Zhernovkov V E, Pal'mina N P
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, Russia.
Bull Exp Biol Med. 2007 Aug;144(2):185-7. doi: 10.1007/s10517-007-0285-6.
The spin probe method was employed to study in vitro the effect of regulatory peptide thyroliberin on structural state of surface (0.8 nm) and deep (2 nm) lipid layers of the plasma membranes in mouse liver and brain. Thyroliberin in a concentration range of 10(-3)-10(-18) M enhanced structural order of surface lipids, the maximum effect was observed at 10(-9)-10(-10) M. The dose-effect dependencies for microviscosity of deep lipids were nonlinear and had 3 extrema at 10(-4)-10(-7) M, 10(-9) M, and 10(-14)-10(-16) M. The greatest changes in lipid microviscosity produced by 10(-9) M thyroliberin are explained by lipid-receptor interaction.
采用自旋探针法在体外研究调节肽促甲状腺素释放激素对小鼠肝脏和大脑质膜表面(0.8纳米)和深层(2纳米)脂质层结构状态的影响。浓度范围为10^(-3)-10^(-18) M的促甲状腺素释放激素增强了表面脂质的结构有序性,在10^(-9)-10^(-10) M时观察到最大效应。深层脂质微粘度的剂量-效应依赖性是非线性的,在10^(-4)-10^(-7) M、10^(-9) M和10^(-14)-10^(-16) M时有3个极值。10^(-9) M促甲状腺素释放激素引起的脂质微粘度最大变化是由脂质-受体相互作用解释的。