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感觉和上下文信息的皮层代表的调制是厌恶联想学习的基础。

Modulation of cortical representations of sensory and contextual information underlies aversive associative learning.

机构信息

Department of Zoology and Physiology, University of Wyoming, Laramie, WY 82071, USA; Wyoming Sensory Biology Center of Biomedical Research Excellence, University of Wyoming, Laramie, WY 82071, USA.

Department of Zoology and Physiology, University of Wyoming, Laramie, WY 82071, USA; Wyoming Sensory Biology Center of Biomedical Research Excellence, University of Wyoming, Laramie, WY 82071, USA.

出版信息

Cell Rep. 2024 Sep 24;43(9):114672. doi: 10.1016/j.celrep.2024.114672. Epub 2024 Aug 27.

DOI:10.1016/j.celrep.2024.114672
PMID:39196779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11472654/
Abstract

Cortical neurons encode both sensory and contextual information, yet it remains unclear how experiences modulate these cortical representations. Here, we demonstrate that trace eyeblink conditioning (TEC), an aversive associative-learning paradigm linking conditioned (CS) with unconditioned stimuli (US), finely tunes cortical coding at both population and single-neuron levels. Initially, we show that the primary somatosensory cortex (S1) is necessary for TEC acquisition, as evidenced by local muscimol administration. At the population level, TEC enhances activity in a small subset (∼20%) of CS- or US-responsive primary neurons (rPNs) while diminishing activity in non-rPNs, including locomotion-tuned or unresponsive PNs. Crucially, TEC learning modulates the encoding of sensory versus contextual information in single rPNs: CS-responsive neurons become less responsive, while US-responsive neurons gain responses to CS. Moreover, we find that the cholinergic pathway, via nicotinic receptors, underlies TEC-induced modulations. These findings suggest that experiences dynamically tune cortical representations through cholinergic pathways.

摘要

皮质神经元编码感觉和上下文信息,但经验如何调节这些皮质表示仍不清楚。在这里,我们证明了痕迹性眨眼条件反射(TEC),一种将条件刺激(CS)与非条件刺激(US)联系起来的厌恶联想学习范式,可以在群体和单个神经元水平上精细地调整皮质编码。最初,我们表明初级体感皮层(S1)是 TEC 获得所必需的,这一点可以通过局部 muscimol 给药得到证明。在群体水平上,TEC 增强了一小部分(约 20%)对 CS 或 US 有反应的初级神经元(rPN)的活动,同时减少了非 rPN 的活动,包括运动调谐或无反应的 PN。至关重要的是,TEC 学习调节了单个 rPN 中感觉与上下文信息的编码:CS 反应神经元的反应性降低,而 US 反应神经元对 CS 的反应性增加。此外,我们发现,通过烟碱型受体,胆碱能通路是 TEC 诱导的调节的基础。这些发现表明,经验通过胆碱能通路动态地调整皮质表示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/db9683db46ec/nihms-2025355-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/dc17420b9faa/nihms-2025355-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/8137d4122d69/nihms-2025355-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/45472e1f826e/nihms-2025355-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/ea83d300b6c5/nihms-2025355-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/db9683db46ec/nihms-2025355-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/dc17420b9faa/nihms-2025355-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/8137d4122d69/nihms-2025355-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/45472e1f826e/nihms-2025355-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/ea83d300b6c5/nihms-2025355-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/11472654/db9683db46ec/nihms-2025355-f0006.jpg

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