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Am J Physiol Endocrinol Metab 291: E1083-E1091, 2006. First published June 27, 2006; doi:10.1152/ajpendo.00159.2006
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Trafficking of dietary fat in obesity-prone and obesity-resistant rats

Matthew R. Jackman,1 Robert E. Kramer,2 Paul S. MacLean,1 and Daniel H. Bessesen1,3

1Department of Medicine, Division of Endocrinology, Metabolism, and Diabetes, University of Colorado at Denver and Health Sciences Center, Aurora, Colorado; 2Department of Pediatrics, Division of Pediatric Gastroenterology and Nutrition, Leonard M. Miller School of Medicine, University of Miami, Miami, Florida; and 3Denver Health Medical Center, Aurora, Colorado

Submitted 3 April 2006 ; accepted in final form 13 June 2006

The trafficking of dietary fat was assessed in obesity-prone (OP) and obesity-resistant (OR) male and female rats. Test meals containing [1-14C]palmitate were delivered through gastric feeding tubes while rats consumed a high-carbohydrate diet (HCD) or after 5 days of a high-fat diet (HFD). Over the subsequent 24 h, the appearance of 14C was followed in the GI tract, skeletal muscles (SM), liver, adipose tissues (AT), and expired CO2. There was no difference in the production of 14CO2 between OP and OR rats consuming a HCD. However, after 5 days on HFD, OR rats produced significantly more 14CO2 after the test meal than OP rats (P < 0.001 females, P = 0.03 males). The differential oxidation of dietary fat between OP and OR rats on HFD was not due to differences in absorption but rather was associated with preferential disposition of tracer to AT in OP rats. Measurements of lipoprotein lipase in part explained increased tracer uptake by AT in OP rats but were not consistent with increased SM tracer uptake in OR rats. Surprisingly, female rats oxidized more tracer than male rats irrespective of phenotype or diet. These results are consistent with the notion that differences in the partitioning of dietary fat between storage in AT and oxidation in SM and liver that develop shortly after the introduction of a HFD may in part underlie the differential tendency for OR and OP rats to gain weight on this diet.

thinness; lipoprotein lipase; sex differences; dietary fat; high-fat diet



Address for reprint requests and other correspondence: M. R. Jackman, Univ. of Colorado at Denver and Health Sciences Center, PO Box 6511, F-8305, Aurora, CO 80045 (e-mail: matthew.jackman{at}uchsc.edu)




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