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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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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