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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Inhibition of acid-sensing ion channel currents by propofol in rat dorsal root ganglion neurons
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Inhibition of acid-sensing ion channel currents by propofol in rat dorsal root ganglion neurons

机译:异丙酚对大鼠背根神经节神经元酸敏感离子通道电流的抑制作用

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Acid-sensing ion channels (ASICs), part of the epithelial sodium channel/degenerin family, are activated by extracellular protons. The ASICs play a significant role in the acidosis-mediated perception of pain. The anaesthetic agent propofol also exerts antinociceptive effects, but the underlying mechanisms for this effect are not clear. We used whole-cell patch clamping to investigate the effect of propofol on proton-gated currents in: (i) rat dorsal root ganglion (DRG) neurons; and (ii) HEK293 cells transfected with either ASIC1a or ASIC3. Propofol inhibited the amplitude of proton-gated currents in DRG neurons, but did not change the sensitivity of ASICs to H+. Notably, propofol altered acid-evoked excitability of rat DRG neurons and decreased the number of action potentials induced by acid stimuli. In addition, we demonstrated that propofol inhibited ASICs by directly binding with these channels in HEK293 cells. These results suggest that propofol inhibits proton-gated currents in DRG neurons and that inhibition of proton-gated currents explains, in part, the antinociceptive effects of propofol in primary afferent neurons.
机译:酸敏感离子通道(ASICs)是上皮钠通道/去骨素家族的一部分,被细胞外质子激活。 ASIC在酸中毒介导的疼痛感知中起着重要作用。麻醉药丙泊酚也具有镇痛作用,但这种作用的潜在机制尚不清楚。我们使用全细胞膜片钳研究了异丙酚对以下情况中质子门控电流的影响:(i)大鼠背根神经节(DRG)神经元; (ii)用ASIC1a或ASIC3转染的HEK293细胞。异丙酚可抑制DRG神经元中质子门控电流的幅度,但不会改变ASIC对H +的敏感性。值得注意的是,异丙酚改变了大鼠DRG神经元的酸诱发兴奋性,并降低了酸刺激诱导的动作电位数量。此外,我们证明了丙泊酚通过直接与HEK293细胞中的这些通道结合而抑制了ASIC。这些结果表明,丙泊酚抑制DRG神经元中的质子门控电流,并且对质子门控电流的抑制部分解释了丙泊酚对原发传入神经元的镇痛作用。

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