Department of Physical Chemistry, Universitat de Barcelona, Barcelona, Spain.
J Phys Chem B. 2011 Mar 24;115(11):2527-35. doi: 10.1021/jp110699h. Epub 2011 Feb 25.
Molecular dynamics simulations are used to study the influence of chloroform in two different lipid membranes: one representative of a liquid-disordered phase and another one mixed with cholesterol and representative of a liquid-ordered phase. When chloroform is added to the cholesterol-containing membrane, a strong chain disordering is induced. In both cases, chloroform laterally disorganizes the membranes. The analysis of the main structural and dynamical membrane properties reveals that the interaction with cholesterol is the main factor to explain the strong disordering effect of chloroform in liquid-ordered phases. The results support and provide a molecular explanation to the observations of Regen et al. ( J. Am. Chem. Soc. 2009 , 131 , 5068 ) that suggest that chloroform loosens cholesterol-containing bilayers, thus changing their lateral lipid organization. This lipid-mediated mechanism is conjectured by Regen et al. to be responsible for the anesthetic effect of chloroform and other small volatile anesthetic compounds. This proposal is also discussed.
一种代表无序相,另一种与胆固醇混合,代表有序相。当氯仿被添加到含胆固醇的膜中时,会引起强烈的链无序。在这两种情况下,氯仿都会侧向扰乱膜。对主要结构和动力学膜性质的分析表明,与胆固醇的相互作用是解释氯仿在有序相中强烈无序效应的主要因素。研究结果支持并提供了分子解释,说明了 Regen 等人的观察结果(J. Am. Chem. Soc. 2009, 131, 5068 ),即氯仿会使含有胆固醇的双层膜松动,从而改变其侧向脂质组织。Regen 等人推测,这种脂质介导的机制是氯仿和其他小分子挥发性麻醉化合物产生麻醉作用的原因。该提议也进行了讨论。