Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication

Phencyclidine (PCP) produces schizophrenia-like psychosis and acute PCP-intoxications; however, whether glutamate/NMDA-receptor blockade by PCP modulates or not these mechanisms has remained to be clarified. To clarify this mechanism, we determined interaction among voltage-gated Na+-channel inhibit...

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Main Authors: Gang Zhu, Motohiro Okada, Daishi Uchiyama, Tadashi Ohkubo, Shukuko Yoshida, Sunao Kaneko
Format: Article
Language:English
Published: Elsevier 2004-01-01
Series:Journal of Pharmacological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1347861319324399
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spelling doaj-21f9cc2f93f9477faef94885d371a5022020-11-25T01:20:32ZengElsevierJournal of Pharmacological Sciences1347-86132004-01-01952214227Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine IntoxicationGang Zhu0Motohiro Okada1Daishi Uchiyama2Tadashi Ohkubo3Shukuko Yoshida4Sunao Kaneko5Department of Neuropsychiatry, Hirosaki University School of Medicine, Hirosaki 036-8562, JapanDepartment of Neuropsychiatry, Hirosaki University School of Medicine, Hirosaki 036-8562, Japan; Corresponding author. FAX: +81-172-395067 E-mail: okadamot@cc.hirosaki-u.ac.jpCenter for Joint Research, Hirosaki University, Hirosaki 036-8560, JapanClinical Research Center, Hirosaki University Hospital, Hirosaki 036-8563, JapanDepartment of Neuropsychiatry, Hirosaki University School of Medicine, Hirosaki 036-8562, Japan; Institute of Neuroscience and Molecular Biology, Shibata BIOTEC, Hirosaki 036-8084, JapanDepartment of Neuropsychiatry, Hirosaki University School of Medicine, Hirosaki 036-8562, JapanPhencyclidine (PCP) produces schizophrenia-like psychosis and acute PCP-intoxications; however, whether glutamate/NMDA-receptor blockade by PCP modulates or not these mechanisms has remained to be clarified. To clarify this mechanism, we determined interaction among voltage-gated Na+-channel inhibitor, tetrodotoxin (TTX), Golgi-disturbing-agent, brefeldin-A (BFA), and PCP on releases of glutamate, GABA, and monoamine in prefrontal-cortex (pFC), using microdialysis. PCP increased basal monoamine release, whereas it decreased basal GABA release, without affecting glutamate release. PCP increased K+-evoked monoamine release, whereas it decreased K+-evoked glutamate and GABA releases. TTX reduced basal monoamine and GABA releases without affecting glutamate release, whereas BFA did not affect them. Interestingly, BFA and TTX inhibited PCP-associated basal monoamine release and abolished PCP-induced reduction of basal GABA release without affecting glutamate release. BFA and TTX reduced K+-evoked releases of all neurotransmitters. BFA inhibited PCP-associated K+-evoked monoamine release, but TTX did not affect them. PCP-induced reduction of K+-evoked GABA and glutamate releases was abolished by TTX and BFA. These results indicate that PCP reduces GABAergic transmission via NMDA-receptor blockade and activates intracellular endoplasmic-reticulum-associated signal-transduction, resulting in enhancement of monoaminergic transmission in pFC. Thus, these PCP properties support the hypothesis that mechanisms of the neurological symptoms of acute PCP-intoxication, convulsion, and rhabdomyolysis may be involved in both reduction of GABAergic-transmission and activation of endoplasmic-reticulum-associated signal-transduction induced by PCP. Keywords:: phencyclidine, exocytosis, endoplasmic-reticulum, schizophrenia, microdialysishttp://www.sciencedirect.com/science/article/pii/S1347861319324399
collection DOAJ
language English
format Article
sources DOAJ
author Gang Zhu
Motohiro Okada
Daishi Uchiyama
Tadashi Ohkubo
Shukuko Yoshida
Sunao Kaneko
spellingShingle Gang Zhu
Motohiro Okada
Daishi Uchiyama
Tadashi Ohkubo
Shukuko Yoshida
Sunao Kaneko
Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
Journal of Pharmacological Sciences
author_facet Gang Zhu
Motohiro Okada
Daishi Uchiyama
Tadashi Ohkubo
Shukuko Yoshida
Sunao Kaneko
author_sort Gang Zhu
title Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
title_short Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
title_full Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
title_fullStr Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
title_full_unstemmed Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
title_sort hyperactivity of endoplasmic reticulum associated exocytosis mechanism contributes to acute phencyclidine intoxication
publisher Elsevier
series Journal of Pharmacological Sciences
issn 1347-8613
publishDate 2004-01-01
description Phencyclidine (PCP) produces schizophrenia-like psychosis and acute PCP-intoxications; however, whether glutamate/NMDA-receptor blockade by PCP modulates or not these mechanisms has remained to be clarified. To clarify this mechanism, we determined interaction among voltage-gated Na+-channel inhibitor, tetrodotoxin (TTX), Golgi-disturbing-agent, brefeldin-A (BFA), and PCP on releases of glutamate, GABA, and monoamine in prefrontal-cortex (pFC), using microdialysis. PCP increased basal monoamine release, whereas it decreased basal GABA release, without affecting glutamate release. PCP increased K+-evoked monoamine release, whereas it decreased K+-evoked glutamate and GABA releases. TTX reduced basal monoamine and GABA releases without affecting glutamate release, whereas BFA did not affect them. Interestingly, BFA and TTX inhibited PCP-associated basal monoamine release and abolished PCP-induced reduction of basal GABA release without affecting glutamate release. BFA and TTX reduced K+-evoked releases of all neurotransmitters. BFA inhibited PCP-associated K+-evoked monoamine release, but TTX did not affect them. PCP-induced reduction of K+-evoked GABA and glutamate releases was abolished by TTX and BFA. These results indicate that PCP reduces GABAergic transmission via NMDA-receptor blockade and activates intracellular endoplasmic-reticulum-associated signal-transduction, resulting in enhancement of monoaminergic transmission in pFC. Thus, these PCP properties support the hypothesis that mechanisms of the neurological symptoms of acute PCP-intoxication, convulsion, and rhabdomyolysis may be involved in both reduction of GABAergic-transmission and activation of endoplasmic-reticulum-associated signal-transduction induced by PCP. Keywords:: phencyclidine, exocytosis, endoplasmic-reticulum, schizophrenia, microdialysis
url http://www.sciencedirect.com/science/article/pii/S1347861319324399
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