Popoli P, Reggio R, Pèzzola A, Scotti de Carolis A
Pharmacology Department, Istituto Superiore di Sanità, Roma, Italy.
Psychopharmacology (Berl). 1995 Jul;120(2):156-61. doi: 10.1007/BF02246188.
The influence of cholecystokinin (CCK), bilaterally injected into the rostral nucleus accumbens, on the EEG and behavioural effects induced by phencyclidine (PCP) has been studied in rats. CCK (10 ng) significantly inhibited PCP-induced EEG effects (increase of spectral power with respect to pre-drug tracing; increase of relative power distribution in the slowest frequency bands), and behavioural effects (circling and ataxia). The inhibitory effects of CCK were completely antagonized by 1 ng PD 135-158, a selective CCKB receptor antagonist, but not by lorglumide (1 microgram), a selective CCKA receptor antagonist. Since the effects induced by PCP in rodents have been proposed to be an experimental correlate of the psychotic symptoms it induces in humans, these results indicate that CCK may act as a neuroleptic. They also suggest that CCKB receptors located in the rostral nucleus accumbens may be involved in the neuroleptic-like activity of CCK.
已在大鼠中研究了双侧注射到伏隔核嘴侧的胆囊收缩素(CCK)对苯环利定(PCP)诱导的脑电图(EEG)和行为效应的影响。CCK(10纳克)显著抑制PCP诱导的EEG效应(相对于给药前描记,频谱功率增加;最慢频段相对功率分布增加)和行为效应(转圈和共济失调)。CCK的抑制作用被1纳克的选择性CCKB受体拮抗剂PD 135 - 158完全拮抗,但未被1微克的选择性CCKA受体拮抗剂洛谷胺拮抗。由于PCP在啮齿动物中诱导的效应被认为是其在人类中诱导的精神症状的实验相关指标,这些结果表明CCK可能作为一种抗精神病药物起作用。它们还表明位于伏隔核嘴侧的CCKB受体可能参与了CCK的抗精神病样活性。