GABA neurons in the ventral tegmental area responding to peripheral sensory input.

Dopamine (DA) neurons in the ventral tegmental area (VTA) not only participate in reward processing, but also respond to aversive stimuli. Although GABA neurons in this area are actively involved in regulating the firing of DA neurons, few data exist concerning the responses of these neurons to aver...

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Main Authors: Chang-Liang Liu, Ming Gao, Guo-Zhang Jin, Xuechu Zhen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3519727?pdf=render
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spelling doaj-5c9298634a5748d7beb8913bbfe3f8f32020-11-24T21:26:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5150710.1371/journal.pone.0051507GABA neurons in the ventral tegmental area responding to peripheral sensory input.Chang-Liang LiuMing GaoGuo-Zhang JinXuechu ZhenDopamine (DA) neurons in the ventral tegmental area (VTA) not only participate in reward processing, but also respond to aversive stimuli. Although GABA neurons in this area are actively involved in regulating the firing of DA neurons, few data exist concerning the responses of these neurons to aversive sensory input. In this study, by employing extracellular single-unit recording and spectral analysis techniques in paralyzed and ventilated rats, we found that the firing pattern in 44% (47 of 106) of GABA cells in the VTA was sensitive to the sensory input produced by the ventilation, showing a significant ventilation-associated oscillation in the power spectra. Detailed studies revealed that most ventilation-sensitive GABA neurons (38 of 47) were excited by the stimuli, whereas most ventilation-sensitive DA neurons (11 of 14) were inhibited. When the animals were under anesthesia or the sensory pathways were transected, the ventilation-associated oscillation failed to appear. Systemic administration of non-competitive N-methyl-D-aspartase (NMDA) receptor antagonist MK-801 completely disrupted the association between the firing of GABA neurons and the ventilation. Interestingly, local MK-801 injection into the VTA dramatically enhanced the sensitivity of GABA neurons to the ventilation. Our data demonstrate that both GABA and DA neurons in the VTA can be significantly modulated by sensory input produced by the ventilation, which may indicate potential functional roles of VTA in processing sensation-related input.http://europepmc.org/articles/PMC3519727?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Chang-Liang Liu
Ming Gao
Guo-Zhang Jin
Xuechu Zhen
spellingShingle Chang-Liang Liu
Ming Gao
Guo-Zhang Jin
Xuechu Zhen
GABA neurons in the ventral tegmental area responding to peripheral sensory input.
PLoS ONE
author_facet Chang-Liang Liu
Ming Gao
Guo-Zhang Jin
Xuechu Zhen
author_sort Chang-Liang Liu
title GABA neurons in the ventral tegmental area responding to peripheral sensory input.
title_short GABA neurons in the ventral tegmental area responding to peripheral sensory input.
title_full GABA neurons in the ventral tegmental area responding to peripheral sensory input.
title_fullStr GABA neurons in the ventral tegmental area responding to peripheral sensory input.
title_full_unstemmed GABA neurons in the ventral tegmental area responding to peripheral sensory input.
title_sort gaba neurons in the ventral tegmental area responding to peripheral sensory input.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Dopamine (DA) neurons in the ventral tegmental area (VTA) not only participate in reward processing, but also respond to aversive stimuli. Although GABA neurons in this area are actively involved in regulating the firing of DA neurons, few data exist concerning the responses of these neurons to aversive sensory input. In this study, by employing extracellular single-unit recording and spectral analysis techniques in paralyzed and ventilated rats, we found that the firing pattern in 44% (47 of 106) of GABA cells in the VTA was sensitive to the sensory input produced by the ventilation, showing a significant ventilation-associated oscillation in the power spectra. Detailed studies revealed that most ventilation-sensitive GABA neurons (38 of 47) were excited by the stimuli, whereas most ventilation-sensitive DA neurons (11 of 14) were inhibited. When the animals were under anesthesia or the sensory pathways were transected, the ventilation-associated oscillation failed to appear. Systemic administration of non-competitive N-methyl-D-aspartase (NMDA) receptor antagonist MK-801 completely disrupted the association between the firing of GABA neurons and the ventilation. Interestingly, local MK-801 injection into the VTA dramatically enhanced the sensitivity of GABA neurons to the ventilation. Our data demonstrate that both GABA and DA neurons in the VTA can be significantly modulated by sensory input produced by the ventilation, which may indicate potential functional roles of VTA in processing sensation-related input.
url http://europepmc.org/articles/PMC3519727?pdf=render
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