Liu Juan, Li Tingting, Li Ruihong, Wang Jie, Li Pengyan, Niu Ming, Zhang Le, Li Chunyu, Wang Tao, Xiao Xiaohe, Wang Jia-Bo, Wang Yunfang
Hepato-Pancreato-Biliary Center, Beijing Tsinghua Changgung Hospital, Tsinghua University, Beijing, China.
Integrative Medical Center, The Fifth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Front Pharmacol. 2022 May 17;13:862830. doi: 10.3389/fphar.2022.862830. eCollection 2022.
The complexity of chemical components of herbal medicines often causes great barriers to toxicity research. In our previous study, we have found the critical divergent hepatotoxic potential of a pair of stilbene isomers in a famous traditional Chinese herb, (Heshouwu in Chinese). However, the high-throughput evaluation for such stereoisomerism-dependent hepatotoxicity is a critical challenge. In this study, we used a hepatic organoids-based hepatotoxic evaluation system in conjunction with using high content imaging to differentiate organ hepatotoxicity of the 2,3,5,4'-tetrahydroxy-stilbene-2-O-β-glucoside () and its isomer (). By using such an organoid platform, we successfully differentiated the two stereoisomers' hepatotoxic potentials, which were in accordance with their differences in rodents and humans. The lesion mechanism of the toxic isomer () was further found as the mitochondrial injury by high-content imaging, and its hepatotoxicity could be dose-dependently inhibited by the mitochondrial protective agent. These results demonstrated the utility of the organoids-based high-content imaging approach in evaluating and predicting organ toxicity of natural products in a low-cost and high-throughput way. It also suggested the rationale to use long-term cultured organoids as an alternative toxicology platform to identify early and cautiously the hepatotoxic new drug candidates in the preclinical phase.
草药化学成分的复杂性常常给毒性研究带来巨大障碍。在我们之前的研究中,我们发现了一种著名的传统中药(中文名为何首乌)中一对芪异构体具有关键的不同肝毒性潜力。然而,对这种依赖立体异构的肝毒性进行高通量评估是一项严峻挑战。在本研究中,我们使用了基于肝类器官的肝毒性评估系统,并结合高内涵成像来区分2,3,5,4'-四羟基二苯乙烯-2-O-β-葡萄糖苷()及其异构体()的肝毒性。通过使用这样的类器官平台,我们成功区分了这两种立体异构体的肝毒性潜力,这与它们在啮齿动物和人类中的差异一致。通过高内涵成像进一步发现有毒异构体()的损伤机制是线粒体损伤,其肝毒性可被线粒体保护剂剂量依赖性地抑制。这些结果证明了基于类器官的高内涵成像方法在以低成本和高通量方式评估和预测天然产物的器官毒性方面的实用性。这也为使用长期培养的类器官作为替代毒理学平台以在临床前阶段早期且谨慎地识别肝毒性新药候选物提供了理论依据。