A- and D-type potassium currents regulate axonal action potential repolarization in midbrain dopamine neurons

被引:10
|
作者
Xiao, Yujie [1 ,2 ]
Yang, Jun [1 ,2 ]
Ji, Wenliang [3 ]
He, Quansheng [4 ]
Mao, Lanqun [3 ]
Shu, Yousheng [4 ]
机构
[1] Beijing Normal Univ, State Key Lab Cognit Neurosci & Learning, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, IDG McGovern Inst Brain Res, Beijing 100875, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Key Lab Analyt Chem Living Biosyst, Beijing 100190, Peoples R China
[4] Fudan Univ, State Key Lab Med Neurobiol, Inst Translat Brain Res, MOE Frontiers Ctr Brain Sci,Dept Neurol,Huashan H, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Dopamine neuron; Axon; A-type K+ current; D-type K+ current; Action potential; K+ CHANNELS; SUBCELLULAR-LOCALIZATION; SUBSTANTIA-NIGRA; MOLECULAR-BASIS; KV1; EXCITABILITY; PROPAGATION; MODULATION; FREQUENCY;
D O I
10.1016/j.neuropharm.2020.108399
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 wholecell 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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页数:9
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