Wang Bing-Ying, Wang Bo, Cao Bo, Gu Ling-Ling, Chen Jiayu, He Hua, Zhao Zheng, Chen Fujun, Wang Zhiru
Institute and Key Laboratory of Brain Functional Genomics of Chinese Ministry of Education, Shanghai Key Laboratory of Brain Functional Genomics, School of Life Sciences, East China Normal University, Shanghai, 200062, China.
Department of Neurosurgery, Third Affiliated Hospital of Navy Military Medical University, Shanghai, 200438, China.
Neurosci Bull. 2025 Apr;41(4):649-664. doi: 10.1007/s12264-024-01327-7. Epub 2024 Nov 27.
Learning-associated functional plasticity at hippocampal synapses remains largely unexplored. Here, in a single session of reward-based trace conditioning, we examine learning-induced synaptic plasticity in the dorsal CA1 hippocampus (dCA1). Local field-potential recording combined with selective optogenetic inhibition first revealed an increase of dCA1 synaptic responses to the conditioned stimulus (CS) induced during conditioning at both Schaffer collaterals to the stratum radiatum (Rad) and temporoammonic input to the lacunosum moleculare (LMol). At these dCA1 inputs, synaptic potentiation of CS-responding excitatory synapses was further demonstrated by locally blocking NMDA receptors during conditioning and whole-cell recording sensory-evoked synaptic responses in dCA1 neurons from naive animals. An overall similar time course of the induction of synaptic potentiation was found in the Rad and LMol by multiple-site recording; this emerged later and saturated earlier than conditioned behavioral responses. Our experiments demonstrate a cued memory-associated dCA1 synaptic plasticity induced at both Schaffer collaterals and temporoammonic pathways.
海马体突触处与学习相关的功能可塑性在很大程度上仍未得到探索。在此,在一次基于奖励的痕迹条件反射实验中,我们研究了背侧CA1海马体(dCA1)中学习诱导的突触可塑性。局部场电位记录结合选择性光遗传学抑制首先揭示,在条件反射过程中,从施affer侧支到辐射层(Rad)以及从颞叶-海马输入到分子层(LMol)的dCA1突触对条件刺激(CS)的反应增加。在这些dCA1输入处,通过在条件反射过程中局部阻断NMDA受体并对来自未经历过实验的动物的dCA1神经元进行全细胞记录感觉诱发的突触反应,进一步证明了CS反应性兴奋性突触的突触增强。通过多位点记录在Rad和LMol中发现了突触增强诱导的总体相似时间进程;这比条件性行为反应出现得晚且饱和得早。我们的实验证明了在施affer侧支和颞叶-海马通路中均诱导出与线索记忆相关的dCA1突触可塑性。