Molecular Imaging and Neurovascular Research (MINER) Laboratory, Department of Neurology, Dongguk University Ilsan Hospital, Dongguk University College of Medicine, 814 Siksa-dong, Goyang, Korea.
Photochem Photobiol Sci. 2011 Oct;10(10):1587-92. doi: 10.1039/c0pp00363h. Epub 2011 Jul 12.
Photodynamic therapy (PDT) has been used to eliminate undesired cells by using a combination of photosensitizers and light illumination to generate reactive oxygen species. There is great interest in applying PDT to atherosclerosis; preferential destruction of pro-inflammatory macrophages in atheromata might attenuate plaque growth or rupture-prone vulnerability. Here, we report on a previously unknown interaction between cardiovascular drugs that are commonly prescribed for atherosclerosis patients and the cytolytic effects of photodynamic therapy using Cathepsin B activatable photosensitizer L-SR15 on murine macrophage Raw 264.7 cells in culture. Atorvastatin and clopidogrel significantly interfered with in vitro photosensitization effect while aspirin did this to a lesser extent; these drugs did not change the efficiency of cellular uptake of L-SR15 after in vitro photosensitization. A photosensitization interference effect of atorvastatin and clopidogrel was also observed when using a conventional photosensitizer free Ce6 or NCI-H1299 cancer cells. Considering the clinical implications of PDT, our study merits further investigation in clinical settings as well as in animal models.
光动力疗法(PDT)已被用于通过将光敏剂和光照结合使用来消除不需要的细胞,以产生活性氧。将 PDT 应用于动脉粥样硬化具有很大的兴趣;在动脉粥样斑块中优先破坏促炎巨噬细胞可能会减轻斑块生长或易破裂的脆弱性。在这里,我们报告了一种以前未知的相互作用,即心血管药物与细胞溶解性光动力疗法之间的相互作用,该作用使用 Cathepsin B 可激活的光敏剂 L-SR15 在培养的鼠巨噬细胞 Raw 264.7 细胞上进行。阿托伐他汀和氯吡格雷在体外显着干扰光敏化作用,而阿司匹林的干扰作用较小;这些药物在体外光敏化后不会改变 L-SR15 的细胞摄取效率。当使用常规的无 Ce6 光敏剂或 NCI-H1299 癌细胞时,阿托伐他汀和氯吡格雷也观察到光敏化干扰作用。鉴于 PDT 的临床意义,我们的研究值得在临床环境以及动物模型中进一步研究。