Obesity is a complex and multifactorial disease representing a major public health challenge. Indeed, overweight and obese people carry a major risk of developing insulin resistance and type 2 diabetes mellitus. It has been demonstrated that polyphenols could be used to counteract some of the mechanisms involved in the generation of insulin resistance. The model of overfeeding represents a very good study model of the metabolic complications of obesity, since it has been shown to induce a transient state of insulin resistance in the human. The purpose of this research is to study the effects of a overfeeding (+50% of daily caloric needs over 31 days) with or without polyphenols supplementation (2g/days over 31 days) on insulin sensitivity measured in the setting of a hyperinsulinemic euglycemic clamp and on post prandial partitioning of exogenous lipids after a test meal. During 31 days, the volunteers will consume chocolate bars, chips, chocolate breads and cola in addition to their usual diet and will be supplemented with 2g of grape polyphenols extract or with placebo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Enrollment
42
Men will have to consume daily 2g of grape polyphenol extract during the 31 days of overfeeding.
Men will have to consume daily 2g of placebo during the 31 days of overfeeding.
Rhône Alpes Human Nutrition Center (CRNH Rhône-Alpes)
Pierre-Bénite, France
Peripheral insulin sensitivity
Volunteers will have peripheral and hepatic insulin sensitivity determined by using a two-stage hyperinsulinemic euglycemic clamp with stable isotopically labeled tracer infusion.
Time frame: During 31 days
Hepatic insulin sensitivity
Endogenous glucose production (EGP) will be determined during the last 30 minutes of the low-dose insulin infusion.
Time frame: before and after the 31 days of overfeeding
Change in genes expression in adipose and muscle tissues
RT-PCR
Time frame: Before and after the 31 days of overfeeding
Anthropometry, Fat quantification and Abdominal fat distribution
Weight, height, waist and hip circumferences, fat mass using dual x-ray absorptiometry (DEXA) and abdominal fat distribution using resonance magnetic imaging (RMI).
Time frame: During 31 days
Fasting and Postprandial partitioning of exogenous lipid
13C enrichment will be measured in blood samples and breath test during a test meal performed before and after the 31 days of overfeeding.
Time frame: Fasting and during all the postprandial period (0-300 minutes)
Modification in intestinal microbiota
Feces analyses
Time frame: Before and after the 31 days of overfeeding
Energy expenditure and substrate oxidation with indirect calorimetry
Energy metabolism will be measured before and after the 31 days of overfeeding.
Time frame: Fasting and during all the postprandial period (0-300 minutes)
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