Hauet Nathalie, Artzner Franck, Boucher François, Grabielle-Madelmont Cécile, Cloutier Isabelle, Keller Gérard, Lesieur Pierre, Durand Dominique, Paternostre Maïté
Equipe Physicochimie des Systèmes Polyphasés, UMR 8612, Université Paris Sud, F-92296 Châtenay Malabry, France.
Biophys J. 2003 May;84(5):3123-37. doi: 10.1016/S0006-3495(03)70037-X.
The structural modifications of the dipalmitoylphosphatidylcholine (DPPC) organization induced by increasing concentration of the volatile anesthetic enflurane have been studied by differential scanning calorimetry, small-angle, and wide-angle x-ray scattering. The interaction of enflurane with DPPC depends on at least two factors: the enflurane-to-lipid concentration ratio and the initial organization of the lipids. At 25 degrees C (gel state), the penetration of enflurane within the lipids induces the apparition of two different mixed lipid phases. At low anesthetic-to-lipid molar ratio, the smectic distance increases whereas the direction of the chain tilt changes from a tilt toward next-neighbors to a tilt between next-neighbors creating a new gel phase called L(beta')(2NNN). At high ratio, the smectic distance is much smaller than for the pure L(beta') DPPC phase, i.e., 50 A compared to 65 A, the aliphatic chains are perpendicular to the membrane and the fusion temperature of the phase is 33 degrees C. The electron profile of this phase that has been called L(beta)(i), indicates that the lipids are fully interdigitated. At 45 degrees C (fluid state), a new melted phase, called L(alpha)(2), was found, in which the smectic distance decreased compared to the initial pure L(alpha)(1) DPPC phase. The thermotropic behavior of the mixed phases has also been characterized by simultaneous x-ray scattering and differential scanning calorimetry measurements using the Microcalix calorimeter of our own. Finally, titration curves of enflurane effect in the mixed lipidic phase has been obtained by using the fluorescent lipid probe Laurdan. Measurements as a function of temperature or at constant temperature, i.e., 25 degrees C and 45 degrees C give, for the maximal effect, an enflurane-to-lipid ratio (M/M), within the membrane, of 1 and 2 for the L(alpha)(2) and the L(beta)(i) lamellar phase respectively. All the results taken together allowed to draw a pseudo-binary phase diagram of enflurane-dipalmitoylphosphatidylcholine in excess water.
通过差示扫描量热法、小角和广角X射线散射研究了挥发性麻醉剂恩氟烷浓度增加对二棕榈酰磷脂酰胆碱(DPPC)结构组织的影响。恩氟烷与DPPC的相互作用至少取决于两个因素:恩氟烷与脂质的浓度比以及脂质的初始组织状态。在25℃(凝胶态)时,恩氟烷在脂质中的渗透导致出现两种不同的混合脂质相。在低麻醉剂与脂质摩尔比时,近晶距离增加,而链倾斜方向从向相邻分子倾斜变为相邻分子之间倾斜,形成一种新的凝胶相,称为L(β')(2NNN)。在高比例时,近晶距离比纯L(β') DPPC相小得多,即50 Å 对比65 Å,脂肪链垂直于膜,该相的融合温度为33℃。这个被称为L(β)(i)相的电子轮廓表明脂质完全交错排列。在45℃(流体态)时,发现了一种新的熔融相,称为L(α)(2),其中近晶距离比初始纯L(α)(1) DPPC相减小。混合相的热致行为也通过使用我们自己的微量量热计进行的同步X射线散射和差示扫描量热测量来表征。最后,通过使用荧光脂质探针劳丹获得了混合脂质相中恩氟烷效应的滴定曲线。在温度变化或恒温(即25℃和45℃)下测量,对于最大效应,在膜内,L(α)(2)和L(β)(i)层状相的恩氟烷与脂质比(M/M)分别为1和2。综合所有结果绘制了过量水中恩氟烷 - 二棕榈酰磷脂酰胆碱的拟二元相图。