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A Thurkauf

2 papers in the library · publishing 1990-1991

Papers

[3H]1-[2-(2-thienyl)cyclohexyl]piperidine labels two high-affinity binding sites in human cortex: further evidence for phencyclidine binding sites associated with the biogenic amine reuptake complex.

Synapse (New York, N.Y.) August 1, 1991 H C Akunne, A A Reid, A Thurkauf et al.

The brain contains two types of PCP binding sites: site 1 (linked to the NMDA receptor) and site 2 (linked to the dopamine reuptake complex). This work examined brain membranes from multiple species and found detectable site 2 in guinea pig, rabbit, pig, mouse, sheep, and human, but not in rat or chicken. In human cortex, site 2 was the predominant binding site. Dopamine and serotonin uptake inhibitors produced a wash-resistant inhibition of [3H]TCP binding to site 2 but not site 1. The results suggest human cortex possesses high-affinity PCP binding sites associated with biogenic reuptake binding sites, and that guinea pig, but not rat, may be an appropriate animal model for studying PCP site 2 in human brain.

Specificity of phencyclidine-like drugs and benzomorphan opiates for two high affinity phencyclidine binding sites in guinea pig brain.

Neuropharmacology September 1, 1990 A A Reid, M V Mattson, B R De Costa et al.

Phencyclidine (PCP) and its analog TCP bind non-selectively to two high-affinity binding sites in guinea pig brain: one coupled to the NMDA glutamate receptor (site 1) and the other associated with the dopamine reuptake carrier (site 2). The compound (+)MK801 is highly selective for site 1 and produces minimal psychotomimetic effects in humans at doses that reduce seizures, whereas PCP produces psychotomimetic effects. This suggests that (+)MK801 can serve as a marker for site 1 and that PCP's psychotomimetic effects may be mediated by site 2.