Chronic intraparaventricular nuclear administration of orexin A in male rats does not alter thyroid axis or uncoupling protein-1 in brown adipose tissue

Regul Pept. 2002 Mar 15;104(1-3):61-8. doi: 10.1016/s0167-0115(01)00349-4.

Abstract

Orexin A, synthesised in the posterolateral hypothalamus, has widespread distribution including the paraventricular nucleus (PVN), which is rich in thyrotropin-releasing hormone (TRH) neurones. Nerve fibres in the PVN synapse on neurones that send polysynaptic projections to brown adipose tissue (BAT), which is important in thermogenesis. A number of observations suggests orexin A may be involved in regulation of metabolism and thermogenesis. We investigated the effect of orexin A injected intracerebroventricularly (ICV) on thyroid-stimulating hormone (TSH) and thyroid hormones in male rats. We then examined the effect of chronic iPVN injections of orexin A on plasma TSH and uncoupling protein-1 (UCP-1) protein in BAT. Orexin A (3 nmol) administered ICV significantly suppressed plasma TSH at 10 and 90 min. Orexin A (0.3 nmol) administered into the PVN twice daily for 3 days significantly increased day-time 2-h food intake, but did not significantly alter nocturnal food intake. Though chronic iPVN orexin A altered diurnal food intake, there was no effect on 24-h food intake or body weight. Furthermore, orexin A administered chronically into the PVN did not alter UCP-1 level in BAT, or plasma hormones relative to saline injected animals. Chronic iPVN orexin A does not appear to influence thermogenesis through activation of UCP-1 or the thyroid axis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism
  • Animals
  • Body Weight / drug effects
  • Carrier Proteins / administration & dosage
  • Carrier Proteins / metabolism*
  • Carrier Proteins / pharmacology*
  • Eating / drug effects*
  • Injections, Intraventricular / methods
  • Intracellular Signaling Peptides and Proteins*
  • Ion Channels
  • Male
  • Membrane Proteins / metabolism*
  • Mitochondrial Proteins
  • Neuropeptides / administration & dosage
  • Neuropeptides / pharmacology*
  • Orexins
  • Pituitary Hormones / blood
  • Rats
  • Rats, Wistar
  • Thyroid Gland / drug effects*
  • Thyrotropin / blood
  • Thyroxine / blood
  • Triiodothyronine / blood
  • Uncoupling Protein 1

Substances

  • Carrier Proteins
  • Intracellular Signaling Peptides and Proteins
  • Ion Channels
  • Membrane Proteins
  • Mitochondrial Proteins
  • Neuropeptides
  • Orexins
  • Pituitary Hormones
  • Ucp1 protein, rat
  • Uncoupling Protein 1
  • Triiodothyronine
  • Thyrotropin
  • Thyroxine