Evaluating Drug-Induced Liver Injury and Its Remission via Discrimination and Imaging of HClO and H2S with a Two-Photon Fluorescent Probe

化学 肝损伤 体内 药品 内生 药理学 戒毒(替代医学) 抗抑郁药 氟西汀 荧光 内科学 生物化学 病理 医学 海马体 血清素 替代医学 受体 生物技术 物理 生物 量子力学
作者
Xiaoyun Jiao,Yongsheng Xiao,Yong Li,Muwen Liang,Xilei Xie,Xu Wang,Bo Tang
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:90 (12): 7510-7516 被引量:114
标识
DOI:10.1021/acs.analchem.8b01106
摘要

Drug-induced liver injury (DILI) has aroused wide concern. Finding new markers or indicators as well as detoxification molecules for DILI is of great significance and good application prospect, which can help develop effective preclinical screening methodology and corresponding treatment protocols. Herein, in this article, DILI caused by antidepressant drugs of duloxetine and fluoxetine and its remission were evaluated by a two-photon fluorescent probe, RPC-1, through discriminating and imaging HClO and H2S simultaneously. By being applied both in vitro and in vivo, RPC-1 revealed slight up-regulation of HClO and negligible liver damage after administration of either of the two drugs. In contrast, an apparent up-regulation of HClO and obvious liver damage was observed after combined administration of the drugs. Meanwhile, the pretreatment of N-acetyl cysteine (NAC) resulted in the increasing of endogenous H2S level, which contributed to the remission of DILI. The histological analysis and serological test both gave good consistency with the imaging results. These findings demonstrate that HClO may be an appropriate indicator of DILI, and H2S plays an important role in the antidotal effect of NAC. We envision that RPC-1 can be used as a powerful tool to predict clinical DILI and study the effect of antidote, as well as explore the molecular mechanisms involved.
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