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

被引:117
作者
Jiao, Xiaoyun [1 ]
Xiao, Yongsheng [1 ]
Li, Yong [1 ]
Liang, Muwen [1 ]
Xie, Xilei [1 ]
Wang, Xu [1 ]
Tang, Bo [1 ]
机构
[1] Shandong Normal Univ, Collaborat Innovat Ctr Functionalized Probes Chem, Coll Chem Chem Engn & Mat Sci,Univ Shandong, Key Lab Mol & Nano Probes,Minist Educ,Inst Mol &, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGEN-SULFIDE; LIVING CELLS; HYPOCHLOROUS-ACID; INDUCED HEPATOTOXICITY; HIGH-SENSITIVITY; UNITED-STATES; STRATEGY; STRESS; PEROXIDE; ANIMALS;
D O I
10.1021/acs.analchem.8b01106
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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.
引用
收藏
页码:7510 / 7516
页数:7
相关论文
共 52 条
[1]   A dual responsive "turn-on'' fluorophore for orthogonal selective sensing of biological thiols and hydrogen peroxide [J].
Ang, Chung Yen ;
Tan, Si Yu ;
Wu, Shaojue ;
Qu, Qiuyu ;
Wong, Mun Fei Eddy ;
Luo, Zhong ;
Li, Pei-Zhou ;
Selvan, Subramanian Tamil ;
Zhao, Yanli .
JOURNAL OF MATERIALS CHEMISTRY C, 2016, 4 (14) :2761-2774
[2]   A Ratiometric Two-Photon Fluorescent Probe Reveals Reduction in Mitochondrial H2S Production in Parkinson's Disease Gene Knockout Astrocytes [J].
Bae, Sung Keun ;
Heo, Cheol Ho ;
Choi, Dong Joo ;
Sen, Debabrata ;
Joe, Eun-Hye ;
Cho, Bong Rae ;
Kim, Hwan Myung .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (26) :9915-9923
[3]   Fluorescent probe for highly selective and sensitive detection of hydrogen sulfide in living cells and cardiac tissues [J].
Chen, Bifeng ;
Li, Wei ;
Lv, Cong ;
Zhao, Manman ;
Jin, Hongwei ;
Jin, Hongfang ;
Du, Junbao ;
Zhang, Liangren ;
Tang, Xinjing .
ANALYST, 2013, 138 (03) :946-951
[4]   FDA-approved drug labeling for the study of drug-induced liver injury [J].
Chen, Minjun ;
Vijay, Vikrant ;
Shi, Qiang ;
Liu, Zhichao ;
Fang, Hong ;
Tong, Weida .
DRUG DISCOVERY TODAY, 2011, 16 (15-16) :697-703
[5]   A Single Fluorescent Probe to Visualize Hydrogen Sulfide and Hydrogen Polysulfides with Different Fluorescence Signals [J].
Chen, Wei ;
Pacheco, Armando ;
Takano, Yoko ;
Day, Jacob J. ;
Hanaoka, Kenjiro ;
Xian, Ming .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (34) :9993-9996
[6]   Investigation of Drug-Induced Hepatotoxicity and Its Remediation Pathway with Reaction-Based Fluorescent Probes [J].
Cheng, Dan ;
Xu, Wang ;
Yuan, Lin ;
Zhang, Xiaobing .
ANALYTICAL CHEMISTRY, 2017, 89 (14) :7693-7700
[7]   Duloxetine Reduces Oxidative Stress, Apoptosis, and Ca2+ Entry Through Modulation of TRPM2 and TRPV1 Channels in the Hippocampus and Dorsal Root Ganglion of Rats [J].
Demirdas, Arif ;
Naziroglu, Mustafa ;
Ovey, Ishak Suat .
MOLECULAR NEUROBIOLOGY, 2017, 54 (06) :4683-4695
[8]   Risks in new drug development: Approval success rates for investigational drugs [J].
DiMasi, JA .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (05) :297-307
[9]  
Ding SS, 2015, ANALYST, V140, P4687, DOI [10.1039/c5an00465a, 10.1039/C5AN00465A]
[10]  
Holoman J, 2002, Bratisl Lek Listy, V103, P70