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Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat

The biogenic amine serotonin is a signaling molecule in the gastrointestinal tract, platelets, and nervous tissue. In nervous system, serotonin and its metabolites are under the control of the circadian timing system, but it is not known if daily variations of serotonin exist in the liver. To explor...

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Autores principales: Valdés-Fuentes, Marlen, Vera-Rivera, Gabriela, De Ita-Pérez, Dalia, Méndez, Isabel, Miranda, María Isabel, Díaz-Muñoz, Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463822/
https://www.ncbi.nlm.nih.gov/pubmed/25948822
http://dx.doi.org/10.14814/phy2.12389
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author Valdés-Fuentes, Marlen
Vera-Rivera, Gabriela
De Ita-Pérez, Dalia
Méndez, Isabel
Miranda, María Isabel
Díaz-Muñoz, Mauricio
author_facet Valdés-Fuentes, Marlen
Vera-Rivera, Gabriela
De Ita-Pérez, Dalia
Méndez, Isabel
Miranda, María Isabel
Díaz-Muñoz, Mauricio
author_sort Valdés-Fuentes, Marlen
collection PubMed
description The biogenic amine serotonin is a signaling molecule in the gastrointestinal tract, platelets, and nervous tissue. In nervous system, serotonin and its metabolites are under the control of the circadian timing system, but it is not known if daily variations of serotonin exist in the liver. To explore this possibility, we tested if the rhythmic pattern of serotonin metabolism was regulated by daytime restricted feeding (DRF) which is a protocol associated to the expression of the food entrained oscillator (FEO). The DRF involved food access for 2 h each day for 3 weeks. Control groups included food ad libitum (AL) as well as acute fasting and refeeding. Serotonin-related metabolites were measured by high pressure liquid chromatography, the anabolic and catabolic enzymes were evaluated by western blot, qPCR, and immunohistochemistry to generate 24-h profiles. The results showed in the AL group, liver serotonin, tryptophan hydroxylase-1 activity, and protein abundance as well as serotonin in plasma and serum were rhythmic and coordinated. The DRF protocol disrupted this coordinated response and damped the rhythmic profile of these parameters. We demonstrated the daily synthesis and the degradation of serotonin as well as its transport in blood. This rhythm could influence the physiological role played by serotonin in peripheral organs. DRF caused an uncoordinated response in the liver and blood serotonin rhythm. This modification could be a part of the physiology of the FEO
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spelling pubmed-44638222015-06-16 Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat Valdés-Fuentes, Marlen Vera-Rivera, Gabriela De Ita-Pérez, Dalia Méndez, Isabel Miranda, María Isabel Díaz-Muñoz, Mauricio Physiol Rep Original Research The biogenic amine serotonin is a signaling molecule in the gastrointestinal tract, platelets, and nervous tissue. In nervous system, serotonin and its metabolites are under the control of the circadian timing system, but it is not known if daily variations of serotonin exist in the liver. To explore this possibility, we tested if the rhythmic pattern of serotonin metabolism was regulated by daytime restricted feeding (DRF) which is a protocol associated to the expression of the food entrained oscillator (FEO). The DRF involved food access for 2 h each day for 3 weeks. Control groups included food ad libitum (AL) as well as acute fasting and refeeding. Serotonin-related metabolites were measured by high pressure liquid chromatography, the anabolic and catabolic enzymes were evaluated by western blot, qPCR, and immunohistochemistry to generate 24-h profiles. The results showed in the AL group, liver serotonin, tryptophan hydroxylase-1 activity, and protein abundance as well as serotonin in plasma and serum were rhythmic and coordinated. The DRF protocol disrupted this coordinated response and damped the rhythmic profile of these parameters. We demonstrated the daily synthesis and the degradation of serotonin as well as its transport in blood. This rhythm could influence the physiological role played by serotonin in peripheral organs. DRF caused an uncoordinated response in the liver and blood serotonin rhythm. This modification could be a part of the physiology of the FEO BlackWell Publishing Ltd 2015-05-06 /pmc/articles/PMC4463822/ /pubmed/25948822 http://dx.doi.org/10.14814/phy2.12389 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Valdés-Fuentes, Marlen
Vera-Rivera, Gabriela
De Ita-Pérez, Dalia
Méndez, Isabel
Miranda, María Isabel
Díaz-Muñoz, Mauricio
Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
title Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
title_full Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
title_fullStr Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
title_full_unstemmed Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
title_short Effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
title_sort effect of daytime-restricted feeding in the daily variations of liver metabolism and blood transport of serotonin in rat
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463822/
https://www.ncbi.nlm.nih.gov/pubmed/25948822
http://dx.doi.org/10.14814/phy2.12389
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