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麻醉剂和阿维菌素对哺乳动物背根神经节神经元中GABAA氯离子通道的作用。

Actions of anaesthetics and avermectin on GABAA chloride channels in mammalian dorsal root ganglion neurones.

作者信息

Robertson B

机构信息

Department of Physiology, John Curtin School of Medical Research, Australian National University, Canberra.

出版信息

Br J Pharmacol. 1989 Sep;98(1):167-76. doi: 10.1111/j.1476-5381.1989.tb16878.x.

Abstract
  1. The gamma-aminobutyric acid (GABA)-mimetic actions of some anaesthetics and the antehelminthic avermectin B1a were examined on freshly isolated mammalian dorsal root ganglion (DRG) neurones by use of suction electrodes and a single electrode voltage clamp. 2. Pentobarbitone (60 microM-3 mM), chloralose (600 microM-1 mM), etomidate (10-100 microM), alphaxalone (10-60 microM) and avermectin (10-60 microM) directly activated chloride channels in GABA-sensitive DRG neurones. The agonist action was sensitive to block by bicuculline and picrotoxinin. 3. Steady-state current-voltage (I-V) curves for the anaesthetics were either linear, or rectified in the opposite direction to steady-state I-V curves obtained with GABA. Current relaxations in response to voltage jumps were also of the opposite direction. An extra surge of current ('bounce') was commonly observed on washout of some of these agonists. 4. Pentobarbitone was ineffective as an agonist at alkali pH (10.4 and 9.4), but was approximately twice as effective at acid (5.4) than at normal (7.4) pH values. 5. These results suggest that some anaesthetics and avermectin are capable of 'blocking' GABA channels in addition to activating them.
摘要
  1. 利用吸力电极和单电极电压钳,对一些麻醉剂和抗蠕虫药阿维菌素B1a在新鲜分离的哺乳动物背根神经节(DRG)神经元上的γ-氨基丁酸(GABA)模拟作用进行了研究。2. 戊巴比妥(60微摩尔/升 - 3毫摩尔/升)、氯醛糖(600微摩尔/升 - 1毫摩尔/升)、依托咪酯(10 - 100微摩尔/升)、α-香酮(10 - 60微摩尔/升)和阿维菌素(10 - 60微摩尔/升)直接激活了GABA敏感的DRG神经元中的氯离子通道。激动剂作用对荷包牡丹碱和印防己毒素的阻断敏感。3. 麻醉剂的稳态电流-电压(I-V)曲线要么是线性的,要么与用GABA获得的稳态I-V曲线在相反方向上整流。对电压阶跃的电流弛豫也在相反方向。在洗脱其中一些激动剂时,通常会观察到额外的电流激增(“反弹”)。4. 戊巴比妥在碱性pH(10.4和9.4)下作为激动剂无效,但在酸性(5.4)pH值下的效力约为正常(7.4)pH值下的两倍。5. 这些结果表明,一些麻醉剂和阿维菌素除了激活GABA通道外,还能够“阻断”它们。

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