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Melatonin decreases human adipose tissue insulin sensitivity.
Zambrano, Carolina; Garitaonaindia, Mireia Tena; Salmerón, Diego; Pérez-Sanz, Fernando; Tchio, Cynthia; Picinato, María Cecilia; de Medina, Fermín Sánchez; Luján, Juan; Scheer, Frank A J L; Saxena, Richa; Martínez-Augustin, Olga; Garaulet, Marta.
Afiliación
  • Zambrano C; Department of Physiology, Regional Campus of International Excellence, University of Murcia, Murcia, Spain.
  • Garitaonaindia MT; Research Biomedical Institute of Murcia (IMIB)-Arrixaca, Murcia, Spain.
  • Salmerón D; Department of Biochemistry and Molecular Biology II, Centro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBERehd), Ibs Granada, Instituto de Nutrición y Tecnología de los Alimentos (INYTA) José Mataix, University of Granada, Granada, Spain.
  • Pérez-Sanz F; Research Biomedical Institute of Murcia (IMIB)-Arrixaca, Murcia, Spain.
  • Tchio C; Health and Social Sciences Department, University of Murcia, Murcia, Spain.
  • Picinato MC; Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), Madrid, Spain.
  • de Medina FS; Research Biomedical Institute of Murcia (IMIB)-Arrixaca, Murcia, Spain.
  • Luján J; Center for Genomic Medicine, Massachusetts General Hospital, Cambridge, Massachusetts, USA.
  • Scheer FAJL; Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
  • Saxena R; Department of Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Martínez-Augustin O; Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta, Georgia, USA.
  • Garaulet M; University Federal do Oeste da Bahia, Barreiras, Brazil.
J Pineal Res ; 76(5): e12965, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38860494
ABSTRACT
Melatonin is a pineal hormone that modulates the circadian system and exerts soporific and phase-shifting effects. It is also involved in many other physiological processes, such as those implicated in cardiovascular, endocrine, immune, and metabolic functions. However, the role of melatonin in glucose metabolism remains contradictory, and its action on human adipose tissue (AT) explants has not been demonstrated. We aimed to assess whether melatonin (a pharmacological dose) influences insulin sensitivity in human AT. This will help better understand melatonin administration's effect on glucose metabolism. Abdominal AT (subcutaneous and visceral) biopsies were obtained from 19 participants with severe obesity (age 42.84 ± 12.48 years; body mass index 43.14 ± 8.26 kg/m2) who underwent a laparoscopic gastric bypass. AT biopsies were exposed to four different treatments control (C), insulin alone (I) (10 nM), melatonin alone (M) (5000 pg/mL), and insulin plus melatonin combined (I + M). All four conditions were repeated in both subcutaneous and visceral AT, and all were performed in the morning at 8 a.m. (n = 19) and the evening at 8 p.m. (in a subsample of n = 12). We used western blot analysis to determine insulin signaling (using the pAKT/tAKT ratio). Furthermore, RNAseq analyses were performed to better understand the metabolic pathways involved in the effect of melatonin on insulin signaling. As expected, insulin treatment (I) increased the pAKT/tAKT ratio compared with control (p < .0001). Furthermore, the addition of melatonin (I + M) resulted in a decrease in insulin signaling as compared with insulin alone (I); this effect was significant only during the evening time (not in the morning time). Further, RNAseq analyses in visceral AT during the evening condition (at 8 p.m.) showed that melatonin resulted in a prompt transcriptome response (around 1 h after melatonin addition), particularly by downregulating the insulin signaling pathway. Our results show that melatonin reduces insulin sensitivity in human AT during the evening. These results may partly explain the previous studies showing a decrease in glucose tolerance after oral melatonin administration in the evening or when eating late when endogenous melatonin is present.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Resistencia a la Insulina / Melatonina Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Pineal Res Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Resistencia a la Insulina / Melatonina Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Pineal Res Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: España