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首页> 外文期刊>Behavioral neuroscience >Effects of dopaminergic drugs on innate pheromone-mediated reward in female mice: A new case of dopamine-independent 'liking'
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Effects of dopaminergic drugs on innate pheromone-mediated reward in female mice: A new case of dopamine-independent 'liking'

机译:多巴胺能药物对雌性小鼠先天性信息素介导的奖赏的影响:新的多巴胺非依赖性“喜欢”病例

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摘要

Male sexual pheromones are innately rewarding to adult female mice, but the role of dopamine in this natural reward is unknown. The authors have tackled this issue by assessing the effects of intraperitoneal injections of dopamine D, (SCH 23390, 0.02-0.05mg/kg) and D-2 (sulpiride, 20.00 mg/kg) antagonists. a dopamine releasing agent (amphetamine. 0.50-2.00 mg/kg, and D, (SKF 38393. 10.00-20.00 mg/kg) and D-2 (quinpirole, 0.20-1.00 mg/kg) agonists on the chernoinvestigation displayed by female mice in male- versus female-soiled bedding 2-choice tests. Dopamine antagonists and quinpirole failed to affect the unconditioned preference displayed by females towards male chemosignals, whereas both amphetamine and SKF 38393 abolished it. Finally, D, and D, antagonists did not block the induction of operant place conditioning by male chemosignals. As the female mice were tested in their first encounter with male sexual pheromones, their behavior can only be influenced by the "liking" component of reward. Therefore. the results suggest that dopamine mediates neither the hedonic properties of male sexual pheromones nor the acquisition of conditioned place preference. However, dopamine acting on D, receptors might inhibit female mice attraction towards male chemosignals.
机译:男性性信息素天生会奖励成年雌性小鼠,但多巴胺在这种自然奖励中的作用尚不清楚。作者通过评估腹膜内注射多巴胺D(SCH 23390,0.02-0.05mg / kg)和D-2(舒必利,20.00 mg / kg)拮抗剂的作用解决了这个问题。多巴胺释放剂(苯丙胺。0.50-2.00mg / kg,和D,(SKF38393。10.00-20.00mg / kg)和D-2(喹吡罗,0.20-1.00 mg / kg)激动剂对雌性小鼠显示的切尔诺作在男性和女性弄脏的床上用品2选择测试中,多巴胺拮抗剂和喹吡罗不能影响女性对男性化学信号的无条件偏爱,而苯丙胺和SKF 38393都消除了它;最后,D和D拮抗剂没有阻止当雄性化学信息素首次与雌性小鼠相遇时,对雌性小鼠进行了测试,因此它们的行为只能受到奖励的“喜好”成分的影响,因此,结果表明,多巴胺既不介导多巴胺雄性性信息素的享乐特性或条件位置偏好的获得,但是,多巴胺作用于D1受体可能会抑制雌性小鼠对雄性化学信号的吸引。

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