GIRK1-mediated inwardly rectifying potassium current suppresses the epileptiform burst activities and the potential antiepileptic effect of ML297
Copyright © 2018 Elsevier Masson SAS. All rights reserved..
G protein-gated inwardly rectifying potassium (GIRK) channels are important inhibitory regulators of neuronal excitability in central nervous system, and the impairment of GIRK channel function has been reported to be associated with the susceptibility of epilepsy. However, the dynamics of GIRK channels in the pathogenesis of epilepsy are still unclear. In this study, our results showed that cyclothiazide, a potent convulsant, dose dependently increased the epileptiform bursting activities and suppressed the baclofen induced GIRK currents. In addition, TPQ, a selective GIRK antagonist, significantly decreased the total inwardly rectifying potassium (Kir) current, and increased the neuronal epileptiform activities. In contrast, ML297, a potent and selective GIRK channel agonist, reversed the cyclothiazide induced decrease of GIRK currents and the increase of neuronal excitability in cultured hippocampal neurons. Further investigation revealed that GIRK1, but not GIRK2, played a key role in suppressing epileptic activities. Finally, in pilocarpine mice seizure model, we demonstrated that ML297 significantly suppressed the seizure behavior. In summary, our current results indicate that GIRK channels, especially GIRK1-containing channels, are involved in epileptic activities and ML297 has a potential antiepileptic effect.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2018 |
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| Erschienen: |
2018 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:101 |
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| Enthalten in: |
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie - 101(2018) vom: 15. Mai, Seite 362-370 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Huang, Yian [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Completed 12.09.2018 Date Revised 12.09.2018 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1016/j.biopha.2018.02.114 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM281565856 |
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| 245 | 1 | 0 | |a GIRK1-mediated inwardly rectifying potassium current suppresses the epileptiform burst activities and the potential antiepileptic effect of ML297 |
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| 520 | |a G protein-gated inwardly rectifying potassium (GIRK) channels are important inhibitory regulators of neuronal excitability in central nervous system, and the impairment of GIRK channel function has been reported to be associated with the susceptibility of epilepsy. However, the dynamics of GIRK channels in the pathogenesis of epilepsy are still unclear. In this study, our results showed that cyclothiazide, a potent convulsant, dose dependently increased the epileptiform bursting activities and suppressed the baclofen induced GIRK currents. In addition, TPQ, a selective GIRK antagonist, significantly decreased the total inwardly rectifying potassium (Kir) current, and increased the neuronal epileptiform activities. In contrast, ML297, a potent and selective GIRK channel agonist, reversed the cyclothiazide induced decrease of GIRK currents and the increase of neuronal excitability in cultured hippocampal neurons. Further investigation revealed that GIRK1, but not GIRK2, played a key role in suppressing epileptic activities. Finally, in pilocarpine mice seizure model, we demonstrated that ML297 significantly suppressed the seizure behavior. In summary, our current results indicate that GIRK channels, especially GIRK1-containing channels, are involved in epileptic activities and ML297 has a potential antiepileptic effect | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Epileptiform burst | |
| 650 | 4 | |a GIRK channel | |
| 650 | 4 | |a GIRK1 subunit | |
| 650 | 4 | |a Hippocampal cultured neuron | |
| 650 | 4 | |a ML297 | |
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| 700 | 1 | |a Zhang, Yuwen |e verfasserin |4 aut | |
| 700 | 1 | |a Kong, Shuzhen |e verfasserin |4 aut | |
| 700 | 1 | |a Zang, Kai |e verfasserin |4 aut | |
| 700 | 1 | |a Jiang, Shize |e verfasserin |4 aut | |
| 700 | 1 | |a Wan, Li |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Lulan |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Guoxiang |e verfasserin |4 aut | |
| 700 | 1 | |a Jiang, Min |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Xin |e verfasserin |4 aut | |
| 700 | 1 | |a Hu, Jie |e verfasserin |4 aut | |
| 700 | 1 | |a Wang, Yun |e verfasserin |4 aut | |
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