 是神经元活性的标志物。在这些脑区中,mPFC 中的 D1 敲低降低了延伸杏仁核的后连合前肢间核(IPAC)中的社交挫败应激诱导的 c-Fos 表达,IPAC 是延伸杏仁核的一个亚区。使用逆行腺相关病毒载体和在 D1 启动子下表达 Cre 重组酶的转基因小鼠,我们还发现 mPFC 中的 D1 表达深层层锥体神经元向 IPAC 发出直接投射。这些发现表明,社交挫败应激特异性地激活了不同脑区中的神经元,其中 IPAC 可能通过直接投射受到 mPFC 中多巴胺 D1 受体的调节。因此,这项研究为确定介导应激诱导的 mPFC 中多巴胺 D1 受体信号的抗抑郁样作用的神经回路提供了线索。