Evidence map›Paper›PMID 38361126›Full record

ArticleMolecular psychiatry2024

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

Julien Castel, Guangping Li, Oriane Onimus, Emma Leishman, Patrice D Cani, Heather Bradshaw, Ken Mackie, Amandine Everard, Serge Luquet, Giuseppe Gangarossa

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Neural circuits regulating activity-based anorexia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Julien CastelUniversité Paris Cité, CNRS, Unité de Biologie Fonctionnelle et Adaptative, F-75013, Paris, France.ORCID 0000-0003-4309-701X
Guangping LiUniversité Paris Cité, CNRS, Unité de Biologie Fonctionnelle et Adaptative, F-75013, Paris, France.
Oriane OnimusUniversité Paris Cité, CNRS, Unité de Biologie Fonctionnelle et Adaptative, F-75013, Paris, France.ORCID 0000-0002-1758-1265
Emma LeishmanDepartment of Psychological and Brain Sciences, Indiana University Bloomington, Bloomington, IN, USA.
Patrice D CaniMetabolism and Nutrition Research group, Louvain Drug Research Institute (LDRI), UCLouvain, Université catholique de Louvain, Brussels, Belgium.ORCID 0000-0003-2040-2448
Heather BradshawDepartment of Psychological and Brain Sciences, Indiana University Bloomington, Bloomington, IN, USA.
Ken MackieDepartment of Psychological and Brain Sciences, Indiana University Bloomington, Bloomington, IN, USA.ORCID 0000-0001-8501-6199
Amandine EverardUniversité Paris Cité, CNRS, Unité de Biologie Fonctionnelle et Adaptative, F-75013, Paris, France.
Serge Luquet *Université Paris Cité, CNRS, Unité de Biologie Fonctionnelle et Adaptative, F-75013, Paris, France. serge.luquet@u-paris.fr.
Giuseppe Gangarossa *Université Paris Cité, CNRS, Unité de Biologie Fonctionnelle et Adaptative, F-75013, Paris, France. giuseppe.gangarossa@u-paris.fr.ORCID 0000-0001-9045-2139
Centre National de la Recherche Scientifique · FRIndiana University Bloomington · USWalloon Excellence in Lifesciences and Biotechnology · BE

Funding

CB2 Cannabinoid Mechanisms for Suppressing Opioid Tolerance and DependenceR01DA047858 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI HOHMANN, ANDREA GRACE, MACKIE, KENNETH · 2019 to 2023
$2.6M
Agence Nationale de la Recherche (French National Research Agency) ANR-19-CE37-0020-02Agence Nationale de la Recherche (French National Research Agency) ANR-21-CE14-0021-01Agence Nationale de la Recherche (French National Research Agency) ANR-23-CE14-0014-02Fondation pour la Recherche Médicale (Foundation for Medical Research in France) EQU202003010155Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) 40007505Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) J.0075.22Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) WELBIO-CR-2019S-03R"la Caixa" Foundation (Caixa Foundation) NeuroGutNIDA NIH HHS R01 DA047858Nutricia Research Foundation 2022-E7U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) DA047858
6 · The paper itself

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.

Indexed as

DopamineFeeding BehaviorHomeostasisNucleus AccumbensPhospholipase DRewardVentral Tegmental AreaAnimalsDopaminergic NeuronsEnergy MetabolismEthanolaminesMaleMiceMice, Inbred C57BLObesityPhosphatidylethanolaminesDopamineEthanolaminesN-acylethanolaminesPhosphatidylethanolaminesPhospholipase D

Identifiers

PMID38361126
OpenAlexW4391843187

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.