A central role of the BK potassium channel in behavioral responses to ethanol in C-elegans

被引:276
作者
Davies, AG
Pierce-Shimomura, JT
Kim, H
VanHoven, MK
Thiele, TR
Bonci, A
Bargmann, CI
McIntire, SL [1 ]
机构
[1] Univ Calif San Francisco, Ernest Gallo Clin, Emeryville, CA 94608 USA
[2] Univ Calif San Francisco, Res Ctr, Dept Neurol, Program Neurosci, Emeryville, CA 94608 USA
[3] Univ Calif San Francisco, Res Ctr, Dept Neurol, Program Biomed Sci, Emeryville, CA 94608 USA
[4] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Biochem & Biophys, Dept Anat, San Francisco, CA 94143 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1016/S0092-8674(03)00979-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The activities of many neuronal proteins are modulated by ethanol, but the fundamental mechanisms underlying behavioral effects of ethanol remain unclear. To identify mechanisms responsible for intoxication, we screened for Caenorhabditis elegans mutants with altered behavioral responses to ethanol. We found that slo-1 mutants, which were previously recognized as having slightly uncoordinated movement, are highly resistant to ethanol in two behavioral assays. Numerous loss-of-function slo-1 alleles emerged from our screens, indicating that slo-1 has a central role in ethanol responses. slo-1 encodes the BK potassium channel. Electrophysiological analysis shows that ethanol activates the channel in vivo, which would inhibit neuronal activity. Moreover, behaviors of slo-1 gain-of-function mutants resemble those of ethanol-intoxicated animals. These results demonstrate that selective activation of BK channels is responsible for acute intoxicating effects of ethanol in C. elegans. BK channel activation may explain a variety of behavioral responses to ethanol in invertebrate and vertebrate systems.
引用
收藏
页码:655 / 666
页数:12
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