Lack of aquaporin-4 water transport inhibition by antiepileptics and arylsulfonamides

被引:66
作者
Yang, Baoxue
Zhang, Hua
Verkman, A. S. [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
water transport; aquaporin; AQP4; antiepileptics; carbonic anhydrase;
D O I
10.1016/j.bmc.2008.06.005
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
Inhibitors of brain glial water channel aquaporin-4 (AQP4) are of potential clinical utility, as they are predicted to modulate brain edema, neuroexcitation and glial scarring. Recently, Huber et al. (Bioorg. Med. Chem. 2007, 17, 1270-1273; in press) reported that a series of arylsulfonamides, antiepileptics, and related small molecules strongly inhibited AQP4 water transport with IC(50)s down to 1 mu M. We retested the compounds with greatest reported potencies, including acetylsulfanilamide, acetazolamide, 6-ethoxybenzothiazole-2- sulfonamide, topiramate, zonisamide, phenytoin, lamotrigine, and sumatriptan, in AQP4-transfected mammalian cells and primary cultures of brain glial cells, using several sensitive assays of osmotic water permeability. Contrary to the findings of Huber et al., in our studies we found no significant inhibition of AQP4 water permeability by any of the compounds at concentrations up to 100 mu M. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7489 / 7493
页数:5
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