Demonstration of the Prebiotic-like Effects of Camu-camu Consumption Against Obesity-related Disorders in Humans
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Overweight
- Sponsor
- Laval University
- Enrollment
- 35
- Locations
- 1
- Primary Endpoint
- Change in Gut Microbiota Composition and Diversity
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
Previous work of the investigators demonstrated the anti-obesity and anti-steatosis potential of the Amazonian fruit camu-camu (CC) in a mouse model of diet-induced obesity [1]. It was demonstrated that the prebiotic role of CC was directly linked to higher energy expenditure stimulated by the fruit since fecal transplantation from CC-treated mice to germ-free mice was sufficient to reproduce the effects.
The full protection against hepatic steatosis observed in CC-treated mice is of particular importance since nonalcoholic fatty liver disease (NAFLD) is one of the most common causes of chronic liver disease. Thirty percent of adults in developed countries have excess fat accumulation in the liver, and this figure can be as high as 80% in obese subjects. NAFLD is an umbrella term encompassing simple steatosis, as well as non-alcoholic steatohepatitis which can lead to cirrhosis and hepatocellular carcinoma in up to 20% of cases. Up to now, except for lifestyle changes, no effective drug treatment are available. Previous work has suggested that CC possesses anti-inflammatory properties and could acutely reduce blood pressure and glycemia after a single intake. While CC could represent a promising treatment for obesity and fatty liver, no studies have thoroughly tested this potential in humans. Therefore, a robust clinical proof of concept study is needed to provide convincing evidence for a microbiome-based therapeutic strategy to counteract obesity and its associated metabolic disorders.
The mechanism of action of CC could involve bile acid (BA) metabolism. BA are produced in the liver and metabolized in the intestine by the gut microbiota. Conversely, they can modulate gut microbial composition. BA and particularly, primary BA, are powerful regulators of metabolism. Indeed, mice treated orally with the primary BA α, β muricholic (αMCA, βMCA) and cholic acids (CA) were protected from diet-induced obesity and hepatic lipid accumulation. Interestingly, the investigators reported that administration of CC to mice increased the levels of αMCA, βMCA and CA. Primary BA are predominantly secreted conjugated to amino acids and that deconjugation rely on the microbial enzymatic machinery of gut commensals. The increased presence of the deconjugated primary BA in CC-treated mice indicate that a cluster of microbes selected by CC influence the BA pool composition. These data therefore point to an Interplay between BA and gut microbiota mediating the health effects of CC.
Polyphenols and in particular procyanidins and ellagitannins in CC can also be responsible for the modulation of BA that can impact on the gut microbiota. Indeed, it has been reported that ellagitannins containing food like walnuts modulate secondary BA in humans whereas procyanidins can interact with farnesoid X receptors and alter BA recirculation to reduce hypertriglyceridemia. These effects are likely mediated by the remodeling of the microbiota by the polyphenols.
In accordance with the hypothesis that the ultimate effect of CC is directly linked to a modification of the microbiota, fecal transplantation from CC-treated mice to germ-free mice was sufficient to recapitulate the lower weight gain and the higher energy expenditure seen in donor mice.
Investigators
André Marette
Professor
Laval University
Eligibility Criteria
Inclusion Criteria
- •BMI between 25 and 40 kg/m2
- •Fasting triglyceride \> 1,35 mmol/L
- •Understanding of spoken and written french
- •Accept to follow study instructions
Exclusion Criteria
- •Medication affecting glucose metabolism, blood lipid levels or blood pressure
- •Metabolic disorders requiring treatment
- •Diabetic subjects presenting HbA1c \>6.5% or fasting glycemia \>7 mmol/L
- •Consumption of fruit or polyphenol supplements in the last 3 months
- •Allergy or intolerance for camu camu or for an ingredient of the placebo
- •Alcohol consumption of \> 2 drinks / day
- •Weight change \> 5% of body weight in the last 3 months
- •Major surgical operation in the last 3 months or planned in the next months
- •Pregnant or breastfeeding women or women planning pregnancy in the next months
- •Antibiotics intake in the last 3 months
Outcomes
Primary Outcomes
Change in Gut Microbiota Composition and Diversity
Time Frame: Change between the beginning and the end of each treatment (12 weeks each)
Global variation of the fecal microbiota
Change in fat accumulation in the liver
Time Frame: Change between the beginning and the end of each treatment (12 weeks each)
Evaluation of fat accumulation by magnetic resonance imaging (MRI)
Secondary Outcomes
- Change in Endotoxemia(Change between the beginning and the end of each treatment (12 weeks each))
- Change in gut health(Change between the beginning and the end of each treatment (12 weeks each))
- Change in stool consistency(Change between the beginning and the end of each treatment (12 weeks each))
- Change in Glucose homeostasis(Change between the beginning and the end of each treatment (12 weeks each))
- Change in anthropometric measurements(Change between the beginning and the end of each treatment (12 weeks each))
- Change in chronic inflammation(Change between the beginning and the end of each treatment (12 weeks each))
- Change in gene expression levels(Change between the beginning and the end of each treatment (12 weeks each))
- Change in Inflammation state of the tissue(Change between the beginning and the end of each treatment (12 weeks each))
- Change in Lipid profile(Change between the beginning and the end of each treatment (12 weeks each))
- Change in body composition(Change between the beginning and the end of each treatment (12 weeks each))
- Change in Intestinal permeability(Change between the beginning and the end of each treatment (12 weeks each))
- Change in Short chain and branched chain fatty acids in the feces(Change between the beginning and the end of each treatment (12 weeks each))
- Change in camu camu-derived metabolites present in stool(Change between the beginning and the end of each treatment (12 weeks each))
- Change in blood pressure(Change between the beginning and the end of each treatment (12 weeks each))
- Change in circulating levels of plasma metabolites(Change between the beginning and the end of each treatment (12 weeks each))
- Change in liver health(Change between the beginning and the end of each treatment (12 weeks each))