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CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis

OBJECTIVES: Therapeutic effects of physical therapy in neurologic disorders mostly rely on the promotion of use-dependent synaptic plasticity in damaged neuronal circuits. Genetic differences affecting the efficiency of synaptic plasticity mechanisms could explain why some patients do not respond ad...

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Autores principales: Mori, Francesco, Ljoka, Concetta, Nicoletti, Carolina G., Kusayanagi, Hajime, Buttari, Fabio, Giordani, Laura, Rossi, Silvia, Foti, Calogero, Centonze, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268035/
https://www.ncbi.nlm.nih.gov/pubmed/25520956
http://dx.doi.org/10.1212/NXI.0000000000000048
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author Mori, Francesco
Ljoka, Concetta
Nicoletti, Carolina G.
Kusayanagi, Hajime
Buttari, Fabio
Giordani, Laura
Rossi, Silvia
Foti, Calogero
Centonze, Diego
author_facet Mori, Francesco
Ljoka, Concetta
Nicoletti, Carolina G.
Kusayanagi, Hajime
Buttari, Fabio
Giordani, Laura
Rossi, Silvia
Foti, Calogero
Centonze, Diego
author_sort Mori, Francesco
collection PubMed
description OBJECTIVES: Therapeutic effects of physical therapy in neurologic disorders mostly rely on the promotion of use-dependent synaptic plasticity in damaged neuronal circuits. Genetic differences affecting the efficiency of synaptic plasticity mechanisms could explain why some patients do not respond adequately to the treatment. It is known that physical exercise activates the endocannabinoid system and that stimulation of cannabinoid CB1 receptors (CB1Rs) promotes synaptic plasticity in both rodents and humans. We thus tested whether CB1R genetic variants affect responsiveness to exercise therapy. METHODS: We evaluated the effect of a genetic variant of the CB1R associated with reduced receptor expression (patients with long AAT trinucleotide short tandem repeats in the CNR1 gene) on long-term potentiation (LTP)–like cortical plasticity induced by transcranial magnetic theta burst stimulation (TBS) of the motor cortex and, in parallel, on clinical response to exercise therapy in patients with multiple sclerosis. RESULTS: We found that patients with long AAT CNR1 repeats do not express TBS-induced LTP-like cortical plasticity and show poor clinical benefit after exercise therapy. CONCLUSIONS: Our results provide the first evidence that genetic differences within the CB1R may influence clinical responses to exercise therapy, and they strengthen the hypothesis that CB1Rs are involved in the regulation of synaptic plasticity and in the control of spasticity in humans. This information might be of great relevance for patient stratification and personalized rehabilitation treatment programs.
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spelling pubmed-42680352014-12-17 CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis Mori, Francesco Ljoka, Concetta Nicoletti, Carolina G. Kusayanagi, Hajime Buttari, Fabio Giordani, Laura Rossi, Silvia Foti, Calogero Centonze, Diego Neurol Neuroimmunol Neuroinflamm Article OBJECTIVES: Therapeutic effects of physical therapy in neurologic disorders mostly rely on the promotion of use-dependent synaptic plasticity in damaged neuronal circuits. Genetic differences affecting the efficiency of synaptic plasticity mechanisms could explain why some patients do not respond adequately to the treatment. It is known that physical exercise activates the endocannabinoid system and that stimulation of cannabinoid CB1 receptors (CB1Rs) promotes synaptic plasticity in both rodents and humans. We thus tested whether CB1R genetic variants affect responsiveness to exercise therapy. METHODS: We evaluated the effect of a genetic variant of the CB1R associated with reduced receptor expression (patients with long AAT trinucleotide short tandem repeats in the CNR1 gene) on long-term potentiation (LTP)–like cortical plasticity induced by transcranial magnetic theta burst stimulation (TBS) of the motor cortex and, in parallel, on clinical response to exercise therapy in patients with multiple sclerosis. RESULTS: We found that patients with long AAT CNR1 repeats do not express TBS-induced LTP-like cortical plasticity and show poor clinical benefit after exercise therapy. CONCLUSIONS: Our results provide the first evidence that genetic differences within the CB1R may influence clinical responses to exercise therapy, and they strengthen the hypothesis that CB1Rs are involved in the regulation of synaptic plasticity and in the control of spasticity in humans. This information might be of great relevance for patient stratification and personalized rehabilitation treatment programs. Lippincott Williams & Wilkins 2014-12-11 /pmc/articles/PMC4268035/ /pubmed/25520956 http://dx.doi.org/10.1212/NXI.0000000000000048 Text en © 2014 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-Noncommercial No Derivative 3.0 License, which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Article
Mori, Francesco
Ljoka, Concetta
Nicoletti, Carolina G.
Kusayanagi, Hajime
Buttari, Fabio
Giordani, Laura
Rossi, Silvia
Foti, Calogero
Centonze, Diego
CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
title CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
title_full CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
title_fullStr CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
title_full_unstemmed CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
title_short CB1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
title_sort cb1 receptor affects cortical plasticity and response to physiotherapy in multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268035/
https://www.ncbi.nlm.nih.gov/pubmed/25520956
http://dx.doi.org/10.1212/NXI.0000000000000048
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