Ketones are natural substances normally produced by the body during prolonged fasting and starvation, or in response to a "ketogenic" diet to be used as fuel by the brain and muscles. Ketones are therefore similar to dietary proteins, carbohydrates and fats since they represent a source of energy for the body. In addition to serving as a source of energy, ketones have also been shown to stimulate increased rates of muscle protein synthesis in humans. The ingestion of dietary protein is well established to stimulate an increase in the rate of protein synthesis in skeletal muscle. The rate of muscle protein synthesis can be maximized following the intake of 20g of protein. As a result, smaller doses of protein (i.e. 10g) represent a sub-optimal dose of protein because there is still room for improvement concerning muscle protein synthesis. Recently ketone-containing food products have become available that elevate ketone levels in the body without the need for ketogenic diets or prolonged fasting. Therefore, the purpose of this study is to measure skeletal muscle protein synthesis rates after ingesting the following: 1. Ketone monoester 2. Ketone monoester supplemented with sub-optimal dose of whey protein 3. Sub-optimal dose of whey protein It is hypothesized that muscle protein synthesis rates will increase following the ingestion of a ketone-containing beverage. Further, muscle protein synthesis rates will be enhanced when the ketone-containing beverage and sub-optimal protein dose are taken together.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
36
* Ketone monoester supplement (R)-3-hydroxybutyl (R)-3-hydroxybutyrate based on participants' body weight (0.36g/kg body weight) * Isocaloric carbohydrate control: dextrose + vanilla flavouring
* Ketone monoester supplement (R)-3-hydroxybutyl (R)-3-hydroxybutyrate based on participants' body weight (0.36g/kg body weight) * 10g Whey Protein * L-\[ring-2H5\]-phenylalanine tracer (enriched to 4%)
* Isocaloric carbohydrate control: dextrose + stevia * 10g Whey Protein * L-\[ring-2H5\]-phenylalanine tracer (enriched to 4%)
Exercise Metabolism and Nutrition Research Laboratory
Montreal, Quebec, Canada
Fractional synthetic rate of muscle protein synthesis (myofibrillar)
Time frame: 0-5 hours in the post-prandial period
Fractional synthetic rate of muscle protein synthesis (myofibrillar)
Time frame: 0-3 hours in the pre-prandial period; 0-2 hours, and 2-5 hours into the post-prandial period
Plasma enrichments (in moles percent excess) of L-[ring-2H5]-phenylalanine
Time frame: 3 hours pre-prandial to 5 hours post-prandial
Plasma glucose concentration (mmol/L)
Time frame: 3 hours pre-prandial to 5 hours post-prandial
Plasma insulin concentration (pmol/L)
Time frame: 3 hours pre-prandial to 5 hours post-prandial
Plasma amino acid concentrations (mmol/L)
Time frame: 3 hours pre-prandial to 5 hours post-prandial
Capillary blood Beta-OHB concentrations (mmol/L)
Time frame: 0-5 hours in the post-prandial period
Signaling molecule phosphorylation status
The use of Western blots to measure the phosphorylation status of signaling molecules involved in protein synthesis ie. mTOR, p70S6k, 4E-BP1
Time frame: 0, 2, and 5 hours into the post-prandial period
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