Key Laboratory of Human Disease Comparative Medicine, National Health Commission of China (NHC), Beijing Engineering Research Center for Experimental Animal Models of Human Diseases, Institute of Laboratory Animal Science, Peking Union Medicine College, Chinese Academy of Medical Sciences, Beijing 100021, China.
Department of Psychology and Program in Neuroscience, Florida State University, Tallahassee, FL 32306, USA.
Horm Behav. 2020 Mar;119:104638. doi: 10.1016/j.yhbeh.2019.104638. Epub 2019 Nov 30.
Social behavior plays a significant role in the formation of social structure and population regulation in both animals and humans. Oxytocin (OXT) and its receptor (OXTR) are well known for regulating social behaviors, but their upstream regulating factors are rarely investigated. We hypothesized that the phosphorylation of the signal transducer and activator of transcription 3 (p-Stat3) may regulate social and aggressive behaviors via the OXT system in the nucleus accumbens (NAc). To test this hypothesis, OXT, p-Stat3 inhibitor, OXTR antagonist, and OXT plus p-Stat3 inhibitor were infused, respectively, into the NAc in the brain of male Brandt's voles (Lasiopodomys brandtii) - a social rodent species in grassland of Inner Mongolia, China. Our data showed that blockage of p-Stat3-Tyr signaling pathway in the NAc not only increased aggressive behavior but also impaired social recognition of male Brandt's voles via its effects on the expression of local OXT and OXTR. These results have illustrated a novel signaling pathway of p-Stat3-Tyr in regulating social behaviors via the OXT system.
社会行为在动物和人类的社会结构形成和种群调节中起着重要作用。催产素(OXT)及其受体(OXTR)是调节社会行为的众所周知的物质,但它们的上游调节因子很少被研究。我们假设,信号转导和转录激活因子 3(p-Stat3)的磷酸化可能通过核 accumbens(NAc)中的 OXT 系统来调节社会和攻击行为。为了验证这一假设,我们分别将 OXT、p-Stat3 抑制剂、OXTR 拮抗剂和 OXT 加 p-Stat3 抑制剂注入中国内蒙古草原的社会性啮齿动物布氏田鼠(Lasiopodomys brandtii)的大脑中的 NAc。我们的数据表明,NAc 中 p-Stat3-Tyr 信号通路的阻断不仅增加了攻击行为,还通过影响局部 OXT 和 OXTR 的表达损害了雄性布氏田鼠的社会识别。这些结果说明了 p-Stat3-Tyr 通过 OXT 系统调节社会行为的新信号通路。