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The Association of Resistance Exercise With the Inflammasome Activation in Obesity Subjects

The Potential Role of Resistance Exercise on Inflammasome Activation and Cytokines Levels in Obese Subjects

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05482178
Enrollment
20
Registered
2022-08-01
Start date
2022-05-31
Completion date
2022-12-16
Last updated
2022-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Activity, Resistance Exercise, Inflammation, Obesity

Keywords

Resistance training, inflammasome, Obesity

Brief summary

The intervention study consist in 3 months of follow up to evaluate the effect of resistance exercise on NLRP3 and interleukin-18 (IL-18) gene expression, and IL-18 and IL-1b cytokines levels in obese subjects, due to, the current evidence has been suggested that aerobic physical exercise could reduce the low-grade chronic inflammation through the downregulation of the NLRP3 inflammasome in obesity subjects, however, there are not enough evidence with resistance protocol. The investigator randomized into two intervention groups: a) group with resistance exercise training plus hypocaloric diet, and b) group with hypocaloric diet. The blood sample was taken fasting at baseline and final intervention (3rd month). The serum was separated for biochemical analyzes and the quantification of cytokines levels. The RNA was obtained from leukocytes to expression assay.

Detailed description

Obesity is a metabolic condition with a high worldwide prevalence. It is characterized by low-grade chronic inflammation and high cytokines level as consequence of the excessive accumulation of adipose tissue. The NLRP3 protein is part of the NLRP3 inflammasome, a multiprotein complex related to inflammation and the risk of developing metabolic disorders. In this sense, the evidence has been suggested that physical exercise could reduce the inflammation through the downregulation of the NLRP3 inflammasome. The aim of this study is evaluate the effect of resistance exercise on NLRP3 and IL-18 gene expression and and IL-18 and IL-1b cytokines levels in obese subjects. This is an experimental study with 3 months of follow up. Participants were randomized into two intervention groups: a) group with resistance exercise plus hypocaloric diet, and b) group with hypocaloric diet. The exercise program was design by certified personal trained, and consisted in 3 phases: conditioning, development and maintenance. Dietary information was collect by validated retrospective questionnaires (24-hour record and 3-days dietary diary) and analyzed in Nutritionist Pro software. Body composition was evaluated by bioimpedance. The biochemical analyzes were performed on serum sample using spectrophotometry equipment. RNA was obtained from leukocytes from peripheral blood, cDNA synthesis was performed with a ThermoFisher kit, and the expression assay was performed by real-time polymerase chain reaction (PCR) using Taqman probes with the 2-ΔΔcq relative quantification method. Cytokines quantification were perform using a commercial ELISA kit. Statistical analysis will be using the Statistical Package for Social Sciences (SPSS v.25) software and a value of p\<0.05 will be considered statistically significant.

Interventions

BEHAVIORALResistance exercise training plus hypocaloric diet

The exercise program included 3 phases of progressive intervention: 1) Adaptation which included 3-4 days per week at 60% of maximum heart rate, 2) Development phase which included 5 days per week at 75-85% of maximum heart rate and the last one, 3) Maintenance phase which included 5 days per week at 75-90% of maximum heart rate. The control and follow up will be through text message exchanges at least once a week or as many as necessary. On the other hand, the diet intervention consisted a caloric restriction of 20% of total energy estimated with Mifflin formula. The nutrients distributions are 50% for carbohydrates, 20% for protein and 30% for lipids, ensuring a sufficient intake of fiber (\>25g per day).

The diet intervention consisted a caloric restriction of 20% of total energy estimated with Mifflin formula. The nutrients distributions are 50% for carbohydrates, 20% for protein and 30% for lipids, ensuring a sufficient intake of fiber (\>25g per day).

Sponsors

Elisa Barron-Cabrera
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Experimental

Eligibility

Sex/Gender
ALL
Age
25 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Both sex * Older than 25 years old * Women with waist circumference ≥ 80cm and men with ≥ 90cm * Subjects with BMI between 30 and 40 kg/m2

Exclusion criteria

* Subjects with diagnosis of metabolic alterations * Subjects with chronic pharmacological treatment * Subjects with anti-inflammatories drugs prescription

Design outcomes

Primary

MeasureTime frameDescription
NLRP3 gene expressionChange from baseline NLRP3 gene expression at 3 monthsAssay expression will be performed by real-time PCR using Taqman probes with the 2-ΔΔcq relative quantification method
IL-18 gene expressionChange from baseline IL-18 gene expression at 3 monthsAssay expression will be performed by real-time PCR using Taqman probes with the 2-ΔΔcq relative quantification method
IL-18 cytokineChange from baseline IL-18 cytokine at 3 monthscommercial ELISA kit
IL-1b cytokineChange from baseline IL-1b cytokine at 3 monthscommercial ELISA kit

Secondary

MeasureTime frameDescription
WeightChange from baseline weight at 3 monthsWeighing machine using bioimpedance technology
Body fat massChange from baseline body fat mass at 3 monthsWeighing machine using bioimpedance technology
Serum triglyceridesChange from baseline serum triglycerides at 3 monthsLiquid chemistry using spectrum equipment
Serum cholesterolChange from baseline serum cholesterol at 3 monthsLiquid chemistry using spectrum equipment
Serum glucoseChange from baseline serum glucose at 3 monthsLiquid chemistry using spectrum equipment

Countries

Mexico

Contacts

Primary ContactMelissa Vega, PhD
melissa.vega@uas.edu.mx+526677545353
Backup ContactMarcela Vergara, PhD
mjvergara@uas.edu.mx+526677545353

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026