前边缘皮质兴奋性过度驱动和抑制性欠驱动伴随着寻找食物的环境抑制。

Kate Z Peters, Zuzana Pedan, Romarua Agbude, Emily C Woods, Oliver G Steele, Nobuyoshi Suto, Scott B Kinghorn, Olga Tsaponina, Eisuke Koya
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引用次数: 0

摘要

与食物有关的线索,如快餐广告,会激发人们对食物的渴望,并可能导致不健康的暴饮暴食。增强认知和身体刺激的环境富集(EE)可以减少线索诱发的小鼠蔗糖寻找和调节食欲行为的前边缘皮层(PL)中蔗糖线索反应神经元或“神经元集合”的募集。因此,情感表达为我们提供了行为模型和神经元目标,以识别“反渴望”相关机制。在这里,我们在PL中研究了EE如何调节线索反应神经元群体中的神经元兴奋性和活动模式。对PL中线索反应神经元的化学发生抑制阻断了线索诱发的蔗糖寻找,从而证实了这些神经元在蔗糖线索记忆中的功能。EE提高了PL中“最初”或在暴露于EE之前的线索反应性兴奋锥体细胞的基线兴奋性。此外,它们的蔗糖线索特异性丧失-导致它们持续激活和非线索选择性激活或“兴奋过度”。此外,EE减少了线索反应性、抑制性中间神经元的募集,反映了“抑制性欠驱动”。综上所述,前额皮质兴奋性“过度驱动”和抑制性“欠驱动”同时导致的神经元食物线索处理受损,可能是情感表达抗渴望作用的基础,因此可以作为开发有助于控制食物渴望的新型药物的潜在神经生理学靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prelimbic cortical excitatory overdrive and inhibitory underdrive accompany environmental suppression of food seeking.

Cues associated with food, such as fast-food advertising, can provoke food cravings and may lead to unhealthy overeating. Environmental enrichment (EE) that enhances cognitive and physical stimulation can reduce cue-evoked sucrose seeking in mice and recruitment of sucrose cue-reactive neurons or 'neuronal ensembles' in the prelimbic cortex (PL), which regulates appetitive behaviors. Hence, EE provides us with a behavioral model and neuronal targets to identify 'anti-craving' relevant mechanisms. Here, we investigated in the PL how EE modulated neuronal excitability and activity patterns in cue-reactive neuronal populations. Chemogenetic inhibition of cue-reactive neurons in PL blocked cue-evoked sucrose seeking, thereby confirming the function of these neurons in sucrose cue memory. EE boosted the baseline excitability of 'originally', or before EE exposure, cue-reactive, excitatory pyramidal cells in PL. Furthermore, their sucrose cue-specificity was lost - resulting in their persistent activation and non-cue selective activation or 'excitatory overdrive'. Furthermore, EE reduced recruitment of cue-reactive, inhibitory interneurons reflecting 'inhibitory underdrive'. Taken together, impaired neuronal food cue processing due to simultaneous prefrontal cortical excitatory 'overdrive' and inhibitory 'underdrive' likely underlies EE's anti-craving action, thereby serving as potential neurophysiological targets to develop novel medications that help control food cravings.

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