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Astrocytes and Huntington’s Disease
Authors:Baljit S Khakh  Michael V Sofroniew
Institution:Departments of Physiology, Neurobiology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California 90095-1751, United States
Abstract:In this Viewpoint, we summarize and discuss the recent serendipitous discovery of an astrocyte Kir4.1 potassium channel dysfunction in two mouse models of Huntington’s disease (HD). Restoration of Kir4.1 channels within astrocytes in vivo attenuated neuronal dysfunction, some aspects of motor dysfunction and increased survival time in a HD mouse model. Overall, the data show that aspects of altered neuronal excitability associated with HD may be secondary to changes in astrocyte-mediated K+ homeostasis, thereby revealing a new striatal neural microcircuit mechanism in HD, and Kir4.1 channels and astrocytes as potential therapeutic targets for drug development.
Keywords:Huntington’  s disease  astrocyte  striatum  potassium channel  microcircuit  basal ganglia  Kir4  1
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