Effects of the altered serotonergic signalling by neonatal treatment with 5,7-dihydroxytryptamine, ritanserin or clomipramine on the adrenocortical stress response and the glucocorticoid receptor binding in the hippocampus in adult rats

J Neural Transm Gen Sect. 1994;96(2):113-23. doi: 10.1007/BF01277933.

Abstract

The aim of the present study is to investigate the effect of neonatal alterations in 5-HT signalling on the regulation of endocrine stress response in adult rats. The neonatal blockade of 5-HT transmission by 5,7-DHT or ritanserin treatment did not alter the density of glucocorticoid receptor (GR) binding sites in the hippocampus, although a 5,7-DHT-induced lesion was clearly shown to decrease in 5-HT content by greater than 80% in the hippocampus. In addition, the animals pretreated with the blockade of 5-HT transmission during early life did not exhibit a hyperresponsiveness of the adrenocortical response to stress. On the other hand, the neonatal administration of the 5-HT uptake inhibitor, clomipramine, was shown to lower the stress responsiveness of the adrenocortical axis in adulthood.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5,7-Dihydroxytryptamine / administration & dosage
  • 5,7-Dihydroxytryptamine / pharmacology
  • 5,7-Dihydroxytryptamine / toxicity*
  • Adrenal Cortex / growth & development
  • Adrenal Cortex / physiology*
  • Animals
  • Animals, Newborn
  • Brain Chemistry / drug effects
  • Clomipramine / administration & dosage
  • Clomipramine / pharmacology*
  • Dexamethasone / pharmacology
  • Feedback
  • Hippocampus / drug effects*
  • Hippocampus / growth & development
  • Hippocampus / metabolism
  • Hydrocortisone / metabolism*
  • Hypothalamo-Hypophyseal System / physiopathology
  • Pituitary-Adrenal System / physiopathology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Glucocorticoid / metabolism*
  • Restraint, Physical
  • Ritanserin / administration & dosage
  • Ritanserin / pharmacology*
  • Serotonin / physiology*
  • Stress, Physiological / physiopathology

Substances

  • Receptors, Glucocorticoid
  • Ritanserin
  • 5,7-Dihydroxytryptamine
  • Serotonin
  • Dexamethasone
  • Clomipramine
  • Hydrocortisone