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Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults

Homoeostatic metaplasticity is a neuroprotective physiological feature that counterbalances Hebbian forms of plasticity to prevent network destabilization and hyperexcitability. Recent animal models highlight dysfunctional homoeostatic metaplasticity in the pathogenesis of Alzheimer’s disease. Howev...

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Autores principales: Sundman, Mark H, Lim, Koeun, Ton That, Viet, Mizell, Jack-Morgan, Ugonna, Chidi, Rodriguez, Rudolph, Chen, Nan-Kuei, Fuglevand, Andrew J, Liu, Yilin, Wilson, Robert C, Fellous, Jean-Marc, Rapcsak, Steven, Chou, Ying-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750948/
https://www.ncbi.nlm.nih.gov/pubmed/33376989
http://dx.doi.org/10.1093/braincomms/fcaa203
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author Sundman, Mark H
Lim, Koeun
Ton That, Viet
Mizell, Jack-Morgan
Ugonna, Chidi
Rodriguez, Rudolph
Chen, Nan-Kuei
Fuglevand, Andrew J
Liu, Yilin
Wilson, Robert C
Fellous, Jean-Marc
Rapcsak, Steven
Chou, Ying-Hui
author_facet Sundman, Mark H
Lim, Koeun
Ton That, Viet
Mizell, Jack-Morgan
Ugonna, Chidi
Rodriguez, Rudolph
Chen, Nan-Kuei
Fuglevand, Andrew J
Liu, Yilin
Wilson, Robert C
Fellous, Jean-Marc
Rapcsak, Steven
Chou, Ying-Hui
author_sort Sundman, Mark H
collection PubMed
description Homoeostatic metaplasticity is a neuroprotective physiological feature that counterbalances Hebbian forms of plasticity to prevent network destabilization and hyperexcitability. Recent animal models highlight dysfunctional homoeostatic metaplasticity in the pathogenesis of Alzheimer’s disease. However, the association between homoeostatic metaplasticity and cognitive status has not been systematically characterized in either demented or non-demented human populations, and the potential value of homoeostatic metaplasticity as an early biomarker of cognitive impairment has not been explored in humans. Here, we report that, through pre-conditioning the synaptic activity prior to non-invasive brain stimulation, the association between homoeostatic metaplasticity and cognitive status could be established in a population of non-demented human subjects (older adults across cognitive spectrums; all within the non-demented range). All participants (n = 40; age range, 65–74, 47.5% female) underwent a standardized neuropsychological battery, magnetic resonance imaging and a transcranial magnetic stimulation protocol. Specifically, we sampled motor-evoked potentials with an input/output curve immediately before and after repetitive transcranial magnetic stimulation to assess neural plasticity with two experimental paradigms: one with voluntary muscle contraction (i.e. modulated synaptic activity history) to deliberately introduce homoeostatic interference, and one without to serve as a control condition. From comparing neuroplastic responses across these experimental paradigms and across cohorts grouped by cognitive status, we found that (i) homoeostatic metaplasticity is diminished in our cohort of cognitively impaired older adults and (ii) this neuroprotective feature remains intact in cognitively normal participants. This novel finding suggests that (i) future studies should expand their scope beyond just Hebbian forms of plasticity that are traditionally assessed when using non-invasive brain stimulation to investigate cognitive ageing and (ii) the potential value of homoeostatic metaplasticity in serving as a biomarker for cognitive impairment should be further explored.
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spelling pubmed-77509482020-12-28 Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults Sundman, Mark H Lim, Koeun Ton That, Viet Mizell, Jack-Morgan Ugonna, Chidi Rodriguez, Rudolph Chen, Nan-Kuei Fuglevand, Andrew J Liu, Yilin Wilson, Robert C Fellous, Jean-Marc Rapcsak, Steven Chou, Ying-Hui Brain Commun Original Article Homoeostatic metaplasticity is a neuroprotective physiological feature that counterbalances Hebbian forms of plasticity to prevent network destabilization and hyperexcitability. Recent animal models highlight dysfunctional homoeostatic metaplasticity in the pathogenesis of Alzheimer’s disease. However, the association between homoeostatic metaplasticity and cognitive status has not been systematically characterized in either demented or non-demented human populations, and the potential value of homoeostatic metaplasticity as an early biomarker of cognitive impairment has not been explored in humans. Here, we report that, through pre-conditioning the synaptic activity prior to non-invasive brain stimulation, the association between homoeostatic metaplasticity and cognitive status could be established in a population of non-demented human subjects (older adults across cognitive spectrums; all within the non-demented range). All participants (n = 40; age range, 65–74, 47.5% female) underwent a standardized neuropsychological battery, magnetic resonance imaging and a transcranial magnetic stimulation protocol. Specifically, we sampled motor-evoked potentials with an input/output curve immediately before and after repetitive transcranial magnetic stimulation to assess neural plasticity with two experimental paradigms: one with voluntary muscle contraction (i.e. modulated synaptic activity history) to deliberately introduce homoeostatic interference, and one without to serve as a control condition. From comparing neuroplastic responses across these experimental paradigms and across cohorts grouped by cognitive status, we found that (i) homoeostatic metaplasticity is diminished in our cohort of cognitively impaired older adults and (ii) this neuroprotective feature remains intact in cognitively normal participants. This novel finding suggests that (i) future studies should expand their scope beyond just Hebbian forms of plasticity that are traditionally assessed when using non-invasive brain stimulation to investigate cognitive ageing and (ii) the potential value of homoeostatic metaplasticity in serving as a biomarker for cognitive impairment should be further explored. Oxford University Press 2020-11-27 /pmc/articles/PMC7750948/ /pubmed/33376989 http://dx.doi.org/10.1093/braincomms/fcaa203 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Sundman, Mark H
Lim, Koeun
Ton That, Viet
Mizell, Jack-Morgan
Ugonna, Chidi
Rodriguez, Rudolph
Chen, Nan-Kuei
Fuglevand, Andrew J
Liu, Yilin
Wilson, Robert C
Fellous, Jean-Marc
Rapcsak, Steven
Chou, Ying-Hui
Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
title Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
title_full Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
title_fullStr Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
title_full_unstemmed Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
title_short Transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
title_sort transcranial magnetic stimulation reveals diminished homoeostatic metaplasticity in cognitively impaired adults
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750948/
https://www.ncbi.nlm.nih.gov/pubmed/33376989
http://dx.doi.org/10.1093/braincomms/fcaa203
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