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Cortical Excitability, Cognitive Functions, and Peripheral Signaling Molecules

Not Applicable
Completed
Conditions
Healthy
Interventions
Behavioral: Exercise
Registration Number
NCT05689606
Lead Sponsor
Ankara City Hospital Bilkent
Brief Summary

It is widely known that exercise creates structural and functional changes in the brain. Synaptic plasticity develops through exercise, thus improving brain functions. It is suggested that skeletal muscle contraction and peripheral signal molecules secreted from various tissues, especially skeletal muscle, contribute to exercise's effect on the brain's structure and function. These signals synthesized and released from skeletal muscle are called myokines. Brain-derived neurotrophic factor (BDNF) and Cathepsin B are two of these myokines, which have been reported to cross the blood-brain barrier following secretion in the periphery and affect the structure and functions of the brain. Transcranial magnetic stimulation (TMS) allows to evaluate the synaptic plasticity responses of the motor cortex to exercise, while cognitive function responses are evaluated via cognitive tests. Additionally, exercise type and intensity influence the responses of cortical excitability and cognitive function. This research proposal aims to investigate how acute high-intensity intermittent exercise (HIIT) changes primary motor cortex (M1) excitability, M1-related cognitive functions, and peripheral BDNF and Cathepsin B levels in healthy sedentary adults and to investigate the relationship between these neurophysiological parameters. All parameters will be measured before and after the acute exercise. M1 excitability will be evaluated through resting motor threshold, short interval intracortical inhibition, and input-output curve measurements. Cognitive functions will be evaluated through mental rotation and working memory tasks, and peripheral signal responses will be measured by serum levels of BDNF and Cathepsin B. Our hypotheses are: 1) Acute HIIT will increase peripheral BDNF and CTSB level, cortical excitability, and M1-specific cognitive function performance. 2) M1 excitability, cognitive function performance, and peripheral BDNF and CTSB increase will be related following exercise. Our findings will have the potential to be a guide for the integration of exercise into daily life and will provide cortical and peripheral data on the neurophysiological basis of the relationship between exercise and cognition.

Detailed Description

Participants Twenty-eight healthy young adults (female\|male:14\|14) aged 20-30 years will have participated in the study.

Participants will be at least undergraduate students, right-handed dominant, exercising \<150 minutes per week in the last six months. Before the experiment, the participants will be evaluated for their background, family history, and whether they have any health complaints that prevent them from exercising.

With the adult transcranial magnetic stimulation safety screening questionnaire, participants in the risk group for brain stimulation, those with intracranial implants and contraindications, and those with a history of any psychiatric or neurological disease, seizures, any serious medical condition, or pregnancy will be excluded. The hand preference questionnaire will evaluate hand preference, and physical activity status will be evaluated by the short version of the international physical activity questionnaire. The cardiorespiratory fitness will be assessed with the graded maximal exercise stress test. The N-back test is a continuous performance test used to assess working memory capacity. The mental rotation test will evaluate the mental rotation score. The research team designed both tests.

Transcranial magnetic stimulation will be used to assess corticomotor excitability. Resting Motor Threshold (RMT), Short Interval Intracortical Inhibition (SICI), and input-output curve measurements will be performed on all participants in our study for the TMS study.

BDNF and CTSB measurements of the participants will be made both at baseline and following the acute exercise.

HIIT exercise lasting 23 minutes will be performed on the bicycle ergometer. Participants will make 3 visits to the laboratory. First session: Cardiorespiratory fitness assessment, all questionnaires. Second session: TMS analyses, cognitive assessments, HIIT, myokine assessments Third session: TMS analyses, cognitive assessments, control (watching a nature documentary).

The second and third sessions will be performed by cross-over design. Data analysis will be performed with two-way repeated ANOVA to determine the effect of within-group factors (control and HIIT) and time (PRE and POST) on corticospinal excitability and other parameters. When the effect size was calculated as ɳp2 \>0.26, the sample size was calculated a priori as n = 22. Considering possible data losses, the number of participants was determined as 28.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
23
Inclusion Criteria
  • Being right-handed
  • Aged between 20 and 30 years
  • Being sedentary
Exclusion Criteria
  • having intracranial implants
  • history of psychiatric or neurological disease, seizure, any serious medical condition or pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Exercise groupExerciseThe exercise group performs acute high-intensity interval training.
Primary Outcome Measures
NameTimeMethod
Short interval intracortical inhibitionChange from Baseline short interval intracortical inhibition immediately following acute exercise

The relative amplitude reduction of motor evoked potentials by subthreshold conditioning stimuli.

Input output curveChange from Baseline input output curve immediately following acute exercise

The input-output curve is a sigmoid-shaped relation between the MEP amplitude at incremented TMS intensities. Higher scores mean a better outcome.

Serum BDNFChange from Baseline serum BDNF immediately following acute exercise

Serum level of BDNF. Higher scores mean a better outcome.

Mental rotationChange from Baseline mental rotation score immediately following acute exercise

The ability to transform a mental representation of an object so as to accurately predict how the object would look from a different angle. Higher scores mean a better outcome.

Working memoryChange from Baseline working memory score immediately following acute exercise

The small amount of information that can be held in mind and used in the execution of cognitive tasks. Higher scores mean a better outcome.

Resting motor thresholdChange from Baseline resting motor threshold immediately following acute exercise

The amount of transcranial magnetic stimulation machine output necessary to produce a motor-evoked potential that exceeds a defined peak-to-peak amplitude. Lower scores mean a better outcome.

Serum Cathepsin BChange from Baseline serum Cathepsin B immediately following acute exercise

Serum level of Cathepsin B. Higher scores mean a better outcome.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ankara City Hospital

🇹🇷

Ankara, Turkey

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