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The effects of inert gases and other general anaesthetics on the release of acetylcholine from the guinea-pig ileum

机译:惰性气体和其他全身麻醉药对豚鼠回肠中乙酰胆碱释放的影响

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>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.
机译:> 1 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,方法是设计成可将组织维持在较高生理条件下的超融合系统> 2 。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,但所需浓度与他们的全身麻醉药能力不符。施加氦气的压力并不会改变其在体内的全身麻醉作用,改变并没有改变。> 3 氨基甲酸酯(50.5 mM和101 mM,但没有16.8 mM)降低了乙酰胆碱的释放速率,并且这种作用不会被氦气压力逆转。> 4 辛醇(1.0 mM,但不是0.124 mM或0.496 mM)会降低乙酰胆碱的产量。氦气压力不能逆转这种作用。对河豚毒素处理过的组织中乙酰胆碱释放的影响不足,表明这种变化是通过阻断动作电位传导而产生的。> 5 苯巴比妥(0.4 mM但不是0.2 mM)也降低了乙酰胆碱的输出。尽管所需的浓度低于先前显示的阻断轴突传导的浓度,但在河豚毒素治疗的组织中未见变化。当施加氦气压力时,降幅小于在大气压力下,但未见到体内发生全压逆转。> 6 。麻醉药对乙酰胆碱输出的影响并未反映出它们的一般情况。在所需浓度,所产生变化的方向或对氦气压力的响应中具有麻醉作用。它们代表可能导致体内麻醉药的生理作用之间出现个体差异的特定作用。

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