Grabacka M, Waligorski P, Zapata A, Blake D A, Wyczechowska D, Wilk A, Rutkowska M, Vashistha H, Ayyala R, Ponnusamy T, John V T, Culicchia F, Wisniewska-Becker A, Reiss K
Department of Food Biotechnology, Faculty of Food Technology, University of Agriculture in Cracow, Cracow, Poland.
J Physiol Pharmacol. 2015 Apr;66(2):233-47.
Fenofibrate, a well-known normolipidemic drug, has been shown to exert strong anticancer effects against tumors of neuroectodermal origin including glioblastoma. Although some pharmacokinetic studies were performed in the past, data are still needed about the detailed subcellular and tissue distribution of fenofibrate (FF) and its active metabolite, fenofibric acid (FA), especially in respect to the treatment of intracranial tumors. We used high performance liquid chromatography (HPLC) to elucidate the intracellular, tissue and body fluid distribution of FF and FA after oral administration of the drug to mice bearing intracranial glioblastoma. Following the treatment, FF was quickly cleaved to FA by blood esterases and FA was detected in the blood, urine, liver, kidney, spleen and lungs. We have also detected small amounts of FA in the brains of two out of six mice, but not in the brain tumor tissue. The lack of FF and FA in the intracranial tumors prompted us to develop a new method for intracranial delivery of FF. We have prepared and tested in vitro biodegradable poly-lactic-co-glycolic acid (PLGA) polymer wafers containing FF, which could ultimately be inserted into the brain cavity following resection of the brain tumor. HPLC-based analysis demonstrated a slow and constant diffusion of FF from the wafer, and the released FF abolished clonogenic growth of glioblastoma cells. On the intracellular level, FF and FA were both present in the cytosolic fraction. Surprisingly, we also detected FF, but not FA in the cell membrane fraction. Electron paramagnetic resonance spectroscopy applied to spin-labeled phospholipid model-membranes revealed broadening of lipid phase transitions and decrease of membrane polarity induced by fenofibrate. Our results indicate that the membrane-bound FF could contribute to its exceptional anticancer potential in comparison to other lipid-lowering drugs, and advocate for intracranial delivery of FF in the combined pharmacotherapy against glioblastoma.
非诺贝特是一种著名的降血脂药物,已被证明对包括胶质母细胞瘤在内的神经外胚层起源的肿瘤具有强大的抗癌作用。尽管过去进行了一些药代动力学研究,但仍需要有关非诺贝特(FF)及其活性代谢物非诺贝酸(FA)在亚细胞和组织中的详细分布数据,特别是在颅内肿瘤治疗方面。我们使用高效液相色谱法(HPLC)来阐明口服该药物给患有颅内胶质母细胞瘤的小鼠后FF和FA在细胞内、组织和体液中的分布。治疗后,FF被血液酯酶迅速裂解为FA,并且在血液、尿液、肝脏、肾脏、脾脏和肺中检测到了FA。我们还在六只小鼠中的两只小鼠的大脑中检测到了少量的FA,但在脑肿瘤组织中未检测到。颅内肿瘤中缺乏FF和FA促使我们开发一种新的FF颅内给药方法。我们制备并在体外测试了含有FF的可生物降解聚乳酸-乙醇酸共聚物(PLGA)聚合物薄片,最终可在切除脑肿瘤后将其插入脑腔。基于HPLC的分析表明FF从薄片中缓慢且持续地扩散,并且释放的FF消除了胶质母细胞瘤细胞的克隆生长。在细胞内水平,FF和FA都存在于胞质部分。令人惊讶的是,我们在细胞膜部分也检测到了FF,但未检测到FA。应用于自旋标记磷脂模型膜的电子顺磁共振光谱显示非诺贝特诱导脂质相变变宽和膜极性降低。我们的结果表明,与其他降脂药物相比,膜结合的FF可能有助于其特殊的抗癌潜力,并主张在胶质母细胞瘤的联合药物治疗中进行FF的颅内给药。