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吸入性麻醉剂的假定受体。

Postulated receptors for inhalational anesthetic agents.

作者信息

Halsey M J

出版信息

Acta Anaesthesiol Belg. 1979;30 Suppl:45-50.

PMID:547664
Abstract

It is postulated that some, if not all, anesthetic actions can be explained on the basis of interaction between anesthetics and hydrophobic areas of protein molecules in addition to their effects on membrane lipids. We have studied molecular perturbations using high resolution nuclear magnetic resonance techniques and changes of activity of enzymes and oxygen affinity of hemoglobin. Although the specific cellular and molecular mechanisms of anesthesia are unknown at present, useful information on the physical properties of the "drug receptor sites" can be inferred from interactions of anesthetics with pressure in intact animals. The present evidence indicates that different anesthetics have different specific molecular sites with only a limited degree of occupancy. These differences between agents at a molecular level of action are relevant both to the effects on the central nervous system and also to the many "side effects" of anesthetics.

摘要

据推测,即使不是所有的麻醉作用,至少部分麻醉作用除了对膜脂的影响外,还可以基于麻醉剂与蛋白质分子疏水区域之间的相互作用来解释。我们使用高分辨率核磁共振技术研究了分子扰动以及酶活性和血红蛋白氧亲和力的变化。尽管目前麻醉的具体细胞和分子机制尚不清楚,但可以从麻醉剂与完整动物压力的相互作用中推断出有关“药物受体位点”物理性质的有用信息。目前的证据表明,不同的麻醉剂具有不同的特定分子位点,且占据程度有限。这些药物在分子作用水平上的差异与对中枢神经系统的影响以及麻醉剂的许多“副作用”都有关。

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