Ion transport blockers inhibit human rhinovirus 2 release

被引:17
作者
Gazina, EV [1 ]
Harrison, DN
Jefferies, M
Tan, H
Williams, D
Anderson, DA
Petrou, S
机构
[1] Univ Melbourne, Howard Florey Inst Expt Physiol & Med, Melbourne, Vic 3010, Australia
[2] Macfarlane Burnet Inst, Prahran, Vic 3181, Australia
[3] Univ Melbourne, Dept Physiol, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会;
关键词
ion transport blockers; rhinovirus;
D O I
10.1016/j.antiviral.2005.05.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Picornavirus replication causes leakage of cytoplasmic K+ and an influx of Na+ and Ca2+. In this study, we have explored the possibility that a blockade of Ca2+ and Na+ influx would reduce rhinovirus production and/or release. The Ca2+-channel blockers, verapamil and diltiazem, as well as the blocker of Na+/H+ exchange and the epithelial Na' channel, EIPA, inhibited both virus production and release. The effect on vir-us release was more pronounced than the effect on production, thus raising the possibility that rhinovirus release may serve as a target for antiviral agents. Unexpectedly, our results also showed that the antiviral activity of the Ca2+-channel blockers was not due to the block of Ca2+ influx. Similarly, the antiviral activity of EIPA appeared to be unrelated to the blockade of cellular Na+/H+ exchanger or the epithelial Na+ channel. Potential alternative mechanisms of the antiviral activity of these compounds are discussed. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 106
页数:9
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