MNOP: Mirror Neurons in Older Participants
Study Details
Study Description
Brief Summary
A critical problem facing aging adults is muscle weakness. Whereas scientists have traditionally attributed the loss of muscle strength with aging to muscle atrophy, emerging evidence suggests that impairments in the neuromuscular system's ability to voluntarily generate force plays a more central role than previously appreciated. One area that has not yet been investigated includes the role that observing another's actions - thereby activating mirror neurons - plays in muscle force generation. Therefore, the purpose of this study is to examine the acute effects of action observation on muscular strength, voluntary muscle activation, and cortical excitability and inhibition in older adults.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
A critical problem facing aging adults is muscle weakness. Whereas scientists have traditionally attributed the loss of muscle strength with aging to atrophic effects, emerging evidence suggests that impairments in the neuromuscular system's ability to voluntarily generate force plays a more central role than previously appreciated. One area that has not yet been investigated includes the role that observing another's actions - thereby activating mirror neurons - plays in muscle force generation. Therefore, the purpose of this study is to examine the acute effects of action observation on muscular strength, voluntary activation, and cortical excitability and inhibition in older adults. Following a thorough familiarization visit, twenty-five men and women ≥60 years of age will complete three action observation sessions in a randomized, counterbalanced manner: 1) observation of very strong hand/wrist contractions, 2) observation of very weak hand/wrist contractions, and 3) a control condition. Maximal voluntary contractions (MVCs) of the wrist flexors will be performed before and after observation sessions. Percent voluntary activation will be determined via the interpolated twitch technique. Single-pulse transcranial magnetic stimulation (TMS) and electromyographic (EMG) recordings from the flexor carpi radialis and first dorsal interosseous will be used to quantify cortical excitability and inhibition, via motor evoked potential amplitude and silent period duration, respectively. The hypothesis of this study is that observation of strong muscle contractions will acutely increase muscle strength, and such changes will be facilitated by enhanced corticospinal excitability and decreased inhibition. In contrast, it is hypothesized that observation of very weak contractions will cause no such efforts or even acute muscle weakness. Collectively, we propose that manipulation of mirror neurons is a worthwhile strategy for clinicians hoping to induce neuromuscular adaptations in older adults, particularly in settings where movement of a joint is painful or infeasible (e.g., bedrest or immobilization).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: Muscle strength condition
|
Other: Action Observation
Strength, voluntary activation, and cortical responses to three conditions will be measured: 1) action observation of very strong, forceful contractions of the hand and wrist flexors 2) action observation of very weak, feeble contractions of the hand and wrist flexors 3) no action observation. Experimental conditions will be randomized and counterbalanced.
|
| Other: Muscle weakness condition
|
Other: Action Observation
Strength, voluntary activation, and cortical responses to three conditions will be measured: 1) action observation of very strong, forceful contractions of the hand and wrist flexors 2) action observation of very weak, feeble contractions of the hand and wrist flexors 3) no action observation. Experimental conditions will be randomized and counterbalanced.
|
| No Intervention: Control
|
Outcome Measures
Primary Outcome Measures
- Muscle Strength [5 minutes]
Isometric muscle strength of the non-dominant hand and wrist flexors will be assessed during maximal voluntary contractions (MVCs).
Secondary Outcome Measures
- Voluntary Activation [5 minutes]
Percent voluntary activation will be quantified during the MVCs to determine each participant's ability to maximally activate their wrist flexor muscles voluntarily.
- Corticospinal excitability [5 minutes]
Transcranial magnetic stimulation will be used to quantify corticospinal excitability throughout the study.
Eligibility Criteria
Criteria
Inclusion Criteria:
- Healthy men and women ≥60 years of age
Exclusion Criteria:
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Neuromuscular disease (e.g. Parkinson's, MS, ALS)
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Metabolic disease (e.g. diabetes, thyroid disorder, metabolic syndrome)
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Arthritis in the upper limbs (hands, arms, shoulders)
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Trouble using or controlling one's muscles
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History of cancer
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History of stroke
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History of heart attack
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Use of an assistive walking device or other mobility aids
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Physician mandated contraindication to exercise within the last 6 months
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Epilepsy or history of convulsions/seizures
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History of fainting or syncope
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History of head trauma that was diagnosed as concussion or was associated with loss of consciousness
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History of hearing problems or tinnitus
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Cochlear implants
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Implanted metal in the brain, skull, or elsewhere in the body
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Implanted neurotransmitter
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Cardiac pacemaker or intracardiac lines
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Medication infusion device
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Past problems with brain stimulation
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Past problems with MRI
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Use of muscle relaxants or benzodiazepines
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Allergy to rubbing alcohol
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Any other health related illnesses that would prohibit a participant from physical performance testing
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Lack of transportation to and from the laboratory
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UCF Neuromuscular Plasticity Laboratory | Orlando | Florida | United States | 32826 |
Sponsors and Collaborators
- University of Central Florida
Investigators
- Principal Investigator: Matt S. Stock, Ph.D., University of Central Florida
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- SBE-18-14657