Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology

We investigated the alterations of hippocampal and reticulo-thalamic (RT) GABAergic parvalbumin (PV) interneurons and their synaptic re-organizations underlying the prodromal local sleep disorders in the distinct rat models of Parkinson’s disease (PD). We demonstrated for the first time that REM sle...

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Main Authors: Ljiljana Radovanovic, Jelena Petrovic, Jasna Saponjic
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:International Journal of Molecular Sciences
Subjects:
rat
Online Access:https://www.mdpi.com/1422-0067/22/16/8922
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spelling doaj-ed4ad1ed848141e49c7d45f32b07fd552021-08-26T13:53:17ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-08-01228922892210.3390/ijms22168922Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease NeuropathologyLjiljana Radovanovic0Jelena Petrovic1Jasna Saponjic2Institute for Biological Research “Sinisa Stankovic”, National Institute of Republic of Serbia, Department of Neurobiology, University of Belgrade, 11060 Belgrade, SerbiaInstitute for Biological Research “Sinisa Stankovic”, National Institute of Republic of Serbia, Department of Neurobiology, University of Belgrade, 11060 Belgrade, SerbiaInstitute for Biological Research “Sinisa Stankovic”, National Institute of Republic of Serbia, Department of Neurobiology, University of Belgrade, 11060 Belgrade, SerbiaWe investigated the alterations of hippocampal and reticulo-thalamic (RT) GABAergic parvalbumin (PV) interneurons and their synaptic re-organizations underlying the prodromal local sleep disorders in the distinct rat models of Parkinson’s disease (PD). We demonstrated for the first time that REM sleep is a predisposing state for the high-voltage sleep spindles (HVS) induction in all experimental models of PD, particularly during hippocampal REM sleep in the hemiparkinsonian models. There were the opposite underlying alterations of the hippocampal and RT GABAergic PV+ interneurons along with the distinct MAP2 and PSD-95 expressions. Whereas the PD cholinopathy enhanced the number of PV+ interneurons and suppressed the MAP2/PSD-95 expression, the hemiparkinsonism with PD cholinopathy reduced the number of PV+ interneurons and enhanced the MAP2/PSD-95 expression in the hippocampus. Whereas the PD cholinopathy did not alter PV+ interneurons but partially enhanced MAP2 and suppressed PSD-95 expression remotely in the RT, the hemiparkinsonism with PD cholinopathy reduced the PV+ interneurons, enhanced MAP2, and did not change PSD-95 expression remotely in the RT. Our study demonstrates for the first time an important regulatory role of the hippocampal and RT GABAergic PV+ interneurons and the synaptic protein dynamic alterations in the distinct rat models of PD neuropathology.https://www.mdpi.com/1422-0067/22/16/8922Parkinson’s diseaseratprodromal sleep disorderssleep spindle dynamicshippocampusreticulo-thalamic nucleus
collection DOAJ
language English
format Article
sources DOAJ
author Ljiljana Radovanovic
Jelena Petrovic
Jasna Saponjic
spellingShingle Ljiljana Radovanovic
Jelena Petrovic
Jasna Saponjic
Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology
International Journal of Molecular Sciences
Parkinson’s disease
rat
prodromal sleep disorders
sleep spindle dynamics
hippocampus
reticulo-thalamic nucleus
author_facet Ljiljana Radovanovic
Jelena Petrovic
Jasna Saponjic
author_sort Ljiljana Radovanovic
title Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology
title_short Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology
title_full Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology
title_fullStr Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology
title_full_unstemmed Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology
title_sort hippocampal and reticulo-thalamic parvalbumin interneurons and synaptic re-organization during sleep disorders in the rat models of parkinson’s disease neuropathology
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-08-01
description We investigated the alterations of hippocampal and reticulo-thalamic (RT) GABAergic parvalbumin (PV) interneurons and their synaptic re-organizations underlying the prodromal local sleep disorders in the distinct rat models of Parkinson’s disease (PD). We demonstrated for the first time that REM sleep is a predisposing state for the high-voltage sleep spindles (HVS) induction in all experimental models of PD, particularly during hippocampal REM sleep in the hemiparkinsonian models. There were the opposite underlying alterations of the hippocampal and RT GABAergic PV+ interneurons along with the distinct MAP2 and PSD-95 expressions. Whereas the PD cholinopathy enhanced the number of PV+ interneurons and suppressed the MAP2/PSD-95 expression, the hemiparkinsonism with PD cholinopathy reduced the number of PV+ interneurons and enhanced the MAP2/PSD-95 expression in the hippocampus. Whereas the PD cholinopathy did not alter PV+ interneurons but partially enhanced MAP2 and suppressed PSD-95 expression remotely in the RT, the hemiparkinsonism with PD cholinopathy reduced the PV+ interneurons, enhanced MAP2, and did not change PSD-95 expression remotely in the RT. Our study demonstrates for the first time an important regulatory role of the hippocampal and RT GABAergic PV+ interneurons and the synaptic protein dynamic alterations in the distinct rat models of PD neuropathology.
topic Parkinson’s disease
rat
prodromal sleep disorders
sleep spindle dynamics
hippocampus
reticulo-thalamic nucleus
url https://www.mdpi.com/1422-0067/22/16/8922
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AT jasnasaponjic hippocampalandreticulothalamicparvalbumininterneuronsandsynapticreorganizationduringsleepdisordersintheratmodelsofparkinsonsdiseaseneuropathology
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