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[3H]PCP-3-OH and (+)[3H]SKF 10047 binding sites in rat brain membranes: evidence of multiplicity.

作者信息

Itzhak Y

出版信息

Eur J Pharmacol. 1987 Apr 14;136(2):231-4. doi: 10.1016/0014-2999(87)90715-1.

DOI:10.1016/0014-2999(87)90715-1
PMID:3036548
Abstract

Specific binding of one of the most potent analogs of phencyclidine (PCP), [3H]PCP-3-OH, in rat brain membranes revealed the labeling of high (Kd = 0.5 nM) and low (Kd = 16 nM) affinity binding sites. (+)SKF 10047 potently inhibited high, but not low, affinity [3H]PCP-3-OH binding. (+)[3H]SKF 10047 apparently labeled the high affinity PCP-3-OH binding site and also an additional site, sensitive to haloperidol, which is distinct from the two sites labeled by [3H]PCP-3-OH.

摘要

相似文献

1
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