Evidence map›Paper›PMID 24561386›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Nucleus accumbens-specific interventions in RGS9-2 activity modulate responses to morphine.

Sevasti Gaspari, Maria M Papachatzaki, Ja Wook Koo, Fiona B Carr, Maria-Efstratia Tsimpanouli, Eugenia Stergiou, Rosemary C Bagot, Deveroux Ferguson, Ezekiell Mouzon, Sumana Chakravarty and 3 more

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genetic mouse models in opioid research: current status and future directions.Journal of neural transmission (Vienna, Austria : 1996) · 2024
    Review
  5. Review
  6. Tianeptine promotes lasting antiallodynic effects in a mouse model of neuropathic pain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Opioid use disorder.Nature reviews. Disease primers · 2020
    Review
  14. Review
  15. Review
  16. Article
  17. Selective Role of RGS9-2 in Regulating Retrograde Synaptic Signaling of Indirect Pathway Medium Spiny Neurons in Dorsal Striatum.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  18. Article
  19. Suppression of RGSz1 function optimizes the actions of opioid analgesics by mechanisms that involve the Wnt/β-catenin pathway.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  20. RGS9-2 Modulates Responses to Oxycodone in Pain-Free and Chronic Pain States.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    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

13 authors at 6 institutions in 3 countries.

Sevasti GaspariDepartment of Basic Sciences, Faculty of Medicine, University of Crete, Heraklion, Greece.
Maria M PapachatzakiDepartment of Basic Sciences, Faculty of Medicine, University of Crete, Heraklion, Greece.
Ja Wook KooFishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA.
Fiona B CarrFishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA.
Maria-Efstratia TsimpanouliDepartment of Basic Sciences, Faculty of Medicine, University of Crete, Heraklion, Greece.
Eugenia StergiouDepartment of Basic Sciences, Faculty of Medicine, University of Crete, Heraklion, Greece.
Rosemary C BagotFishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA.
Deveroux FergusonFishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA.
Ezekiell MouzonFishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA.
Sumana ChakravartyDivision of Chemical Biology, Indian Institute of Chemical Technology, Hyderabad, India.
Karl DeisserothDepartments of Bioengineering and Physiology and Behavioural Sciences, Stanford Univerity, Stanford, CA, USA.
Mary Kay LoboDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Venetia Zachariou1] Department of Basic Sciences, Faculty of Medicine, University of Crete, Heraklion, Greece [2] Fishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA [3] Department of Pharmacology and Systems Therapeutics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Allen Institute for Brain Science · USUniversity of Crete · GRIcahn School of Medicine at Mount Sinai · USIndian Institute of Chemical Technology · INStanford University · USUniversity of Maryland, Baltimore · US

Funding

Novel Role for Sirtuin Signaling Mechanisms and Downstream Targets in DepressionK99MH094405 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FERGUSON, DEVEROUX · 2012 to 2013
$180k
NIMH NIH HHS K99 MH094405
6 · The paper itself

Abstract

Regulator of G protein signalling 9-2 (Rgs9-2) modulates the actions of a wide range of CNS-acting drugs by controlling signal transduction of several GPCRs in the striatum. RGS9-2 acts via a complex mechanism that involves interactions with Gα subunits, the Gβ5 protein, and the adaptor protein R7BP. Our recent work identified Rgs9-2 complexes in the striatum associated with acute or chronic exposures to mu opioid receptor (MOR) agonists. In this study we use several new genetic tools that allow manipulations of Rgs9-2 activity in particular brain regions of adult mice in order to better understand the mechanism via which this protein modulates opiate addiction and analgesia. We used adeno-associated viruses (AAVs) to express forms of Rgs9-2 in the dorsal and ventral striatum (nucleus accumbens, NAc) in order to examine the influence of this protein in morphine actions. Consistent with earlier behavioural findings from constitutive Rgs9 knockout mice, we show that Rgs9-2 actions in the NAc modulate morphine reward and dependence. Notably, Rgs9-2 in the NAc affects the analgesic actions of morphine as well as the development of analgesic tolerance. Using optogenetics we demonstrate that activation of Channelrhodopsin2 in Rgs9-2-expressing neurons, or in D1 dopamine receptor (Drd1)-enriched medium spiny neurons, accelerates the development of morphine tolerance, whereas activation of D2 dopamine receptor (Drd2)-enriched neurons does not significantly affect the development of tolerance. Together, these data provide new information on the signal transduction mechanisms underlying opiate actions in the NAc.

Indexed as

Analgesics, OpioidAnimalsMaleMiceMice, Inbred C57BLMorphineNeostriatumNeuronsNucleus AccumbensOptogeneticsReceptors, Dopamine D1Receptors, Dopamine D2RewardRGS ProteinsSignal TransductionAnalgesics, OpioidMorphineReceptors, Dopamine D1Receptors, Dopamine D2regulator of g-protein signaling 9RGS Proteins

Identifiers

PMID24561386
PMCPMC4059906
OpenAlexW1985264299

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.