Key Laboratory of Drug Quality Control and Pharmacovigilance (China Pharmaceutical University), Ministry of Education, Nanjing 210009, China; Department of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing 210009, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Apr 1;1142:122019. doi: 10.1016/j.jchromb.2020.122019. Epub 2020 Feb 3.
In recent years, depression occurs frequently. Given the long duration of the disease and the high risk of recurrence, the treatment of depression requires long-term medication. Zhi-Zi-Hou-Po Decoction (ZZHPD) has been used in clinical treatment of depression and related diseases for many years, and the potential toxic damage caused by its long-term use has gradually emerged. Existing research methods that expose toxicity by a one-time administration of large doses cannot provide a reference for clinical safe drug use. In this study, the potential toxicity of ZZHPD in repeated administration was studied by urinary metabolomics with nondestructive sampling. Based on ultra-high performance liquid chromatography-quadruple-Exactive Orbitrap mass spectrometry (UHPLC-Q-Exactive Orbitrap-MS) and chemometrics, 33 differential biomarkers, such as 3-hydroxybutyric acid, indole sulfuric acid, hippuric acid and citric acid, were screened and dynamically tracked. The changes of some endogenous substances showed obvious time dependence. Further analysis of these time-dependent components in combination with network pharmacology revealed that the potential hepatotoxicity and nephrotoxicity of ZZHPD were related to the disorders of amino acid metabolism, energy metabolism, lipid metabolism, nucleotide metabolism and gut microflora metabolism pathway. This study can better grasp the occurrence and development of drug toxicity, and provide reference for rational and safe drug use and potential toxicity prevention of ZZHPD.
近年来,抑郁症的发病率居高不下。鉴于该病的病程长、复发风险高,抑郁症的治疗需要长期用药。自子厚坡汤(ZZHPD)在临床治疗抑郁症及相关疾病中应用多年以来,其长期使用所带来的潜在毒性损伤逐渐显现。现有的大剂量一次性给药暴露毒性的研究方法,无法为临床安全用药提供参考。本研究采用非损伤性采样的尿代谢组学方法,研究 ZZHPD 重复给药的潜在毒性。基于超高效液相色谱-四极杆-静电场轨道阱质谱联用(UHPLC-Q-Exactive Orbitrap-MS)和化学计量学,筛选并动态跟踪了 33 个差异生物标志物,如 3-羟基丁酸、吲哚硫酸、马尿酸和柠檬酸。一些内源性物质的变化表现出明显的时间依赖性。进一步分析这些随时间变化的成分,并结合网络药理学,揭示了 ZZHPD 的潜在肝毒性和肾毒性与氨基酸代谢、能量代谢、脂质代谢、核苷酸代谢和肠道微生物群代谢途径的紊乱有关。该研究可以更好地掌握药物毒性的发生和发展,为 ZZHPD 的合理安全用药和潜在毒性预防提供参考。