Evidence map›Paper›PMID 17551543›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2008

Acute amphetamine exposure selectively desensitizes kappa-opioid receptors in the nucleus accumbens.

Yan-fang Xia, Li He, Jennifer L Whistler, Gregory O Hjelmstad

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Relative Timing Between Kappa Opioid Receptor Activation and Cocaine Determines the Impact on Reward and Dopamine Release.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
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  7. Article
  8. Review
  9. Article
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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

4 authors at 2 institutions in 1 country.

Yan-fang XiaErnest Gallo Clinic and Research Center, University of California, San Francisco, CA 94608, USA.
Li He
Jennifer L Whistler
Gregory O Hjelmstad
Ernest Gallo Clinic and Research Center · USUniversity of California, San Francisco · US

Funding

Trafficking and signaling of opioid receptor subtypes and heterodimersR01DA015232 · NIDA · ERNEST GALLO CLINIC AND RESEARCH CENTER · PI WHISTLER, JENNIFER L · 2003 to 2010
$2.0M
Plasticity of Kappa Opioid Function in Reward CircuitryR01DA015686 · NIDA · ERNEST GALLO CLINIC AND RESEARCH CENTER · PI HJELMSTAD, GREGORY OLAF · 2003 to 2007
$1.2M
NIDA NIH HHS DA15232NIDA NIH HHS DA15686NIDA NIH HHS R01 DA015232NIDA NIH HHS R01 DA015686
6 · The paper itself

Abstract

In the present study, we investigated the effects of psychostimulant exposure on kappa-opioid peptide (KOP) receptor signaling in the rat mesolimbic system. A single subcutaneous (s.c.) injection of amphetamine (2.5 mg/kg) reduced the KOP receptor-mediated inhibition of glutamate release in the nucleus accumbens shell, as a consequence of KOP receptor desensitization. This effect was blocked by dopamine (DA) receptor antagonists or the nonselective opioid antagonist, naltrexone (1 mg/kg, s.c.), and mimicked by the KOP receptor agonists U69593 (0.32 mg/kg, s.c.) and dynorphin (1 microM), indicating that an amphetamine-induced release of dynorphin is producing a long-lasting desensitization of the KOP receptor. Despite the fact that amphetamine also increases dynorphin release in the ventral tegmental area (VTA), KOP receptor function in this region was not affected by amphetamine; there was no difference in the KOP receptor-mediated change in firing rate or resting membrane potential measured in VTA neurons from saline- or amphetamine-treated animals. This study demonstrates that amphetamine can produce regionally selective adaptations in KOP receptor signaling, which may, in turn, alter the effects of subsequent drug exposure.

Indexed as

AmphetamineAnalgesics, OpioidAnalysis of VarianceAnimalsBenzeneacetamidesCentral Nervous System StimulantsDopamine AgentsDose-Response Relationship, DrugDrug InteractionsDynorphinsElectric StimulationEnkephalin, Ala(2)-MePhe(4)-Gly(5)-Excitatory Postsynaptic PotentialsGene Expression RegulationMaleNarcotic AntagonistsAmphetamineAnalgesics, OpioidBenzeneacetamidesCentral Nervous System StimulantsDopamine AgentsDynorphinsEnkephalin, Ala(2)-MePhe(4)-Gly(5)-Narcotic AntagonistsPyrrolidinesReceptors, Opioid, kappaU 69593

Identifiers

PMID17551543
PMCPMC2268619
OpenAlexW2057810468

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.