Cinnamyl-3,4-dihydroxy-α-cyanocinnamate and nordihydroguaiaretic acid inhibit human Kv1.5 currents independently of lipoxygenase

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• 作者：Ying-Zi Gong ; Wei-Guang Ding ; Jie Wu ; Keiko Tsuji ; Minoru Horie ; Hiroshi Matsuura
• 关键词：Kv1.5 ; I_Kur ; CDC ; NDGA ; Lipoxygenase ; Open channel block ; Site-directed mutagenesis
• 刊名：European Journal of Pharmacology
• 出版年：2008
• 出版时间：14 December 2008
• 年：2008
• 卷：600
• 期：1-3
• 页码：18-25
• 全文大小：784 K

文摘

In humans, Kv1.5 (hKv1.5) channels conduct the ultra-rapid delayed rectifier K⁺ current (I_Kur) that is important for the repolarization of cardiac action potentials. We aimed at examining the effect of lipoxygenase inhibitors cinnamyl-3,4-dihydroxy-α-cyanocinnamate (CDC), nordihydroguaiaretic acid (NDGA), and gossypol on hKv1.5 wild-type and mutant channels heterologously expressed in Chinese hamster ovary (CHO) cells, by use of the site-directed mutagenesis and whole-cell patch-clamp method. CDC and NDGA, but not gossypol, a structurally dissimilar inhibitor, reversibly inhibited hKv1.5 current in a concentration-dependent manner with IC₅₀ of 5.7 μM and 16.4 μM, respectively. The blockade evoked by both drugs was voltage-dependent between − 20 and + 10 mV (voltage range of channel opening). Moreover, this blocking action was found to progress with time during depolarizing voltage steps with a more rapid block at higher concentrations. CDC induced slight but significant delay of the deactivation rate. However, NDGA markedly slowed the deactivation time course, resulting in a tail crossover phenomenon. The recovery time constants from current block at repolarizing potentials for CDC and NDGA were 60.9 ms and 129.7 ms, respectively. Mutation of arginine 487 to valine (R487V) in the outer pore region of the channel significantly reduced the CDC action. These results demonstrate for the first time that CDC and NDGA block hKv1.5 channels by binding to the open state of the channels, independently of their effects on lipoxygenase activity. The putative binding site for CDC appears to be related to arginine 487 located in the outer pore region.