Delayed regional metabolic actions of phencyclidine.

Delayed regional metabolic actions of phencyclidine.
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苯环己哌啶的局部代谢作用延迟。

DOI:
10.1016/0014-2999(93)90926-9
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发表时间:
1993
影响因子:
5
通讯作者:
Tamminga,CA
Tamminga,CA
中科院分区:
医学2区
文献类型:
--
作者:
Gao,XM;Shirakawa,O;Du,F;Tamminga,CA

文献摘要

被引文献

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苯环利定(PCP)是一种滥用的拟精神病药物,在人类中产生精神变化和表现,使人联想到精神分裂症,尽管这些作用的机制仍然未知。我们在这里报告了PCP对局部脑葡萄糖代谢作用的双相时间过程,持续时间超过48小时。单次给予PCP(8.6 mg/kg)后,葡萄糖代谢最初增加(3 h),随后降低(24 h),直至48 h才恢复至基线水平。单次较低剂量的五氯苯酚(0.86毫克/千克),被认为是对NMDA-PCP受体具有选择性作用的剂量,不会产生早期代谢变化(3小时),但复制了局部代谢减退,尽管在24小时时强度较低。延迟性脑代谢减退似乎与PCP诱导的压后皮质细胞内空泡化无关。这些代谢变化可能与PCP的拟精神病效应有关,因此可能与人类精神病有关。
Phencyclidine (PCP), a psychotomimetic drug of abuse, produces mental changes and manifestations in humans which are reminiscent of schizophrenia, though the mechanism of these actions remains unknown. We report here a biphasic time course of PCP action on regional cerebral glucose metabolism extending over 48 h. A single dose of PCP (8.6 mg/kg) produces an initial increase in glucose metabolism (at 3 h) and a later decrease in glucose metabolism (at 24 h) without a return to baseline until 48 h. A single lower dose of PCP (0.86 mg/kg), a dose which is considered selective for action at the NMDA-PCP receptor, produces no early metabolic change (at 3 h), but replicates the regional hypometabolism albeit less intense at 24 h. The delayed cerebral hypometabolism does not appear to be related to PCP-induced intracellular vacuolization, seen in the retrosplenial cortex. These metabolic changes may be associated with the psychotomimetic effects of PCP and thus may be relevant to psychosis in humans.