| Title: | Neuropeptide S Attenuates the Alarm Pheromone-Evoked Defensive and Risk Assessment Behaviors Through Activation of Cognate Receptor-Expressing Neurons in the Posterior Medial Amygdala |
| Author(s): | Shao YF; Wang C; Rao XP; Wang HD; Ren YL; Li J; Dong CY; Xie JF; Yang XW; Xu FQ; Hou YP; |
| Address: | "Departments of Neuroscience, Anatomy, Histology, and Embryology, Key Laboratory of Preclinical Study for New Drugs of Gansu Province, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China. Key Lab of Neurology of Gansu Province, Lanzhou University, Lanzhou, China. Center of Brain Science, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, National Center for Magnetic Resonance in Wuhan, Key Laboratory of Magnetic Resonance in Biological Systems, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, Wuhan, China. Shenzhen Key Lab of Neuropsychiatric Modulation and Collaborative Innovation Center for Brain Science, Guangdong Provincial Key Laboratory of Brain Connectome and Behavior, CAS Key Laboratory of Brain Connectome and Manipulation, Brain Cognition and Brain Disease Institute (BCBDI), Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions, Shenzhen, China. Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, China. Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China" |
| DOI: | 10.3389/fnmol.2021.752516 |
| ISSN/ISBN: | 1662-5099 (Print) 1662-5099 (Electronic) 1662-5099 (Linking) |
| Abstract: | "Neuropeptide S (NPS) acts by activating its cognate receptor (NPSR). High level expression of NPSR in the posterior medial amygdala suggests that NPS-NPSR system should be involved in regulation of social behaviors induced by social pheromones. The present study was undertaken to investigate the effects of central administration of NPS or with NPSR antagonist on the alarm pheromone (AP)-evoked defensive and risk assessment behaviors in mice. Furthermore, H129-H8, a novel high-brightness anterograde multiple trans-synaptic virus, c-Fos and NPSR immunostaining were employed to reveal the involved neurocircuits and targets of NPS action. The mice exposed to AP displayed an enhancement in defensive and risk assessment behaviors. NPS (0.1-1 nmol) intracerebroventricular (i.c.v.) injection significantly attenuated the AP-evoked defensive and risk assessment behaviors. NPSR antagonist [D-Val(5)]NPS at the dose of 40 nmol completely blocked the effect of 0.5 nmol of NPS which showed the best effective among dose range. The H129-H8-labeled neurons were observed in the bilateral posterodorsal medial amygdala (MePD) and posteroventral medial amygdala (MePV) 72 h after the virus injection into the unilateral olfactory bulb (OB), suggesting that the MePD and MePV receive olfactory information inputs from the OB. The percentage of H129-H8-labeled neurons that also express NPSR were 90.27 +/- 3.56% and 91.67 +/- 2.46% in the MePD and MePV, respectively. NPS (0.5 nmol, i.c.v.) remarkably increased the number of Fos immunoreactive (-ir) neurons in the MePD and MePV, and the majority of NPS-induced Fos-ir neurons also expressed NPSR. The behavior characteristic of NPS or with [D-Val(5)]NPS can be better replicated in MePD/MePV local injection within lower dose. The present findings demonstrated that NPS, via selective activation of the neurons bearing NPSR in the posterior medial amygdala, attenuates the AP-evoked defensive and risk assessment behaviors in mice" |
| Keywords: | alarm pheromone antagonist c-Fos herpes simplex virus neural circuit tracing neuropeptide S neuropeptide S receptor posterior medial amygdala;neuroscience; |
| Notes: | "PubMed-not-MEDLINEShao, Yu-Feng Wang, Can Rao, Xiao-Ping Wang, Hua-Dong Ren, Yan-Li Li, Jing Dong, Chao-Yu Xie, Jun-Fan Yang, Xing-Wen Xu, Fu-Qiang Hou, Yi-Ping eng Switzerland 2022/01/11 Front Mol Neurosci. 2021 Dec 24; 14:752516. doi: 10.3389/fnmol.2021.752516. eCollection 2021" |
