Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/51154
Title: Unraveling a new circuitry for sleep regulation in Parkinson's disease
Authors: Targa, Adriano D. S.
Rodrigues, Lais S.
Noseda, Ana Carolina D.
Aurich, Mariana F.
Andersen, Monica L. [UNIFESP]
Tufik, Sergio [UNIFESP]
da Cunha, Claudio
Lima, Marcelo M. S.
Keywords: Sleep regulation
Parkinson's disease
Dopamine
Pedunculopontine nucleus
Substantia nigra pars compacta
Striatum
Issue Date: 2016
Publisher: Pergamon-Elsevier Science Ltd
Citation: Neuropharmacology. Oxford, v. 108, p. 161-171, 2016.
Abstract: Sleep disturbances are among the most disabling non-motor symptoms in Parkinson's disease. The pedunculopontine tegmental nucleus and basal ganglia are likely involved in these dysfunctions, as they are affected by neurodegeneration in Parkinson's disease and have a role in sleep regulation. To investigate this, we promoted a lesion in the pedunculopontine tegmental nucleus or substantia nigra pars compacta of male rats, followed by 24 h of REM sleep deprivation. Then, we administrated a dopaminergic D2 receptor agonist, antagonist or vehicle directly in the striatum. After a period of 24 h of sleep wake recording, we observed that the ibotenic acid infusion in the pedunculopontine tegmental nucleus blocked the so-called sleep rebound effect mediated by REM sleep deprivation, which was reversed by striatal D2 receptors activation. Rotenone infusion in the substantia nigra pars compacta also blocked the sleep rebound, however, striatal D2 receptors activation did not reverse it. In addition, rotenone administration decreased the time spent in NREM sleep, which was corroborated by positive correlations between dopamine levels in both substantia nigra pars compacta and striatum and the time spent in NREM sleep. These findings suggest a new circuitry for sleep regulation in Parkinson's disease, involving the triad composed by pedunculopontine nucleus, substantia nigra pars compacta and striatum, evidencing a potential therapeutic target for the sleep disturbances associated to this pathology. (C) 2016 Elsevier Ltd. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/51154
ISSN: 0028-3908
Other Identifiers: http://dx.doi.org/10.1016/j.neuropharm.2016.04.018
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