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Mitochondrial Energy Metabolism in Obese Women

Not Applicable
Completed
Conditions
Metabolism Disorder
Mitochondrial Alteration
Physical Activity
Obesity
Interventions
Other: Physical Training
Registration Number
NCT03119350
Lead Sponsor
University of Sao Paulo
Brief Summary

Considering that the failure of the treatment of obesity is justified by the multifactorial pathophysiology of this morbidity, the present project has the following hypotheses:

1. The occurrence of obesity is due to the derange,ent of mitochondrial energy metabolism ;

2. The unbalance is therapeutically modified through physical training ;

3. Obesity courses with the break-down in energy metabolism mitochondrial disease associated with systemic inflammatory characteristics that can be corrected through a combined long-term physical training program.

This study have as objective : to analyse changes in mitochondrial function, inflammatory profile, oxidative stress and energy metabolism caused by concurrent physical training in obese women.

Detailed Description

Specific objectives:

Body composition by deuterium oxide; Metabolic rate of resting and oxidation of substrates by indirect calorimetry; Proinflammatory cytokines Anti-inflammatory cytokines Oxidative Stress: Malondialdehyde, Superoxide Dismutase, Glutathione-Peroxidase; Fatty acids: ceramide and palmitate; Mitochondrial respiration and citrate synthase enzyme; Quantify and qualify: mitochondrial number, endoplasmic reticulum structure, adipose cell size; Gene expression, quantify by microscopy and analyze the protein by western blot.

The study began with 20 women, however, there was withdrawal of 6, ending with 14 women.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
14
Inclusion Criteria
  • This study included women with obesity (BMI of 30 to 40 kg / m²), sedentary, with no associated comorbidity, convenience sample
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Exclusion Criteria
  • Women who have undergone bariatric surgery, menopause, cancer or any metabolic disease, smokers, alcoholics, who are in use of drugs that act directly on the metabolism and that have medical impediment to the practice of physical exercise.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Physical TrainingPhysical TrainingThere was concurrent physical training intervention: strength and aerobic exercises in the same session. Duration: 2 weeks of adaptation and learning to exercise, 8 weeks of physical training. Frequency: 3 times per week Duration: 55 minutes each session. Intensity: 75 to 90% of maximum heart rate.
Primary Outcome Measures
NameTimeMethod
Changes inflammatory cytokinesTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Collected in lithium heparin tubes, they were centrifuged.

Changes Physical PerformanceTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Based on the Shuttle Walking Test adaptation.

Changes Telomere lengthTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

peripheral blood in ethylenediaminetetraacetic acid tubes and genomic DNA was automatically extracted from Peripheral Blood Mononuclear Cell. The relative quantification of Telomere length was determined using the telomere to single copy gene ratio by Quantitative Polymerase Chain Reaction (qPCR).

Changes in fatty acidsTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Collected in lithium heparin tubes, they were centrifuged.

Changes in total cholesterolTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Collected in lithium heparin tubes, they were centrifuged.

Changes in Determination of LactateTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Blood samples were collected by manual puncture of the earlobe in previously calibrated and heparinized capillary tubes, stored in eppendorf with sodium fluoride. Analyzed by electrochemical lactate analyser.

Changes Nitrogen BalanceTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Through the collection of urine of 24 hours the dosage of urinary nitrogen will be made by the chemiluminescence method for determination of protein nitrogen.

Changes Indirect calorimetryTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

With a gas analyzer (indirect calorimeter), we evaluated the metabolic rate and rest (REE) and oxidation of substrates (Lipids and carbohydrates).

Changes oxidative stressTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Collected in lithium heparin tubes, they were centrifuged.

Changes Food intakeTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Food registry of 3 days, the quantification of the daily intake of nutrients will still be made using software.

Changes Body weightTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

Body weight was measured by digital balance before and after the intervention

Changes Body compositionTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

The change in body composition through deuterium oxide was evaluated.

Changes White adipose tissue biopsyTwo times: (1) First day and (2) 10 weeks after adaptation and intervention

A subcutaneous tissue sample was collected for analysis of: mitochondrial respiration, citrate synthase enzyme, gene expression (UCP1, 2 and 3).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Camila Fernanda Cunha Brandão

🇧🇷

Ribeirao Preto, SP, Brazil

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