Neuromuscular Electrical Stimulation Clinical Trial
Official title:
Can Branched Chain Amino Acids Supplementation Reduce Muscle Damage Induced by Neuromuscular Electrical Stimulation ? A Combined Functional and Metabolic Non-invasive Investigation in Healthy Humans.
Neuromuscular electrical stimulation (NMES) is commonly used in rehabilitation contexts in
order to increase or restore muscle capacities of hypoactive patients or patients with
articular trauma. Although this technique seems to be particularly adapted to muscle
rehabilitation, growing evidence is emerging regarding potential damaging effects of
electrically- induced isometric contractions in healthy humans. Recent studies have reported
a 10 to 30-fold increase in creatine kinase (CK) activity coupled to significantly increased
muscle soreness and impaired force production as a result of NMESs. On that basis, further
studies should be conducted on these deleterious effects which might limit the clinical
application of NMES.
Over the last decade, many studies paid attention to branched-chain amino acids (BCAA)
supplementation as a potential prophylactic/therapeutic approach. The rationale of this
approach is that BCAA might increase protein synthesis and reduce protein breakdown through
physiological mechanisms involving mTOR regulation pathway (mammalian Target of Rapamycin).
Additionally, BCAA could also be used as energetic substrate during exercise when glycogen
stores are depleted. Overall, previous results have supported the efficacy of BCAA
supplementation in attenuating muscle damage. Nevertheless, comprehensive studies
investigating the effect of amino acid supplementation on markers of muscle damage are still
scarce.
Magnetic resonance imaging (IRM) and phosphorus 31 magnetic resonance spectroscopy (31P-MRS)
are powerful non invasive tools allowing the exploration of skeletal muscle structure and
energy metabolism.
This ambitious project is devoted to the anatomical, functional and metabolic
characterization of BCAA supplementation after NMES using MRI and 31P-MRS. Various markers
of muscle damage, including maximal voluntary force production, T2 values and apparent
diffusion coefficient (obtained by MRI) and energy metabolism assessed at rest and during
exercise (using 31P-MRS), will be obtained before and after NMES. This project is of utmost
importance for improving our knowledge of anatomic, metabolic and functional events related
to BCAA supplementation in the context of exercise-induced muscle damage
Status | Completed |
Enrollment | 20 |
Est. completion date | January 2014 |
Est. primary completion date | June 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 35 Years |
Eligibility |
Inclusion Criteria: - Male - Between 18 and 35 years - Subjects will have to be unhurt: - Any general disease - Psychiatric disorders(confusions) - Any infectious, inflammatory, tumoral, vascular, degenerative or traumatic pathology - They will have to follow no chronic treatment - They will have to be unhurt of any history of alcoholism or drug addiction Exclusion Criteria: - Contraindications for an examination MRI - Suffering from claustrophobia - Having stimulating one cardiac, carriers of a system Holter, carriers of hook(staple) (clip) surgical metallic, carriers of a prosthesis or a metallic implant (or quite other metallic foreign bodies), carriers of a prosthesis dental (device), carriers of a hearing aid, carriers of an insulin pump - Having been hurt by pieces of shrapnel or lead - Having had a dislocation, a fracture or a recent surgical operation (less than 6 months before the inclusion) - Having followed a treatment with anti-inflammatory drugs during the last 3 months - Having followed a treatment with amino acids during the last 3 months - Having followed a treatment(processing) with anabolic steroids during the last 3 months - Having participated in a program of body-building of lower limbs during the last 6 months |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)
Country | Name | City | State |
---|---|---|---|
France | Assistance Publique Hopitaux de Marseille | Marseille |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique Hopitaux De Marseille |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | evaluation of the muscular responsiveness | 24 MONTHS | No | |
Secondary | evaluation of the effects of a supplementation in AAB | on the physiological aspects | 24 MONTTHS | No |
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