Halliday D J, Little H J, Paton W D
Br J Pharmacol. 1979 Oct;67(2):229-37. doi: 10.1111/j.1476-5381.1979.tb08671.x.
1 The actions of a range of general anaesthetic agents on the rates of release of acetylcholine from the guinea-pig ileum were tested, by means of a superfusion system designed to maintain the tissues under physiological conditions in a high pressure chamber.2 Anaesthetic pressures of nitrous oxide, nitrogen, argon, sulphur hexafluoride and carbon tetrafluoride caused increases in acetylcholine ouput but the concentrations required did not parallel their general anaesthetic potencies. The changes were not altered by the application of a pressure of helium which reverses their general anaesthetic actions in vivo.3 Urethane (50.5 mM and 101 mM, but not 16.8 mM) decreased acetylcholine release rates and this effect was not reversed by helium pressure.4 Octanol (1.0 mM, but not 0.124 mM or 0.496 mM) decreased the acetylcholine output. This action was not reversed by helium pressure. The lack of effect on acetylcholine release from tetrodotoxin-treated tissues suggested that the changes were produced by blockade of action potential conduction.5 Phenobarbitone (0.4 mM but not 0.2 mM) also decreased acetylcholine output. Although the concentrations required were lower than those which have been previously shown to block axonal conduction, no changes were seen in tetrodotoxin-treated tissues. The decreases were less when helium pressure was applied than at atmospheric pressure but full pressure reversal, as occurs in vivo, was not seen.6 The effects on acetylcholine output exerted by the anaesthetics studied did not reflect their general anaesthetic action in the concentrations required, the direction of the changes produced or in the response to helium pressure. They represent specific actions which are likely to contribute to the individual differences which are seen between the physiological actions of the anaesthetics in vivo.
通过一个旨在将组织维持在生理条件下的高压室中的灌注系统,测试了一系列全身麻醉剂对豚鼠回肠乙酰胆碱释放速率的作用。
一氧化二氮、氮气、氩气、六氟化硫和四氟化碳的麻醉压力导致乙酰胆碱输出增加,但所需浓度与它们的全身麻醉效力不平行。氦气压力的施加并没有改变这些变化,而氦气在体内可逆转它们的全身麻醉作用。
乌拉坦(50.5 mM和101 mM,但不是16.8 mM)降低了乙酰胆碱释放速率,并且这种作用不会被氦气压力逆转。
辛醇(1.0 mM,但不是0.124 mM或0.496 mM)降低了乙酰胆碱输出。这种作用不会被氦气压力逆转。对经河豚毒素处理的组织中乙酰胆碱释放缺乏影响表明,这些变化是由动作电位传导的阻断引起的。
苯巴比妥(0.4 mM但不是0.2 mM)也降低了乙酰胆碱输出。尽管所需浓度低于先前显示可阻断轴突传导的浓度,但在经河豚毒素处理的组织中未见变化。施加氦气压力时的降低幅度比在大气压下小,但未观察到如在体内发生的完全压力逆转。
所研究的麻醉剂对乙酰胆碱输出的影响在所需浓度、产生变化的方向或对氦气压力的反应方面均未反映出它们的全身麻醉作用。它们代表了特定的作用,这些作用可能导致了在体内麻醉剂生理作用之间所观察到的个体差异。