Dopamine neuron activity evoked by sucrose and sucrose-predictive cues is augmented by peripheral and central manipulations of glucose availability

Eur J Neurosci. 2024 May;59(10):2419-2435. doi: 10.1111/ejn.16214. Epub 2023 Dec 6.

Abstract

Food deprivation drives eating through multiple signals and circuits. Decreased glucose availability (i.e., cytoglucopenia) drives eating and also increases the value of sucrose. Ventral tegmental area (VTA) dopamine neurons (DANs) contribute to the evaluation of taste stimuli, but their role in integrating glucoprivic signals remains unknown. We monitored VTA DAN activity via Cre-dependent expression of a calcium indicator with in vivo fibre photometry. In ad libitum fed rats, intraoral sucrose evoked a phasic increase in DAN activity. To manipulate glucose availability, we administered (intraperitoneal, lateral or fourth ventricular) the antiglycolytic agent 5-thio-D-glucose (5TG), which significantly augmented the phasic DAN activity to sucrose. 5TG failed to alter DAN activity to water or saccharin, suggesting the response was selective for caloric stimuli. 5TG enhancement of sucrose-evoked DAN activity was stronger after fourth ventricular administration, suggesting a critical node of action within the hindbrain. As 5TG also increases blood glucose, in a separate study, we used peripheral insulin, which stimulates eating, to decrease blood glucose-which was associated with increased DAN activity to intraoral sucrose. DAN activity developed to a cue predictive of intraoral sucrose. While 5TG augmented cue-evoked DAN activity, its action was most potent when delivered to the lateral ventricle. Together, the studies point to central glucose availability as a key modulator of phasic DAN activity to food and food-cues. As glucose sensing neurons are known to populate the hypothalamus and brainstem, results suggest differential modulation of cue-evoked and sucrose-evoked DAN activity.

Keywords: appetitive; consummatory; fibre photometry; reward; ventral tegmental area.

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Cues*
  • Dopaminergic Neurons* / drug effects
  • Dopaminergic Neurons* / metabolism
  • Dopaminergic Neurons* / physiology
  • Glucose* / metabolism
  • Insulin / metabolism
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Sucrose* / pharmacology
  • Ventral Tegmental Area* / drug effects
  • Ventral Tegmental Area* / metabolism
  • Ventral Tegmental Area* / physiology