伏隔核在食物奖励寻求和睡眠调节中的动态。

IF 5.8 1区 医学 Q1 PSYCHIATRY
Ana L Almeida Rojo, Li Cai, Tyler R Barnhardt, Yanhua H Huang
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引用次数: 0

摘要

寻求奖励的行为是生存所必需的,它在很大程度上受到经验、内在状态和睡眠等生理因素的影响。伏隔核(NAc)是奖赏处理中枢,整合外部和内部信号来调节奖赏寻求行为。然而,在寻求奖励的过程中,NAc活动如何受到学习经验的影响,以及它在多大程度上受睡眠等生理调节的影响,目前还不清楚。在这里,我们使用体内纤维光度法来监测接受蔗糖自我给药(SA)训练的雄性和雌性小鼠NAc中钙(Ca2+)的活性。我们发现蔗糖SA期间NAc Ca2+动态与行为结果有关,并在不同的训练阶段进化。此外,急性睡眠剥夺增加了蔗糖SA,同时降低了NAc Ca2+反应,并抑制了其对奖励更新的敏感性。因此,我们的研究结果表明,自然寻求奖励过程中的NAc反应是动态的,适应于学习经验,并且可以通过急性睡眠剥夺而减弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleus accumbens dynamics in food reward seeking and regulation by sleep.

Reward-seeking behavior is essential for survival and is greatly influenced by experience, internal states, and physiological factors such as sleep. The nucleus accumbens (NAc) is reward processing hub that integrates external and internal signals to regulate reward-seeking behaviors. However, it is not well understood how NAc activities during reward seeking may be shaped by learning experience, and to what extent that it may be subject to physiological regulations such as sleep. Here, we used in vivo fiber photometry to monitor calcium (Ca2+) activities in the NAc of male and female mice undergoing sucrose self-administration (SA) training. We found that the NAc Ca2+ dynamics during sucrose SA were related to the behavioral outcome and evolved over different training stages. Moreover, acute sleep deprivation increased sucrose SA while reduced NAc Ca2+ responses and dampened its sensitivity to reward update. Thus, our findings suggest that the NAc response during natural reward seeking is dynamic, adaptive to learning experience, and can be blunted by acute sleep deprivation.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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