Hayden Dustin J, Finnie Peter S B, Thomazeau Aurore, Li Alyssa Y, Cooke Samuel F, Bear Mark F
bioRxiv. 2023 Jan 25:2023.01.25.524429. doi: 10.1101/2023.01.25.524429.
In mouse primary visual cortex (V1), familiar stimuli evoke significantly altered responses when compared to novel stimuli. This stimulus-selective response plasticity (SRP) was described originally as an increase in the magnitude of visual evoked potentials (VEPs) elicited in layer (L) 4 by familiar phase-reversing grating stimuli. SRP is dependent on NMDA receptors (NMDAR) and has been hypothesized to reflect potentiation of thalamocortical synapses in L4. However, recent evidence indicates that the synaptic modifications that manifest as SRP do not occur on L4 principal cells. To shed light on where and how SRP is induced and expressed, the present study had three related aims: (1) to confirm that NMDAR are required specifically in glutamatergic principal neurons of V1, (2) to investigate the consequences of deleting NMDAR specifically in L6, and (3) to use translaminar electrophysiological recordings to characterize SRP expression in different layers of V1. We find that knockout of NMDAR in L6 principal neurons disrupts SRP. Current-source density analysis of the VEP depth profile shows augmentation of short latency current sinks in layers 3, 4 and 6 in response to phase reversals of familiar stimuli. Multiunit recordings demonstrate that increased peak firing occurs to in response to phase reversals of familiar stimuli across all layers, but that activity between phase reversals is suppressed. Together, these data reveal important aspects of the underlying phenomenology of SRP and generate new hypotheses for the expression of experience-dependent plasticity in V1.
Repeated exposure to stimuli that portend neither reward nor punishment leads to behavioral habituation, enabling organisms to dedicate attention to novel or otherwise significant features of the environment. The neural basis of this process, which is so often dysregulated in neurological and psychiatric disorders, remains poorly understood. Learning and memory of stimulus familiarity can be studied in mouse visual cortex by measuring electrophysiological responses to simple phase-reversing grating stimuli. The current study advances knowledge of this process by documenting changes in visual evoked potentials, neuronal spiking activity, and oscillations in the local field potentials across all layers of mouse visual cortex. In addition, we identify a key contribution of a specific population of neurons in layer 6 of visual cortex.
在小鼠初级视觉皮层(V1)中,与新刺激相比,熟悉的刺激会引起显著改变的反应。这种刺激选择性反应可塑性(SRP)最初被描述为在第4层(L4)中由熟悉的相位反转光栅刺激引发的视觉诱发电位(VEP)幅度增加。SRP依赖于NMDA受体(NMDAR),并且据推测反映了L4中丘脑皮质突触的增强。然而,最近的证据表明,表现为SRP的突触修饰并非发生在L4主细胞上。为了阐明SRP在何处以及如何被诱导和表达,本研究有三个相关目标:(1)确认V1的谷氨酸能主神经元中特异性需要NMDAR;(2)研究在L6中特异性删除NMDAR的后果;(3)使用跨层电生理记录来表征V1不同层中的SRP表达。我们发现L6主神经元中NMDAR的敲除会破坏SRP。VEP深度剖面的电流源密度分析显示,在响应熟悉刺激的相位反转时,第3、4和6层中短潜伏期电流汇增强。多单元记录表明,在所有层中,响应熟悉刺激的相位反转时峰值放电增加,但相位反转之间的活动受到抑制。这些数据共同揭示了SRP潜在现象学的重要方面,并为V1中经验依赖性可塑性的表达产生了新的假设。
反复暴露于既不预示奖励也不预示惩罚的刺激会导致行为习惯化,使生物体能够将注意力投入到环境的新特征或其他重要特征上。这个过程的神经基础在神经和精神疾病中常常失调,仍然知之甚少。通过测量对简单相位反转光栅刺激的电生理反应,可以在小鼠视觉皮层中研究刺激熟悉度的学习和记忆。本研究通过记录小鼠视觉皮层所有层中视觉诱发电位、神经元放电活动和局部场电位振荡的变化,推进了对这一过程的认识。此外,我们确定了视觉皮层第6层中特定神经元群体的关键作用。