Department of Life System, Institute of Technology and Science, Graduate School, The University of Tokushima, Minamijosanjimacho-2, Tokushima, 770-8506, Japan.
Adv Exp Med Biol. 2013;789:385-389. doi: 10.1007/978-1-4614-7411-1_51.
We describe our solution for removal of the low-density lipoprotein (LDL) depot contained in proteins and lipids as a 'druggable' target for atherosclerotic cardiovascular diseases by neutron dynamic therapy (NDT), which we developed using boron tracedrugs for NDT against bovine serum albumin as a model protein. Thus, we examined, among our developed boron tracedrugs, a boron-containing curcuminoid derivative UTX-51, to destroy freshly isolated human LDL dynamically under irradiated thermal neutron to obtain a decreased intensity of band of LDL treated with UTX-51 and thermal neutron irradiation in their SDS-PAGE and electrophoresis analysis. These results suggest that UTX-51 might be a novel candidate of 'beyond chemical' therapeutic agents for atherosclerotic cardiovascular disease.
我们描述了我们的解决方案,通过中子动态治疗(NDT)去除蛋白质和脂质中包含的低密度脂蛋白(LDL)库,这是动脉粥样硬化性心血管疾病的“可药物”靶点,我们使用硼示踪剂开发了针对牛血清白蛋白的 NDT。因此,我们在我们开发的硼示踪剂中研究了一种含硼姜黄素衍生物 UTX-51,以在辐照热中子下动态破坏新鲜分离的人 LDL,以获得在 SDS-PAGE 和电泳分析中用 UTX-51 和热中子辐照处理的 LDL 条带强度降低。这些结果表明,UTX-51 可能是动脉粥样硬化性心血管疾病的“超越化学”治疗剂的新型候选药物。