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全身麻醉药对鱿鱼巨轴突的兴奋作用。

Excitation of the squid giant axon by general anaesthetics.

作者信息

Haydon D A, Simon A J

机构信息

Physiological Laboratory, Cambridge.

出版信息

J Physiol. 1988 Aug;402:375-89. doi: 10.1113/jphysiol.1988.sp017210.

Abstract
  1. The effects of 'clinical' concentrations of some general anaesthetics on the minimum stimulus required to produce an action potential in the squid giant axon have been examined as a function of time from exposure to the anaesthetic. The resting potential in these experiments was also monitored. 2. The minimum stimulus varied with time in different ways for different anaesthetics. For chloroform, diethyl ether, n-pentanol, halothane and cyclopropane the stimulus initially declined, reached a minimum after about 3 min and then recovered to near-normal values at 10-15 min. For n-pentane, cyclopentane and, to a lesser extent methoxyflurane, the stimulus often declined to such low values that the axon exhibited spontaneous action potentials which persisted until the anaesthetic was removed. For one substance, the experimental local anaesthetic diheptanoyl phosphatidylcholine, the stimulus increased considerably over the 10-15 min required to reach the steady state. In all instances the axons reverted to normal behaviour after removal of the anaesthetic although the time course by which they did so was more variable than for the initial exposure. 3. For all anaesthetics the resting potential changed in the positive direction monotonically by ca. 1-5 mV and reached a steady state in approximately 3 min. On removal of the anaesthetic the resting potential returned to normal, also monotonically. 4. The voltage-gated Na+ and K+ currents were significantly affected even at the low anaesthetic concentrations used. Estimates of the changes in the Hodgkin-Huxley parameters were obtained partly by direct experiment and partly from results previously obtained for higher anaesthetic concentrations. 5. The time dependencies of the minimum stimuli have been accounted for semi-quantitatively in terms of the resting potential changes and the voltage shifts in the Na+ current steady-state activation, and the time dependencies respectively of these two parameters. 6. Quantitative calculations of the resting potential changes for comparison with experiment have been made based on the changes in K+ conductance determined in the preceding paper (Haydon, Requena & Simon, 1988) and changes in the Hodgkin-Huxley parameters of the Na+ and delayed-rectifier K+ currents. 7. Calculations of the minimum stimulus in the steady state have been made from the experimental resting potential changes and from the anaesthetic-affected Hodgkin-Huxley parameters. Good agreement with the experimental stimuli was found, especially in the prediction of high and low values.
摘要
  1. 研究了一些全身麻醉剂的“临床”浓度对枪乌贼巨大轴突产生动作电位所需最小刺激的影响,并将其作为暴露于麻醉剂后时间的函数进行考察。这些实验中还监测了静息电位。2. 不同麻醉剂的最小刺激随时间变化的方式不同。对于氯仿、乙醚、正戊醇、氟烷和环丙烷,刺激最初下降,约3分钟后达到最小值,然后在10 - 15分钟时恢复到接近正常的值。对于正戊烷、环戊烷以及在较小程度上的甲氧氟烷,刺激常常下降到很低的值,以至于轴突表现出自发动作电位,这种电位一直持续到麻醉剂被移除。对于一种物质,即实验性局部麻醉剂二庚酰磷脂酰胆碱,在达到稳态所需的10 - 15分钟内刺激显著增加。在所有情况下,麻醉剂移除后轴突恢复正常行为,尽管其恢复过程的时间进程比初始暴露时更具变异性。3. 对于所有麻醉剂,静息电位正向单调变化约1 - 5 mV,并在大约3分钟内达到稳态。麻醉剂移除后,静息电位也单调恢复正常。4. 即使在使用的低麻醉剂浓度下,电压门控的Na⁺和K⁺电流也受到显著影响。霍奇金 - 赫胥黎参数变化的估计部分通过直接实验获得,部分来自先前在较高麻醉剂浓度下获得的结果。5. 最小刺激的时间依赖性已根据静息电位变化和Na⁺电流稳态激活中的电压偏移以及这两个参数各自的时间依赖性进行了半定量解释。6. 基于前一篇论文(Haydon,Requena & Simon,1988)中确定的K⁺电导变化以及Na⁺和延迟整流K⁺电流的霍奇金 - 赫胥黎参数变化,对静息电位变化进行了定量计算,以便与实验进行比较。7. 根据实验性静息电位变化和受麻醉剂影响的霍奇金 - 赫胥黎参数对稳态下的最小刺激进行了计算。发现与实验刺激结果吻合良好,尤其是在预测高值和低值方面。

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本文引用的文献

1
Convulsive phenomena in hyperthermic dogs during anesthesia.麻醉期间高热犬的惊厥现象。
Anesthesiology. 1961 Nov-Dec;22:893-6. doi: 10.1097/00000542-196111000-00004.
2
Abnormal motor movements during divinyl ether anesthesia.
Anesthesiology. 1956 Mar;17(2):353-7. doi: 10.1097/00000542-195603000-00015.

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