Evidence map›Paper›PMID 26585290›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

Role of β4* Nicotinic Acetylcholine Receptors in the Habenulo-Interpeduncular Pathway in Nicotine Reinforcement in Mice.

Lauriane Harrington, Xavier Viñals, Andrea Herrera-Solís, Africa Flores, Carole Morel, Stefania Tolu, Philippe Faure, Rafael Maldonado, Uwe Maskos, Patricia Robledo

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Impact of the gut microbiome on nicotine's motivational effects and glial cells in the ventral tegmental area in male mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  7. Chemical Flavorants in Vaping Products Alter Neurobiology in a Sex-Dependent Manner to Promote Vaping-Related Behaviors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  8. Article
  9. Dynamic activity of interpeduncular nucleus GABAergic neurons controls expression of nicotine withdrawal in male mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  10. Review
  11. Article
  12. β4-Nicotinic Receptors Are Critically Involved in Reward-Related Behaviors and Self-Regulation of Nicotine Reinforcement.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. Mu opioid receptors in the medial habenula contribute to naloxone aversion.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  14. Review
  15. Article
  16. Chrna5-Expressing Neurons in the Interpeduncular Nucleus Mediate Aversion Primed by Prior Stimulation or Nicotine Exposure.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Lauriane HarringtonUnité Neurobiologie Intégrative des Systèmes Cholinergiques, Département de Neuroscience, Institut Pasteur, Paris Cedex, France.
Xavier ViñalsLaboratory of Neuropharmacology, Department of Experimental and Health Sciences, Pompeu Fabra University (UPF), Barcelona, Spain.
Andrea Herrera-SolísLaboratory of Neuropharmacology, Department of Experimental and Health Sciences, Pompeu Fabra University (UPF), Barcelona, Spain.
Africa FloresLaboratory of Neuropharmacology, Department of Experimental and Health Sciences, Pompeu Fabra University (UPF), Barcelona, Spain.
Carole MorelNeuroscience Paris Seine NPS, CNRS UMR8246, INSERM U1130 UPMC UM 119, Equipe Neurophysiologie et comportement (NPC), Université P. et M. Curie, Paris, France.
Stefania ToluNeuroscience Paris Seine NPS, CNRS UMR8246, INSERM U1130 UPMC UM 119, Equipe Neurophysiologie et comportement (NPC), Université P. et M. Curie, Paris, France.
Philippe FaureNeuroscience Paris Seine NPS, CNRS UMR8246, INSERM U1130 UPMC UM 119, Equipe Neurophysiologie et comportement (NPC), Université P. et M. Curie, Paris, France.
Rafael MaldonadoLaboratory of Neuropharmacology, Department of Experimental and Health Sciences, Pompeu Fabra University (UPF), Barcelona, Spain.
Uwe MaskosUnité Neurobiologie Intégrative des Systèmes Cholinergiques, Département de Neuroscience, Institut Pasteur, Paris Cedex, France.
Patricia RobledoLaboratory of Neuropharmacology, Department of Experimental and Health Sciences, Pompeu Fabra University (UPF), Barcelona, Spain.
Pompeu Fabra University · ESCentre National de la Recherche Scientifique · FRInserm · FRHospital del Mar Research Institute · ESNeurosciences Paris-Seine

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nicotine exerts its psychopharmacological effects by activating the nicotinic acetylcholine receptor (nAChR), composed of alpha and/or beta subunits, giving rise to a diverse population of receptors with a distinct pharmacology. β4-containing (β4*) nAChRs are located almost exclusively in the habenulo-interpeduncular pathway. We examined the role of β4* nAChRs in the medial habenula (MHb) and the interpeduncular nucleus (IPN) in nicotine reinforcement using behavioral, electrophysiological, and molecular techniques in transgenic mice. Nicotine intravenous self-administration (IVSA) was lower in constitutive β4 knockout (KO) mice at all doses tested (7.5, 15, 30, and 60 μg/kg/infusion) compared with wild-type (WT) mice. In vivo microdialysis showed that β4KO mice have higher extracellular dopamine (DA) levels in the nucleus accumbens than in WT mice, and exhibit a differential sensitivity to nicotine-induced DA outflow. Furthermore, electrophysiological recordings in the ventral tegmental area (VTA) demonstrated that DA neurons of β4KO mice are more sensitive to lower doses of nicotine than that of WT mice. Re-expression of β4* nAChRs in IPN neurons fully restored nicotine IVSA, and attenuated the increased sensitivity of VTA DA neurons to nicotine. These findings suggest that β4* nAChRs in the IPN have a role in maintaining nicotine IVSA.

Indexed as

Reinforcement, PsychologyAction PotentialsAnimalsConditioning, OperantDopamineDose-Response Relationship, DrugGreen Fluorescent ProteinsHabenulaInterpeduncular NucleusMaleMiceMice, Inbred C57BLMice, TransgenicMicrodialysisNerve Tissue ProteinsNicotineChrnb4 protein, mouseDopamineenhanced green fluorescent proteinGreen Fluorescent ProteinsNerve Tissue ProteinsNicotineNicotinic AgonistsPhosphoglycerate KinaseReceptors, Nicotinic

Identifiers

PMID26585290
PMCPMC4869047
OpenAlexW2177600480

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.