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水通道蛋白4的缺失会在小鼠海马体突触刺激期间增加细胞外钾离子浓度。

Deletion of aquaporin-4 increases extracellular K(+) concentration during synaptic stimulation in mouse hippocampus.

作者信息

Haj-Yasein Nadia Nabil, Bugge Cecilie Elisabeth, Jensen Vidar, Østby Ivar, Ottersen Ole Petter, Hvalby Øivind, Nagelhus Erlend Arnulf

机构信息

Letten Centre, Institute of Basic Medical Sciences, University of Oslo, 0317, Oslo, Norway.

出版信息

Brain Struct Funct. 2015 Jul;220(4):2469-74. doi: 10.1007/s00429-014-0767-z. Epub 2014 Apr 18.

Abstract

The coupling between the water channel aquaporin-4 (AQP4) and K(+) transport has attracted much interest. In this study, we assessed the effect of Aqp4 deletion on activity-induced [K(+)]o changes in acute slices from hippocampus and corpus callosum of adult mice. We show that Aqp4 deletion has a layer-specific effect on [K(+)]o that precisely mirrors the known effect on extracellular volume dynamics. In CA1, the peak [K(+)]o in stratum radiatum during 20 Hz stimulation of Schaffer collateral/commissural fibers was significantly higher in Aqp4 (-/-) mice than in wild types, whereas no differences were observed throughout the [K(+)]o recovery phase. In stratum pyramidale and corpus callosum, neither peak [K(+)]o nor post-stimulus [K(+)]o recovery was affected by Aqp4 deletion. Our data suggest that AQP4 modulates [K(+)]o during synaptic stimulation through its effect on extracellular space volume.

摘要

水通道蛋白4(AQP4)与钾离子(K⁺)转运之间的耦合引起了广泛关注。在本研究中,我们评估了成年小鼠海马体和胼胝体急性切片中Aqp4基因缺失对活动诱导的细胞外钾离子浓度([K⁺]o)变化的影响。我们发现,Aqp4基因缺失对[K⁺]o具有层特异性影响,这与对细胞外体积动力学的已知影响精确对应。在CA1区,当刺激海马体联合纤维/连合纤维时,Aqp4基因敲除(-/-)小鼠的辐射层中[K⁺]o峰值在20Hz刺激时显著高于野生型小鼠,而在整个[K⁺]o恢复阶段未观察到差异。在锥体层和胼胝体中,Aqp4基因缺失对[K⁺]o峰值和刺激后[K⁺]o恢复均无影响。我们的数据表明,AQP4通过对细胞外空间体积的影响在突触刺激期间调节[K⁺]o。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dabf/4481334/b962813891a8/429_2014_767_Fig1_HTML.jpg

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