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口渴通过脑下器官神经元招募相位多巴胺信号。

Thirst recruits phasic dopamine signaling through subfornical organ neurons.

机构信息

Department of Psychology, University of Illinois at Chicago, Chicago, IL 60607.

Graduate Program in Neuroscience, University of Illinois at Chicago, Chicago, IL 60607.

出版信息

Proc Natl Acad Sci U S A. 2020 Dec 1;117(48):30744-30754. doi: 10.1073/pnas.2009233117. Epub 2020 Nov 16.

Abstract

Thirst is a highly potent drive that motivates organisms to seek out and consume balance-restoring stimuli. The detection of dehydration is well understood and involves signals of peripheral origin and the sampling of internal milieu by first order homeostatic neurons within the lamina terminalis-particularly glutamatergic neurons of the subfornical organ expressing CaMKIIa (SFO). However, it remains unknown whether mesolimbic dopamine pathways that are critical for motivation and reinforcement integrate information from these "early" dehydration signals. We used in vivo fiber photometry in the ventral tegmental area and measured phasic dopamine responses to a water-predictive cue. Thirst, but not hunger, potentiated the phasic dopamine response to the water cue. In euvolemic rats, the dipsogenic hormone angiotensin II, but not the orexigenic hormone ghrelin, potentiated the dopamine response similarly to that observed in water-deprived rats. Chemogenetic manipulations of SFO revealed bidirectional control of phasic dopamine signaling during cued water reward. Taking advantage of within-subject designs, we found predictive relationships between changes in cue-evoked dopamine response and changes in behavioral responses-supporting a role for dopamine in motivation induced by homeostatic need. Collectively, we reveal a putative mechanism for the invigoration of goal-directed behavior: internal milieu communicates to first order, need state-selective circuits to potentiate the mesolimbic dopamine system's response to cues predictive of restorative stimuli.

摘要

口渴是一种强烈的驱动力,促使生物寻找和摄入平衡恢复刺激物。脱水的检测已被充分理解,涉及起源于外围的信号和一级体内平衡神经元对内环境的采样,特别是表达 CaMKIIa 的穹窿下器官中的谷氨酸能神经元(SFO)。然而,目前尚不清楚对于动机和强化至关重要的中脑边缘多巴胺途径是否整合了这些“早期”脱水信号的信息。我们使用腹侧被盖区的活体光纤光度法测量了对水预测线索的相位多巴胺反应。口渴而非饥饿会增强对水线索的相位多巴胺反应。在等容大鼠中,促饮激素血管紧张素 II,但不是食欲激素胃饥饿素,同样增强了多巴胺反应,类似于在缺水大鼠中观察到的反应。SFO 的化学遗传操作揭示了在提示性水奖励期间相位多巴胺信号的双向控制。利用个体内设计,我们发现线索诱发的多巴胺反应变化与行为反应变化之间存在预测关系,这支持了多巴胺在由体内平衡需求引起的动机中的作用。总的来说,我们揭示了一种激发目标导向行为的潜在机制:内环境向一级、需要状态选择性回路传达信息,以增强中脑边缘多巴胺系统对恢复性刺激预测线索的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151d/7720158/5570809a56d1/pnas.2009233117fig01.jpg

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