• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

吸入麻醉药对质子/羟基跨脂质囊泡流动的增强作用。

The enhancement of proton/hydroxyl flow across lipid vesicles by inhalation anesthetics.

作者信息

Raines D E, Cafiso D S

机构信息

Department of Chemistry, University of Virginia, Charlottesville 22901.

出版信息

Anesthesiology. 1989 Jan;70(1):57-63. doi: 10.1097/00000542-198901000-00013.

DOI:10.1097/00000542-198901000-00013
PMID:2536253
Abstract

When pH gradients are created across model lipid membranes, there is a well-documented electrogenic flow of protons, which results in the development of a transmembrane potential. As a result, protons come to electrochemical equilibrium across lipid vesicles within tens of minutes. The ability of a series of inhalation anesthetics to enhance the conduction of protons across model membranes was examined. When clinically relevant concentrations of halothane, isoflurane, enflurane, or chloroform were equilibrated with sonicated lipid vesicles, significant increases in the proton conduction were found. However, for even high anesthetic concentrations (above 8 MAC) of ether and cyclopropane, no increases in proton conduction could be detected. These results rule out a common mechanism for general anesthesia involving enhanced proton conduction across membranes.

摘要

当在模型脂质膜上形成pH梯度时,质子会发生有充分记录的生电流动,这会导致跨膜电位的产生。结果,质子会在数十分钟内在脂质囊泡内达到电化学平衡。研究了一系列吸入麻醉剂增强质子跨模型膜传导的能力。当将临床相关浓度的氟烷、异氟烷、恩氟烷或氯仿与经超声处理的脂质囊泡平衡时,发现质子传导显著增加。然而,即使对于高浓度麻醉剂(高于8倍最低肺泡有效浓度)的乙醚和环丙烷,也未检测到质子传导增加。这些结果排除了全身麻醉涉及增强质子跨膜传导的常见机制。

相似文献

1
The enhancement of proton/hydroxyl flow across lipid vesicles by inhalation anesthetics.吸入麻醉药对质子/羟基跨脂质囊泡流动的增强作用。
Anesthesiology. 1989 Jan;70(1):57-63. doi: 10.1097/00000542-198901000-00013.
2
Interfacial preference of anesthetic action upon the phase transition of phospholipid bilayers and partition equilibrium of inhalation anesthetics between membrane and deuterium oxide.麻醉作用对磷脂双层膜相变及吸入麻醉药在膜与重水间分配平衡的界面偏好性。
Biochim Biophys Acta. 1981 Jul 20;645(2):237-42. doi: 10.1016/0005-2736(81)90194-2.
3
Anesthetic potencies and the unitary theory of narcosis.麻醉效能与麻醉单一理论
Anesth Analg. 1981 Jun;60(6):380-4.
4
Anesthetics reduce the magnitude of the membrane dipole potential. Measurements in lipid vesicles using voltage-sensitive spin probes.麻醉剂会降低膜偶极子电位的幅度。使用电压敏感自旋探针在脂质囊泡中进行的测量。
Biochemistry. 1995 Apr 25;34(16):5536-43. doi: 10.1021/bi00016a027.
5
Lipid protein interactions in mitochondria. VIII. Effect of general anesthetics on the mobility of spin labels in lipid vesicles and mitochondrial membranes.线粒体中的脂蛋白相互作用。VIII. 全身麻醉剂对脂质囊泡和线粒体膜中自旋标记物流动性的影响。
J Bioenerg Biomembr. 1979 Apr;11(1-2):17-32. doi: 10.1007/BF00743158.
6
The effect of general anesthetics on the proton and potassium permeabilities of liposomes.全身麻醉药对脂质体质子和钾通透性的影响。
Biochim Biophys Acta. 1985 Oct 10;819(2):161-9. doi: 10.1016/0005-2736(85)90170-1.
7
[Comparative effects of inhalation anesthetics on atrioventricular conduction with and without calcium entry blockers].[吸入麻醉药在有和无钙通道阻滞剂情况下对房室传导的比较作用]
Hokkaido Igaku Zasshi. 1989 Jan;64(1):43-54.
8
Alcohol effects on lipid bilayer permeability to protons and potassium: relation to the action of general anesthetics.酒精对脂质双分子层质子和钾离子通透性的影响:与全身麻醉药作用的关系。
Biochim Biophys Acta. 1988 Sep 15;944(1):40-8. doi: 10.1016/0005-2736(88)90314-8.
9
Membrane expansion and inhalation anesthetics. Mean excess volume hypothesis.膜扩张与吸入麻醉药。平均过量容积假说。
Mol Pharmacol. 1984 Jan;25(1):123-30.
10
A conformational model for the action of general anesthetics at the membrane level. II. Experimental observations on the effects of anesthetics on lipid fluidity and lipid protein interactions.全身麻醉药在膜水平作用的构象模型。II. 麻醉药对脂质流动性和脂质-蛋白质相互作用影响的实验观察
Ital J Biochem. 1978 Nov-Dec;27(6):401-30.

引用本文的文献

1
Competitive Antagonism of Anesthetic Action at the γ-Aminobutyric Acid Type A Receptor by a Novel Etomidate Analog with Low Intrinsic Efficacy.一种具有低内在活性的新型依托咪酯类似物对γ-氨基丁酸A型受体麻醉作用的竞争性拮抗
Anesthesiology. 2017 Nov;127(5):824-837. doi: 10.1097/ALN.0000000000001840.