ATP-activated channels in excitable cells.

B P Bean, D D Friel
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引用次数: 106

Abstract

Extracellular ATP is an activator or modulator of ionic channels in a wide variety of excitable cells. There appears to be a class of related cation-permeable ATP-activated channels in skeletal muscle, cardiac muscle, smooth muscle, and neurons; the channels in the different cell types appear to be similar, but not identical, in their ionic selectivity, receptor selectivity, and pharmacology. In all cases, these channels reverse near 0 mV and activation by ATP produces an excitatory effect. Much remains to be learned about these channels, their possible existence and roles in other cell types, and their relation to other types of ligand-gated channels. It will be especially important to develop more specific pharmacological blockers (and activators) in order to distinguish subtypes and to assess their physiological role. Another type of channel, so far described only in cardiac atrial cells, is identical to the channels in cardiac atrial cells activated by ACh receptors; it will be interesting to see if this type of receptor-channel complex is also found in neurons or other cells. In a variety of cells, ATP also acts as a modulator of voltage-dependent channels and of channels activated by other transmitters. It seems very likely that more instances of such modulation will be described in years to come. Possible second-messenger pathways mediating such modulation remain to be elucidated.

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可兴奋细胞中的atp激活通道。
细胞外ATP是多种可兴奋细胞中离子通道的激活剂或调节剂。在骨骼肌、心肌、平滑肌和神经元中似乎存在一类相关的阳离子渗透性atp激活通道;不同细胞类型中的通道在离子选择性、受体选择性和药理学上似乎相似,但不完全相同。在所有情况下,这些通道在0毫伏附近反转,ATP的激活产生兴奋效应。关于这些通道,它们在其他细胞类型中的可能存在和作用,以及它们与其他类型配体门控通道的关系,还有很多有待了解的地方。为了区分亚型和评估其生理作用,开发更具体的药理学阻滞剂(和激活剂)将是特别重要的。另一种类型的通道,到目前为止只在心房细胞中描述过,与心房细胞中被乙酰胆碱受体激活的通道相同;看看这种类型的受体-通道复合物是否也存在于神经元或其他细胞中,这将是一件有趣的事情。在多种细胞中,ATP还作为电压依赖性通道和由其他递质激活的通道的调制器。在未来的几年里,似乎很有可能会出现更多这样的调制实例。可能介导这种调节的第二信使通路仍有待阐明。
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