Evidence map›Paper›PMID 16162929›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Genetic enhancement of visual learning by activation of protein kinase C pathways in small groups of rat cortical neurons.

Guo-Rong Zhang, Xiaodan Wang, Lingxin Kong, Xiu-Gui Lu, Brian Lee, Meng Liu, Mei Sun, Corinna Franklin, Robert G Cook, Alfred I Geller

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Review
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  19. Identified circuit in rat postrhinal cortex encodes essential information for performing specific visual shape discriminations.Proceedings of the National Academy of Sciences of the United States of America · 2010
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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

10 authors.

Guo-Rong ZhangDepartment of Neurology, West Roxbury Veterans Affairs Hospital, Harvard Medical School, West Roxbury, Massachusetts 02132, USA.
Xiaodan Wang
Lingxin Kong
Xiu-Gui Lu
Brian Lee
Meng Liu
Mei Sun
Corinna Franklin
Robert G Cook
Alfred I Geller

Funding

Promoters for Long-term Expression from HSV-1 VectorsR01NS045855 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GELLER, ALFRED I. · 2003 to 2011
$2.0M
GENE THERAPY FOR AGING DISORDERSR01AG016777 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GELLER, ALFRED I. · 2000 to 2004
$1.4M
High-titer helper virus-free HSV-1 vectorsR01AG021193 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GELLER, ALFRED I. · 2003 to 2007
$1.3M
Enhanced HSV-1 Vector Particles for Neural Gene TherapyR01NS043107 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GELLER, ALFRED I. · 2001 to 2004
$1.1M
Gene therapy for Parkinson's DiseaseK01AG020177 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SUN, MEI · 2002 to 2006
$592k
NIA NIH HHS AG021193NIA NIH HHS AG16777NIA NIH HHS AG20177NIA NIH HHS K01 AG020177NIA NIH HHS R01 AG016777NIA NIH HHS R01 AG021193NINDS NIH HHS NS045855NINDS NIH HHS NS43107NINDS NIH HHS R01 NS043107NINDS NIH HHS R01 NS045855
6 · The paper itself

Abstract

Although learning and memory theories hypothesize that memories are encoded by specific circuits, it has proven difficult to localize learning within a cortical area. Neural network theories predict that activation of a small fraction of the neurons in a circuit can activate that circuit. Consequently, altering the physiology of a small group of neurons might potentiate a specific circuit and enhance learning, thereby localizing learning to that circuit. In this study, we activated protein kinase C (PKC) pathways in small groups of neurons in rat postrhinal (POR) cortex. We microinjected helper virus-free herpes simplex virus vectors that expressed a constitutively active PKC into POR cortex. This PKC was expressed predominantly in glutamatergic and GABAergic neurons in POR cortex. This intervention increased phosphorylation of five PKC substrates that play critical roles in neurotransmitter release (GAP-43 and dynamin) or glutamatergic neurotransmission (specific subunits of AMPA or NMDA receptors and myristoylated alanine-rich C kinase substrate). Additionally, activation of PKC pathways in cultured cortical neurons supported activation-dependent increases in release of glutamate and GABA. This intervention enhanced the learning rate and accuracy of visual object discriminations. In individual rats, the numbers of transfected neurons positively correlated with this learning. During learning, neuronal activity was increased in neurons proximal to the transfected neurons. These results demonstrate that potentiating small groups of glutamatergic and GABAergic neurons in POR cortex enhances visual object learning. More generally, these results suggest that learning can be mediated by specific cortical circuits.

Indexed as

Photic StimulationAnimalsCerebral CortexEnzyme ActivationLearningModels, AnimalNeuronsProtein Kinase CRatsProtein Kinase C

Identifiers

PMID16162929
PMCPMC2581869

What OpenQuestion holds

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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.