首页> 美国卫生研究院文献>The Journal of Physiology >One-way cross-desensitization between P2X purinoceptors and vanilloid receptors in adult rat dorsal root ganglion neurones
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One-way cross-desensitization between P2X purinoceptors and vanilloid receptors in adult rat dorsal root ganglion neurones

机译:成年大鼠背根神经节神经元中P2X嘌呤受体与类香草醇受体之间的单向交叉脱敏

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摘要

class="enumerated" style="list-style-type:decimal">Capsaicin and ATP can activate ligand-gated cation channels in nociceptive rat dorsal root ganglion (DRG) neurones. We have studied cross-desensitization between these two agents in rat isolated DRG neurones using the whole-cell voltage-clamp technique.ATP (10 μM) activated an inward current in DRG neurones at a holding potential of −60 mV. ATP evoked ‘fast’ responses that underwent rapid activation and desensitization, ‘slow’ responses that activated and desensitized more slowly, or responses that displayed a mixture of these two characteristics. The time course of the response to ATP was not related obviously to capsaicin sensitivity.Prior application of capsaicin (0·5 μM) increased the proportion of cells displaying only fast responses to ATP (10 μM) suggesting that cross-desensitization had occurred between capsaicin and the slow component of the ATP response. Prior desensitization to ATP had no apparent effect on the inward current response to capsaicin (0·5 μM).Cross-desensitization between capsaicin and ATP was Ca2+ dependent.Changing the membrane holding potential (Vh) to +40 mV for a brief period before applying ATP at −60 mV had a similar effect to capsaicin, i.e. the proportion of cells displaying only fast responses to ATP was increased significantly. This effect of depolarization was not Ca2+ dependent.The heterogenity of responses to ATP is probably due to co-expression of homomeric P2X3 receptors and heteromeric receptors comprising P2X3 subunits with other P2X subunits. We propose that the change in time course of the ATP response produced by prior desensitization to capsaicin is due to selective cross-desensitization with the heteromeric P2X receptors.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 辣椒素和ATP可以激活伤害性大鼠背根神经节(DRG)神经元中的配体门控阳离子通道。我们已经使用全细胞电压钳技术研究了大鼠分离的DRG神经元中这两种药物之间的交叉脱敏。 ATP(10μM)在保持电位为−的情况下激活了DRG神经元中的内向电流。 60毫伏。 ATP引发了“快速”响应,这些响应经历了快速激活和脱敏,“缓慢”响应则激活和脱敏速度变慢,或者显示了这两种特征的混合。 ATP响应的时间进程与辣椒素敏感性没有明显关系。 辣椒碱(0·5μM)的应用增加了仅对ATP(10μM)表现出快速响应的细胞比例。辣椒素和ATP反应的慢成分之间发生了交叉脱敏。事先对ATP脱敏对辣椒素的内向电流响应(0·5μM)没有明显影响。 辣椒素与ATP之间的交叉脱敏依赖于Ca 2 + 。 / li> li在施加-60 mV的ATP之前,将膜保持电位(Vh)短暂更改为+40 mV具有与辣椒素相似的作用,即仅对ATP表现出快速反应的细胞比例显着增加。去极化的这种作用不依赖于Ca 2 + 对ATP响应的异质性可能是由于同源P2X3受体和包含P2X3亚基的异聚受体与其他受体的共表达P2X亚基。我们认为,先对辣椒素脱敏后产生的ATP反应的时程变化是由于与异聚P2X受体选择性交叉脱敏所致。

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