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VTA GABA neurons modulate specific learning behaviors through the control of dopamine and cholinergic systems

Overview of attention for article published in Frontiers in Behavioral Neuroscience, January 2014
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Title
VTA GABA neurons modulate specific learning behaviors through the control of dopamine and cholinergic systems
Published in
Frontiers in Behavioral Neuroscience, January 2014
DOI 10.3389/fnbeh.2014.00008
Pubmed ID
Authors

Meaghan C. Creed, Niels R. Ntamati, Kelly R. Tan

Abstract

The mesolimbic reward system is primarily comprised of the ventral tegmental area (VTA) and the nucleus accumbens (NAc) as well as their afferent and efferent connections. This circuitry is essential for learning about stimuli associated with motivationally-relevant outcomes. Moreover, addictive drugs affect and remodel this system, which may underlie their addictive properties. In addition to dopamine (DA) neurons, the VTA also contains approximately 30% γ-aminobutyric acid (GABA) neurons. The task of signaling both rewarding and aversive events from the VTA to the NAc has mostly been ascribed to DA neurons and the role of GABA neurons has been largely neglected until recently. GABA neurons provide local inhibition of DA neurons and also long-range inhibition of projection regions, including the NAc. Here we review studies using a combination of in vivo and ex vivo electrophysiology, pharmacogenetic and optogenetic manipulations that have characterized the functional neuroanatomy of inhibitory circuits in the mesolimbic system, and describe how GABA neurons of the VTA regulate reward and aversion-related learning. We also discuss pharmacogenetic manipulation of this system with benzodiazepines (BDZs), a class of addictive drugs, which act directly on GABAA receptors located on GABA neurons of the VTA. The results gathered with each of these approaches suggest that VTA GABA neurons bi-directionally modulate activity of local DA neurons, underlying reward or aversion at the behavioral level. Conversely, long-range GABA projections from the VTA to the NAc selectively target cholinergic interneurons (CINs) to pause their firing and temporarily reduce cholinergic tone in the NAc, which modulates associative learning. Further characterization of inhibitory circuit function within and beyond the VTA is needed in order to fully understand the function of the mesolimbic system under normal and pathological conditions.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 334 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 6 2%
France 3 <1%
Brazil 1 <1%
Germany 1 <1%
United Kingdom 1 <1%
Finland 1 <1%
Canada 1 <1%
Poland 1 <1%
Unknown 319 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 86 26%
Researcher 60 18%
Student > Bachelor 42 13%
Student > Master 31 9%
Student > Doctoral Student 23 7%
Other 41 12%
Unknown 51 15%
Readers by discipline Count As %
Neuroscience 108 32%
Agricultural and Biological Sciences 82 25%
Psychology 27 8%
Medicine and Dentistry 24 7%
Biochemistry, Genetics and Molecular Biology 11 3%
Other 20 6%
Unknown 62 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 22 February 2019.
All research outputs
#20,144,873
of 25,626,416 outputs
Outputs from Frontiers in Behavioral Neuroscience
#2,646
of 3,483 outputs
Outputs of similar age
#235,462
of 320,611 outputs
Outputs of similar age from Frontiers in Behavioral Neuroscience
#46
of 57 outputs
Altmetric has tracked 25,626,416 research outputs across all sources so far. This one is in the 18th percentile – i.e., 18% of other outputs scored the same or lower than it.
So far Altmetric has tracked 3,483 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 12.7. This one is in the 17th percentile – i.e., 17% of its peers scored the same or lower than it.
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We're also able to compare this research output to 57 others from the same source and published within six weeks on either side of this one. This one is in the 17th percentile – i.e., 17% of its contemporaries scored the same or lower than it.