4.7 Article

Increasing skeletal muscle carnitine content in older individuals increases whole-body fat oxidation during moderate-intensity exercise

期刊

AGING CELL
卷 20, 期 2, 页码 -

出版社

WILEY
DOI: 10.1111/acel.13303

关键词

carnitine; fat oxidation; insulin resistance; intramyocellular lipid; older adults; skeletal muscle

资金

  1. Dunhill Medical Trust [R211/0711]

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Increasing muscle total carnitine content in older men can enhance fat oxidation and intramyocellular lipid utilization during exercise. However, this intervention did not lead to improvements in resting insulin-stimulated whole-body or skeletal muscle glucose disposal. Further research is needed to explore the potential metabolic benefits of carnitine supplementation in older adults with impaired lipid turnover.
Intramyocellular lipid (IMCL) utilization is impaired in older individuals, and IMCL accumulation is associated with insulin resistance. We hypothesized that increasing muscle total carnitine content in older men would increase fat oxidation and IMCL utilization during exercise, and improve insulin sensitivity. Fourteen healthy older men (69 +/- 1 year, BMI 26.5 +/- 0.8 kg/m(2)) performed 1 h of cycling at 50% VO(2)max and, on a separate occasion, underwent a 60 mU/m(2)/min euglycaemic hyperinsulinaemic clamp before and after 25 weeks of daily ingestion of a 220 ml insulinogenic beverage (44.4 g carbohydrate, 13.8 g protein) containing 4.5 g placebo (n = 7) or L-carnitine L-tartrate (n = 7). During supplementation, participants performed twice-weekly cycling for 1 h at 50% VO(2)max. Placebo ingestion had no effect on muscle carnitine content or total fat oxidation during exercise at 50% VO(2)max. L-carnitine supplementation resulted in a 20% increase in muscle total carnitine content (20.1 +/- 1.2 to 23.9 +/- 1.7 mmol/kg/dm; p < 0.01) and a 20% increase in total fat oxidation (181.1 +/- 15.0 to 220.4 +/- 19.6 J/kg lbm/min; p < 0.01), predominantly due to increased IMCL utilization. These changes were associated with increased expression of genes involved in fat metabolism (ACAT1, DGKD & PLIN2; p < 0.05). There was no change in resting insulin-stimulated whole-body or skeletal muscle glucose disposal after supplementation. This is the first study to demonstrate that a carnitine-mediated increase in fat oxidation is achievable in older individuals. This warrants further investigation given reduced lipid turnover is associated with poor metabolic health in older adults.

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