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Lemon Verbena Extract Oxidative Stress and Muscle Damage

Not Applicable
Completed
Conditions
Muscle Injury
Muscle Soreness
Interventions
Dietary Supplement: maltodextrin
Dietary Supplement: Lvemon verbena extract
Registration Number
NCT04742244
Lead Sponsor
National Taiwan Sport University
Brief Summary

In the present study, investigators investigated whether supplementation with lemon verbena extract (LVE) could improve muscle damage and biochemical indicators after exhaustive exercise challenge. Based on maximum jump heights, 60 subjects (30 males and 30 females) were equally divided into a placebo group (0 mg/human/day) and an LVE supplement group (400 mg/human/day), with gender-equal distribution. All subjects started supplementation 10 days before exhaustive exercise and continued it until all tests were completed. Before the intervention, after the exhaustive exercise, and on the following 3 days, the participants underwent 12-minute Cooper running/walking; blood collection; assessments of pain, muscle stiffness, maximum jump heights, and isometric maximum muscle strength; and anaerobic strength tests.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • health
  • Must be able to swallow tablets
Exclusion Criteria
  • non-smokers
  • no musculoskeletal
  • medical
  • metabolic disease
  • women not on the reproductive cycle
  • high blood pressure, asthma
  • skeletal neuromuscular injuries in the upper or lower extremities

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebomaltodextrin0 mg LVE/capsule, 2capsule/day, 14days
Lemon Verbena extractLvemon verbena extract200 mg LVE/capsule, 2capsule/day, 14days
Primary Outcome Measures
NameTimeMethod
Clinical Biochemistry of CK level10 days

To assess muscle damage, volunteers fasted for at least 8 hours before performing muscle exhaustion exercises. At designated time points in the recovery period, including baseline (0) and 3h, 24h, and 48 after exercise, blood samples were collected with brachial venous catheters. Serum CK (U/L), were assessed for monitoring physiological adaptation. All biochemical indices were assessed using an autoanalyzer (Hitachi 7060, Tokyo, Japan).

Assessment of muscle stiffness10 days

3 h, 24h, 48h after exhausting exercise, use Myoton machine to evaluate muscle stiffness (N/m) (Myoton, Tallinn, Estonia)

inflammation of IL-6 level10 days

To assess inflammation indicators, volunteers fasted for at least 8 hours before performing muscle exhaustion exercises. At designated time points in the recovery period, including baseline (0) and 3h, 24h, and 48 after exercise, blood samples were collected with brachial venous catheters. Assess serum IL-6 levels (pg/ml) to monitor physiological fitness. Used commercial kit human IL-6 immunoassay (R\&D system, Minnesota, USA) and Elisa reader (PerkinElmer, Massachusetts, USA) for analysis

Stress hormones 8-Hydroxy-2'-Deoxyguanosine (8-OHdG) in Urine10 days

Subjects' urine was collected 24 hours after the exhaustive exercise for analysis. Used commercial kit human 8-OHdG (Cayman, Mich, USA) and Elisa reader (PerkinElmer, Massachusetts, USA) for analysis

Visual Analogue Scale (VAS) evaluation10 days

3 h, 24h, 48h after exhausting exercise, use VAS questionnaire to record muscle pain. the minimum is 0 and maximum is 10, and whether higher scores mean more pain

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

National Taiwan Sport University

🇨🇳

Taoyuan, Taiwan

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