Faculty of Psychology, Southwest University, Chongqing, China; Key Laboratory of Cognition and Personality (Southwest University), Ministry of Education, China; Chongqing Collaborative Innovation Center for Brain Science, Chongqing, China.
Faculty of Psychology, Southwest University, Chongqing, China; Key Laboratory of Cognition and Personality (Southwest University), Ministry of Education, China.
Pharmacol Biochem Behav. 2019 May;180:32-43. doi: 10.1016/j.pbb.2019.03.003. Epub 2019 Mar 21.
Serotonin 5-HT receptors are expressed throughout the mesolimbic and mesocortical dopamine pathways, and manipulation of this receptor system has a profound impact on dopamine functions and dopamine-mediated behaviors. It is highly likely that 5-HT receptors may also modulate the D-mediated maternal effects. The present study investigated this issue and also explored the possible behavioral mechanisms. We tested the effects of two D drugs (an agonist quinpirole: 0.5, 1.0 mg/kg, and a potent D antagonist haloperidol: 0.05, 0.10 mg/kg, sc) and their combinations with two 5-HT drugs (a selective 5-HT agonist TCB-2: 2.5 mg/kg, and 5-HT antagonist MDL100907, 1.0 mg/kg, sc) on maternal behavior in Sprague-Dawley postpartum females. Individually, TCB-2 (2.5 mg/kg, sc) and quinpirole (0.5 and 1.0 mg/kg, sc) reduced pup preference and disrupted home-cage maternal behavior. In contrast, haloperidol (0.10 mg/kg, sc) only disrupted home-cage maternal behavior, but did not suppress pup preference. MDL100907 (1.0 mg/kg, sc) by itself had no effect on either pup preference or maternal behavior. When administered in combination, pretreatment of TCB-2 did not alter quinpirole's disruption of pup preference and home-cage maternal behavior (possibly due to the floor effect), however, it did enhance haloperidol's disruption of pup retrieval in the home cage. MDL100907 had no effect both quinpirole's and haloperidol's disruption of pup preference and home-cage maternal behavior. Interestingly, haloperidol attenuated TCB-2's disruptive effect on pup preference. These findings suggest that activation of 5-HT receptors tends to enhance D-mediated maternal disruption, whereas blockade of 5-HT receptors is less effective. They also suggest that 5-HT receptors may have a direct effect on maternal behavior independent of their interaction with D receptors. The possible behavioral and neural mechanisms by which 5-HT- and D2-mediated maternal effects and their interaction are discussed.
5-羟色胺 5-HT 受体存在于中脑边缘多巴胺和中脑皮质多巴胺通路上,该受体系统的操纵对多巴胺功能和多巴胺介导的行为有深远影响。很可能 5-HT 受体也可以调节 D 介导的母性行为。本研究探讨了这个问题,并探索了可能的行为机制。我们测试了两种 D 药物(激动剂喹吡罗:0.5、1.0mg/kg 和强效 D 拮抗剂氟哌啶醇:0.05、0.10mg/kg,sc)及其与两种 5-HT 药物(选择性 5-HT 激动剂 TCB-2:2.5mg/kg 和 5-HT 拮抗剂 MDL100907,1.0mg/kg,sc)组合对 Sprague-Dawley 产后雌性动物母性行为的影响。单独使用 TCB-2(2.5mg/kg,sc)和喹吡罗(0.5 和 1.0mg/kg,sc)会降低幼仔偏好并破坏笼内母性行为。相反,氟哌啶醇(0.10mg/kg,sc)仅破坏笼内母性行为,但不抑制幼仔偏好。MDL100907(1.0mg/kg,sc)本身对幼仔偏好或母性行为均无影响。联合给药时,TCB-2 的预处理并未改变喹吡罗对幼仔偏好和笼内母性行为的破坏作用(可能是由于地板效应),但确实增强了氟哌啶醇在笼内对幼仔检索的破坏作用。MDL100907 对喹吡罗和氟哌啶醇破坏幼仔偏好和笼内母性行为均无影响。有趣的是,氟哌啶醇减弱了 TCB-2 对幼仔偏好的破坏作用。这些发现表明,5-HT 受体的激活往往会增强 D 介导的母性行为破坏,而 5-HT 受体的阻断则效果较差。它们还表明,5-HT 受体可能对母性行为有直接影响,而与其与 D 受体的相互作用无关。讨论了 5-HT-和 D2 介导的母性行为及其相互作用的可能行为和神经机制。