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A- and D-type potassium currents regulate axonal action potential repolarization in midbrain dopamine neurons.
Xiao, Yujie; Yang, Jun; Ji, Wenliang; He, Quansheng; Mao, Lanqun; Shu, Yousheng.
Affiliation
  • Xiao Y; State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, 100875, China.
  • Yang J; State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, 100875, China.
  • Ji W; Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
  • He Q; Department of Neurology, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institute for Translational Brain Research, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, 200032, China.
  • Mao L; Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China. Electronic address: lqmao@iccas.ac.cn.
  • Shu Y; Department of Neurology, Huashan Hospital, State Key Laboratory of Medical Neurobiology, Institute for Translational Brain Research, MOE Frontiers Center for Brain Science, Fudan University, Shanghai, 200032, China. Electronic address: yousheng@fudan.edu.cn.
Neuropharmacology ; 185: 108399, 2021 03 01.
Article in En | MEDLINE | ID: mdl-33400937
ABSTRACT
Midbrain dopamine neurons (DANs) regulate various brain functions such as motor control and motivation. Alteration of spiking activities of these neurons could contribute to severe brain disorders including Parkinson's disease and depression. Previous studies showed important roles of somatodendritic voltage-gated K+ channels (Kv) of DANs in governing neuronal excitability and dopamine release. However, it remains largely unclear about the biophysical properties and the function of Kv channels distributed at DAN axons. We performed whole-cell recordings from the axons of DANs in acute mouse midbrain and striatal slices. We detected both rapidly activating/inactivating Kv current (i.e. A-current) and rapidly activating but slowly inactivating current (i.e. D-current) in DAN axons. Pharmacological experiments with channel blockers revealed that these currents are predominantly mediated by Kv1.4 and Kv1.2 subunits, respectively. Blocking these currents could substantially prolong axonal action potentials (APs) via a reduction of their repolarization slope. Together, our results show that Kv channels mediating A- and D-currents shape AP waveforms in midbrain DAN axons, through this regulation they may control dopamine release at the axonal terminals. Therefore, these axonal Kv channels could be drug targets for brain disorders with abnormal dopamine release.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Axons / Action Potentials / Mesencephalon / Kv1.3 Potassium Channel / Kv1.4 Potassium Channel / Dopaminergic Neurons Limits: Animals Language: En Journal: Neuropharmacology Year: 2021 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Axons / Action Potentials / Mesencephalon / Kv1.3 Potassium Channel / Kv1.4 Potassium Channel / Dopaminergic Neurons Limits: Animals Language: En Journal: Neuropharmacology Year: 2021 Document type: Article Affiliation country: China