Modulatory effect of antidepressants on peripheral-type benzodiazepine receptors

Eur J Pharmacol. 1993 Dec 7;250(2):289-94. doi: 10.1016/0014-2999(93)90393-v.

Abstract

The effect of 21 days of imipramine hydrochloride (10 mg/kg) and phenelzine sulfate (10 mg/kg) administration followed by a 7-day period of withdrawal on peripheral-type benzodiazepine receptors was studied in male Sprague-Dawley rats. Both imipramine and phenelzine down-regulated adrenal peripheral-type benzodiazepine receptors (-18% P < 0.05; and -32%, P < 0.01, respectively) and up-regulated hepatic peripheral-type benzodiazepine receptors (+27%, P < 0.05; and +76%, P < 0.0001, respectively), while no alteration was observed in the kidney. Adrenal peripheral-type benzodiazepine receptors decreased further (-30% versus controls) after withdrawal from imipramine, while full restoration to normal values occurred following phenelzine withdrawal. [3H]PK 11195 binding to the liver did not differ significantly from the control values after withdrawal from either drug. The observed changes can be explained as adaptive responses to antidepressant-induced hormonal and cellular alterations.

MeSH terms

  • Adrenal Glands / drug effects
  • Adrenal Glands / metabolism
  • Animals
  • Antidepressive Agents / pharmacology*
  • Down-Regulation / drug effects
  • Imipramine / pharmacology
  • In Vitro Techniques
  • Isoquinolines / pharmacokinetics
  • Kidney / drug effects
  • Kidney / metabolism
  • Kinetics
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Membranes / drug effects
  • Membranes / metabolism
  • Organ Specificity
  • Peripheral Nervous System / drug effects*
  • Phenelzine / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA-A / drug effects*
  • Up-Regulation / drug effects

Substances

  • Antidepressive Agents
  • Isoquinolines
  • Receptors, GABA-A
  • Phenelzine
  • Imipramine
  • PK 11195