Evidence map›Paper›PMID 22828798›Full record

ArticleMolecular pharmacology2012

A role for kalirin in the response of rat medium spiny neurons to cocaine.

Xin-Ming Ma, Jian-Ping Huang, Xiaonan Xin, Yan Yan, Richard E Mains, Betty A Eipper

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. SIRT1-FOXO3a regulate cocaine actions in the nucleus accumbens.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Kalirin-7 mediates cocaine-induced AMPA receptor and spine plasticity, enabling incentive sensitization.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  10. Neuronal Rho GEFs in synaptic physiology and behavior.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2013
    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

6 authors at 1 institution in 1 country.

Xin-Ming MaDepartment of Neuroscience, University of Connecticut Health Center, 263 Farmington Ave., MC-3401, Farmington, CT, USA. ma@nso.uchc.edu
Jian-Ping Huang
Xiaonan Xin
Yan Yan
Richard E Mains
Betty A Eipper
UConn Health · US

Funding

Dissecting the role of one neuronal RhoGEF amongst many: the Kalirin-7 null mouseR01DA023082 · NIDA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAINS, RICHARD E · 2008 to 2012
$1.6M
GDP/GTP Exchange Factors: Nucleus Accumbens PlasticityR01DA015464 · NIDA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI EIPPER, ELIZABETH ANNE · 2004 to 2008
$1.6M
Constructing a Conditional Kalirin Null MouseR21DA018274 · NIDA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAINS, RICHARD E · 2004 to 2005
$290k
NIDA NIH HHS DA15464NIDA NIH HHS R01 DA015464NIDA NIH HHS R01 DA023082NIDA NIH HHS R21 DA018274
6 · The paper itself

Abstract

Kalirin-7 (Kal7), the major kalirin isoform in adult brain, plays a key role in the formation of dendritic spines in hippocampal/cortical neurons. Its role in the GABAergic medium spiny neurons (MSNs) of the nucleus accumbens (NAc) and striatum, the areas known to play a key role in the common reward pathway, is not as well understood. Although Kal7 expression in mouse NAc increased in response to cocaine, MSN dendritic spine density did not differ from that for the wild type in Kal7-null mice. Unlike wild-type mice, Kal7-null mice did not respond to cocaine with an increase in MSN dendritic spine density. To explore further the role of Kal7 in cocaine-induced alterations in MSN morphology, we turned to the rat. Based on immunostaining, both Kal7 and Kal12 are expressed at moderate levels in the MSNs of the NAc and striatum. Expression of Kal7 and Kal12 in MSNs of both areas increases after repeated cocaine treatments. Overexpression of Kal7 in cultured MSN neurons increases dendritic spine density, as observed in rats after long-term cocaine administration. Reducing endogenous expression of all major kalirin isoforms in cultured MSN neurons causes a decrease in total dendritic length and dendritic spine density. These data suggest that kalirin is essential for maintaining spine density in NAc MSNs under normal conditions and that Kal7 is an obligatory intermediate in the response of MSNs to repeated exposure to cocaine.

Indexed as

AnimalsCells, CulturedCocaineCorpus StriatumDendritic SpinesGuanine Nucleotide Exchange FactorsMaleNeuronsNucleus AccumbensProtein IsoformsRatsRats, Sprague-DawleyTime FactorsCocaineGuanine Nucleotide Exchange FactorsKalrn protein, ratProtein Isoforms

Identifiers

PMID22828798
PMCPMC3463218
OpenAlexW2122118862

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.