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Modulation of the Activities of Neuronal Ion Channels by Fatty Acid-Derived Pro-Resolvents

机译:脂肪酸衍生的亲溶剂对神经元离子通道活性的调节

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摘要

Progress of inflammation depends on the balance between two biological mechanisms: pro-inflammatory and pro-resolving processes. Many extracellular and intracellular molecular components including cytokines, growth factors, steroids, neurotransmitters, and lipidergic mediators and their receptors contribute to the two processes, generated from cellular participants during inflammation. Fatty acid-derived mediators are crucial in directing the inflammatory phase and orchestrating heterogeneous reactions of participants such as inflamed cells, innate immune cells, vascular components, innervating neurons, etc. As well as activating specific types of receptor molecules, lipidergic mediators can actively control the functions of various ion channels via direct binding and/or signal transduction, thereby altering cellular functions. Lipid mediators can be divided into two classes based on which of the two processes they promote: pro-inflammatory, which includes prostaglandins and leukotrienes, and pro-resolving, which includes lipoxins, resolvins, and maresins. The research on the modulations of neuronal ion channels regarding the actions of the pro-inflammatory class has begun relatively earlier while the focus is currently expanding to cover the ion channel interaction with pro-resolvents. As a result, knowledge of inhibitory mechanisms by the pro-resolvents, historically seldom found for other known endogenous modulators or pro-inflammatory mediators, is accumulating particularly upon sensory neuronal cation channels. Diverse mechanistic explanations at molecular levels are being proposed and refined. Here we overviewed the interactions of lipidergic pro-resolvents with neuronal ion channels and outcomes from the interactions, focusing on transient receptor potential (TRP) ion channels. We also discuss unanswered hypotheses and perspectives regarding their interactions.
机译:炎症的进展取决于两种生物学机制之间的平衡:促炎和解决过程。许多细胞外和细胞内分子成分,包括细胞因子,生长因子,类固醇,神经递质和脂质能介体及其受体,对炎症过程中细胞参与者产生的两个过程都有贡献。脂肪酸来源的介体对于指导炎症阶段和协调参与者的异质反应至关重要,例如炎症细胞,先天免疫细胞,血管成分,神经支配神经元等。除了激活特定类型的受体分子,脂质能介体还可以主动控制通过直接结合和/或信号转导来改变各种离子通道的功能,从而改变细胞功能。脂质介体可根据其促进的两种过程中的哪一种而分为两类:促炎性药物(包括前列腺素和白三烯)和促溶性药物(包括脂蛋白,RESOLVINS和Maresins)。关于促炎类别的作用的神经元离子通道调节的研究相对较早地开始,而目前的重点是扩大以涵盖离子通道与促溶剂的相互作用。结果,在历史上很少发现其他已知的内源调节剂或促炎性介质对前溶剂的抑制机制的知识,尤其是在感觉神经元阳离子通道上积累。在分子水平上的各种力学解释正在被提出和完善。在这里,我们概述了脂能亲溶剂与神经元离子通道的相互作用以及相互作用的结果,重点是瞬时受体电位(TRP)离子通道。我们还将讨论关于它们之间相互作用的未定假设和观点。

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