Amphotericin B is a very effective antifungal drug,but it has an adverse reaction to the membrane of mammals＇ cells.The interaction between Am B and cholesterol（Chol） causes the formation of pores on the membrane t...Amphotericin B is a very effective antifungal drug,but it has an adverse reaction to the membrane of mammals＇ cells.The interaction between Am B and cholesterol（Chol） causes the formation of pores on the membrane to destroy its integrity.In particular,Am B has a significant effect on the permeability of membrane for K~＋ions.It has been reported that Na＋ions and Ca^（2＋）ions may have some influence on the interaction between amphotericin B and lipid molecules.In this work,the effects of these metal cations on the physical state and intermolecular interaction of the Cholesterol/Dipalmitoylphosphatidylcholine（Chol/DPPC） monolayer with and without Am B have been investigated.The addition of Am B induces the change of physical state of the lipid monolayer from liquid-gel phase to liquid phase.Different metal cations could influence the phase transition of the Am B-lipid monolayer.The K~＋ions and Ca2＋ions make the obvious phase transition disappear.However,the presence of Na＋ions has little influence on the phase transition of the Am B-lipid monolayer.The addition of Am B and the presence of different metal cations weaken the attractive force on the monolayers.After addition of Am B,the force between the molecules is the strongest in the environment of K＋ions,thus is the weakest in the environment of Ca^（2＋）ions,which may be due to the distribution of these metal cations inside and outside of cells.A large number of K＋ions distribute inside of the cells,thus most of Na＋and Ca^（2＋）ions exist out of the cells.Hence,it may be possible that when Am B molecules are out of the cells,the reaction between the drug and lipid molecules is weaker than that inside the cells.These results may have a great reference value for further studying the toxicity mechanism of Am B and the influence of metal cations on the membrane.展开更多
基金Project supported by the National Natural Science Foundation of China(Grant Nos.21402114 and 11544009)the Natural Science Basic Research Plan in Shaanxi Province of China(Grant No.2016JM2010)the Fundamental Research Funds for the Central Universities of China(Grant No.GK201603026)
文摘Amphotericin B is a very effective antifungal drug,but it has an adverse reaction to the membrane of mammals＇ cells.The interaction between Am B and cholesterol（Chol） causes the formation of pores on the membrane to destroy its integrity.In particular,Am B has a significant effect on the permeability of membrane for K~＋ions.It has been reported that Na＋ions and Ca^（2＋）ions may have some influence on the interaction between amphotericin B and lipid molecules.In this work,the effects of these metal cations on the physical state and intermolecular interaction of the Cholesterol/Dipalmitoylphosphatidylcholine（Chol/DPPC） monolayer with and without Am B have been investigated.The addition of Am B induces the change of physical state of the lipid monolayer from liquid-gel phase to liquid phase.Different metal cations could influence the phase transition of the Am B-lipid monolayer.The K~＋ions and Ca2＋ions make the obvious phase transition disappear.However,the presence of Na＋ions has little influence on the phase transition of the Am B-lipid monolayer.The addition of Am B and the presence of different metal cations weaken the attractive force on the monolayers.After addition of Am B,the force between the molecules is the strongest in the environment of K＋ions,thus is the weakest in the environment of Ca^（2＋）ions,which may be due to the distribution of these metal cations inside and outside of cells.A large number of K＋ions distribute inside of the cells,thus most of Na＋and Ca^（2＋）ions exist out of the cells.Hence,it may be possible that when Am B molecules are out of the cells,the reaction between the drug and lipid molecules is weaker than that inside the cells.These results may have a great reference value for further studying the toxicity mechanism of Am B and the influence of metal cations on the membrane.
