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伏隔核内cAMP依赖性蛋白激酶的抑制会损害食欲性工具性学习。

Appetitive instrumental learning is impaired by inhibition of cAMP-dependent protein kinase within the nucleus accumbens.

作者信息

Baldwin Anne E, Sadeghian Kenneth, Holahan Matthew R, Kelley Ann E

机构信息

Neuroscience Training Program, University of Wisconsin-Madison Medical School, 53719-1176, USA.

出版信息

Neurobiol Learn Mem. 2002 Jan;77(1):44-62. doi: 10.1006/nlme.2000.4002.

Abstract

The medium spiny neurons of the nucleus accumbens receive a unique convergence of dopaminergic and glutamatergic inputs from regions associated with motivational, cognitive, and sensory processes. Long-term forms of plasticity in the nucleus accumbens associated with such processes as appetitive learning and drug addiction may require coactivation of both dopamine D1 and glutamate N-methyl-D-aspartate (NMDA) receptors. This notion implies that an intracellular mechanism is likely to be involved in these long-term neuroadaptive processes. The present series of experiments examined the effects of intra-accumbens microinfusion of protein kinase inhibitors on acquisition of an instrumental task, lever-pressing for food. Male Sprague-Dawley rats were bilaterally implanted with chronic indwelling cannulae aimed at the nucleus accumbens core. Following recovery, animals were food-restricted and subsequently trained for operant responding. The broad-based serine/threonine kinase inhibitor H-7 (5 or 27 nmol per side) dose-dependently impaired learning when infused immediately after testing on days 1-4. Rp-cAMPS, a cAMP-dependent protein kinase (PKA) inhibitor, also impaired learning regardless of whether it was infused immediately before (5 or 20 nmol) or immediately after (10 nmol) testing on days 1-4. Rp-cAMPS (10 nmol) also inhibited learning when infused 1 h after testing, though to a lesser extent than when administered before or immediately after testing. The PKA stimulator Sp-cAMPS (5 or 20 nmol) also impaired learning when infused before testing, suggesting that there is an optimal level of PKA activity required for learning. None of the drugs used produced nonspecific motor or feeding effects. These results provide evidence supporting the involvement of nucleus accumbens PKA in appetitive learning and suggest that this kinase may be involved in long-term changes associated with this and other motivationally based neuroadaptive processes.

摘要

伏隔核的中等多棘神经元从与动机、认知和感觉过程相关的区域接收多巴胺能和谷氨酸能输入的独特汇聚。与诸如奖赏学习和药物成瘾等过程相关的伏隔核长期可塑性形式可能需要多巴胺D1受体和谷氨酸N-甲基-D-天冬氨酸(NMDA)受体的共同激活。这一观点意味着细胞内机制可能参与了这些长期神经适应性过程。本系列实验研究了向伏隔核内微量注射蛋白激酶抑制剂对工具性任务(按压杠杆获取食物)习得的影响。雄性Sprague-Dawley大鼠双侧植入针对伏隔核核心的慢性留置套管。恢复后,对动物进行食物限制,随后训练其操作性反应。在第1 - 4天测试后立即注射时,广谱丝氨酸/苏氨酸激酶抑制剂H-7(每侧5或27 nmol)剂量依赖性地损害学习。Rp-cAMPS,一种环磷酸腺苷依赖性蛋白激酶(PKA)抑制剂,无论在第1 - 4天测试前(5或20 nmol)还是测试后立即(10 nmol)注射,都会损害学习。Rp-cAMPS(10 nmol)在测试后1小时注射时也会抑制学习,尽管程度比在测试前或测试后立即给药时要小。PKA刺激剂Sp-cAMPS(5或20 nmol)在测试前注射时也会损害学习,表明学习需要最佳水平的PKA活性。所使用的药物均未产生非特异性运动或进食影响。这些结果提供了证据支持伏隔核PKA参与奖赏学习,并表明该激酶可能参与与此及其他基于动机的神经适应性过程相关的长期变化。

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