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新奇性有选择地允许腹侧被盖区-海马-前额叶回路中与学习相关的可塑性。

Novelty selectively permits learning-associated plasticity in ventral tegmental-hippocampal-prefrontal circuitry.

作者信息

Park Alan Jung

机构信息

Department of Physiology, Seoul National University College of Medicine, Seoul, Republic of Korea.

Neuroscience Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

出版信息

Front Behav Neurosci. 2023 Jan 9;16:1091082. doi: 10.3389/fnbeh.2022.1091082. eCollection 2022.

Abstract

Modifying established behavior in novel situations is essential, and patients with neuropsychiatric disorders often lack this flexibility. Understanding how novelty affects behavioral flexibility therefore has therapeutic potential. Here, novelty differentially impacts connectivity within the ventral tegmental-hippocampal-medial prefrontal (VTA-HPC-mPFC) circuit, thereby enhancing the ability of mice to overcome established behavioral bias and adapt to new rules. Circuit connectivity was measured by local field potential (LFP) coherence. As mice exposed to novelty learned to overcome previously established spatial bias, the ventral HPC (vHPC) strengthens its coherence with the VTA and mPFC in theta frequency (4-8 Hz). Novelty or learning did not affect circuits involving the dorsal HPC (dHPC). Without novelty, however, mice continued following established spatial bias and connectivity strength remained stable in the VTA-HPC-mPFC circuit. Pharmacologically blocking dopamine D1-receptors (D1Rs) in the vHPC abolished the behavioral and physiological impacts of novelty. Thus, novelty promotes behavioral adaptation by permitting learning-associated plasticity in the vHPC-mPFC and VTA-vHPC circuit, a process mediated by D1Rs in the vHPC.

摘要

在新环境中改变既定行为至关重要,而神经精神疾病患者往往缺乏这种灵活性。因此,了解新奇性如何影响行为灵活性具有治疗潜力。在此,新奇性对腹侧被盖区-海马-内侧前额叶(VTA-HPC-mPFC)回路内的连通性产生不同影响,从而增强小鼠克服既定行为偏差并适应新规则的能力。通过局部场电位(LFP)相干性来测量回路连通性。当暴露于新奇环境的小鼠学会克服先前建立的空间偏差时,腹侧海马(vHPC)在θ频率(4-8赫兹)下增强了其与VTA和mPFC的相干性。新奇性或学习并未影响涉及背侧海马(dHPC)的回路。然而,在没有新奇性的情况下,小鼠继续遵循既定的空间偏差,并且VTA-HPC-mPFC回路中的连通性强度保持稳定。药理学上阻断vHPC中的多巴胺D1受体(D1Rs)消除了新奇性的行为和生理影响。因此,新奇性通过允许vHPC-mPFC和VTA-vHPC回路中与学习相关的可塑性来促进行为适应,这一过程由vHPC中的D1Rs介导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90a9/9868659/6c89ac7c9606/fnbeh-16-1091082-g001.jpg

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