Evidence map›Paper›PMID 21228905›Full record

ArticleFrontiers in neuroanatomy2010

Heterogeneity and diversity of striatal GABAergic interneurons.

James M Tepper, Fatuel Tecuapetla, Tibor Koós, Osvaldo Ibáñez-Sandoval

Abstract read
In one paragraph

Article in Frontiers in neuroanatomy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 275 papers.

0numbers the graph read from it
0cells of the map it votes in
275citing 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

275 citing papers in PubMed.

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215 more citing papers are in PubMed but not listed here.

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.

James M TepperCenter for Molecular and Behavioral Neuroscience, Rutgers University Newark, NJ, USA.
Fatuel Tecuapetla
Tibor Koós
Osvaldo Ibáñez-Sandoval

Funding

Nigrostriatal Dopamine FunctionR01NS034865 · NINDS · RUTGERS THE STATE UNIV OF NJ NEWARK · PI KOOS, TIBOR, TEPPER, JAMES M · 1997 to 2022
$9.3M
Dopamine modulation of the neostriatal feedback circuitryR01NS052370 · NINDS · RUTGERS THE STATE UNIV OF NJ NEWARK · PI KOOS, TIBOR · 2006 to 2010
$1.6M
Nigrostriatal dopamine functionR56NS034865 · NINDS · RUTGERS THE STATE UNIV OF NJ NEWARK · PI TEPPER, JAMES M · 2008 to 2009
$485k
NINDS NIH HHS R01 NS034865NINDS NIH HHS R01 NS052370NINDS NIH HHS R56 NS034865
6 · The paper itself

Abstract

The canonical view of striatal GABAergic interneurons has evolved over several decades of neuroanatomical/neurochemical and electrophysiological studies. From the anatomical studies, three distinct GABAergic interneuronal subtypes are generally recognized. The best-studied subtype expresses the calcium-binding protein, parvalbumin. The second best known interneuron type expresses a number of neuropeptides and enzymes, including neuropeptide Y, somatostatin, and nitric oxide synthase. The last GABAergic interneuron subtype expresses the calcium binding protein, calretinin. There is no overlap or co-localization of these three different sets of markers. The parvalbumin-immunoreactive GABAergic interneurons have been recorded in vitro and shown to exhibit a fast-spiking phenotype characterized by short duration action potentials with large and rapid spike AHPs. They often fire in a stuttering pattern of high frequency firing interrupted by periods of silence. They are capable of sustained firing rates of over 200 Hz. The NPY/SOM/NOS interneurons have been identified as PLTS cells, exhibiting very high input resistances, low threshold spike and prolonged plateau potentials in response to intracellular depolarization or excitatory synaptic stimulation. Thus far, no recordings from identified CR interneurons have been obtained. Recent advances in technological approaches, most notably the generation of several BAC transgenic mouse strains which express a fluorescent marker, enhanced green fluorescent protein, specifically and selectively only in neurons of a certain genetic makeup (e.g., parvalbumin-, neuropeptide Y-, or tyrosine hydroxylase-expressing neurons etc.) have led to the ability of electrophysiologists to visualize and patch specific neuron types in brain slices with epifluorescence illumination. This has led to a rapid expansion of the number of neurochemically and/or electrophysiologically identified interneuronal cell types in the striatum and elsewhere. This article will review the anatomy, neurochemistry, electrophysiology, synaptic connections, and function of the three "classic" striatal GABAergic interneurons as well as more recent data derived from in vitro recordings from BAC transgenic mice as well as recent in vivo data.

Indexed as

EGFPGABAergicinterneuronneostriatumNOSNPYSOMtyrosine hydroxylase

Identifiers

PMID21228905
PMCPMC3016690

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.