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麻醉机制——从分子层面到生物学层面

Anaesthetic mechanism--from molecular to biological aspects.

作者信息

Ogli K, Tsukamoto I, Yokono S, Nogaya J

机构信息

Department of Anesthesiology & Emergency Medicine, Kagawa Medical School, Japan.

出版信息

Ann Acad Med Singap. 1994 Jul;23(4):536-45.

PMID:7979129
Abstract

The mechanism of anaesthesia is still a black box, although many investigators have been concerned about this theme since the 19th century. It is too complex to clarify the mode of anaesthetic action, as a variety of compounds have been adopted as anaesthetics. Hill coefficients calculated from the righting reflex dose-response curve in enflurane, isoflurane sevoflurane and halothane anaesthesia in a certain strain of mice were from 14 to 56. It shows that many factors are related to the mechanisms of anaesthetic actions. In this review, we adduce from our previous studies 2 approaches to study the anaesthetic mechanism. The pharmacogenetical approach is concerned with the mode of genetics in anaesthetic sensitivities in ddN and C57BL, 2 strains of mice and their hybrids, and distributions of neurotransmitters in each mouse brain. The sensitivity rates in enflurane and isoflurane anaesthesia are both 1.4 between ddN and C57BL. The rate is highest compared with precedent data. The F1 males from ddN females x C57BL males had a significantly higher ED50 than F1 males from the reciprocal crosses for both enflurane and isoflurane, indicating that enflurane resistance and isoflurane resistance are controlled by genes on the sex (X) chromosome. In the F2 progeny, we hypothesized that 1 gene was on the X chromosome and another gene was on the autosome. Although there were several differences among ddN, C57BL and their hybrids and several anaesthetics concerning distributions of neurotransmitters, neuropeptide Y, serotonine and methionine-enkephalin in the mouse brain, the relationship to the genetical analysis has been chaotic. The physicochemical approach is concerned with the confirmation of the action site of volatile anaesthetics in phospholipid bilayer membranes. It is suspected from Overton's experiment that the action site is not in the core of lipid bilayer but on the surface of membrane. It was demonstrated by 2 methodologies. Two-dimensional nuclear Overhauser effect spectrum in H1-NMR spectra of dipalmitoyl phosphatidylcholine (DPPC) vesicle membrane in the presence of methoxyflurane revealed from the existence of the cross-peak between the methoxy-proton and the choline methyl-proton that methoxyflurane molecule interacted only to the polar head of lipid membrane at lower temperatures.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

尽管自19世纪以来许多研究人员就关注这一主题,但麻醉机制仍是一个未知领域。由于多种化合物被用作麻醉剂,阐明麻醉作用方式过于复杂。在某一品系小鼠中,根据恩氟烷、异氟烷、七氟烷和氟烷麻醉下翻正反射剂量 - 反应曲线计算出的希尔系数为14至56。这表明许多因素与麻醉作用机制相关。在本综述中,我们从之前的研究中提出两种研究麻醉机制的方法。药物遗传学方法关注ddN和C57BL这两种品系小鼠及其杂交种对麻醉敏感性的遗传模式,以及每只小鼠大脑中神经递质的分布。ddN和C57BL对恩氟烷和异氟烷麻醉的敏感率均为1.4。与先前数据相比,该比率最高。ddN雌性×C57BL雄性的F1雄性对恩氟烷和异氟烷的半数有效剂量(ED50)均显著高于反交组合的F1雄性,这表明恩氟烷抗性和异氟烷抗性由性(X)染色体上的基因控制。在F2后代中,我们假设一个基因位于X染色体上,另一个基因位于常染色体上。尽管在ddN、C57BL及其杂交种之间,以及几种麻醉剂对小鼠大脑中神经递质、神经肽Y、血清素和甲硫氨酸脑啡肽的分布存在一些差异,但与遗传分析的关系一直很混乱。物理化学方法关注挥发性麻醉剂在磷脂双分子层膜中的作用位点的确认。从奥弗顿实验推测作用位点不在脂质双分子层的核心,而在膜表面。这通过两种方法得到了证实。在甲氧氟烷存在下,二棕榈酰磷脂酰胆碱(DPPC)囊泡膜的H1 - NMR谱中的二维核Overhauser效应谱显示,在较低温度下,甲氧氟烷分子仅与脂质膜的极性头部相互作用,这从甲氧基质子和胆碱甲基质子之间存在交叉峰得以揭示。

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