Department of Analytical Chemistry, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan 24100, Turkey.
Department of Analytical Chemistry, Faculty of Pharmacy, Atatürk University, Erzurum, Turkey.
Ann Pharm Fr. 2024 Nov;82(6):1150-1162. doi: 10.1016/j.pharma.2024.08.002. Epub 2024 Aug 8.
Precision medicine, which looks for high efficacy and low toxicity in therapies, has increased in popularity with omics technology. This work aims to discover novel and low-toxicity therapy options by examining the complex relationship between silodosin-induced side effects and the metabolomic profiles associated with its administration.
The plasma samples of the control group and silodosin-treated rats were analyzed by LC-Q-TOF-MS/MS. Employing XCMS and MetaboAnalyst software, MS/MS data processed to detect compounds and investigate metabolic pathways. MATLAB 2019b was used for data categorization and multivariate analysis. A thorough comparison of METLIN and HMDB databases revealed 41m/z values with significant differences between the drug-treated and control groups (p <0.01 and fold analysis≥1.5).
According to multivariate data analysis, 17-β-estradiol, taurocholic acid, L-kynurenine, N-formylkynurenine, D-glutamine, L-arginine, prostaglandin H2, prostaglandine G2, 15-keto-prostaglandin E2, calcidiol, thromboxane A2, 5'-methylthioadenosine, L-methionine and S-adenosylmethionine levels changed significantly compared to the control group. Differences in the metabolisms of glycerophospholipid, tyrosine, phenylalanine, arachidonic acid, cysteine and methionine, and biosynthesis of phenylalanine, tyrosine, and tryptophan, and aminoacyl-tRNA have been successfully demonstrated by metabolic pathway analysis. According to this study, vitamin D, D-glutamine, and L-arginine supplements can be recommended to prevent side effects such as fatigue, intraoperative floppy iris syndrome, blurred vision, and dizziness in the treatment of silodosin. Silodosin treatment negatively affected the immune system by affecting the kynurenine and tryptophan metabolism pathways.
The study is a guide for silodosin treatments that offer low side effects and high therapeutic effect within the scope of precision medicine.
随着组学技术的发展,精准医学越来越受到重视,它旨在寻找高效低毒的治疗方法。本研究旨在通过研究司多司琼诱导的副作用与药物代谢组学之间的复杂关系,发现新的、低毒性的治疗方法。
采用 LC-Q-TOF-MS/MS 对对照组和司多司琼处理组大鼠的血浆样本进行分析。运用 XCMS 和 MetaboAnalyst 软件对 MS/MS 数据进行处理,以检测化合物并研究代谢途径。使用 MATLAB 2019b 对数据进行分类和多元分析。通过对 METLIN 和 HMDB 数据库的详细比较,发现药物处理组和对照组之间有 41 个 m/z 值存在显著差异(p<0.01,倍数分析≥1.5)。
根据多元数据分析,与对照组相比,17-β-雌二醇、牛磺胆酸、L-犬尿氨酸、N-甲酰基犬尿氨酸、D-谷氨酰胺、L-精氨酸、前列腺素 H2、前列腺素 G2、15-酮-前列腺素 E2、胆钙化醇、血栓烷 A2、5'-甲基硫腺苷、L-蛋氨酸和 S-腺苷甲硫氨酸水平有显著变化。通过代谢途径分析,成功证明了甘油磷脂、酪氨酸、苯丙氨酸、花生四烯酸、半胱氨酸和蛋氨酸的代谢以及苯丙氨酸、酪氨酸和色氨酸的生物合成和氨酰-tRNA 的变化。根据本研究,建议在治疗司多司琼时补充维生素 D、D-谷氨酰胺和 L-精氨酸,以预防疲劳、术中虹膜松软综合征、视力模糊和头晕等副作用。司多司琼治疗通过影响犬尿氨酸和色氨酸代谢途径对免疫系统产生负面影响。
本研究为司多司琼治疗提供了指导,在精准医学范围内实现了低副作用和高治疗效果。