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大麻素通过在功能上使海马体CA1与CA3分离来破坏记忆编码。

Cannabinoids disrupt memory encoding by functionally isolating hippocampal CA1 from CA3.

作者信息

Sandler Roman A, Fetterhoff Dustin, Hampson Robert E, Deadwyler Sam A, Marmarelis Vasilis Z

机构信息

Department of Biomedical Engineering, University of Southern California, Los Angeles, California, United States of America.

Department of Physiology & Pharmacology, Wake Forest University, Winston-Salem, North Carolina, United States of America.

出版信息

PLoS Comput Biol. 2017 Jul 7;13(7):e1005624. doi: 10.1371/journal.pcbi.1005624. eCollection 2017 Jul.

Abstract

Much of the research on cannabinoids (CBs) has focused on their effects at the molecular and synaptic level. However, the effects of CBs on the dynamics of neural circuits remains poorly understood. This study aims to disentangle the effects of CBs on the functional dynamics of the hippocampal Schaffer collateral synapse by using data-driven nonparametric modeling. Multi-unit activity was recorded from rats doing an working memory task in control sessions and under the influence of exogenously administered tetrahydrocannabinol (THC), the primary CB found in marijuana. It was found that THC left firing rate unaltered and only slightly reduced theta oscillations. Multivariate autoregressive models, estimated from spontaneous spiking activity, were then used to describe the dynamical transformation from CA3 to CA1. They revealed that THC served to functionally isolate CA1 from CA3 by reducing feedforward excitation and theta information flow. The functional isolation was compensated by increased feedback excitation within CA1, thus leading to unaltered firing rates. Finally, both of these effects were shown to be correlated with memory impairments in the working memory task. By elucidating the circuit mechanisms of CBs, these results help close the gap in knowledge between the cellular and behavioral effects of CBs.

摘要

许多关于大麻素(CBs)的研究都集中在其在分子和突触水平上的作用。然而,CBs对神经回路动力学的影响仍知之甚少。本研究旨在通过使用数据驱动的非参数建模来厘清CBs对海马体谢弗侧支突触功能动力学的影响。在对照实验以及外源性给予四氢大麻酚(THC,大麻中发现的主要CB)影响下,记录了执行工作记忆任务的大鼠的多单元活动。结果发现,THC并未改变放电率,只是略微降低了θ振荡。然后,根据自发的尖峰活动估计的多变量自回归模型被用于描述从CA3到CA1的动态转换。结果显示,THC通过减少前馈兴奋和θ信息流,在功能上将CA1与CA3隔离开来。CA1内反馈兴奋的增加补偿了这种功能隔离,从而使放电率保持不变。最后,这两种效应都被证明与工作记忆任务中的记忆损伤有关。通过阐明CBs的回路机制,这些结果有助于填补CBs细胞效应和行为效应之间的知识空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8be7/5521875/5992a4cdbf0b/pcbi.1005624.g001.jpg

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