Muller Jeff M, Moore Holly, Myers Michael M, Shair Harry N
Division of Developmental Neuroscience, New York State Psychiatric Institute, 1051 Riverside Drive, Unit 40, New York, NY 10032, USA.
Dev Psychobiol. 2009 Mar;51(2):158-72. doi: 10.1002/dev.20355.
Mammalian infant behavior directed toward caregivers is critical to survival and may play a role in establishing social bonds. Most mammalian infants vocalize when isolated. Rat pups vocalize at a higher rate when isolated following an interaction with an adult female than after an interaction with littermates, a phenomenon termed maternal potentiation. We previously reported that the D2 receptor family agonist quinpirole disrupts maternal potentiation at a dose that does not alter vocalization rate following contact with littermates. Here we further examine the role of dopamine in maternal potentiation by testing effects of both D1 and D2 receptor family ligands, alone and in combination, on maternal potentiation. We tested the drugs' effects on isolation vocalization subsequent to littermate contact and then another isolation preceded by a brief "reunion" period of exposure either to the anesthetized dam or a handling-only "pickup" condition. D2 receptor stimulation blocked the increase in vocalizations following reunion with the dam. The D2 agonist effect in the dam-reunion condition was much larger than its small effect in the pickup condition, providing further evidence that D2 receptors exert a selective modulation of maternal potentiation. On the other hand, systemic administration of the D1 agonist SKF81297 reduced isolation vocalizations nonspecifically, across all the experimental conditions. Finally, the D1 and D2 receptor dual antagonist, alpha-flupenthixol, increased isolation vocalizations and disrupted potentiation, but at doses that also inhibited locomotion. We conclude that D2 receptor family activation has a more selective effect of disrupting maternal potentiation than D1 receptor family activation.
哺乳动物幼崽针对照料者的行为对其生存至关重要,且可能在建立社会联系中发挥作用。大多数哺乳动物幼崽在独处时会发出叫声。与成年雌性互动后被隔离的大鼠幼崽比与同窝幼崽互动后被隔离时叫得更频繁,这种现象被称为母性增强。我们之前报道,D2受体家族激动剂喹吡罗以一种不改变与同窝幼崽接触后发声率的剂量破坏母性增强。在此,我们通过单独及联合测试D1和D2受体家族配体对母性增强的影响,进一步研究多巴胺在母性增强中的作用。我们测试了药物对同窝幼崽接触后的隔离发声的影响,然后是在短暂的“团聚”期(暴露于麻醉的母鼠或仅进行处理的“抱起”条件)后再次隔离时的发声影响。D2受体刺激阻断了与母鼠团聚后发声的增加。在母鼠团聚条件下D2激动剂的作用远大于其在抱起条件下的微小作用,这进一步证明D2受体对母性增强发挥选择性调节作用。另一方面,全身性给予D1激动剂SKF81297在所有实验条件下均非特异性地降低隔离发声。最后,D1和D2受体双重拮抗剂氟哌噻吨增加隔离发声并破坏增强作用,但所用剂量也抑制了运动。我们得出结论,与D1受体家族激活相比,D2受体家族激活对破坏母性增强具有更具选择性的作用。