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In-Depth Study of the Interaction Sensitivity and Gating Modulation by PUFAs on K+ Channels; Interaction and New Targets

机译:PUFA在K +通道上的相互作用灵敏度和门控调制的深入研究;互动与新目标

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摘要

Voltage gated potassium channels (KV) are membrane proteins that allow selective flow of K+ ions in a voltage-dependent manner. These channels play an important role in several excitable cells as neurons, cardiomyocytes, and vascular smooth muscle. Over the last 20 years, it has been shown that omega-3 polyunsaturated fatty acids (PUFAs) enhance or decrease the activity of several cardiac KV channels. PUFAs-dependent modulation of potassium ion channels has been reported to be cardioprotective. However, the precise cellular mechanism underlying the cardiovascular benefits remained unclear in part because new PUFAs targets and signaling pathways continue being discovered. In this review, we will focus on recent data available concerning the following aspects of the KV channel modulation by PUFAs: (i) the exact residues involved in PUFAs-KV channels interaction; (ii) the structural PUFAs determinants important for their effects on KV channels; (iii) the mechanism of the gating modulation of KV channels and, finally, (iv) the PUFAs modulation of a few new targets present in smooth muscle cells (SMC), KCa1.1, K2P, and KATP channels, involved in vascular relaxation.
机译:电压门控钾通道(KV)是一种膜蛋白,可允许K + 离子以电压依赖性方式选择性流动。这些通道在神经细胞,心肌细胞和血管平滑肌等几种兴奋性细胞中起重要作用。在过去的20年中,已证明omega-3多不饱和脂肪酸(PUFA)增强或降低了几个心脏KV通道的活性。据报道,PUFAs依赖性的钾离子通道调节具有心脏保护作用。但是,仍不清楚心血管潜在的确切细胞机制,部分原因是继续发现了新的PUFA靶标和信号传导途径。在这篇综述中,我们将重点关注有关PUFA对KV通道调制的以下方面的最新数据:(i)PUFA与KV通道相互作用所涉及的确切残基; (ii)对于其对KV频道的影响而言重要的结构性PUFA; (iii)KV通道的门控调节机制,最后(iv)平滑肌细胞(SMC),KCa1.1,K2P和KATP通道中存在的一些新靶标的PUFA调节,这些靶标涉及血管舒张。

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