Literature DB >> 15072566

Dissociation between adipose tissue signals, behavior and the food-entrained oscillator.

M T Martínez-Merlos1, M Angeles-Castellanos, M Díaz-Muñoz, R Aguilar-Roblero, J Mendoza, C Escobar.   

Abstract

Digestive and metabolic processes are entrained by restricted feeding (RFS) schedules and are thought to be potential elements of a food-entrained oscillator (FEO). Due to the close relationship of leptin with metabolic regulation and because leptin is a relevant communication signal of the individual's peripheral metabolic condition with the central nervous system, we explored whether leptin is an endogenous entraining signal from the periphery to a central element of an FEO. First we characterized in the rat the diurnal rhythm of serum leptin (in rats fed ad libitum (AL)), its adjustment to an RFS and the influence of fasting after RFS, or RFS followed by AL feeding and then total food deprivation (RF-AF) in the persistence of this fluctuating pattern. We also explored the response of free fatty acids and stomach weight under the same entraining conditions. We compared the metabolic response with the behavioral expression of drinking anticipatory activity (AA) under the same conditions. Finally, we tested the effect of daily i.c.v administration of leptin as a putative entraining signal for the generation of AA. Metabolic parameters responded to food entrainment by adjusting their phase to mealtime. However, leptin and free fatty acid rhythms persisted only for a few cycles in fasting conditions and readjusted to the light-darkness cycle after an RF-AF protocol. In contrast, behavioral food-entrained rhythms persisted after both fasting manipulations. Daily leptin i.c.v. administration did not produce AA, nor produce changes in the behavioral free-running rhythm. Stomach weight indicated an adaptive process allowing an extreme stomach distension followed by a slow emptying process, which suggests that the stomach may be playing a relevant role as a storage organ. In conclusion, metabolic signals here studied respond to feeding schedules by adjusting their phase to mealtime, but do only persist for a few cycles in fasting. Leptin does not produce AA and thus is not an entraining signal for FEO. The response of metabolic signals to feeding schedules depends on different mechanisms than the expression of AA.

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Year:  2004        PMID: 15072566     DOI: 10.1677/joe.0.1810053

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  15 in total

1.  Persistence of hormonal and metabolic rhythms during fasting in 7- to 9-day-old rabbits entrained by nursing during the night.

Authors:  Elvira Morgado; Enrique Meza; M Kathleen Gordon; Francis K Y Pau; Claudia Juárez; Mario Caba
Journal:  Horm Behav       Date:  2010-05-20       Impact factor: 3.587

Review 2.  Interactions between light, mealtime and calorie restriction to control daily timing in mammals.

Authors:  Etienne Challet
Journal:  J Comp Physiol B       Date:  2010-02-20       Impact factor: 2.200

Review 3.  Dorsal striatum dopamine oscillations: Setting the pace of food anticipatory activity.

Authors:  Guillaume de Lartigue; Molly McDougle
Journal:  Acta Physiol (Oxf)       Date:  2018-06-27       Impact factor: 6.311

4.  Daytime food restriction alters liver glycogen, triacylglycerols, and cell size. A histochemical, morphometric, and ultrastructural study.

Authors:  Mauricio Díaz-Muñoz; Olivia Vázquez-Martínez; Adrián Báez-Ruiz; Gema Martínez-Cabrera; María V Soto-Abraham; María C Avila-Casado; Jorge Larriva-Sahd
Journal:  Comp Hepatol       Date:  2010-02-23

5.  Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant mice.

Authors:  Nicolas F Berbari; Raymond C Pasek; Erik B Malarkey; S M Zaki Yazdi; Andrew D McNair; Wesley R Lewis; Tim R Nagy; Robert A Kesterson; Bradley K Yoder
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-18       Impact factor: 11.205

6.  Hormonal and metabolic rhythms associated with the daily scheduled nursing in rabbit pups.

Authors:  Elvira Morgado; M Kathleen Gordon; María del Carmen Miñana-Solis; Enrique Meza; Seymour Levine; Carolina Escobar; Mario Caba
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-05-14       Impact factor: 3.619

7.  Leptin-sensitive neurons in the arcuate nucleus integrate activity and temperature circadian rhythms and anticipatory responses to food restriction.

Authors:  Michael F Wiater; Ai-Jun Li; Thu T Dinh; Heiko T Jansen; Sue Ritter
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-08-28       Impact factor: 3.619

8.  Changes in the 24 h Rhythmicity of Liver PPARs and Peroxisomal Markers When Feeding Is Restricted to Two Daytime Hours.

Authors:  Julieta B Rivera-Zavala; Adrián Báez-Ruiz; Mauricio Díaz-Muñoz
Journal:  PPAR Res       Date:  2011-04-05       Impact factor: 4.964

9.  Chronic inhibition of endoplasmic reticulum calcium-release channels and calcium-ATPase lengthens the period of hepatic clock gene Per1.

Authors:  Adrián Báez-Ruiz; Mauricio Díaz-Muñoz
Journal:  J Circadian Rhythms       Date:  2011-07-08

Review 10.  Circadian adaptations to meal timing: neuroendocrine mechanisms.

Authors:  Danica F Patton; Ralph E Mistlberger
Journal:  Front Neurosci       Date:  2013-10-14       Impact factor: 4.677

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