Sakamoto Seiichi, Uto Takuhiro, Shoyama Yukihiro
Department of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Nagasaki International University, 2825-7 Huis Ten Bosch, Sasebo, Nagasaki 859-3298, Japan.
Biochim Biophys Acta. 2015 Feb;1848(2):434-43. doi: 10.1016/j.bbamem.2014.11.014. Epub 2014 Nov 20.
To investigate an interfacial behavior of the aglycon of glycyrrhizin (GC), glycyrrhetinic acid (GA), with a lipid raft model consisting of equimolar ternary mixtures of N-palmitoyl sphingomyelin (PSM), dioleoylphosphatidylcholine (DOPC), and cholesterol (CHOL), Langmuir monolayer techniques were systematically conducted. Surface pressure (π)-molecular area (A) and surface potential (ΔV)-A isotherms showed that the adsorbed GA at the air/water interface was desorbed into the bulk upon compression of the lipid monolayer. In situ morphological analysis by Brewster angle microscopy and fluorescence microscopy revealed that the raft domains became smaller as the concentrations of GA in the subphase (CGA) increased, suggesting that GA promotes the formation of fluid networks related to various cellular processes via lipid rafts. In addition, ex situ morphological analysis by atomic force microscopy revealed that GA interacts with lipid raft by lying down at the surface. Interestingly, the distinctive striped regions were formed at CGA=5.0 μM. This phenomenon was observed to be induced by the interaction of CHOL with adsorbed GA and is involved in the membrane-disrupting activity of saponin and its aglycon. A quantitative comparison of GA with GC (Sakamoto et al., 2013) revealed that GA interacts more strongly with the raft model than GC in the monolayer state. Various biological activities of GA are known to be stronger than those of GC. This fact allows us to hypothesize that differences in the interactions of GA/GC with the model monolayer correlate to their degree of exertion for numerous activities.
为了研究甘草酸(GC)的苷元甘草次酸(GA)与由N-棕榈酰鞘磷脂(PSM)、二油酰磷脂酰胆碱(DOPC)和胆固醇(CHOL)等摩尔三元混合物组成的脂筏模型的界面行为,系统地进行了Langmuir单分子层技术研究。表面压力(π)-分子面积(A)和表面电位(ΔV)-A等温线表明,在空气/水界面吸附的GA在脂质单分子层压缩时解吸到本体相中。通过布鲁斯特角显微镜和荧光显微镜进行的原位形态分析表明,随着亚相中GA浓度(CGA)的增加,筏域变小,这表明GA通过脂筏促进了与各种细胞过程相关的流体网络的形成。此外,通过原子力显微镜进行的异位形态分析表明,GA通过平躺于表面与脂筏相互作用。有趣的是,在CGA = 5.0 μM时形成了独特的条纹区域。观察到这种现象是由CHOL与吸附的GA的相互作用诱导的,并且与皂苷及其苷元的膜破坏活性有关。GA与GC(Sakamoto等人,2013年)的定量比较表明,在单分子层状态下,GA与筏模型的相互作用比GC更强。已知GA的各种生物活性比GC更强。这一事实使我们能够假设,GA/GC与模型单分子层相互作用的差异与其在众多活性中的发挥程度相关。