Quastel D M, Saint D A
Br J Pharmacol. 1986 Aug;88(4):747-56. doi: 10.1111/j.1476-5381.1986.tb16247.x.
A method of local polarization-excitation was used to study changes in motor nerve terminal excitability produced by n-alkanols and volatile anaesthetics in mouse diaphragm preparations. Ethanol and propanol caused an exaggeration of 'accommodation', i.e., the increase in excitation threshold produced by a conditioning depolarization. Butanol, hexanol and octanol had mixed effects, producing a rise in the minimum threshold (threshold after removal of resting accommodation) in addition to an increase in accommodation. Volatile anaesthetics produced effects on excitability at concentrations comparable to minimum alveolar concentration. The action of enflurane was essentially only to increase accommodation while methoxyflurane produced an increase in threshold insensitive to conditioning polarization. Halothane and isoflurane produced intermediate effects. Accommodation curves were little affected by Ba2+ or 4-aminopyridine and were consistent with accommodation being a reflection of inactivation of the Na+ current system. We conclude that volatile anaesthetics, at concentrations comparable to those producing anaesthesia, may substantially modify Na+ channel gating and inactivation.
采用局部极化激发法,研究了正链烷醇和挥发性麻醉剂对小鼠膈肌标本运动神经末梢兴奋性的影响。乙醇和丙醇导致“适应性”增强,即条件性去极化引起的兴奋阈值升高。丁醇、己醇和辛醇具有混合效应,除了适应性增加外,还导致最小阈值(去除静息适应性后的阈值)升高。挥发性麻醉剂在与最低肺泡浓度相当的浓度下对兴奋性产生影响。恩氟烷的作用主要只是增加适应性,而甲氧氟烷则产生对条件性极化不敏感的阈值升高。氟烷和异氟烷产生中间效应。适应性曲线受Ba2+或4-氨基吡啶的影响很小,并且与适应性反映Na+电流系统失活一致。我们得出结论,挥发性麻醉剂在与产生麻醉作用相当的浓度下,可能会显著改变Na+通道的门控和失活。