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扣带回下脚投射至伏隔核壳部和杏仁核调节可卡因消退学习的编码。

Infralimbic Projections to the Nucleus Accumbens Shell and Amygdala Regulate the Encoding of Cocaine Extinction Learning.

机构信息

Interdisciplinary Neuroscience Program, University of Iowa, Iowa City, Iowa 52242

Department of Psychological and Brain Sciences, University of Iowa, Iowa City, Iowa 52242.

出版信息

J Neurosci. 2023 Feb 22;43(8):1348-1359. doi: 10.1523/JNEUROSCI.2023-22.2022. Epub 2023 Jan 19.

Abstract

Prior evidence indicates that the infralimbic cortex (IL) mediates the ongoing inhibition of cocaine seeking following self-administration and extinction training in rats, specifically through projections to the nucleus accumbens shell (NAshell). Our own data indicate that IL activity immediately following an unreinforced lever press is critical for encoding the extinction contingencies in such procedures. Whether extinction encoding requires activity in the IL exclusively or also activity in its outputs, such as those to the NAshell and amygdala, is unknown. To address this issue, we used a closed-loop optogenetic approach in female and male Sprague Dawley rats to silence IL-NAshell or IL-amygdala activity following an unreinforced lever press during extinction training. Optical illumination (20 s) was given either immediately after a lever press or following a 20 s delay. IL-NAshell inhibition immediately following an unreinforced lever press increased lever pressing during extinction training and impaired retention of extinction learning, as assessed during subsequent extinction sessions without optical inhibition. Likewise, IL-amygdala inhibition given in the same manner impaired extinction retention during sessions without inhibition. Control experiments indicate that critical encoding of extinction learning does not require activity in these pathways beyond the initial 20 s post-lever press period, as delayed IL-NAshell and IL-amygdala inhibition had no effect on extinction learning. These results suggest that a larger network extending from the IL to the NAshell and amygdala is involved in encoding extinction contingencies following cocaine self-administration. Infralimbic cortex (IL) activity following an unreinforced lever press during extinction learning encodes the extinction of cocaine-seeking behavior. However, the larger circuitry controlling such encoding has not been investigated. Using closed-loop optogenetic pathway targeting, we found that inhibition of IL projections to the nucleus accumbens shell and to the amygdala impaired the extinction of cocaine seeking. Importantly, these effects were only observed when activity was disrupted during the first 20 s post-lever press and not when given following a 20 s delay. These findings suggest that successful cocaine extinction encoding requires activity across a larger circuit beyond simply inputs to the IL.

摘要

先前的证据表明,在大鼠自身给药和消退训练后,边缘下皮层(IL)介导可卡因寻求的持续抑制,特别是通过向伏隔核壳(NAshell)投射。我们自己的数据表明,在无强化杆按压后立即进行的 IL 活动对于在这些程序中对消退条件进行编码至关重要。消退编码是否需要 IL 中的活动,还是也需要其输出的活动,例如向 NAshell 和杏仁核的活动,尚不清楚。为了解决这个问题,我们使用雌性和雄性 Sprague Dawley 大鼠的闭环光遗传学方法,在消退训练期间,在无强化杆按压后立即沉默 IL-NAshell 或 IL-杏仁核的活动。光照明(20 秒)要么在杆按压后立即进行,要么在 20 秒延迟后进行。在无强化杆按压后立即进行的 IL-NAshell 抑制增加了消退训练期间的杆按压,并损害了消退学习的保留,如在随后的无抑制消退训练中评估的那样。同样,以相同方式进行的 IL-杏仁核抑制在无抑制期间也损害了消退保留。对照实验表明,在初始的 20 秒后,关键的消退学习编码不需要这些通路中的活动,因为延迟的 IL-NAshell 和 IL-杏仁核抑制对消退学习没有影响。这些结果表明,在可卡因自我给药后,从 IL 延伸到 NAshell 和杏仁核的更大网络参与了消退条件的编码。在消退学习期间,无强化杆按压后的边缘下皮层(IL)活动对可卡因寻求行为的消退进行编码。然而,控制这种编码的更大的电路尚未被研究。使用闭环光遗传学途径靶向,我们发现抑制 IL 投射到伏隔核壳和杏仁核的活动损害了可卡因寻求的消退。重要的是,这些影响仅在杆按压后 20 秒内进行活动干扰时观察到,而不是在 20 秒延迟后进行时观察到。这些发现表明,成功的可卡因消退编码需要在更大的电路中进行活动,而不仅仅是输入到 IL。

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