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BALB/c小鼠中轮跑行为的强化:运动活动和内源性阿片类物质的作用

Reinforcement of wheel running in BALB/c mice: role of motor activity and endogenous opioids.

作者信息

Vargas-Pérez Héctor, Sellings Laurie H L, Paredes Raúl G, Prado-Alcalá Roberto A, Díaz José-Luis

机构信息

Departamento de Neurobiología Conductual y Cognitiva, Instituto de Neurobiología, Universidad Nacional Autónoma de México.

出版信息

J Mot Behav. 2008 Nov;40(6):587-93. doi: 10.3200/JMBR.40.6.587-593.

Abstract

The authors investigated the effect of the opioid antagonist naloxone on wheel-running behavior in Balb/c mice. Naloxone delayed the acquisition of wheel-running behavior, but did not reduce the expression of this behavior once acquired. Delayed acquisition was not likely a result of reduced locomotor activity, as naloxone-treated mice did not exhibit reduced wheel running after the behavior was acquired, and they performed normally on the rotarod test. However, naloxone-blocked conditioned place preference for a novel compartment paired previously with wheel running, suggesting that naloxone may delay wheel-running acquisition by blocking the rewarding or reinforcing effects of the behavior. These results suggest that the endogenous opioid system mediates the initial reinforcing effects of wheel running that are important in acquisition of the behavior.

摘要

作者研究了阿片类拮抗剂纳洛酮对Balb/c小鼠转轮行为的影响。纳洛酮延迟了转轮行为的习得,但一旦习得,并不会减少该行为的表现。延迟习得不太可能是运动活性降低的结果,因为经纳洛酮处理的小鼠在行为习得后并未表现出转轮减少,并且它们在转棒试验中表现正常。然而,纳洛酮阻断了先前与转轮配对的新隔室的条件性位置偏爱,这表明纳洛酮可能通过阻断该行为的奖赏或强化作用来延迟转轮行为的习得。这些结果表明,内源性阿片系统介导了转轮行为最初的强化作用,而这在该行为的习得中很重要。

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