Effects of repeated phencyclidine treatment on serotonin transporter in rat brain

Neurosci Lett. 2000 Feb 11;280(1):53-6. doi: 10.1016/s0304-3940(99)00991-x.

Abstract

Phencyclidine (PCP) is known to be an inhibitor of serotonin (5-HT) uptake and to increase serotonergic activity. The development of tolerance to serotonergic stereotyped behaviors induced by repeated PCP treatment and changes of 5-HT transporters were examined. Backpedalling was significantly reduced in frequency following 14 days PCP treatment (7.5 mg/kg per day). Furthermore, repeated PCP treatment decreased the equilibrium dissociation constant (Kd) of [3H]paroxetine binding to 5-HT transporters in whole brain excluding the cerebellum without any change of maximum number of binding sites (Bmax). Single treatment with PCP failed to change binding parameters. These results indicate that repeated PCP treatment causes tolerance in serotonergic stereotyped behavior and increases affinity of 5-HT transporters for [3H]paroxetine binding. The increased affinity of 5-HT transporters could represent compensatory responses to chronic inhibition of 5-HT uptake by PCP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Brain / drug effects
  • Brain / metabolism*
  • Carrier Proteins / drug effects
  • Carrier Proteins / metabolism*
  • Cell Membrane / metabolism
  • Drug Administration Schedule
  • Kinetics
  • Male
  • Membrane Glycoproteins / drug effects
  • Membrane Glycoproteins / metabolism*
  • Membrane Transport Proteins*
  • Motor Activity / drug effects
  • Nerve Tissue Proteins*
  • Paroxetine / pharmacokinetics
  • Phencyclidine / administration & dosage
  • Phencyclidine / pharmacology*
  • Rats
  • Rats, Wistar
  • Serotonin Plasma Membrane Transport Proteins
  • Stereotyped Behavior / drug effects
  • Time Factors
  • Tritium

Substances

  • Carrier Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • Serotonin Plasma Membrane Transport Proteins
  • Slc6a4 protein, rat
  • Tritium
  • Paroxetine
  • Phencyclidine