Orexinergic input to dopaminergic neurons of the human ventral tegmental area.

The mesolimbic reward pathway arising from dopaminergic (DA) neurons of the ventral tegmental area (VTA) has been strongly implicated in reward processing and drug abuse. In rodents, behaviors associated with this projection are profoundly influenced by an orexinergic input from the lateral hypothal...

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Main Authors: Erik Hrabovszky, Csilla S Molnár, Beáta Á Borsay, Péter Gergely, László Herczeg, Zsolt Liposits
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3869755?pdf=render
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author Erik Hrabovszky
Csilla S Molnár
Beáta Á Borsay
Péter Gergely
László Herczeg
Zsolt Liposits
author_facet Erik Hrabovszky
Csilla S Molnár
Beáta Á Borsay
Péter Gergely
László Herczeg
Zsolt Liposits
author_sort Erik Hrabovszky
collection DOAJ
description The mesolimbic reward pathway arising from dopaminergic (DA) neurons of the ventral tegmental area (VTA) has been strongly implicated in reward processing and drug abuse. In rodents, behaviors associated with this projection are profoundly influenced by an orexinergic input from the lateral hypothalamus to the VTA. Because the existence and significance of an analogous orexigenic regulatory mechanism acting in the human VTA have been elusive, here we addressed the possibility that orexinergic neurons provide direct input to DA neurons of the human VTA. Dual-label immunohistochemistry was used and orexinergic projections to the VTA and to DA neurons of the neighboring substantia nigra (SN) were analyzed comparatively in adult male humans and rats. Orexin B-immunoreactive (IR) axons apposed to tyrosine hydroxylase (TH)-IR DA and to non-DA neurons were scarce in the VTA and SN of both species. In the VTA, 15.0±2.8% of TH-IR perikarya in humans and 3.2±0.3% in rats received orexin B-IR afferent contacts. On average, 0.24±0.05 and 0.05±0.005 orexinergic appositions per TH-IR perikaryon were detected in humans and rats, respectively. The majority (86-88%) of randomly encountered orexinergic contacts targeted the dendritic compartment of DA neurons. Finally, DA neurons of the SN also received orexinergic innervation in both species. Based on the observation of five times heavier orexinergic input to TH-IR neurons of the human, compared with the rat, VTA, we propose that orexinergic mechanism acting in the VTA may play just as important roles in reward processing and drug abuse in humans, as already established well in rodents.
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spelling doaj.art-fc77d88b89e34e1488832dfd542c536e2022-12-22T01:56:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8302910.1371/journal.pone.0083029Orexinergic input to dopaminergic neurons of the human ventral tegmental area.Erik HrabovszkyCsilla S MolnárBeáta Á BorsayPéter GergelyLászló HerczegZsolt LipositsThe mesolimbic reward pathway arising from dopaminergic (DA) neurons of the ventral tegmental area (VTA) has been strongly implicated in reward processing and drug abuse. In rodents, behaviors associated with this projection are profoundly influenced by an orexinergic input from the lateral hypothalamus to the VTA. Because the existence and significance of an analogous orexigenic regulatory mechanism acting in the human VTA have been elusive, here we addressed the possibility that orexinergic neurons provide direct input to DA neurons of the human VTA. Dual-label immunohistochemistry was used and orexinergic projections to the VTA and to DA neurons of the neighboring substantia nigra (SN) were analyzed comparatively in adult male humans and rats. Orexin B-immunoreactive (IR) axons apposed to tyrosine hydroxylase (TH)-IR DA and to non-DA neurons were scarce in the VTA and SN of both species. In the VTA, 15.0±2.8% of TH-IR perikarya in humans and 3.2±0.3% in rats received orexin B-IR afferent contacts. On average, 0.24±0.05 and 0.05±0.005 orexinergic appositions per TH-IR perikaryon were detected in humans and rats, respectively. The majority (86-88%) of randomly encountered orexinergic contacts targeted the dendritic compartment of DA neurons. Finally, DA neurons of the SN also received orexinergic innervation in both species. Based on the observation of five times heavier orexinergic input to TH-IR neurons of the human, compared with the rat, VTA, we propose that orexinergic mechanism acting in the VTA may play just as important roles in reward processing and drug abuse in humans, as already established well in rodents.http://europepmc.org/articles/PMC3869755?pdf=render
spellingShingle Erik Hrabovszky
Csilla S Molnár
Beáta Á Borsay
Péter Gergely
László Herczeg
Zsolt Liposits
Orexinergic input to dopaminergic neurons of the human ventral tegmental area.
PLoS ONE
title Orexinergic input to dopaminergic neurons of the human ventral tegmental area.
title_full Orexinergic input to dopaminergic neurons of the human ventral tegmental area.
title_fullStr Orexinergic input to dopaminergic neurons of the human ventral tegmental area.
title_full_unstemmed Orexinergic input to dopaminergic neurons of the human ventral tegmental area.
title_short Orexinergic input to dopaminergic neurons of the human ventral tegmental area.
title_sort orexinergic input to dopaminergic neurons of the human ventral tegmental area
url http://europepmc.org/articles/PMC3869755?pdf=render
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