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用于药物性肝损伤的循环线粒体生物标志物。

Circulating mitochondrial biomarkers for drug-induced liver injury.

作者信息

Shi Qiang, Yang Xi, Mattes William B, Mendrick Donna L, Harrill Alison H, Beger Richard D

机构信息

Division of Systems Biology, National Center for Toxicological Research, Food & Drug Administration, 3900 NCTR Road, Jefferson, AR 72079, USA.

Regulatory Activities, National Center for Toxicological Research, Food & Drug Administration, 3900 NCTR Road, Jefferson, AR 72079, USA.

出版信息

Biomark Med. 2015;9(11):1215-23. doi: 10.2217/bmm.15.59. Epub 2015 Oct 28.

Abstract

Liver mitochondria affected by drugs can be released into circulation and serve as biomarkers for drug-induced liver injury (DILI). The tissue specificity of ALT was improved by differentiating cytosolic ALT1 and mitochondrial ALT2 isoforms released in circulation. Prior to ALT elevation, mitochondrial cytochrome c, OCT, GLDH, CPS1 and DNA were increased in circulation following DILI. The baseline expression of mt-Nd6 was predictive of individual DILI susceptibility in animals. As mitochondrial DILI biomarkers appeared to be drug or species dependent, they might have value in clinical scenarios when culprit drugs are established, but may not be ideal tools to assess DILI potentials of new drugs.

摘要

受药物影响的肝脏线粒体可释放到循环系统中,并作为药物性肝损伤(DILI)的生物标志物。通过区分循环中释放的胞质ALT1和线粒体ALT2同工型,提高了ALT的组织特异性。在ALT升高之前,DILI后循环中的线粒体细胞色素c、OCT、GLDH、CPS1和DNA会增加。mt-Nd6的基线表达可预测动物个体对DILI的易感性。由于线粒体DILI生物标志物似乎依赖于药物或物种,它们在确定罪魁祸首药物的临床情况下可能有价值,但可能不是评估新药DILI潜力的理想工具。

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