Prepuberal light phase feeding induces neuroendocrine alterations in adult rats

J Endocrinol. 2017 Jan;232(1):15-28. doi: 10.1530/JOE-16-0402. Epub 2016 Oct 11.

Abstract

Feeding patterns are important factors in obesity evolvement. Time-restricted feeding schedules (tRF) during resting phase change energy homeostasis regulation, disrupting the circadian release of metabolism-regulating hormones, such as leptin, insulin and corticosterone and promoting body weight gain. Thyroid (HPT) and adrenal (HPA) axes exhibit a circadian regulation and are involved in energy expenditure, thus studying their parameters in tRF paradigms will elucidate their role in energy homeostasis impairments under such conditions. As tRF in young animals is poorly studied, we subjected prepuberal rats to a tRF either in light (LPF) or in darkness phase (DPF) and analyzed HPT and HPA response when they reach adulthood, as well as their arcuate (ARC) and paraventricular (PVN) hypothalamic nuclei neurons' sensitivity to leptin in subsets of 10-week-old animals after fasting and with i.p. leptin treatment. LPF group showed high body weight and food intake, along with increased visceral fat pads, corticosterone, leptin and insulin serum levels, whereas circulating T4 decreased. HPA axis hyperactivity was demonstrated by their high PVN Crf mRNA expression; the blunted activity of HPT axis, by the decreased hypophysiotropic PVN Trh mRNA expression. Trh impaired expression to the positive energy balance in LPF, accounted for their ARC leptin resistance, evinced by an increased Npy and Socs3 mRNA expression. We concluded that the hyperphagia of prepuberal LPF animals could account for the HPA axis hyperactivity and for the HPT blocked function due to the altered ARC leptin signaling and impaired NPY regulation on PVN TRH neurons.

Keywords: feeding schedules; leptin; proCRF; proTRH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arcuate Nucleus of Hypothalamus / drug effects
  • Arcuate Nucleus of Hypothalamus / metabolism*
  • Body Weight / drug effects
  • Body Weight / physiology
  • Circadian Rhythm / physiology*
  • Corticosterone / blood
  • Corticotropin-Releasing Hormone / metabolism
  • Eating / drug effects
  • Eating / physiology
  • Energy Metabolism / drug effects
  • Energy Metabolism / physiology
  • Feeding Behavior / physiology*
  • Insulin / blood
  • Leptin / blood
  • Leptin / pharmacology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Paraventricular Hypothalamic Nucleus / drug effects
  • Paraventricular Hypothalamic Nucleus / metabolism*
  • Rats
  • Thyroxine / blood

Substances

  • Insulin
  • Leptin
  • Corticotropin-Releasing Hormone
  • Thyroxine
  • Corticosterone