首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Trace Fear Conditioning Differentially Modulates Intrinsic Excitability of Medial Prefrontal Cortex-Basolateral Complex of Amygdala Projection Neurons in Infralimbic and Prelimbic Cortices
【24h】

Trace Fear Conditioning Differentially Modulates Intrinsic Excitability of Medial Prefrontal Cortex-Basolateral Complex of Amygdala Projection Neurons in Infralimbic and Prelimbic Cortices

机译:痕量恐惧条件差异调节下肢和前肢皮质杏仁核投射神经元内侧前额叶皮层-基底外侧复合体的内在兴奋性。

获取原文
获取原文并翻译 | 示例
       

摘要

Neuronal activity in medial prefrontal cortex (mPFC) is critical for the formation of trace fear memory, yet the cellular mechanisms underlying these memories remain unclear. One possibility involves the modulation of intrinsic excitability within mPFC neurons that project to the basolateral complex of amygdala (BLA). The current study used a combination of retrograde labeling and in vitro whole-cell patch-clamp recordings to examine the effect of trace fear conditioning on the intrinsic excitability of layer 5 mPFC-BLA projection neurons in adult rats. Trace fear conditioning significantly enhanced the intrinsic excitability of regular spiking infralimbic (IL) projection neurons, as evidenced by an increase in the number of action potentials after current injection. These changes were also associated with a reduction in spike threshold and an increase in h current. In contrast, trace fear conditioning reduced the excitability of regular spiking prelimbic (PL) projection neurons, through a learning-related decrease of input resistance. Interestingly, the amount of conditioned freezing was (1) positively correlated with excitability of IL-BLA projection neurons after conditioning and (2) negatively correlated with excitability of PL-BLA projection neurons after extinction. Trace fear conditioning also significantly enhanced the excitability of burst spiking PL-BLA projection neurons. In both regions, conditioning-induced plasticity was learning specific (observed in conditioned but not in pseudoconditioned rats), flexible (reversed by extinction), and transient (lasted <10 d). Together, these data suggest that intrinsic plasticity within mPFC-BLA projection neurons occurs in a subregion- and cell-type-specific manner during acquisition, consolidation, and extinction of trace fear conditioning.
机译:内侧前额叶皮层(mPFC)中的神经元活动对于痕量恐惧记忆的形成至关重要,但仍不清楚这些记忆的基础细胞机制。一种可能性涉及调节投射到杏仁核基底外侧复合体(BLA)的mPFC神经元内的固有兴奋性。当前的研究结合了逆行标记和体外全细胞膜片钳记录,以研究痕量恐惧条件对成年大鼠第5层mPFC-BLA投射神经元固有兴奋性的影响。痕量恐惧条件显着增强了常规突刺下肢(IL)投射神经元的内在兴奋性,如电流注射后动作电位数量的增加所证明。这些变化还与尖峰阈值的降低和h电流的增加有关。相反,通过与学习相关的输入阻力降低,痕量恐惧条件降低了规则的尖峰前期(PL)投射神经元的兴奋性。有趣的是,条件冷冻的量与(1)条件调节后的IL-BLA投射神经元的兴奋性正相关,(2)与灭绝后的PL-BLA投射神经元的兴奋性负相关。痕量恐惧调节还显着增强了突发性PL-BLA投射神经元的兴奋性。在这两个区域中,条件诱导的可塑性具有特定的学习能力(在条件条件下的大鼠中观察到,但在假条件条件的大鼠中则未观察到),柔韧性(通过灭绝逆转)和短暂的(持续<10 d)。在一起,这些数据表明mPFC-BLA投射神经元内在的可塑性在痕量恐惧条件的获取,巩固和消灭过程中以亚区域和细胞类型特定的方式发生。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号