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U0126,一种 MEK 抑制剂,在原代培养物和脑片中对钾通道有很强的阻断作用。

Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices.

机构信息

School of Life Sciences, South China Normal University, Guangzhou, 510631, China.

Institute of Neuroscience, Chinese Academy of Sciences, 320 Yue Yang Road, Shanghai, 200031, China.

出版信息

Sci Rep. 2018 Jun 11;8(1):8808. doi: 10.1038/s41598-018-27235-1.

DOI:10.1038/s41598-018-27235-1
PMID:29892075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5995919/
Abstract

U0126 (1,4-diamino-2,3-dicyano-1,4-bis (2-aminophenylthio) butadiene), a widely used mitogen-activated protein kinase kinase (MEK) inhibitor, was found to accelerate voltage-gated K channel (K) inactivation in heterologous cells expressing several types of K. The goal of this study was to examine whether U0126 at a concentration thought to specifically inhibit MEK signaling also inhibits K in native neurons of primary cultures or brain slices. U0126 caused a dose-dependent inhibition of both the transient (I) and sustained (I) components of K currents in hippocampal neurons. U0126 also exhibited much higher potency on the I and I than the classical K blockers 4-aminopyridine (4-AP) and tetraethylammonium (TEA). Consistent with its inhibitory effect on K, U0126 broadened action potential duration, profoundly affected the repolarizing phase, and dramatically reduced firing frequency in response to current pulse injections. Despite the potent and reversible action of U0126 on K channels, PD98059, a structurally-unrelated MEK inhibitor, did not induce such an effect, suggesting U0126 may act independently of MEK inhibition. Together, these results raise cautions for using U0126 as a specific inhibitor for studying MEK signaling in neurons; on the other hand, further studies on the blocking mechanisms of U0126 as a potent inhibitor of K may provide useful insights into the structure-function relationship of K in general.

摘要

U0126(1,4-二氨基-2,3-二氰基-1,4-双(2-氨基苯基硫代)丁二烯)是一种广泛使用的丝裂原活化蛋白激酶激酶(MEK)抑制剂,已被发现可加速表达多种类型 K 的异源细胞中的电压门控 K 通道(K)失活。本研究的目的是检查在浓度上被认为可特异性抑制 MEK 信号的 U0126 是否也会抑制原代培养神经元或脑片中的 K。U0126 导致海马神经元中的瞬时(I)和持续(I)K 电流成分呈剂量依赖性抑制。U0126 对 I 和 I 的抑制作用也比经典的 K 阻断剂 4-氨基吡啶(4-AP)和四乙铵(TEA)高得多。与对 K 的抑制作用一致,U0126 使动作电位持续时间变宽,对复极化阶段产生深远影响,并在电流脉冲注入时大大降低了放电频率。尽管 U0126 对 K 通道具有强大且可逆的作用,但结构上不相关的 MEK 抑制剂 PD98059 并未引起这种作用,表明 U0126 可能独立于 MEK 抑制作用。总之,这些结果对使用 U0126 作为研究神经元中 MEK 信号的特异性抑制剂提出了警告;另一方面,对 U0126 作为 K 有效抑制剂的阻断机制的进一步研究可能为 K 的结构-功能关系提供有用的见解。

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