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PDE10A 缺陷型小鼠表现出食欲和厌恶动机行为以及学习能力受损,表明纹状体信号在评估显著度归因中发挥作用。

Impaired appetitively as well as aversively motivated behaviors and learning in PDE10A-deficient mice suggest a role for striatal signaling in evaluative salience attribution.

机构信息

Laboratory of Biological Psychology, Department of Psychology, University of Leuven, Tiensestraat 102, 3000 Leuven, Belgium.

出版信息

Neurobiol Learn Mem. 2011 Mar;95(3):260-9. doi: 10.1016/j.nlm.2010.11.018. Epub 2010 Dec 2.

DOI:10.1016/j.nlm.2010.11.018
PMID:21130175
Abstract

Phosphodiesterase 10A (PDE10A) hydrolyzes both cAMP and cGMP, and is a key element in the regulation of medium spiny neuron (MSN) activity in the striatum. In the present report, we investigated the effects of targeted disruption of PDE10A on spatial learning and memory as well as aversive and appetitive conditioning in C57BL/6J mice. Because of its putative role in motivational processes and reward learning, we also determined the expression of the immediate early gene zif268 in striatum and anterior cingulate cortex. Animals showed decreased response rates in scheduled appetitive operant conditioning, as well as impaired aversive conditioning in a passive avoidance task. Morris water maze performance revealed not-motor related spatial learning and memory deficits. Anxiety and social explorative behavior was not affected in PDE10A-deficient mice. Expression of zif268 was increased in striatum and anterior cingulate cortex, which suggests alterations in the neural connections between striatum and anterior cingulate cortex in PDE10A-deficient mice. The changes in behavior and plasticity in these PDE10A-deficient mice were in accordance with the proposed role of striatal MSNs and corticostriatal connections in evaluative salience attribution.

摘要

磷酸二酯酶 10A(PDE10A)可水解 cAMP 和 cGMP,是纹状体中型多棘神经元(MSN)活性调节的关键因素。在本报告中,我们研究了靶向敲除 PDE10A 对 C57BL/6J 小鼠空间学习和记忆以及厌恶和奖赏条件作用的影响。由于其在动机过程和奖赏学习中的潜在作用,我们还确定了纹状体和前扣带皮层中即刻早期基因 zif268 的表达。动物在预期奖赏操作性条件作用中表现出反应率降低,在被动回避任务中表现出厌恶条件作用受损。Morris 水迷宫性能显示出与运动无关的空间学习和记忆缺陷。PDE10A 缺陷型小鼠的焦虑和社交探索行为不受影响。PDE10A 缺陷型小鼠纹状体和前扣带皮层中的 zif268 表达增加,这表明 PDE10A 缺陷型小鼠纹状体和前扣带皮层之间的神经连接发生了改变。这些 PDE10A 缺陷型小鼠的行为和可塑性变化与纹状体 MSN 和皮质纹状体连接在评价显著归因中的作用一致。

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