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光遗传刺激杏仁核基底外侧核传入的内嗅皮层对条件性恐惧和消退的影响。

Effects of optogenetic photoexcitation of infralimbic cortex inputs to the basolateral amygdala on conditioned fear and extinction.

机构信息

Laboratory of Behavioral and Genomic Neuroscience, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD, USA.

Laboratory of Behavioral and Genomic Neuroscience, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD, USA.

出版信息

Behav Brain Res. 2021 Jan 1;396:112913. doi: 10.1016/j.bbr.2020.112913. Epub 2020 Sep 18.

DOI:10.1016/j.bbr.2020.112913
PMID:32950607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8299731/
Abstract

Deficiencies in the ability to extinguish fear is a hallmark of Trauma- and stressor-related disorders, Anxiety disorders, and certain other neuropsychiatric conditions. Hence, a greater understanding of the brain mechanisms involved in the inhibition of fear is of significant translational relevance. Previous studies in rodents have shown that glutamatergic projections from the infralimbic prefrontal cortex (IL) to basolateral amygdala (BLA) play a crucial instructional role in the formation of extinction memories, and also indicate that variation in the strength of this input correlates with extinction efficacy. To further examine the relationship between the IL→BLA pathway and extinction we expressed three different titers of the excitatory opsin, channelrhodopsin (ChR2), in IL neurons and photostimulated their projections in the BLA during partial extinction training. The behavioral effects of photoexcitation differed across the titer groups: the low titer had no effect, the medium titer selectively facilitated extinction memory formation, and the high titer produced both an acute suppression of fear and a decrease in fear during (light-free) extinction retrieval. We discuss various possible explanations for these titer-specific effects, including the possibility of IL-mediated inhibition of BLA fear-encoding neurons under conditions of sufficiently strong photoexcitation. These findings further support the role of IL→BLA pathway in regulating fear and highlight the importance of methodological factors in optogenetic studies of neural circuits underling behavior.

摘要

无法消除恐惧是创伤和应激相关障碍、焦虑障碍和某些其他神经精神疾病的一个显著特征。因此,深入了解大脑中涉及恐惧抑制的机制具有重要的转化意义。先前在啮齿动物中的研究表明,来自边缘下前额皮质 (IL) 的谷氨酸能投射到基底外侧杏仁核 (BLA) 在形成消退记忆中起着至关重要的指导作用,并且还表明这种输入的强度变化与消退效果相关。为了进一步研究 IL→BLA 通路与消退之间的关系,我们在 IL 神经元中表达了三种不同效价的兴奋性光感受器通道视紫红质 (ChR2),并在部分消退训练期间对其在 BLA 中的投射进行光刺激。光激发的行为效应在效价组之间存在差异:低效价没有影响,中效价选择性促进了消退记忆的形成,而高效价则在急性抑制恐惧的同时,也降低了在(无光)消退检索期间的恐惧。我们讨论了这些效价特异性效应的各种可能解释,包括在足够强的光激发条件下,IL 介导的对 BLA 恐惧编码神经元的抑制的可能性。这些发现进一步支持了 IL→BLA 通路在调节恐惧中的作用,并强调了在研究行为相关神经回路的光遗传学研究中方法学因素的重要性。

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