Unbound MEDLINE

Protein intake induced an increase in exercise stimulated fat oxidation during stable body weight.

Abstract

BACKGROUND
Protein-rich weight-loss diets spare fat-free mass at the cost of fat mass. The objective was to examine if there is a change in stimulated fat oxidation related to protein intake during stable body weight.
METHODS
Subjects' (BMI 22±2kg/m(2), age 25±8 years) maximal fat oxidation (Fat(max)) was assessed during a graded bicycle test, before and after a 3-month dietary-intervention of 2MJ/day supplements exchanged with 2MJ/d of habitual energy intake. The parallel design consisted of protein-rich supplements in the protein group and an isocaloric combination of carbohydrate and fat supplements in the control group. Daily protein intake was determined according to 24-h urine nitrogen. Body composition was measured according to a 4-compartment model by a combination of underwater-weighing technique, deuterium-dilution technique and whole-body dual-energy X-ray absorptiometry (DXA).
RESULTS
Subjects were weight stable and did not change their physical activity. The protein group (n=12) increased protein intake (11±14g, P<0.05) and had significantly higher daily protein intake vs. control (n=4) (80±21 vs.59±11g, P<0.05). Fat(max) increased significantly in the protein group (0.08±0.08g/min, P<0.01). Fat-free mass increased independent of change in body weight (P<0.01), and fat mass and fat percentage decreased (P<0.05). Change in Fat(max) was a function of change in protein intake (r=0.623, P<0.05), and not of changes in body composition or VO(2)max.
CONCLUSION
Increased stimulated fat oxidation was related to increased protein intake.

Links

  • Publisher Full Text
  • Authors

    Soenen S, Plasqui G, Smeets AJ, Westerterp-Plantenga MS

    Source

    Physiology & behavior 101:5 2010 Dec 2 pg 770-4

    MeSH

    Absorptiometry, Photon
    Adult
    Body Composition
    Body Weight
    Dietary Proteins
    Energy Intake
    Exercise
    Fats
    Humans

    Pub Type(s)

    Journal Article
    Randomized Controlled Trial
    Research Support, Non-U.S. Gov't

    Language

    eng

    PubMed ID

    20826169