Achterberg E J Marijke, van Kerkhof Linda W M, Servadio Michela, van Swieten Maaike M H, Houwing Danielle J, Aalderink Mandy, Driel Nina V, Trezza Viviana, Vanderschuren Louk J M J
Department of Animals in Science and Society, Division of Behavioural Neuroscience, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
Neuropsychopharmacology. 2016 Feb;41(3):858-68. doi: 10.1038/npp.2015.212. Epub 2015 Jul 15.
Social play behavior, abundant in the young of most mammalian species, is thought to be important for social and cognitive development. Social play is highly rewarding, and as such, the expression of social play depends on its pleasurable and motivational properties. Since the motivational properties of social play have only sporadically been investigated, we developed a setup in which rats responded for social play under a progressive ratio schedule of reinforcement. Dopaminergic neurotransmission plays a key role in incentive motivational processes, and both dopamine and noradrenaline have been implicated in the modulation of social play behavior. Therefore, we investigated the role of dopamine and noradrenaline in the motivation for social play. Treatment with the psychostimulant drugs methylphenidate and cocaine increased responding for social play, but suppressed its expression during reinforced play periods. The dopamine reuptake inhibitor GBR-12909 increased responding for social play, but did not affect its expression, whereas the noradrenaline reuptake inhibitor atomoxetine decreased responding for social play as well as its expression. The effects of methylphenidate and cocaine on responding for social play, but not their play-suppressant effects, were blocked by pretreatment with the dopamine receptor antagonist α-flupenthixol. In contrast, pretreatment with the α2-adrenoceptor antagonist RX821002 prevented the play-suppressant effect of methylphenidate, but left its effect on responding for social play unaltered. In sum, the present study introduces a novel method to study the incentive motivational properties of social play behavior in rats. Using this paradigm, we demonstrate dissociable roles for dopamine and noradrenaline in social play behavior: dopamine stimulates the motivation for social play, whereas noradrenaline negatively modulates the motivation for social play behavior and its expression.
社交玩耍行为在大多数哺乳动物幼崽中很常见,被认为对社交和认知发展很重要。社交玩耍极具奖赏性,因此,社交玩耍的表现取决于其愉悦性和动机特性。由于社交玩耍的动机特性只是偶尔被研究,我们开发了一种装置,让大鼠在渐进性比率强化程序下为社交玩耍做出反应。多巴胺能神经传递在激励动机过程中起关键作用,多巴胺和去甲肾上腺素都与社交玩耍行为的调节有关。因此,我们研究了多巴胺和去甲肾上腺素在社交玩耍动机中的作用。使用精神兴奋药物哌甲酯和可卡因进行治疗增加了对社交玩耍的反应,但在强化玩耍期间抑制了其表现。多巴胺再摄取抑制剂GBR - 12909增加了对社交玩耍的反应,但不影响其表现,而去甲肾上腺素再摄取抑制剂托莫西汀减少了对社交玩耍的反应及其表现。哌甲酯和可卡因对社交玩耍反应的影响,而非其玩耍抑制作用,被多巴胺受体拮抗剂α - 氟哌噻吨预处理所阻断。相反,α2 - 肾上腺素能受体拮抗剂RX821002预处理可防止哌甲酯的玩耍抑制作用,但不改变其对社交玩耍反应的影响。总之,本研究引入了一种新方法来研究大鼠社交玩耍行为的激励动机特性。使用这种范式,我们证明了多巴胺和去甲肾上腺素在社交玩耍行为中的不同作用:多巴胺刺激社交玩耍的动机,而去甲肾上腺素对社交玩耍行为的动机及其表现起负性调节作用。