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Effects of repeated phencyclidine treatment on serotonin transporter in rat brain.

T Hori, S Abe, A Baba, T Suzuki, H Shiraishi

Neuroscience Letters February 11, 2000 DOI: 10.1016/s0304-3940(99)00991-x (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Rats (implied by typical PCP studies, but not explicitly stated in text)
Intervention Phencyclidine (PCP)
Dose 7.5 mg/kg per day
Duration 14 days
Measures [3H]paroxetine binding
Topics Serotonin
Key findings Repeated PCP treatment reduces serotonergic stereotyped behavior and increases the affinity of serotonin transporters for [3H]paroxetine binding.

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.

Comparable studies

Other preclinical and animal studies on serotonin, most cited first.

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