Journal of Applied Physiology
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J Appl Physiol 102: 1065-1070, 2007. First published November 30, 2006; doi:10.1152/japplphysiol.01011.2006
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Carbohydrate ingestion augments L-carnitine retention in humans

Francis B. Stephens, Claire E. Evans, Dumitru Constantin-Teodosiu, and Paul L. Greenhaff

Centre for Integrated Systems Biology and Medicine, School of Biomedical Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, United Kingdom

Submitted 11 September 2006 ; accepted in final form 27 November 2006

Maintaining hyperinsulinemia (~150 mU/l) during steady-state hypercarnitinemia (~550 µmol/l) increases skeletal muscle total carnitine (TC) content by ~15% within 5 h. The present study aimed to investigate whether an increase in whole body carnitine retention can be achieved through L-carnitine feeding in conjunction with a dietary-induced elevation in circulating insulin. On two randomized visits (study A), eight men ingested 3 g/day L-carnitine followed by 4 x 500-ml solutions, each containing flavored water (Con) or 94 g simple sugars (glucose syrup; CHO). In addition, 14 men ingested 3 g/day L-carnitine followed by 2 x 500 ml of either Con or CHO for 2 wk (study B). Carbohydrate ingestion in study A resulted in a fourfold greater serum insulin area under the curve when compared with Con (P < 0.001) and in a lower plasma TC concentration throughout the CHO visit (P < 0.05). Twenty-four-hour urinary TC excretion in the CHO visit was lower than in the Con visit in study A (155.0 ± 10.7 vs. 212.1 ± 17.2 mg; P < 0.05). In study B, daily urinary TC excretion increased after 3 days (65.9 ± 18.0 to 281.0 ± 35.0 mg; P < 0.001) and remained elevated throughout the Con trial. During the CHO trial, daily urinary TC excretion increased from a similar basal value of 53.8 ± 9.2 to 166.8 ± 17.3 mg after 3 days (P < 0.01), which was less than during the Con trial (P < 0.01), and it remained lower over the course of the study (P < 0.001). The difference in plasma TC concentration in study A and 24-h urinary TC excretion in both studies suggests that insulin augmented the retention of carnitine in the CHO trials.

novel organic cation transporter 2; insulin; skeletal muscle



Address for reprint requests and other correspondence: F. B. Stephens, E Floor, School of Biomedical Sciences, Univ. of Nottingham Medical School, Queen's Medical Centre, Nottingham, NG7 2UH, UK (e-mail: francis.stephens{at}nottingham.ac.uk)







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