Ontology highlight
ABSTRACT: Objective
Swertiamarin (STM) belongs to iridoid class of compounds, and the heat-transformed products (HTPS) are produced by STM in the process of drug processing. The purpose of this study was to explore the protective effect and mechanism of STM or HTPS on acetaminophen (APAP)-induced hepatotoxicity.Methods
Mice and L-O2 cells were given APAP to establish the hepatotoxicity model in vivo and in vitro. The effects of STM or HTPS on oxidative stress, inflammation, and apoptosis induced by APAP were evaluated, with N-acetylcysteine (NAC) as a positive control.Results
STM or HTPS reduced the APAP-induced apoptosis of L-O2 cells and significantly alleviated the liver injury index induced by APAP (p < 0.01, 0.005) Interestingly, HTPS had better protective effect against APAP-induced hepatotoxicity than STM (p < 0.05). In addition STM or HTPS improved the histological abnormalities; inhibited lipid peroxidation and reduced the level of inflammatory mediators. They also activated the defense system of nuclear factor erythroid 2 related factor 2 (Nrf-2) and inhibited nuclear factor-κ B (NF-κB).
SUBMITTER: Zhou Q
PROVIDER: S-EPMC10404768 | biostudies-literature | 2023 Aug
REPOSITORIES: biostudies-literature
Zhou Qian Q Zhou Qixiu Q Xia Rui R Zhang Peng P Xie Yanqing Y Yang Zhuya Z Khan Afsar A Zhou Zhihong Z Tan Wenhong W Liu Lu L
Heliyon 20230727 8
<h4>Objective</h4>Swertiamarin (STM) belongs to iridoid class of compounds, and the heat-transformed products (HTPS) are produced by STM in the process of drug processing. The purpose of this study was to explore the protective effect and mechanism of STM or HTPS on acetaminophen (APAP)-induced hepatotoxicity.<h4>Methods</h4>Mice and L-O2 cells were given APAP to establish the hepatotoxicity model <i>in vivo</i> and <i>in vitro</i>. The effects of STM or HTPS on oxidative stress, inflammation, a ...[more]