Beaver R W, Brauer R W, Lahser S
J Appl Physiol Respir Environ Exerc Physiol. 1977 Aug;43(2):221-9. doi: 10.1152/jappl.1977.43.2.221.
The interactions of phenobarbital, barbital, and pentobarbital with high pressures of heliox were explored. Principal features of the complex results include: double peaks in the time course of convulsion thresholds (Pc); an early peak and a shoulder in the time course of pressures reversing anesthesia (Pa); far steeper dose-response curves for Pa than for Pc; selectively greater anticonvulsant effect for phenobarbital than for the other barbiturates; and enhancement of Pa with simultaneous depression of Pc by reserpine in phenobarbital-pretreated mice. The data indicate the existence of at least two discrete sites of interaction between barbiturates and high pressure, reflected by Pc and Pa. The implications of the data for the development of biophysical theories of pressure reversal of anesthesia and anti-high-pressure neurological syndrome action of anesthetics are discussed, together with implications for the experimental study of convulsant and anticonvulsant agents, and their applications to underwater physiology.
研究了苯巴比妥、巴比妥和戊巴比妥与高浓度氦氧混合气之间的相互作用。复杂结果的主要特征包括:惊厥阈值(Pc)随时间变化出现双峰;压力逆转麻醉(Pa)随时间变化出现一个早期峰值和一个肩峰;Pa的剂量反应曲线比Pc陡峭得多;苯巴比妥的抗惊厥作用选择性地强于其他巴比妥类药物;在苯巴比妥预处理的小鼠中,利血平可增强Pa,同时降低Pc。数据表明巴比妥类药物与高压之间至少存在两个离散的相互作用位点,分别由Pc和Pa反映。讨论了这些数据对麻醉压力逆转生物物理理论发展以及麻醉剂抗高压神经综合征作用的意义,以及对惊厥剂和抗惊厥剂实验研究及其在水下生理学中的应用的意义。