The effects of phenelzine and other monoamine oxidase inhibitor antidepressants on brain and liver I2 imidazoline-preferring receptors

Br J Pharmacol. 1995 Feb;114(4):837-45. doi: 10.1111/j.1476-5381.1995.tb13280.x.

Abstract

1. The binding of [3H]-idazoxan in the presence of 10(-6) M (-)-adrenaline was used to quantitate I2 imidazoline-preferring receptors in the rat brain and liver after chronic treatment with various irreversible and reversible monoamine oxidase (MAO) inhibitors. 2. Chronic treatment (7-14 days) with the irreversible MAO inhibitors, phenelzine (1-20 mg kg-1, i.p.), isocarboxazid (10 mg kg-1, i.p.), clorgyline (3 mg kg-1, i.p.) and tranylcypromine (10 mg kg-1, i.p.) markedly decreased (21-71%) the density of I2 imidazoline-preferring receptors in the rat brain and liver. In contrast, chronic treatment (7 days) with the reversible MAO-A inhibitors, moclobemide (1 and 10 mg kg-1, i.p.) or chlordimeform (10 mg kg-1, i.p.) or with the reversible MAO-B inhibitor Ro 16-6491 (1 and 10 mg kg-1, i.p.) did not alter the density of I2 imidazoline-preferring receptors in the rat brain and liver; except for the higher dose of Ro 16-6491 which only decreased the density of these putative receptors in the liver (38%). 3. In vitro, phenelzine, clorgyline, 3-phenylpropargylamine, tranylcypromine and chlordimeform displaced the binding of [3H]-idazoxan to brain and liver I2 imidazoline-preferring receptors from two distinct binding sites. Phenelzine, 3-phenylpropargylamine and tranylcypromine displayed moderate affinity (KiH = 0.3-6 microM) for brain and liver I2 imidazoline-preferring receptors; whereas chlordimeform displayed high affinity (KiH = 6 nM) for these receptors in the two tissues studied, Clorgyline displayed very high affinity for rat brain (KiH = 40 pM) but not for rat liver I2 imidazoline-preferring receptors (KiH = 169 nM). 4. Preincubation of cortical or liver membranes with phenelzine (10-4 M for 30 min) did not alter the total density of I2 imidazoline-preferring receptors, indicating that this irreversible MAO inhibitor does not irreversibly bind to I2 imidazoline-preferring receptors. In contrast, preincubation with 10-6 Mclorgyline reduced by 40% the Bmax of [3H]-idazoxan to brain and liver I2 imidazoline-preferring receptors.5. Chronic treatment (7 days) with the inducers of cytochrome P-450 enzymes phenobarbitone (40 or 80 mg kg-1, i.p.), 3-methylcholanthrene (20 mg kg-1, i.p.) or 2-methylimidazole (40 mg kg-1, i.p.) did not alter the binding parameters of [3H]-idazoxan to brain and liver 12 imidazoline-preferring receptors.The compound SKF 525A, a potent inhibitor of cytochrome P-450 enzymes which forms a tight but reversible complex with the haemoprotein, completely displaced with moderate affinity (KiH = 2-10 microM)the specific binding of [3H]-idazoxan to brain and liver 12 imidazoline-preferring receptors. Preincubation of total liver homogenates with 3 x 10-4 M phenelzine in the presence of 10-3 M NADH, a treatment that irreversibly inactivates the haeme group of cytochrome P-450, did not reduce the density of liver I2 imidazoline-preferring receptors. These results discounted a possible interaction of [3H]-idazoxan with the haeme group of cytochrome P-450 enzymes.6. Together the results indicate that the down-regulation of I2 imidazoline-preferring receptors is associated with an irreversible inactivation of MAO (at least in the brain) that is not related either to the affinity of the MAO inhibitors for I2 imidazoline-preferring receptors or to an irreversible binding to these putative receptors. These findings indicate a novel effect of irreversible MAO inhibitors in the brain and suggest a new target for these compounds that could be of relevance in the treatment of depression, a disease in which an increased density of brain I2 imidazoline-preferring receptors has been reported.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Antagonists / metabolism
  • Animals
  • Antidepressive Agents / administration & dosage
  • Antidepressive Agents / pharmacology*
  • Benzamides / administration & dosage
  • Benzamides / metabolism
  • Benzamides / pharmacology
  • Binding, Competitive
  • Brain / drug effects
  • Brain / metabolism
  • Chlorphenamidine / administration & dosage
  • Chlorphenamidine / pharmacology
  • Clorgyline / administration & dosage
  • Clorgyline / pharmacology
  • Cytochrome P-450 Enzyme System / metabolism
  • Dioxanes / metabolism
  • Idazoxan
  • Imidazoles / metabolism
  • Imidazoline Receptors
  • In Vitro Techniques
  • Injections, Intraperitoneal
  • Isocarboxazid / administration & dosage
  • Isocarboxazid / pharmacology
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Moclobemide
  • Monoamine Oxidase Inhibitors / administration & dosage
  • Monoamine Oxidase Inhibitors / metabolism
  • Monoamine Oxidase Inhibitors / pharmacology*
  • Pargyline / analogs & derivatives
  • Phenelzine / administration & dosage
  • Phenelzine / pharmacology*
  • Propylamines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Drug / drug effects*
  • Receptors, Drug / metabolism
  • Tranylcypromine / administration & dosage
  • Tranylcypromine / pharmacology

Substances

  • Adrenergic alpha-Antagonists
  • Antidepressive Agents
  • Benzamides
  • Dioxanes
  • Imidazoles
  • Imidazoline Receptors
  • Monoamine Oxidase Inhibitors
  • Propylamines
  • Receptors, Drug
  • Isocarboxazid
  • Tranylcypromine
  • 3-phenylpropargylamine
  • Ro 16-6491
  • Cytochrome P-450 Enzyme System
  • Pargyline
  • Chlorphenamidine
  • Clorgyline
  • Phenelzine
  • Moclobemide
  • Idazoxan