Perturbation of hypothalamic microRNA expression patterns in male rats after metabolic distress: impact of obesity and conditions of negative energy balance

Endocrinology. 2014 May;155(5):1838-50. doi: 10.1210/en.2013-1770. Epub 2014 Feb 11.

Abstract

The hypothalamus plays a crucial role in body weight homeostasis through an intricate network of neuronal circuits that are under the precise regulation of peripheral hormones and central transmitters. Although deregulated function of such circuits might be a major contributing factor in obesity, the molecular mechanisms responsible for the hypothalamic control of energy balance remain partially unknown. MicroRNAs (miRNAs) have been recognized as key regulators of different biological processes, including insulin sensitivity and glucose metabolism. However, the roles of miRNA pathways in the control of metabolism have been mostly addressed in peripheral tissues, whereas the potential deregulation of miRNA expression in the hypothalamus in conditions of metabolic distress remains as yet unexplored. In this work, we used high-throughput screening to define to what extent the hypothalamic profiles of miRNA expression are perturbed in two extreme conditions of nutritional stress in male rats, namely chronic caloric restriction and high-fat diet-induced obesity. Our analyses allowed the identification of sets of miRNAs, including let-7a, mir-9*, mir-30e, mir-132, mir-145, mir-200a, and mir-218, whose expression patterns in the hypothalamus were jointly altered by caloric restriction and/or a high-fat diet. The predicted targets of these miRNAs include several elements of key inflammatory and metabolic pathways, including insulin and leptin. Our study is the first to disclose the impact of nutritional challenges on the hypothalamic miRNA expression profiles. These data will help to characterize the molecular miRNA signature of the hypothalamus in extreme metabolic conditions and pave the way for targeted mechanistic analyses of the involvement of deregulated central miRNAs pathways in the pathogenesis of obesity and related disorders.

Publication types

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

MeSH terms

  • Aging*
  • Animals
  • Appetite Depressants / therapeutic use
  • Body Composition
  • Caloric Restriction / adverse effects
  • Computational Biology
  • Diet, High-Fat / adverse effects
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental* / drug effects
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism*
  • Leptin / blood
  • Leptin / therapeutic use
  • Male
  • Malnutrition / blood
  • Malnutrition / etiology
  • Malnutrition / metabolism*
  • MicroRNAs / metabolism*
  • Models, Biological
  • Neurons / drug effects
  • Neurons / metabolism*
  • Obesity / blood
  • Obesity / drug therapy
  • Obesity / etiology
  • Obesity / metabolism*
  • Rats
  • Rats, Wistar
  • Weaning

Substances

  • Appetite Depressants
  • Leptin
  • MicroRNAs