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High-fat feeding inhibits exercise-induced increase in mitochondrial respiratory flux in skeletal muscle.

Journal of applied physiology (Bethesda, Md. : 1985)
June 1, 2011
Mette Skovbro et al. (5 authors)
Journal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine the effects of a high-fat diet on mitochondrial function, exercise-induced respiratory changes, and insulin sensitivity in healthy untrained males.

Results Summary

The high-fat diet altered mitochondrial electron transport system protein content and exercise-induced substrate oxidation rates, but did not affect insulin sensitivity or intramyocellular lipid accumulation. Exercise-induced increases in mitochondrial respiration were abolished in the high-fat diet group, though lipid substrate oxidation remained elevated post-exercise.

Population

21 healthy untrained male subjects

Effective Dosage

55-60% fat, 25-30% carbohydrate, 15% protein (isocaloric, tailored to energy expenditure)

Duration

2.5 weeks

Interactions

None mentioned

Extracted Claims (14)
InterventionDirectionEndpointPopulationDosageImpactClaim #
high-fat diet (HFD)
decrease
exercise-induced increase in state 3 (glycolytic substrates) and uncoupled respiration
healthy untrained male subjects
-
abolished
#1
high-fat diet (HFD)
decrease
complex I protein expression
healthy untrained male subjects
-
decreased
#2
high-fat diet (HFD)
decrease
complex IV protein expression
healthy untrained male subjects
-
decreased
#3
high-fat diet (HFD)
decrease
mitochondrial electron transport system protein content
healthy untrained male subjects
-
induced marked changes
#4
high-fat diet (HFD)
decrease
exercise-induced mitochondrial substrate oxidation rates
healthy untrained male subjects
-
induced marked changes
#5
high-fat diet (HFD)
increase
respiratory rate at recovery with a lipid substrate (octanoyl-carnitine with or without ADP)
healthy untrained male subjects
-
elevated
#6
high-fat diet (HFD)
no change
insulin sensitivity (hyperinsulinemic-euglycemic clamp)
healthy untrained male subjects
-
did not change
#7
high-fat diet (HFD)
no change
intramyocellular triacylglycerol content
healthy untrained male subjects
-
did not change
#8
high-fat diet (HFD)
no change
insulin resistance
healthy untrained male subjects
-
does not cause
#9
normal diet (ND)
no change
insulin sensitivity (hyperinsulinemic-euglycemic clamp)
healthy untrained male subjects
-
did not change
#10
normal diet (ND)
no change
intramyocellular triacylglycerol content
healthy untrained male subjects
-
did not change
#11
bicycle exercise
increase
state 3 (glycolytic substrates) respiration
healthy untrained male subjects
31 ± 11%
increase
#12
bicycle exercise
increase
uncoupled respiration
healthy untrained male subjects
26 ± 9%
increase
#13
bicycle exercise
increase
respiratory rate with a lipid substrate (octanoyl-carnitine with or without ADP)
healthy untrained male subjects
31-62%
increases
#14
Abstract

Twenty one healthy untrained male subjects were randomized to follow a high-fat diet (HFD; 55-60E% fat, 25-30E% carbohydrate, and 15E% protein) or a normal diet (ND; 25-35E% fat, 55-60E% carbohydrate, and 10-15E% protein) for 2(1/2) wk. Diets were isocaloric and tailored individually to match energy expenditure. At 2(1/2) wk of diet, one 60-min bout of bicycle exercise (70% of maximal oxygen uptake) was performed. Muscle biopsies were obtained before and after the diet, immediately after exercise, and after 3-h recovery. Insulin sensitivity (hyperinsulinemic-euglycemic clamp) and intramyocellular triacylglycerol content did not change with the intervention in either group. Indexes of mitochondrial density were similar across the groups and intervention. Mitochondrial respiratory rates, measured in permeabilized muscle fibers, showed a 31 ± 11 and 26 ± 9% exercise-induced increase (P < 0.05) in state 3 (glycolytic substrates) and uncoupled respiration, respectively. However, in HFD this increase was abolished. At recovery, no change from resting respiration was seen in either group. With a lipid substrate (octanoyl-carnitine with or without ADP), similar exercise-induced increases (31-62%) were seen in HFD and ND, but only in HFD was an elevated (P < 0.05) respiratory rate seen at recovery. With HFD complex I and IV protein expression decreased (P < 0.05 and P = 0.06, respectively). A fat-rich diet induces marked changes in the mitochondrial electron transport system protein content and in exercise-induced mitochondrial substrate oxidation rates, with the effects being present hours after the exercise. The effect of HFD is present even without effects on insulin sensitivity and intramyocellular lipid accumulation. An isocaloric high-fat diet does not cause insulin resistance.

Medical Subject Headings (MeSH)
AdultBasal MetabolismBiopsyBlood GlucoseCalorimetry, IndirectCell RespirationDenmarkDietary FatsElectron Transport Complex IElectron Transport Complex IVEnergy IntakeEnergy MetabolismExerciseGlucose Clamp TechniqueGlycolysisHumansInsulinInsulin ResistanceMaleMitochondria, MuscleMuscle, SkeletalOxygen ConsumptionTime FactorsTriglyceridesYoung Adult
Study Links
Quality Scores
Safety85
Efficacy70/10
Quality80/10
Citation Metrics
Total Citations17
Citations/Year1.2
Relative Citation Ratio0.57
NIH Percentile31%
Research Impact Scores
APT Score0.25
Weight Score1.32
Normalized Score0.78
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