Molecular Markers of Neuroplasticity During Exercise in People With Incomplete Spinal Cord Injury

NCT ID: NCT01538693

Last Updated: 2015-05-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-12-31
• Study Completion Date: 2015-05-31

Brief Summary

The purpose of this study is to determine whether exercising (walking) at different intensities increases levels of factors in the blood and saliva that are known to impact neuroplasticity (how the connections in the spinal cord and brain can change) and if these levels are changed by pairing exercise with a single dose of commonly used prescription drugs or by your mood.

Detailed Description

The protein brain-derived neurotrophic factor (BDNF) is known to promote cell survival, improve synaptic function, and induce neuronal morphological changes. Consequently, BDNF plays a major role in neuroplasticity and the ability of the central nervous system to adapt and recover following injury. Regardless of the molecular mechanisms by which this occurs (which are poorly understood), potentiating the expression of BDNF following spinal cord injury has been shown to improve functional outcomes in animals.(1, 2) It is well documented in both animal and human literature that the production BDNF increases with physical exercise in healthy populations and individuals with chronic disease or disability. (3) The literature suggests that this increase is proportional to the intensity of exercise, though the parameters of exercise to maximize this effect are poorly understood. (2, 4-6) From animal research, it has been postulated that serotonin (5HT) plays a role in the mechanism of increase in BDNF expression, (7-9) with findings that specifically demonstrate potentiation of the exercise-induced expression with antidepressant treatment(10)and a blunted response when monoaminergic signaling is blocked.(11) A specific genetic variation in the BDNF gene, found in approximately 30% of the population has also been noted as an important factor in the proper release of BDNF with associated deficits in motor learning. (12, 13) Initial evidence also suggests that this polymorphism may have an impact of the relationship between exercise and BDNF. (14, 15) The objective of this study is the evaluate the response of serum concentrations of brain-derived neurotrophic factor ([BDNF]s) to an acute bout of exercise in ambulatory people with incomplete spinal cord injury; additionally, to examine the effect of pharmacological agents that alter serotonergic (5HT) transmission on this exercise-induced change in [BDNF]s. To achieve this objective we will investigate [BDNF]s during a treadmill test alone and in combination with two commonly used medications; escitalopram oxalate , a selective-5HT reuptake inhibitor (SSRI) and cyproheptadine (CYPRO), a 5HT antagonist.

Studies have also shown a relationship of BDNF to mood, in particular, depression. A secondary study will be performed in parallel with the primary study with the purpose of examining mood and how it correlates with the molecular markers for neuroplasticity as individuals participate in the repeated exercise and the other stated interventions. As the subjects progress over the course of the study time mood may change and may impact the relationship of the BDNF to the primary interventions.

