Literature DB >> 12081827

The effect of etomoxir on 24-h substrate oxidation and satiety in humans.

Vera B Hinderling1, Patrick Schrauwen, Wolfgang Langhans, Margriet S Westerterp-Plantenga.   

Abstract

BACKGROUND: The carnitine O-palmitoyltransferase I (EC 2.3.1.21) inhibitor etomoxir inhibits fatty acid oxidation, and hepatic fatty acid oxidation has been suggested to be a metabolic satiety signal in subjects who consume high-fat diets.
OBJECTIVE: We investigated substrate oxidation and satiety after repeated administrations of etomoxir or placebo in subjects who consumed a high-fat diet.
DESIGN: In a randomized crossover design consisting of three 5-d treatments, we fed 10 healthy men [mean +/- SE age: 25.6 +/- 1.7 y; mean +/- SE body mass index (in kg/m(2)): 21.8 +/- 0.3] a high-fat diet twice and a low-fat diet once. The subjects consumed each diet at home for 3 consecutive days, after which they spent 36 h in energy balance in a respiration chamber. During the chamber stays with the high-fat treatments, etomoxir or placebo was administered in 5 doses (600 mg etomoxir in total). Blood samples were obtained on the mornings of days 4 and 5 of each treatment, and appetite profiles were assessed.
RESULTS: Mean (+/-SE) 24-h respiratory quotients were significantly (P < 0.05) higher with repeated administrations of etomoxir (0.833 +/- 0.004) than with repeated administrations of placebo (0.814 +/- 0.006), and mean (+/-SE) 24-h whole-body fat oxidation tended to be less (13.7%, P = 0.06) with administration of etomoxir (136.0 +/- 5.2 g/d) than with administration of placebo (157.5 +/- 5.6 g/d). With the etomoxir treatment, fat balance was positive (P < 0.0001) and carbohydrate balance was negative (P < 0.001), whereas with the placebo treatment, neither of the balances was significantly different from zero. Hunger and satiety ratings were not affected under these conditions.
CONCLUSIONS: Etomoxir decreased whole-body fat oxidation, as indicated by the respiratory quotients in the healthy subjects. With the current protocol, however, hunger and satiety ratings were not affected.

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Year:  2002        PMID: 12081827     DOI: 10.1093/ajcn/76.1.141

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  7 in total

1.  Enhancing hepatic mitochondrial fatty acid oxidation stimulates eating in food-deprived mice.

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2.  Adipose triglyceride lipase deletion from adipocytes, but not skeletal myocytes, impairs acute exercise performance in mice.

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3.  Augmenting muscle diacylglycerol and triacylglycerol content by blocking fatty acid oxidation does not impede insulin sensitivity.

Authors:  Silvie Timmers; Miranda Nabben; Madeleen Bosma; Bianca van Bree; Ellen Lenaers; Denis van Beurden; Gert Schaart; Margriet S Westerterp-Plantenga; Wolfgang Langhans; Matthijs K C Hesselink; Vera B Schrauwen-Hinderling; Patrick Schrauwen
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-02       Impact factor: 11.205

4.  Glucometabolic consequences of acute and prolonged inhibition of fatty acid oxidation.

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Journal:  J Lipid Res       Date:  2019-11-12       Impact factor: 5.922

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Journal:  Oncogene       Date:  2018-07-11       Impact factor: 9.867

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Review 7.  The Importance of the Fatty Acid Transporter L-Carnitine in Non-Alcoholic Fatty Liver Disease (NAFLD).

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  7 in total

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