Johnson K M
Pharmacol Biochem Behav. 1982 Jul;17(1):53-7. doi: 10.1016/0091-3057(82)90262-3.
Phencyclidine (PCP) is known to have anticholinergic effects in various in vitro test systems and to inhibit the binding of muscarinic antagonists to rat brain membranes. In order to verify the anticholinergic properties of PCP, its interaction with oxotremorine (OXO), a muscarinic agonist, was studied in mice. OXO (1 mg/kg) in combination with PCP (10 mg/kg) was lethal in 100% of the mice studied. The lethality of this combination was completely reversed by 3.3 mg/kg methyl atropine bromide (MA), a quarternary muscarinic antagonist. Therefore, PCP appears to act as a muscarinic agonist in some peripheral systems. The central interactions between PCP and OXO were studied in mice in which the preipheral effects of OXO were blocked by MA. In a test of motor performance, OXO potentiated the effect of PCP at one dose only. Contrary to the effects of PCP in other behavioral measures, no evidence for an anticholinergic effect of PCP was observed. The in vivo anticholinergic potential of PCP was estimated by adding a brain extract from PCP-treated mice to brain muscarinic receptors in the presence of 3H-quinuclidinyl benzilate. These data suggested that PCP, after in vivo administration, does not attain a sufficient brain concentration to directly affect central muscarinic receptors. However, a direct action of PCP on peripheral muscarinic receptors was not discounted.
已知苯环己哌啶(PCP)在各种体外测试系统中具有抗胆碱能作用,并能抑制毒蕈碱拮抗剂与大鼠脑膜的结合。为了验证PCP的抗胆碱能特性,研究了其与毒蕈碱激动剂氧化震颤素(OXO)在小鼠体内的相互作用。OXO(1毫克/千克)与PCP(10毫克/千克)联合使用对100%的受试小鼠具有致死性。这种联合用药的致死性可被3.3毫克/千克的季铵类毒蕈碱拮抗剂甲基溴化阿托品(MA)完全逆转。因此,PCP在某些外周系统中似乎起到了毒蕈碱激动剂的作用。在MA阻断了OXO外周效应的小鼠中研究了PCP与OXO的中枢相互作用。在一项运动性能测试中,OXO仅在一个剂量下增强了PCP的作用。与PCP在其他行为测量中的作用相反,未观察到PCP具有抗胆碱能作用的证据。通过在存在3H-喹核醇基苯甲酸酯的情况下将PCP处理小鼠的脑提取物添加到脑毒蕈碱受体中来评估PCP的体内抗胆碱能潜力。这些数据表明,PCP在体内给药后,大脑中未能达到足以直接影响中枢毒蕈碱受体的浓度。然而,并未排除PCP对外周毒蕈碱受体的直接作用。