bioRxivNeurosciencePreprint
Neurons in the ventral striatopallidal complex modulate lateral hypothalamic orexin/hypocretin neuron activity: Implications for reward-seeking
Caitlin S. MitchelliD, Aida MohammadkhaniiD, Elizabeth E. ManningiD, Erin J. CampbelliD, Simon D. FisheriD, Jiann Wei YeohiD, Amy J. Pearl, Nicholas J. Burton, Min QiaoiD, Jacqueline A. IredaleiD, Jaideep Singh BainsiD, Gavan P. McNallyiD, Zane A. AndrewsiD, Brett Anthony GrahamiD, Thomas E. ScammelliD, Bradford B. LowelliD, Dong KongiD, Stephanie L. BorglandiD, Christopher V. DayasiD
Abstract
Reward-seeking involves the engagement and computation of multiple physiological and motivational parameters. The lateral hypothalamus (LH) is a necessary node in the circuits that control food-seeking and motivation. One group of cells that plays an important yet incompletely understood role in these processes are the orexin/hypocretin (OX/HT) neurons. OX/HT cells are located exclusively within the LH and are implicated in feeding, arousal, and reward-seeking behavior. Importantly, the role of OX/HT neurons in consummatory versus reward-seeking actions is not fully defined, nor are the circuits that control the activity of these neurons under different behavioral states. Here we show that OX/HT neurons respond in real time to food presentation and that this response is modulated by differences in metabolic state. We observed increased OX/HT neuron activity on approach to food, but this activity trended towards pre-approach levels by the start of the consummatory phase. Next, we studied ventrostriatopallidal (VSP) inputs to the OX/HT neurons. Using optogenetics and cell type-specific electrophysiology, we found that ventral pallidum inputs onto OX/HT neurons exert strong inhibitory (and weak excitatory) effects whereas the lateral nucleus accumbens shell provides weaker direct inhibitory connections with OX/HT neurons. These findings reveal that the activity of OX/HT neurons is strongly modulated by metabolic and hedonic state. Further, OX/HT neurons is primarily associated with food approach and that the effect of VSP-terminal output is to suppress OX/HT activity.
- organism: mouse
- assay: electronic health records
- research focus: cell type annotation
- approach: experimental assay
- Citations
- 4
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