Stringer J L, Greenfield L J, Hackett J T, Guyenet P G
Brain Res. 1983 Nov 28;280(1):127-38. doi: 10.1016/0006-8993(83)91180-0.
Long-term potentiation (LTP) of synaptic transmission in the rat hippocampus in vivo and in vitro, was studied using field potentials. Pretreatment with phencyclidine (PCP) or 'sigma' opiates blocked LTP in vivo while mu and kappa opiates and the antagonist naloxone were ineffective. Scopolamine (20 mg/kg i.p.) neither prevented LTP nor antagonized the LTP-blocking effect of PCP. In vitro, PCP up to 100 microM did not alter synaptic activation of CA1 pyramidal cells by stratum radiatum stimulation but blocked LTP in a dose-dependent manner (ED50: 3 microM). The sigma opiate, cyclazocine, also prevented the induction of LTP in vitro while morphine and procaine were ineffective.
利用场电位研究了大鼠海马体内和体外突触传递的长时程增强(LTP)。用苯环己哌啶(PCP)或“σ”阿片类药物预处理可阻断体内的LTP,而μ和κ阿片类药物以及拮抗剂纳洛酮则无效。东莨菪碱(20mg/kg腹腔注射)既不能预防LTP,也不能拮抗PCP的LTP阻断作用。在体外,高达100μM的PCP不会改变辐射层刺激对CA1锥体细胞的突触激活,但以剂量依赖性方式阻断LTP(半数有效剂量:3μM)。σ阿片类药物环唑辛也可在体外阻止LTP的诱导,而吗啡和普鲁卡因则无效。