NAPE-PLD in the ventral tegmental area regulates reward events, feeding and energy homeostasis.
Julien CastelGuangping LiOnimus OrianeEmma LeishmanPatrice D CaniHeather BradshawKen MackieAmandine EverardSerge LuquetGiuseppe GangarossaPublished in: Molecular psychiatry (2024)
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.
Keyphrases
- high fat diet
- prefrontal cortex
- insulin resistance
- systematic review
- metabolic syndrome
- adipose tissue
- type diabetes
- transcription factor
- human health
- spinal cord
- randomized controlled trial
- skeletal muscle
- multiple sclerosis
- dna methylation
- gene expression
- genome wide
- white matter
- high fat diet induced
- tissue engineering
- atomic force microscopy