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对自由活动的大鼠急性给予苯环利定可诱导内侧前额叶皮质神经元的强直性激活。

Acute administration of phencyclidine induces tonic activation of medial prefrontal cortex neurons in freely moving rats.

作者信息

Suzuki Y, Jodo E, Takeuchi S, Niwa S, Kayama Y

机构信息

Department of Physiology, Fukushima Medical University School of Medicine, 1 Hikari-ga-oka, Fukushjima 960-1295, Japan.

出版信息

Neuroscience. 2002;114(3):769-79. doi: 10.1016/s0306-4522(02)00298-1.

DOI:10.1016/s0306-4522(02)00298-1
PMID:12220577
Abstract

Recent studies have reported that acute administration of the psychotomimetic drug phencyclidine results in considerable increases in the amounts of both extracellular glutamate and dopamine in the medial prefrontal cortex (mPFC). However, the effect of phencyclidine on the firing activity of mPFC neurons remains unknown. Here, we report the first data on phencyclidine-induced activation of mPFC neurons in freely moving rats. Unanesthetized rats received an intraperitoneal injection of either phencyclidine (5 mg/kg) or physiological saline (0.5 ml/kg) in order to investigate the impulse activity of mPFC neurons and behavioral activity. The phencyclidine injection induced a remarkable increase (two-fold or more) in the spontaneous discharge rate of the majority of mPFC neurons (20/23), and this increase lasted for more than 70 min. In addition, a considerable augmentation of behavioral activity was observed that nearly paralleled that of the mPFC neuronal activation. In contrast, microiontophoretically applied phencyclidine exerted little influence on the spontaneous firing activity of most mPFC neurons (25/29) in anesthetized rats, although systemically applied phencyclidine produced activation of mPFC neurons even under general anesthesia. These results suggest that the behavioral abnormalities induced by acute administration of phencyclidine may be caused by hyperactivation of mPFC neurons, and that this hyperactivation is elicited through excitatory inputs from brain regions outside the mPFC.

摘要

最近的研究报告称,急性给予拟精神病药物苯环利定会导致内侧前额叶皮质(mPFC)细胞外谷氨酸和多巴胺的量显著增加。然而,苯环利定对mPFC神经元放电活动的影响仍然未知。在此,我们报告了关于苯环利定诱导自由活动大鼠mPFC神经元激活的首批数据。为了研究mPFC神经元的冲动活动和行为活动,未麻醉的大鼠腹腔注射苯环利定(5毫克/千克)或生理盐水(0.5毫升/千克)。注射苯环利定导致大多数mPFC神经元(20/23)的自发放电率显著增加(两倍或更多),且这种增加持续超过70分钟。此外,观察到行为活动有相当大的增强,这几乎与mPFC神经元的激活平行。相比之下,在麻醉大鼠中,微离子透入法施加苯环利定对大多数mPFC神经元(25/29)的自发放电活动影响很小,尽管全身应用苯环利定即使在全身麻醉下也会使mPFC神经元激活。这些结果表明,急性给予苯环利定所诱导的行为异常可能是由mPFC神经元的过度激活引起的,并且这种过度激活是通过来自mPFC以外脑区的兴奋性输入引发的。

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