Abstract |
A specific, saturable, reversible, and selective binding site with Kd = 87 +/- 33 nmol/L, Bmax = 0.78 +/- 0.11 pmol/mg protein was detected in the binding of [3H] phencyclidine (PCP) to porcine cerebral blood vessels. Only ligands of PCP/sigma series were able to bind to the PCP receptors. [3H]PCP bound to its receptors was not displaced by etorphine or norepinephrine 0.1 mmol/L. A specific [3H]PCP binding site was found in porcine brain with Kd = 75 +/- 34 nmol/L, Bmax = 0.61 +/- 0.23 pmol/mg protein. Bioassay in vitro showed PCP enhanced the perfusion pressure of porcine cerebral blood vessels in a dose-dependent manner. This study provides direct evidence for PCP receptors on cerebral blood vessels, and suggests that PCP may produce cerebral vasospasm via PCP receptor interaction.
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Authors | Y F Lu, F Y Sun, L M Zhang, A Z Zhang |
Journal | Zhongguo yao li xue bao = Acta pharmacologica Sinica
(Zhongguo Yao Li Xue Bao)
Vol. 10
Issue 6
Pg. 508-11
(Nov 1989)
ISSN: 0253-9756 [Print] China |
PMID | 2561934
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Receptors, Neurotransmitter
- Receptors, Phencyclidine
- Phencyclidine
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Topics |
- Animals
- Basilar Artery
(drug effects)
- Binding Sites
- Cerebral Arteries
(analysis)
- Perfusion
- Phencyclidine
(metabolism)
- Radioligand Assay
- Receptors, Neurotransmitter
(analysis)
- Receptors, Phencyclidine
- Swine
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