Evidence for a Window of Enhanced Plasticity in the Human Motor Cortex Following Ischemic Stroke

Author:

Hordacre Brenton1ORCID,Austin Duncan2,Brown Katlyn E.2,Graetz Lynton3,Pareés Isabel45,De Trane Stefania678,Vallence Ann-Maree91011,Koblar Simon312,Kleinig Timothy312,McDonnell Michelle N.13,Greenwood Richard8,Ridding Michael C.1,Rothwell John C.2

Affiliation:

1. IIMPACT in Health, Allied Health and Human Performance, University of South Australia, Adelaide, South Australia, Australia

2. UCL Institute of Neurology, London, UK

3. The University of Adelaide, Adelaide, South Australia, Australia

4. Hospital Universitario Ramón y Cajal, Madrid, Spain

5. Hospital Ruber Internacional, Madrid, Spain

6. Queen Mary University of London, London, UK

7. The Royal London Hospital, Barts Health NHS Trust, London, UK

8. National Hospital for Neurology and Neurosurgery, London, UK

9. Discipline of Psychology, College of Science, Health, Engineering, and Education, Murdoch University, Australia

10. Centre for Healthy Ageing, Health Futures Institute, Murdoch University, Australia

11. Centre for Molecular Medicine and Innovative Therapeutics, Health Futures Institute, Murdoch University, Australia

12. Royal Adelaide Hospital, Adelaide, South Australia, Australia

13. The Physio Clinic, Adelaide, South Australia, Australia

Abstract

Background In preclinical models, behavioral training early after stroke produces larger gains compared with delayed training. The effects are thought to be mediated by increased and widespread reorganization of synaptic connections in the brain. It is viewed as a period of spontaneous biological recovery during which synaptic plasticity is increased. Objective To look for evidence of a similar change in synaptic plasticity in the human brain in the weeks and months after ischemic stroke. Methods We used continuous theta burst stimulation (cTBS) to activate synapses repeatedly in the motor cortex. This initiates early stages of synaptic plasticity that temporarily reduces cortical excitability and motor-evoked potential amplitude. Thus, the greater the effect of cTBS on the motor-evoked potential, the greater the inferred level of synaptic plasticity. Data were collected from separate cohorts (Australia and UK). In each cohort, serial measurements were made in the weeks to months following stroke. Data were obtained for the ipsilesional motor cortex in 31 stroke survivors (Australia, 66.6 ± 17.8 years) over 12 months and the contralesional motor cortex in 29 stroke survivors (UK, 68.2 ± 9.8 years) over 6 months. Results Depression of cortical excitability by cTBS was most prominent shortly after stroke in the contralesional hemisphere and diminished over subsequent sessions ( P = .030). cTBS response did not differ across the 12-month follow-up period in the ipsilesional hemisphere ( P = .903). Conclusions Our results provide the first neurophysiological evidence consistent with a period of enhanced synaptic plasticity in the human brain after stroke. Behavioral training given during this period may be especially effective in supporting poststroke recovery.

Funder

National Health and Medical Research Council

Medical Research Council

Australian Research Council

The Stroke Association UK

Natural Science and Engineering Council of Canada

Publisher

SAGE Publications

Subject

General Medicine

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