Department of Biology, Faculty of Arts and Sciences, Duzce University, 81620 Duzce, Turkey(1); Department of Biological Sciences, Middle East Technical University, 06531 Ankara, Turkey.
Department of Biological Sciences, Middle East Technical University, 06531 Ankara, Turkey; Department of Biophysics, Faculty of Medicine, Altinbas University, Bakirkoy, 34147 Istanbul, Turkey(2); Biomedical Sciences Graduate Programme, Institute of Health, Altinbas University, Bakirkoy, Istanbul, Turkey.
Biochim Biophys Acta Biomembr. 2019 Jun 1;1861(6):1240-1251. doi: 10.1016/j.bbamem.2019.04.009. Epub 2019 Apr 25.
Agents capable of scavenging ROS have attracted attention recently because of their potential use as antioxidative agents. Amifostine, a ROS scavenger, has the potential to be used as an antioxidant in therapeutic applications. In this study, the effect of amifostine on neutral zwitterionic dipalmitoylphosphatidylcholine (DPPC) and anionic dipalmitoylphosphatidylglycerol (DPPG) model membranes' structure and dynamics is aimed to be examined by Fourier transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC). Our results revealed that amifostine at concentrations used (1-24 mol%) does not induce any important alteration in the shape of phase transition curve and phase transition temperature in the DPPC and DPPG membranes. High concentrations of amifostine slightly increased the acyl chain flexibility of DPPC membranes in the liquid crystalline phase and DPPG membranes in the gel phase. A lessening in the dynamics of DPPC liposomes was observed for all concentrations of amifostine in both phases but slight dual effect was observed only in the gel phase as a decrease in dynamics at low concentrations and an increase at higher concentrations of amifostine in DPPG liposomes. Additionally, strong hydrogen bonding was observed for both CO and PO groups in case of DPPC and for PO groups in case of DPPG. Dehydration around the CO regions occurred in case of DPPG. Accordingly, amifostine is proposed to be interacting strongly with zwitterionic and negatively charged membrane head groups and glycerol backbone in all concentrations and because of this interaction it causes some changes in lipid order and dynamics especially at high concentrations.
由于其作为抗氧化剂的潜在用途,能够清除活性氧 (ROS) 的试剂最近引起了关注。一种 ROS 清除剂氨磷汀有可能作为治疗应用中的抗氧化剂使用。在这项研究中,通过傅里叶变换红外(FTIR)光谱和差示扫描量热法(DSC),旨在研究氨磷汀对中性两性离子二棕榈酰磷脂酰胆碱(DPPC)和阴离子二棕榈酰磷脂酰甘油(DPPG)模型膜结构和动力学的影响。我们的结果表明,在所用浓度(1-24 mol%)下,氨磷汀不会引起 DPPC 和 DPPG 膜相变曲线和相变温度形状的任何重要变化。高浓度的氨磷汀略微增加了 DPPC 膜在液晶相和 DPPG 膜在凝胶相中的酰基链柔韧性。在两相中,所有浓度的氨磷汀都观察到 DPPC 脂质体的动力学减慢,但仅在凝胶相中观察到双相效应,即在低浓度下降低动力学,在较高浓度下增加动力学在 DPPG 脂质体中。此外,在 DPPC 中观察到 CO 和 PO 基团以及在 DPPG 中观察到 PO 基团的氢键均较强。在 DPPG 中,CO 区域周围发生脱水。因此,氨磷汀被提议与两性离子和带负电荷的膜头部基团以及所有浓度的甘油骨架强烈相互作用,并且由于这种相互作用,它会导致脂质有序性和动力学发生一些变化,尤其是在高浓度时。