Metabolic Fate Modifications of Saturated Fats After an Overfeeding (SURNUT)
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Purpose
The purpose of this study is to determine the partitioning of exogenous lipids in the postprandial period while a study of overfeeding. The method is based on the incorporation of a stable isotopic tracer (d31_palmitic acid, d31_C16) in lipoprotein triglycerides (TG-CHYLOMICRON and TG-VLDL) and in free fatty acids (FFA).
| Condition | Intervention |
|---|---|
|
Obesity Lipid Metabolism Inflammation |
Dietary Supplement: Hyperlipidic overfeeding |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Basic Science |
| Official Title: | Metabolic Fate Modifications of Saturated Fats After an Overfeeding |
- Post prandial partitioning of exogenous lipids [ Time Frame: Before and after overfeeding ] [ Designated as safety issue: No ]
- Genes expression in adipose and muscle tissues [ Time Frame: Before and after overfeeding ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 40 |
| Study Start Date: | September 2005 |
| Study Completion Date: | March 2010 |
| Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
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Dietary Supplement: Hyperlipidic overfeeding
Healthy overweight and lean young men are subjected to an overfeeding during 56 days which corresponds to a supplement of 761 Kcal/day. During two exploration days (before : D0 et after : D56 overfeeding) they have ingested a breakfast with tracer (d31_palmitic acid, d31_C16, 20mg/kg) and blood and urine samples were collected every hour of each exploration day. The enrichment in deuterium was measured by gas chromatography-organic mass spectrometry (GC-OMS) in palmitic acid pool of lipid fractions.
Eligibility| Ages Eligible for Study: | 18 Years to 55 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- 18 to 55 years old
- BMI 18 to 30 kg/m²
- Stable physical activity
- Safety subject during medical consultation
Exclusion Criteria:
- Medical or surgical history which may affect energy expenditure (renal -cardiovascular -hepatic- endocrine-inflammatory diseases)
- Drug use that could affect energy expenditure (steroids, nicotine substitutes, thyroid hormones)
- Eating disorder
- Intensive sportive activity
- Subjects who Smoke
- Claustrophobic subjects
Contacts and Locations| France | |
| Centre de recherche en nutrition humaine Rhone-Alpes | |
| Pierre-Bénite, France, 69495 | |
| Study Director: | Martine Laville, PhD, MD | Centre de recherche en nutrition humaine Rhône-Alpes |
More Information
No publications provided by Centre de Recherche en Nutrition Humaine Rhone-Alpe
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Martine Laville PhD, MD, CRNHRA |
| ClinicalTrials.gov Identifier: | NCT00905892 History of Changes |
| Other Study ID Numbers: | CRNHRA-09-002 |
| Study First Received: | May 20, 2009 |
| Last Updated: | June 22, 2011 |
| Health Authority: | France: Direction Générale de la Santé |
Keywords provided by Centre de Recherche en Nutrition Humaine Rhone-Alpe:
|
overfeeding stable isotopes lipoprotein metabolism lipid oxidation |
fat distribution gene expression endotoxemia mass spectrometry/gas chromatography |
Additional relevant MeSH terms:
|
Inflammation Obesity Pathologic Processes Overnutrition |
Nutrition Disorders Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 23, 2013