NAPE-PLD in the ventral tegmental area regulates reward events, feeding and energy homeostasis

Mol Psychiatry. 2024 May;29(5):1478-1490. doi: 10.1038/s41380-024-02427-6. Epub 2024 Feb 15.

Abstract

The N-acyl phosphatidylethanolamine-specific phospholipase D (NAPE-PLD) catalyzes the production of N-acylethanolamines (NAEs), a family of endogenous bioactive lipids, which are involved in various biological processes ranging from neuronal functions to energy homeostasis and feeding behaviors. Reward-dependent behaviors depend on dopamine (DA) transmission between the ventral tegmental area (VTA) and the nucleus accumbens (NAc), which conveys reward-values and scales reinforced behaviors. However, whether and how NAPE-PLD may contribute to the regulation of feeding and reward-dependent behaviors has not yet been investigated. This biological question is of paramount importance since NAEs are altered in obesity and metabolic disorders. Here, we show that transcriptomic meta-analysis highlights a potential role for NAPE-PLD within the VTA→NAc circuit. Using brain-specific invalidation approaches, we report that the integrity of NAPE-PLD is required for the proper homeostasis of NAEs within the midbrain VTA and it affects food-reward behaviors. Moreover, region-specific knock-down of NAPE-PLD in the VTA enhanced food-reward seeking and reinforced behaviors, which were associated with increased in vivo DA release dynamics in response to both food- and non-food-related rewards together with heightened tropism towards food consumption. Furthermore, midbrain knock-down of NAPE-PLD, which increased energy expenditure and adapted nutrient partitioning, elicited a relative protection against high-fat diet-mediated body fat gain and obesity-associated metabolic features. In conclusion, these findings reveal a new key role of VTA NAPE-PLD in shaping DA-dependent events, feeding behaviors and energy homeostasis, thus providing new insights on the regulation of body metabolism.

MeSH terms

  • Animals
  • Dopamine* / metabolism
  • Dopaminergic Neurons / metabolism
  • Energy Metabolism / physiology
  • Ethanolamines
  • Feeding Behavior* / physiology
  • Homeostasis* / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nucleus Accumbens* / metabolism
  • Obesity / genetics
  • Obesity / metabolism
  • Phosphatidylethanolamines / metabolism
  • Phospholipase D* / genetics
  • Phospholipase D* / metabolism
  • Reward*
  • Ventral Tegmental Area* / metabolism

Substances

  • Phospholipase D
  • Dopamine
  • N-acylethanolamines
  • Phosphatidylethanolamines
  • Ethanolamines