Conditions

Spinal Cord Injury

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

escitalopram oxalate

Exercise testing with escitalopram oxalate dose

Group Type: ACTIVE_COMPARATOR

escitalopram oxalate

Intervention Type: DRUG

10 mg 4.5 hours prior to testing

Graded intensity exercise

Intervention Type: OTHER

modified bruce protocol for peak oxygen consumption testing

cyproheptadine

exercise testing with cyproheptadine dose

Group Type: ACTIVE_COMPARATOR

Cyproheptadine

Intervention Type: DRUG

8mg 4.5 hours prior to testing

Graded intensity exercise

Intervention Type: OTHER

modified bruce protocol for peak oxygen consumption testing

placebo

exercise testing with placebo dose

Group Type: PLACEBO_COMPARATOR

sugar pill

Intervention Type: DRUG

4.5 hour prior to testing

Graded intensity exercise

Intervention Type: OTHER

modified bruce protocol for peak oxygen consumption testing

Interventions

escitalopram oxalate

10 mg 4.5 hours prior to testing

Intervention Type: DRUG

Cyproheptadine

8mg 4.5 hours prior to testing

Intervention Type: DRUG

sugar pill

4.5 hour prior to testing

Intervention Type: DRUG

Graded intensity exercise

modified bruce protocol for peak oxygen consumption testing

Intervention Type: OTHER

Other Intervention Names

Lexapro

Eligibility Criteria

Inclusion Criteria

• Must be motor incomplete spinal cord injury (ASIA C or D) of 1 year or greater duration, with anatomical lesions between C1-T10
• Must be between 18 and 75 years of age
• Must be ambulatory with passive range of motion consistent with normal walking, and must include: ankle dorsiflexion ankle to 10° and plantarflexion to 30°, knee flexion from 0 to 90°, hip flexion/extension to 90° to -10°.
• Must be medically stable with medical clearance to participate, with absence of concurrent severe medical illness including: unhealed decubiti, existing infection, significant cardiovascular or metabolic disease which limits exercise participation, significant osteoporosis (as indicated by history of fractures following injury), active heterotrophic ossification in the lower extremities, known history of peripheral nerve injury in lower legs, history of known traumatic head injury, mental illness, history of pre-existing QT interval prolongation, congenital long QT syndrome, and history of pulmonary complications, including significant obstructive and/or restrictive lung diseases
• May be undergoing concurrent physical therapy
• May be of childbearing potential (for women)
• Men and women will be recruited for participation in the proposed study at rates consistent with national and local average of gender disparities of SCI (80% male, 20% women)
• Individuals of different ethnicities will be recruited at rates similar to the national and local ethnicity rates. Current data since 2005 indicate that of the entire population of SCI, 66.1% are Caucasian, 27.1% are African American, 6.6% are of Hispanic origin, and 2.0% are Asian.

Exclusion Criteria

• Weighing more than 300lbs
• Ventilator-dependency
• Use of substantial orthopedic bracing to stabilize the cervical or thoracic vertebral column
• Inability to tolerate 10 minutes of standing without orthostasis (decrease in blood pressure by 20 mmHg systolic and 10 mmHg diastolic).
• Women who are pregnant or who are considering becoming pregnant will be excluded due to the trunk and pelvis restraints required for use during locomotion, and secondary to the unknown effects of the pharmacological agents on the developing fetus
• Exhibiting symptoms suggestive of depression according to the Personal health Questionaire (PHQ-9)
• Subjects who exhibit hemoglobin levels consistent with anemia (<13g/dL for men and <12g/dL for women) will be excluded from the study.
• Currently taking prescribed anti-depressant medications, including specific monoaminergic agents, their precursors or their agonists, antipsychotics, medications known to prolong the QT interval, or other medications with known interactions to the SSRIs. All subjects will be excluded from participation unless both attending physician and patient agree to cease all such medications during the evaluation and training period. A 14-day washout period for SSRIs and a 72 hour washout for Tizanidine will be utilized. Subjects will be financially responsible for the physician visits necessary to wean from medication. Completion of appropriate and safe weaning will be confirmed by the patients' physician.
• Currently taking prescribed anti-spastic medications. Specific agents to be excluded include baclofen (Lioresal®) and benzodiazepines (Diazepam®). Selected agents used for pain modulation will be evaluated per subject to ascertain potential interactions with test agent. All subjects will be excluded from participation unless both attending physician and patient agree to cease all such medications during the evaluation and training period. A 72-hour minimum washout period for all such medications will be utilized. Subjects will be financially responsible for the physician visits necessary to wean from medication. Completion of appropriate and safe weaning will be confirmed by the patients' physician.
• Clinically diagnosed liver, renal, or other metabolic disease that may interfere with drug action and/or clearance

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Medicine and Dentistry of New Jersey

OTHER

Sponsor Role: collaborator

Shirley Ryan AbilityLab

OTHER

Sponsor Role: collaborator

T. George Hornby

OTHER

Sponsor Role: lead

Responsible Party

T. George Hornby

Assistant Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Thomas G Hornby, PhD, PT

Role: PRINCIPAL_INVESTIGATOR

University of Illinois at Chicago, Rehabiliation Institute of Chicago, Northwestern University

Locations

Rehabiliation Institute of Chicago

Chicago, Illinois, United States

Countries

United States

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Other Identifiers

STU00056144

Identifier Type: -

Identifier Source: org_study_id