Obesity
Conditions
Keywords
nicotinic acid, lipolysis, training program, adipose tissue inflammation, obese
Brief summary
Our working hypothesis postulates that lipolysis is a determinant of inflammation in adipose tissue (AT). Inhibition of lipolysis, e.g. using the oldest normolipidemic drug, nicotinic acid, has proved valuable to combat the metabolic syndrome. Our proposal will determine whether part of the beneficial effects of this antilipolytic compound is due to a diminution of AT inflammation. To this aim, the effect of nicotinic acid or placebo will be studied in male obese subjects with or without a training program which goal is to enhance lipolysis.
Detailed description
24 male obese insulin resistant subjects will receive nicotinic acid or placebo for 16 weeks. The last 8 weeks, the subjects will follow a training program calculated to optimize use of lipid. Insulin sensitivity and glucose tolerance will be assessed using, respectively, fasting-based estimates of insulin sensitivity (plasma and muscle) and oral glucose tolerance test. Plasma parameters of adipokines and, inflammatory and metabolic parameters will be determined. As an index of AT inflammation, the percentage and the phenotype of macrophages will be determined using flow cytometry of cells of the stromavascular fraction of subcutaneous AT. Macrophage infiltration will be investigated by light microscopy. The characterization of the inflammatory profile of AT will be completed by measurements of the expression of genes that are either specific markers of human AT macrophages or inflammatory and anti-inflammatory adipokines. This combination of approaches has never been carried out during a pharmacological intervention in humans. The following points will be addressed: * determine the influence of lipolysis on AT inflammation, specifically on macrophage activation and adipokine production. * examine the causal relationship between adipocyte FA metabolism, AT inflammation and insulin sensitivity. * establish whether the beneficial effect of antilipolytic drugs may be attributable at least in part to a decrease in AT inflammation.
Interventions
BEHAVIORALtraining
the last 8 weeks, the subjects will follow a training program calculated to optimize use of lipid
DRUGnicotinic acid
Obese subjects will receive nicotinic acid or placebo for 16 weeks
DRUGPlacebo
Obese subjects will receive nicotinic acid or placebo for 16 weeks
Sponsors
University Hospital, Toulouse
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
MALE
Age
25 Years to 45 Years
Healthy volunteers
No
Inclusion criteria
* Signature of informed consent form * Age 25 to 45 year-old * Male, insulin resistant obese subjects (30\<BMI\<40 kg/m2), * Blood arterial pressure\<140/90 mmHg
Exclusion criteria
* History of cardiovascular disease * Treatment with drugs which can interfere with cardiovascular system and autonomic nervous system (i.e. beta blockers). * Treatment with nicotinic acid * Treatment with fibrates, statins, cholestyramine and ezetimibe * Treatment with thiazidics * Fasted hyperglycaemia \> 1,26 g/l (Diabetes) * Triglycerides \>5 g/l * Blood arterial pressure \> 140/90 mm Hg
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of changes of AT inflammation will be measured by gene expression analysis | Visit 1(T0), Visit 2 (T+8 weeks of treatment) and Visit 3 (T+16 weeks of treatment) |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of changes in insulin sensitivity and glucose tolerance | Visit 1(T0), Visit 2 (T+8 weeks of treatment) and Visit 3 (T+16 weeks of treatment) |
Countries
France
Outcome results
None listed