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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Motor-skill learning in a novel running-wheel task is dependent on D1 dopamine receptors in the striatum.
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Motor-skill learning in a novel running-wheel task is dependent on D1 dopamine receptors in the striatum.

机译:在新的跑轮任务中的运动技能学习取决于纹状体中的D1多巴胺受体。

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摘要

Evidence indicates that dopamine receptors regulate processes of procedural learning in the sensorimotor striatum. Our previous studies revealed that the indirect dopamine receptor agonist cocaine alters motor-skill learning-associated gene regulation in the sensorimotor striatum. Cocaine-induced gene regulation in the striatum is principally mediated by D1 dopamine receptors. We investigated the effects of cocaine and striatal D1 receptor antagonism on motor-skill learning. Rats were trained on a running wheel (40-60 min, 2-5 days) to learn a new motor skill, that is, the ability to control the movement of the wheel. Immediately before each training session, the animals received an injection of vehicle or cocaine (25 mg/kg, i.p.), and/or the D1 receptor antagonist SCH-23390 (0, 3, 10 microg/kg, i.p., or 0, 0.3, 1 microg, intrastriatal via chronically implanted cannula). The animal's ability to control/balance the moving wheel (wheel skill) was tested before and repeatedly after the training. Normal wheel-skill memory lasted for at least 4 weeks. Cocaine administered before the training tended to attenuate skill learning. Systemic administration of SCH-23390 alone also impaired skill learning. However, cocaine given in conjunction with the lower SCH-23390 dose (3 microg/kg) reversed the inhibition of skill learning produced by the D1 receptor antagonist, enabling intact skill performance during the whole post-training period. In contrast, when cocaine was administered with the higher SCH-23390 dose (10 microg/kg), skill performance was normalized 1-6 days after the training, but these rats lost their improved wheel skill by day 18 after the training. Similar effects were produced by SCH-23390 (0.3-1 microg) infused into the striatum. Our results indicate that cocaine interferes with normal motor-skill learning, which seems to be dependent on optimal D1 receptor signaling. Furthermore, our findings demonstrate that D1 receptors in the striatum are critical for consolidation of long-term skill memory.
机译:有证据表明,多巴胺受体调节感觉运动纹状体中的程序学习过程。我们以前的研究表明,间接的多巴胺受体激动剂可卡因改变了感觉运动纹状体中与运动技能学习相关的基因调控。可卡因诱导的纹状体基因调控主要是由D1多巴胺受体介导的。我们调查了可卡因和纹状体D1受体拮抗作用对运动技能学习的影响。在跑轮上训练大鼠(40-60分钟,2-5天)以学习新的运动技能,即控制轮子运动的能力。在每次训练之前,立即给动物注射媒介物或可卡因(25 mg / kg,ip)和/或D1受体拮抗剂SCH-23390(0、3、10 microg / kg,ip或0、0.3) ,1微克,通过慢性植入的套管纹状体)。在训练之前和之后反复测试动物控制/平衡动轮的能力(车轮技巧)。正常的车轮技术记忆至少持续4周。训练前服用可卡因往往会削弱技能学习。仅SCH-23390的系统管理也会损害技能学习。但是,可卡因与较低的SCH-23390剂量(3微克/千克)一起使用可逆转D1受体拮抗剂产生的技能学习抑制,从而在整个训练后期间保持完整的技能表现。相反,当以较高的SCH-23390剂量(10微克/千克)给予可卡因时,训练后1-6天技能性能恢复正常,但这些大鼠在训练后第18天丧失了提高的滚轮技能。通过将SCH-23390(0.3-1 microg)注入纹状体,可以产生类似的效果。我们的结果表明,可卡因干扰正常的运动技能学习,这似乎取决于最佳的D1受体信号传导。此外,我们的发现表明,纹状体中的D1受体对于长期技能记忆的巩固至关重要。

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