Literature DB >> 10919937

An endocrine and metabolic definition of the intermeal interval in humans: evidence for a role of leptin on the prandial pattern through fatty acid disposal.

D Chapelot1, R Aubert, C Marmonier, M Chabert, J Louis-Sylvestre.   

Abstract

BACKGROUND: It has been proposed that leptin provides a hormonal link between adipose stores and food intake.
OBJECTIVE: This study investigated the role of leptin in the prandial pattern.
DESIGN: In experiment 1, a spontaneous prandial pattern was recreated in 6 young, normal-weight men who were deprived of time cues and had blood withdrawn continuously at a frequency of one tube every 5 min. Meals were consumed ad libitum and dinner was requested voluntarily. Data from a second experiment, conducted in 8 subjects, were used to confirm the changes in leptin during the intermeal interval (IMI).
RESULTS: Plasma leptin gradually rose to a peak (62 +/- 18% of the lunch concentration) during the IMI and declined before the dinner request (-21 +/- 4% of the peak concentration). This preprandial decline was confirmed in experiment 2 (-15 +/- 9%). The leptin concentration at lunch and fat-free mass were the only significant predictors of the IMI (both: r(2) = 0.91, P = 0.03). With fat intake at lunch, the leptin concentration at lunch was a positive predictor of the area under the curve of plasma fatty acids during the IMI (r(2) = 0.95, P = 0.01). Moreover, the leptin concentration at lunch was negatively correlated with energy intake in the first course of this meal (r = -0.95, P < 0.005). A similar result was found at dinner (r = -0.85, P < 0.05). Last, the change in leptin was predicted accurately by changes in glucose, triacylglycerol, and fatty acids (r(2) = 0.87, P < 10(-5)).
CONCLUSION: Plasma leptin concentrations increase during a spontaneous IMI and decline before the onset of a meal. The results argue for a role of leptin in the prandial pattern through fatty acid peripheral disposal.

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Year:  2000        PMID: 10919937     DOI: 10.1093/ajcn/72.2.421

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


  10 in total

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  10 in total

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