首页> 美国卫生研究院文献>The Journal of Physiology >Enhancement of gamma-aminobutyric acid-activated Cl- currents in cultured rat hippocampal neurones by three volatile anaesthetics.
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Enhancement of gamma-aminobutyric acid-activated Cl- currents in cultured rat hippocampal neurones by three volatile anaesthetics.

机译:三种挥发性麻醉剂可增强培养的大鼠海马神经元中γ-氨基丁酸激活的Cl-电流。

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摘要

1. The effects of the volatile anaesthetics enflurane, halothane and isoflurane on gamma-aminobutyric acid (GABA)A receptor-mediated chloride currents were studied in cultured rat hippocampal neurones. Transient current responses were obtained by brief pressure application of GABA to the cell body of neurones under voltage clamp. 2. All three anaesthetics increased the peak amplitude and duration of current 2. All three anaesthetics increased the peak amplitude and duration of current responses to brief applications of GABA. These effects were fully reversible, and did not involve alterations in the reversal potential for GABA responses. 3. The experimental concentrations of anaesthetics were measured directly using gas chromatography. The enhancement of GABA currents increased with increasing anaesthetic concentration. Clinically effective concentrations of anaesthetics (between 1 and 1.5 times MAC (minimum alveolar concentration) produced significant enhancement of GABA currents. 4. These results demonstrate that the changes in the time course of synaptic inhibition reported in the presence of the volatile anaesthetics are likely to result from modification of the function of postsynaptic GABAA receptor-channel complexes. These findings also support the hypothesis that GABAA receptor complexes serve as common molecular target sites for a variety of structurally diverse anaesthetic molecules.
机译:1.在培养的大鼠海马神经元中研究了挥发性麻醉剂环烷,氟烷和异氟烷对γ-氨基丁酸(GABA)A受体介导的氯离子电流的影响。短暂的电流响应是通过在电压钳位下将GABA短暂施加于神经元细胞体而获得的。 2.所有三种麻醉剂均增加了电流的峰值幅度和持续时间。2.所有三种麻醉剂均增加了对GABA的短暂应用的电流响应的峰值幅度和持续时间。这些作用是完全可逆的,并且不涉及GABA反应的逆转潜力的改变。 3.使用气相色谱法直接测量麻醉剂的实验浓度。 GABA电流的增加随着麻醉剂浓度的增加而增加。临床上有效的麻醉剂浓度(最小MAC浓度的1到1.5倍,MAC产生了GABA电流的增强)4.这些结果表明,在存在挥发性麻醉剂的情况下,突触抑制时间的变化很可能会这些结果也支持以下假设:GABAA受体复合物是多种结构多样的麻醉剂分子的共同分子靶位。

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