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   <subfield code="a">Intramyocellular lipid stores increase markedly in athletes after 1.5days lipid supplementation and are utilized during exercise in proportion to their content</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Monica Zehnder, Emanuel Christ, Michael Ith, Kevin Acheson, Etienne Pouteau, Roland Kreis, Roman Trepp, Peter Diem, Chris Boesch, Jacques Décombaz]</subfield>
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   <subfield code="a">Intramyocellular lipids (IMCL) and muscle glycogen provide local energy during exercise (EX). The objective of this study was to clarify the role of high versus low IMCL levels at equal initial muscle glycogen on fuel selection during EX. After 3h of depleting exercise, 11 endurance-trained males consumed in a crossover design a high-carbohydrate (7gkg−1day−1) low-fat (0.5gkg−1day−1) diet (HC) for 2.5days or the same diet with 3gkg−1day−1 more fat provided during the last 1.5days of diet (four meals; HCF). Respiratory exchange, thigh muscle substrate breakdown by magnetic resonance spectroscopy, and plasma FFA oxidation ([1-13C]palmitate) were measured during EX (3h, 50% W max). Pre-EX IMCL concentrations were 55% higher after HCF. IMCL utilization during EX in HCF was threefold greater compared with HC (P&lt;0.001) and was correlated with aerobic power and highly correlated (P&lt;0.001) with initial content. Glycogen values and decrements during EX were similar. Whole-body fat oxidation (Fatox) was similar overall and plasma FFA oxidation smaller (P&lt;0.05) during the first EX hour after HCF. Myocellular fuels contributed 8% more to whole-body energy demands after HCF (P&lt;0.05) due to IMCL breakdown (27% Fatox). After EX, when both IMCL and glycogen concentrations were again similar across trials, a simulated 20-km time-trial showed no difference in performance between diets. In conclusion, IMCL concentrations can be increased during a glycogen loading diet by consuming additional fat for the last 1.5days. During subsequent exercise, IMCL decrease in proportion to their initial content, partly in exchange for peripheral fatty acids.</subfield>
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   <subfield code="a">Springer-Verlag, 2006</subfield>
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   <subfield code="u">Department of Clinical Research, University and Inselspital, 3010, Bern, Switzerland</subfield>
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   <subfield code="a">Christ</subfield>
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