Nausch Bernhard, Rode Frederik, Jørgensen Susanne, Nardi Antonio, Korsgaard Mads P G, Hougaard Charlotte, Bonev Adrian D, Brown William D, Dyhring Tino, Strøbæk Dorte, Olesen Søren-Peter, Christophersen Palle, Grunnet Morten, Nelson Mark T, Rønn Lars C B
NeuroSearch A/S, Ballerup, Denmark (F.R., S.J., A.N., M.P.G.K., C.H., W.D.B., T.D., D.S., S.-P.O., P.C., M.G., L.C.B.R.); University of Vermont, Department of Pharmacology, Burlington, Vermont (B.N., A.D.B., M.T.N.); and Institute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom (M.T.N.).
NeuroSearch A/S, Ballerup, Denmark (F.R., S.J., A.N., M.P.G.K., C.H., W.D.B., T.D., D.S., S.-P.O., P.C., M.G., L.C.B.R.); University of Vermont, Department of Pharmacology, Burlington, Vermont (B.N., A.D.B., M.T.N.); and Institute of Cardiovascular Sciences, University of Manchester, Manchester, United Kingdom (M.T.N.)
J Pharmacol Exp Ther. 2014 Sep;350(3):520-30. doi: 10.1124/jpet.113.212662. Epub 2014 Jun 20.
Large-conductance Ca(2+)-activated K(+) channels (BK, KCa1.1, MaxiK) are important regulators of urinary bladder function and may be an attractive therapeutic target in bladder disorders. In this study, we established a high-throughput fluorometric imaging plate reader-based screening assay for BK channel activators and identified a small-molecule positive modulator, NS19504 (5-[(4-bromophenyl)methyl]-1,3-thiazol-2-amine), which activated the BK channel with an EC50 value of 11.0 ± 1.4 µM. Hit validation was performed using high-throughput electrophysiology (QPatch), and further characterization was achieved in manual whole-cell and inside-out patch-clamp studies in human embryonic kidney 293 cells expressing hBK channels: NS19504 caused distinct activation from a concentration of 0.3 and 10 µM NS19504 left-shifted the voltage activation curve by 60 mV. Furthermore, whole-cell recording showed that NS19504 activated BK channels in native smooth muscle cells from guinea pig urinary bladder. In guinea pig urinary bladder strips, NS19504 (1 µM) reduced spontaneous phasic contractions, an effect that was significantly inhibited by the specific BK channel blocker iberiotoxin. In contrast, NS19504 (1 µM) only modestly inhibited nerve-evoked contractions and had no effect on contractions induced by a high K(+) concentration consistent with a K(+) channel-mediated action. Collectively, these results show that NS19504 is a positive modulator of BK channels and provide support for the role of BK channels in urinary bladder function. The pharmacologic profile of NS19504 indicates that this compound may have the potential to reduce nonvoiding contractions associated with spontaneous bladder overactivity while having a minimal effect on normal voiding.
大电导钙激活钾通道(BK、KCa1.1、MaxiK)是膀胱功能的重要调节因子,可能是膀胱疾病中一个有吸引力的治疗靶点。在本研究中,我们建立了一种基于高通量荧光成像酶标仪的BK通道激活剂筛选测定法,并鉴定出一种小分子正性调节剂NS19504(5-[(4-溴苯基)甲基]-1,3-噻唑-2-胺),其激活BK通道的EC50值为11.0±1.4μM。使用高通量电生理学(QPatch)进行命中验证,并在表达hBK通道的人胚肾293细胞的手动全细胞和内向外膜片钳研究中进一步表征:NS19504从0.3μM的浓度开始引起明显激活,10μM的NS19504使电压激活曲线左移60 mV。此外,全细胞记录显示NS19504激活了豚鼠膀胱天然平滑肌细胞中的BK通道。在豚鼠膀胱条中,NS19504(1μM)减少了自发性相性收缩,该效应被特异性BK通道阻滞剂iberiotoxin显著抑制。相比之下,NS19504(1μM)仅适度抑制神经诱发的收缩,对高钾浓度诱导的收缩没有影响,这与钾通道介导的作用一致。总体而言,这些结果表明NS19504是BK通道的正性调节剂,并为BK通道在膀胱功能中的作用提供了支持。NS19504的药理学特征表明,该化合物可能有潜力减少与自发性膀胱过度活动相关的非排尿收缩,同时对正常排尿的影响最小。