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Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns

BACKGROUND: In Parkinson’s disease (PD), cerebral dopamine depletion is associated with PD subtype-specific metabolic patterns of hypo- and hypermetabolism. It has been hypothesised that hypometabolism reflects impairment, while hypermetabolism may indicate compensatory activity. In order to associa...

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Autores principales: Kordys, Elena, Apetz, Nadine, Schneider, Katharina, Duncan, Eilidh, Büschbell, Beatriz, Rohleder, Cathrin, Sué, Michael, Drzezga, Alexander, Neumaier, Bernd, Timmermann, Lars, Endepols, Heike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567589/
https://www.ncbi.nlm.nih.gov/pubmed/28831764
http://dx.doi.org/10.1186/s13550-017-0317-9
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author Kordys, Elena
Apetz, Nadine
Schneider, Katharina
Duncan, Eilidh
Büschbell, Beatriz
Rohleder, Cathrin
Sué, Michael
Drzezga, Alexander
Neumaier, Bernd
Timmermann, Lars
Endepols, Heike
author_facet Kordys, Elena
Apetz, Nadine
Schneider, Katharina
Duncan, Eilidh
Büschbell, Beatriz
Rohleder, Cathrin
Sué, Michael
Drzezga, Alexander
Neumaier, Bernd
Timmermann, Lars
Endepols, Heike
author_sort Kordys, Elena
collection PubMed
description BACKGROUND: In Parkinson’s disease (PD), cerebral dopamine depletion is associated with PD subtype-specific metabolic patterns of hypo- and hypermetabolism. It has been hypothesised that hypometabolism reflects impairment, while hypermetabolism may indicate compensatory activity. In order to associate metabolic patterns with pathophysiological and compensatory mechanisms, we combined resting state [(18)F]FDG-PET (to demonstrate brain metabolism in awake animals), [(18)F]FDOPA-PET (dopamine depletion severity) and gait analysis in a unilateral 6-hydroxydopamine rat model. RESULTS: We found unilateral nigro-striatal dopaminergic loss to decrease swing speed of the contralesional forelimb and stride length of all paws in association with depletion severity. Depletion severity was found to correlate with compensatory changes such as increased stance time of the other three paws and diagonal weight shift to the ipsilesional hind paw. [(18)F]FDG-PET revealed ipsilesional hypo- and contralesional hypermetabolism; metabolic deactivation of the ipsilesional network needed for sensorimotor integration (hippocampus/retrosplenial cortex/lateral posterior thalamus) was solely associated with bradykinesia, but hypometabolism of the ipsilesional rostral forelimb area was related to both pathological and compensatory gait changes. Mixed effects were also found for hypermetabolism of the contralesional midbrain locomotor region, while contralesional striatal hyperactivation was linked to motor impairments rather than compensation. CONCLUSIONS: Our results indicate that ipsilesional hypo- and contralesional hypermetabolism contribute to both motor impairment and compensation. This is the first time when energy metabolism, dopamine depletion and gait analysis were combined in a hemiparkinsonian model. By experimentally increasing or decreasing compensational brain activity, its potential and limits can be further investigated.
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spelling pubmed-55675892017-09-11 Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns Kordys, Elena Apetz, Nadine Schneider, Katharina Duncan, Eilidh Büschbell, Beatriz Rohleder, Cathrin Sué, Michael Drzezga, Alexander Neumaier, Bernd Timmermann, Lars Endepols, Heike EJNMMI Res Original Research BACKGROUND: In Parkinson’s disease (PD), cerebral dopamine depletion is associated with PD subtype-specific metabolic patterns of hypo- and hypermetabolism. It has been hypothesised that hypometabolism reflects impairment, while hypermetabolism may indicate compensatory activity. In order to associate metabolic patterns with pathophysiological and compensatory mechanisms, we combined resting state [(18)F]FDG-PET (to demonstrate brain metabolism in awake animals), [(18)F]FDOPA-PET (dopamine depletion severity) and gait analysis in a unilateral 6-hydroxydopamine rat model. RESULTS: We found unilateral nigro-striatal dopaminergic loss to decrease swing speed of the contralesional forelimb and stride length of all paws in association with depletion severity. Depletion severity was found to correlate with compensatory changes such as increased stance time of the other three paws and diagonal weight shift to the ipsilesional hind paw. [(18)F]FDG-PET revealed ipsilesional hypo- and contralesional hypermetabolism; metabolic deactivation of the ipsilesional network needed for sensorimotor integration (hippocampus/retrosplenial cortex/lateral posterior thalamus) was solely associated with bradykinesia, but hypometabolism of the ipsilesional rostral forelimb area was related to both pathological and compensatory gait changes. Mixed effects were also found for hypermetabolism of the contralesional midbrain locomotor region, while contralesional striatal hyperactivation was linked to motor impairments rather than compensation. CONCLUSIONS: Our results indicate that ipsilesional hypo- and contralesional hypermetabolism contribute to both motor impairment and compensation. This is the first time when energy metabolism, dopamine depletion and gait analysis were combined in a hemiparkinsonian model. By experimentally increasing or decreasing compensational brain activity, its potential and limits can be further investigated. Springer Berlin Heidelberg 2017-08-23 /pmc/articles/PMC5567589/ /pubmed/28831764 http://dx.doi.org/10.1186/s13550-017-0317-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Kordys, Elena
Apetz, Nadine
Schneider, Katharina
Duncan, Eilidh
Büschbell, Beatriz
Rohleder, Cathrin
Sué, Michael
Drzezga, Alexander
Neumaier, Bernd
Timmermann, Lars
Endepols, Heike
Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
title Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
title_full Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
title_fullStr Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
title_full_unstemmed Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
title_short Motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
title_sort motor impairment and compensation in a hemiparkinsonian rat model: correlation between dopamine depletion severity, cerebral metabolism and gait patterns
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567589/
https://www.ncbi.nlm.nih.gov/pubmed/28831764
http://dx.doi.org/10.1186/s13550-017-0317-9
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