Convergence Research Center for Diagnosis, Treatment and Care System of Dementia (DTC), Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.
Division of Bio-Medical Science and Technology, KIST School, Korea University of Science and Technology (UST), Seoul, Republic of Korea.
Addict Biol. 2021 May;26(3):e12956. doi: 10.1111/adb.12956. Epub 2020 Aug 6.
Nicotine can diversely affect neural activity and motor learning in animals. However, the impact of chronic nicotine on striatal activity in vivo and motor learning at long-term sparse timescale remains unknown. Here, we demonstrate that chronic nicotine persistently suppresses the activity of striatal fast-spiking parvalbumin interneurons, which mediate nicotine-induced deficit in sparse motor learning. Six weeks of longitudinal in vivo single-unit recording revealed that mice show reduced activity of fast-spiking interneurons in the dorsal striatum during chronic nicotine exposure and withdrawal. The reduced firing of fast-spiking interneurons was accompanied by spike broadening, diminished striatal delta oscillation power, and reduced sample entropy in local field potential. In addition, chronic nicotine withdrawal impaired motor learning with a weekly sparse training regimen but did not affect general locomotion and anxiety-like behavior. Lastly, the excitatory DREADD hM3Dq-mediated activation of striatal fast-spiking parvalbumin interneurons reversed the chronic nicotine withdrawal-induced deficit in sparse motor learning. Taken together, we identified that chronic nicotine withdrawal impairs sparse motor learning via disruption of activity in striatal fast-spiking parvalbumin interneurons. These findings suggest that sparse motor learning paradigm can reveal the subtle effect of nicotine withdrawal on motor function and that striatal fast-spiking parvalbumin interneurons are a neural substrate of nicotine's effect on motor learning.
尼古丁可以在动物中多样化地影响神经活动和运动学习。然而,慢性尼古丁对纹状体体内活动和长期稀疏时间尺度上的运动学习的影响尚不清楚。在这里,我们证明慢性尼古丁持续抑制纹状体中快速放电的 parvalbumin 中间神经元的活动,这种神经元介导了尼古丁诱导的稀疏运动学习缺陷。六周的纵向体内单细胞记录显示,在慢性尼古丁暴露和戒断期间,小鼠在背纹状体中表现出快速放电中间神经元活性降低。快速放电中间神经元的放电减少伴随着尖峰展宽、纹状体 delta 振荡功率降低和局部场电位中样本熵降低。此外,慢性尼古丁戒断会损害每周稀疏训练方案的运动学习,但不会影响一般运动和焦虑样行为。最后,兴奋性 DREADD hM3Dq 介导的纹状体快速放电 parvalbumin 中间神经元的激活逆转了慢性尼古丁戒断引起的稀疏运动学习缺陷。总之,我们发现慢性尼古丁戒断通过破坏纹状体快速放电 parvalbumin 中间神经元的活动来损害稀疏运动学习。这些发现表明,稀疏运动学习范式可以揭示尼古丁戒断对运动功能的微妙影响,并且纹状体快速放电 parvalbumin 中间神经元是尼古丁对运动学习影响的神经基础。