【摘 要】
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The pathogenesis of the second major neurodegenerative disorder,Parkinson\'s disease (PD),is closely associated with the dysfunction of potassium (K+) channels.Therefore,PD is also considered to be an ion channel disease or neuronal channelopathy.Mounti
【机 构】
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Collaborative Innovation Center for Brain Science, Department of Physiology, Shandong Provincial Col
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The pathogenesis of the second major neurodegenerative disorder,Parkinson\'s disease (PD),is closely associated with the dysfunction of potassium (K+) channels.Therefore,PD is also considered to be an ion channel disease or neuronal channelopathy.Mounting evidence has shown that K+ channels play crucial roles in the regulations of neurotransmitter release,neuronal excitability,and cell volume.Inhibition of K+ channels enhances the spontaneous firing frequency of nigral dopamine (DA)neurons,induces a transition from tonic firing to burst discharge,and promotes the release of DA in the striatum.Recently,three K+ channels have been identified to protect DA neurons and to improve the motor and non-motor symptoms in PD animal models:small conductance (SK)channels,A-type K+ channels,and Kv7/KCNQ channels.In this review,we summarize the physiological and pharmacological effects of the three K+ channels.We also describe in detail the laboratory investigations regarding K+ channels as a potential therapeutic target for PD.
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