Differential response of TRHergic neurons of the hypothalamic paraventricular nucleus (PVN) in female animals submitted to food-restriction or dehydration-induced anorexia and cold exposure

Horm Behav. 2008 Feb;53(2):366-77. doi: 10.1016/j.yhbeh.2007.11.003. Epub 2007 Nov 19.

Abstract

TRH neurons of the hypothalamic paraventricular nucleus (PVN), regulate pituitary-thyroid axis (HPT). Fasting activates expression of orexigenic peptides from the arcuate nucleus, increases corticosterone while reduces leptin, and pro-TRH mRNA levels despite low serum thyroid hormone concentration (tertiary hypothyroidism). TRH synthesis is positively regulated by anorexigenic peptides whose expression is reduced in fasting. The model of dehydration-induced anorexia (DIA) leads to decreased voluntary food intake but peptide expression in the arcuate is similar to forced-food restriction (FFR), where animals remain hungered. We compared the response of HPT axis of female Wistar rats submitted to DIA (2.5% saline solution, food ad libitum, 7 days) with FFR (provided with the amount of food ingested by DIA) and naïve (N) group fed ad libitum, as well as their response to acute cold exposure. Pro-TRH and pro-CRH mRNA levels in the PVN were measured by RT-PCR, TRH content, serum concentration of TSH and thyroid hormones by radioimmunoassay. DIA rats reduced 80% their food consumption compared to N, decreased PVN pro-CRH expression, serum estradiol and leptin levels, increased corticosterone similar to FFR. HPT axis of DIA animals failed to adapt: FFR presented tertiary hypothyroidism and DIA, primary. Response to cold stimulation leading to increased pro-TRH mRNA levels and TRH release was preserved under reduced energy availability in FFR rats but not in DIA, although the dynamics of hormonal release differed: TSH release augmented only in naïve; thyroxine in all but highest in DIA, and triiodothyronine in FFR and DIA suggesting a differential regulation of deiodinases.

Publication types

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

MeSH terms

  • Adaptation, Physiological*
  • Aminopeptidases / metabolism
  • Animals
  • Anorexia / etiology
  • Anorexia / metabolism
  • Anxiety / complications
  • Anxiety / metabolism
  • Appetite Regulation / physiology*
  • Body Composition
  • Cold Temperature
  • Corticosterone / blood
  • Dehydration / complications
  • Dehydration / metabolism
  • Disease Models, Animal
  • Female
  • Food Deprivation / physiology*
  • Hypothalamo-Hypophyseal System / metabolism
  • Matched-Pair Analysis
  • Neurons / metabolism*
  • Paraventricular Hypothalamic Nucleus / cytology
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Pituitary Gland, Anterior / metabolism
  • Protein Precursors / metabolism
  • Pyrrolidonecarboxylic Acid / analogs & derivatives
  • Pyrrolidonecarboxylic Acid / metabolism
  • RNA, Messenger / analysis
  • Rats
  • Rats, Wistar
  • Receptors, Thyrotropin-Releasing Hormone / genetics
  • Receptors, Thyrotropin-Releasing Hormone / metabolism
  • Sex Factors
  • Stress, Physiological / complications
  • Stress, Physiological / metabolism
  • Thyroid Gland / metabolism
  • Thyroid Hormones / blood
  • Thyrotropin-Releasing Hormone / metabolism*

Substances

  • Protein Precursors
  • RNA, Messenger
  • Receptors, Thyrotropin-Releasing Hormone
  • Thyroid Hormones
  • Thyrotropin-Releasing Hormone
  • Aminopeptidases
  • pyroglutamyl-peptidase II
  • Pyrrolidonecarboxylic Acid
  • Corticosterone