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The acute effects of olive oil v. cream on postprandial thermogenesis and substrate oxidation in postmenopausal women

Published online by Cambridge University Press:  09 March 2007

M. J. Soares*
Affiliation:
Department of Nutrition, Dietetics and Food Science, School of Public Health, Curtin University of Technology, GPO Box U 1987, Perth WA 6845, Australia
S. J. Cummings
Affiliation:
Department of Human Movement and Exercise Science, University of Western Australia, 151 Stirling Highway, Perth WA 6009, Australia
J. C. L. Mamo
Affiliation:
Department of Nutrition, Dietetics and Food Science, School of Public Health, Curtin University of Technology, GPO Box U 1987, Perth WA 6845, Australia
M. Kenrick
Affiliation:
Department of Nutrition, Dietetics and Food Science, School of Public Health, Curtin University of Technology, GPO Box U 1987, Perth WA 6845, Australia
L. S. Piers
Affiliation:
Menzies School of Health Research, Tiwi, Northern Territory 0810, Australia and Health Surveillance and Evaluation Section, Department of Human Services, Government of Victoria, Level 18, 120 Spencer Street, Melbourne, Victoria 3000, Australia
*
*Corresponding author: Dr Mario J. Soares, fax +61 8 9266 2958, email m.soares@curtin.edu.au
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Abstract

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The influence of the source of dietary fat on postprandial thermogenesis and substrate oxidation rates, was examined in twelve postmenopausal women aged 57–73 years, with BMI 21·9–38·3 kg/m2. A single blind, randomised, paired comparison of two high-fat, isoenergetic, mixed test meals was conducted. The major source of fat was either cream (CREAM) or extra virgin olive oil (EVOO). RMR, diet-induced thermogenesis (DIT) and substrate oxidation rates over 5 h were measured by indirect calorimetry. There were no differences in body weight, RMR, fasting carbohydrate or fat oxidation rates between the two occasions. DIT (EVOO 97 (sd 46) v. CREAM 76 (sd 69) kJ/5 h and EVOO 5·2 (sd 2·5) v. CREAM 4·1 (sd 3·7)% energy) did not differ between the two test meals. The postprandial increase in carbohydrate oxidation rates, relative to their respective fasting values (ΔCOX), was significantly lower following the EVOO meal (EVOO 10·6 (sd 8·3) v. CREAM 17·5 (sd 10) g/5 h; paired t test, P=0·023), while postprandial fat oxidation rates (ΔFOX) were significantly higher (EVOO 0·0 (sd 4·4) v. CREAM -3·6 (sd 4·0) g/5 h; P=0·028). In the eight obese subjects, however, DIT was significantly higher following the EVOO meal (EVOO 5·1 (sd 2·0) v. CREAM 2·5 (sd 2·9) %; P=0·01). This was accompanied by a significantly lower ΔCOX (EVOO 10·9 (sd 9·9) v. CREAM 17·3 (sd 10·5) g/5 h; P=0·03) and significantly higher ΔFOX (EVOO 0·11 (sd 4·4) v. CREAM −4·1 (sd 4·5) g/5 h, P=0·034). The present study showed that olive oil significantly promoted postprandial fat oxidation and stimulated DIT in abdominally obese postmenopausal women.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2004

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