High-fat feeding inhibits exercise-induced increase in mitochondrial respiratory flux in skeletal muscle.
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
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
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 |
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.