Hughes Edel M, Thornton Aoife M, Kerr Daniel M, Smith Karen, Sanchez Connie, Kelly John P, Finn David P, Roche Michelle
Physiology, School of Medicine, National University of Ireland, Galway, Ireland; Galway Neuroscience Centre, National University of Ireland, Galway, Ireland.
Physiology, School of Medicine, National University of Ireland, Galway, Ireland; Pharmacology and Therapeutics, School of Medicine, National University of Ireland, Galway, Ireland.
Neuroscience. 2020 Sep 15;444:9-18. doi: 10.1016/j.neuroscience.2020.07.055. Epub 2020 Aug 5.
The kappa opioid receptor (KOP) system modulates social play responding, however a paucity of studies have examined effects on social motivation and cognition in the absence of play. Prenatal exposure to the anti-epileptic and mood stabiliser valproic acid (VPA) is associated with impaired social responding and altered gene expression of KOP (oprk1) and dynorphin (pdyn) in several brain regions. The present study examined if pharmacological modulation of KOP altered social motivation and cognition, immediate early gene (IEG) and oprk1-pdyn expression in adolescent male rats and rats prenatally exposed to VPA. In control rats, the KOP antagonist DIPPA enhanced sociability, while both DIPPA and the KOP agonist U50488 decreased social novelty preference. In rats exposed prenatally to VPA, neither U50488 nor DIPPA altered sociability or social novelty preference. Analysis of IEG expression revealed that DIPPA reduced expression of egr-1 expression in the prefrontal cortex of control rats and U50488 increased junb expression in the PFC of both control and VPA-exposed rats. VPA-exposed rats exhibited increased expression of oprk1 and pdyn in the prefrontal cortex and amygdala compared with control rats. DIPPA and U50488 increased oprk1 expression in the amygdala of control rats and decreased oprk1 expression in the prefrontal cortex of VPA-exposed rats. Taken together, these data demonstrate that pharmacological modulation of the KOP system alters social motivation and cognition in control rats, an effect not observed in rats prenatally exposed to VPA. These data provide support that prenatal exposure to VPA is associated with alterations in the expression and functionality of KOP system.
κ-阿片受体(KOP)系统调节社交玩耍反应,然而,在缺乏玩耍的情况下,很少有研究考察其对社交动机和认知的影响。产前暴露于抗癫痫和情绪稳定剂丙戊酸(VPA)与社交反应受损以及几个脑区中KOP(oprk1)和强啡肽(pdyn)的基因表达改变有关。本研究考察了KOP的药理学调节是否会改变青春期雄性大鼠以及产前暴露于VPA的大鼠的社交动机和认知、即刻早期基因(IEG)以及oprk1-pdyn表达。在对照大鼠中,KOP拮抗剂DIPPA增强了社交性,而DIPPA和KOP激动剂U50488均降低了对社交新奇性的偏好。在产前暴露于VPA的大鼠中,U50488和DIPPA均未改变社交性或对社交新奇性的偏好。对IEG表达的分析表明,DIPPA降低了对照大鼠前额叶皮层中egr-1的表达,而U50488增加了对照大鼠和暴露于VPA的大鼠前额叶皮层中junb的表达。与对照大鼠相比,暴露于VPA的大鼠在前额叶皮层和杏仁核中oprk1和pdyn的表达增加。DIPPA和U50488增加了对照大鼠杏仁核中oprk1的表达,并降低了暴露于VPA的大鼠前额叶皮层中oprk1的表达。综上所述,这些数据表明,KOP系统的药理学调节改变了对照大鼠的社交动机和认知,而在产前暴露于VPA的大鼠中未观察到这种效应。这些数据支持产前暴露于VPA与KOP系统的表达和功能改变有关。