[Chronobiological aspects of obesity and metabolic syndrome]

Endocrinol Nutr. 2012 Jan;59(1):50-61. doi: 10.1016/j.endonu.2011.08.002. Epub 2011 Nov 18.
[Article in Spanish]

Abstract

Circadian rhythms (approximately 24h) are widely characterized at molecular level and their generation is acknowledged to originate from oscillations in expression of several clock genes and from regulation of their protein products. While general entrainment of organisms to environmental light-dark cycles is mainly achieved through the master clock of the suprachiasmatic nucleus in mammals, this molecular clockwork is functional in several organs and tissues. Some studies have suggested that disruption of the circadian system (chronodisruption (CD)) may be causal for manifestations of the metabolic syndrome. This review summarizes (1) how molecular clocks coordinate metabolism and their specific role in the adipocyte; (2) the genetic aspects of and scientific evidence for obesity as a chronobiological illness; and (3) CD and its causes and pathological consequences. Finally, ideas about use of chronobiology for the treatment of obesity are discussed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • ARNTL Transcription Factors / genetics
  • ARNTL Transcription Factors / physiology
  • Adiponectin / genetics
  • Adiponectin / physiology
  • Adipose Tissue / physiopathology
  • Animals
  • Cardiovascular Diseases / epidemiology
  • Cardiovascular Diseases / etiology
  • Chronotherapy
  • Circadian Rhythm / physiology*
  • Cryptochromes / genetics
  • Cryptochromes / physiology
  • Female
  • Gene Expression Regulation / physiology
  • Humans
  • Jet Lag Syndrome / physiopathology
  • Leptin / physiology
  • Male
  • Mammals / physiology
  • Metabolic Syndrome / epidemiology
  • Metabolic Syndrome / physiopathology*
  • Metabolic Syndrome / therapy
  • Neoplasms / epidemiology
  • Neoplasms / etiology
  • Obesity / epidemiology
  • Obesity / physiopathology*
  • Obesity / therapy
  • PPAR gamma / genetics
  • PPAR gamma / physiology
  • Period Circadian Proteins / genetics
  • Period Circadian Proteins / physiology
  • Receptors, Adiponectin / genetics
  • Receptors, Adiponectin / physiology
  • Receptors, Leptin / physiology

Substances

  • ADIPOQ protein, human
  • ARNTL Transcription Factors
  • BMAL1 protein, human
  • Adiponectin
  • CRY1 protein, human
  • Cryptochromes
  • LEPR protein, human
  • Leptin
  • PER2 protein, human
  • PPAR gamma
  • Period Circadian Proteins
  • Receptors, Adiponectin
  • Receptors, Leptin