Evidence map›Paper›PMID 24513972›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Amphetamine self-administration attenuates dopamine D2 autoreceptor function.

Erin S Calipari, Haiguo Sun, Khalil Eldeeb, Deborah J Luessen, Xin Feng, Allyn C Howlett, Sara R Jones, Rong Chen

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Ventral midbrain astrocytes display unique physiological features and sensitivity to dopamine D2 receptor signaling.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Article
  17. GIRK currents in VTA dopamine neurons control the sensitivity of mice to cocaine-induced locomotor sensitization.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Article
  19. Article
  20. Review
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

8 authors at 1 institution in 1 country.

Erin S CalipariDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Haiguo SunDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Khalil EldeebDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Deborah J LuessenDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Xin FengDepartment of Otolaryngology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Allyn C Howlett1] Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA [2] The Center for Neurobiology of Addiction Treatment, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Sara R Jones1] Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA [2] The Center for Neurobiology of Addiction Treatment, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Rong Chen1] Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston Salem, NC, USA [2] The Center for Neurobiology of Addiction Treatment, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Wake Forest University · US

Funding

TROPANE EVALUATION AND GENERAL SCIENTIFIC SERVICES COREP50DA006634 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI NADER, MICHAEL A · 1991 to 2019
$30.8M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
A Novel Animal Model of Cocaine AddictionR01DA014030 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JONES, SARA RAULERSON · 2001 to 2015
$3.2M
CANNABINOID RECEPTORS IN NEURONAL CELLS AND BRAINR01DA003690 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOWLETT, ALLYN C · 1985 to 2014
$2.8M
Postdoctoral Research, Instruction, and Mentoring Experience (PRIME)K12GM102773 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOWLETT, ALLYN C · 2013 to 2018
$2.6M
NEUROSCIENCE OF DRUG ABUSE TRAINING PROGRAMT32DA007246 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHILDERS, STEVEN R · 1991 to 2011
$2.2M
Dopamine Transporter Changes Following Cocaine Self-AdministrationR01DA021325 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JONES, SARA RAULERSON · 2007 to 2011
$1.4M
Methylphenidate, Serotonin and Dopamine InteractionsR01DA030161 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JONES, SARA RAULERSON · 2010 to 2014
$1.4M
The effect of methylphenidate use and abuse on dopamine system kineticsF31DA031533 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CALIPARI, ERIN · 2012 to 2013
$63k
NIAAA NIH HHS T32 AA007565NIDA NIH HHS DA006634NIDA NIH HHS DA021325NIDA NIH HHS DA030161NIDA NIH HHS DA03690NIDA NIH HHS F31 DA031533NIDA NIH HHS P50 DA006634NIDA NIH HHS R01 DA003690NIDA NIH HHS R01 DA014030NIDA NIH HHS T32 DA007246NIGMS NIH HHS K12 GM102773
6 · The paper itself

Abstract

Dopamine D2 autoreceptors located on the midbrain dopaminergic neurons modulate dopamine (DA) neuron firing, DA release, and DA synthesis through a negative-feedback mechanism. Dysfunctional D2 autoreceptors following repeated drug exposure could lead to aberrant DA activity in the ventral tegmental area (VTA) and projection areas such as nucleus accumbens (NAcc), promoting drug-seeking and -taking behavior. Therefore, it is important to understand molecular mechanisms underlying drug-induced changes in D2 autoreceptors. Here, we reported that 5 days of amphetamine (AMPH) self-administration reduced the ability of D2 autoreceptors to inhibit DA release in the NAcc as determined by voltammetry. Using the antibody-capture [(35)S]GTPγS scintillation proximity assay, we demonstrated for the first time that midbrain D2/D3 receptors were preferentially coupled to Gαi2, whereas striatal D2/D3 receptors were coupled equally to Gαi2 and Gαo for signaling. Importantly, AMPH abolished the interaction between Gαi2 and D2/D3 receptors in the midbrain while leaving striatal D2/D3 receptors unchanged. The disruption of the coupling between D2/D3 receptors and Gαi2 by AMPH is at least partially explained by the enhanced RGS2 (regulator of G-protein signaling 2) activity resulting from an increased RGS2 trafficking to the membrane. AMPH had no effects on the midbrain expression and trafficking of other RGS proteins such as RGS4 and RGS8. Our data suggest that midbrain D2/D3 receptors are more susceptible to AMPH-induced alterations. Reduced D2 autoreceptor function could lead to enhanced DA signaling and ultimately addiction-related behavior. RGS2 may be a potential non-dopaminergic target for pharmacological intervention of dysfunctional DA transmission and drug addiction.

Indexed as

AmphetamineAnimalsAutoreceptorsCorpus StriatumDopamineDopamine Uptake InhibitorsDrug-Seeking BehaviorMaleNucleus AccumbensRatsRats, Sprague-DawleyReceptors, Dopamine D2Receptors, Dopamine D3Self AdministrationSignal TransductionVentral StriatumAmphetamineAutoreceptorsDopamineDopamine Uptake InhibitorsReceptors, Dopamine D2Receptors, Dopamine D3

Identifiers

PMID24513972
PMCPMC4059891
OpenAlexW2068819681

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.