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Idiosyncratic Drug-Induced Liver Injury and the Role of Inflammatory Stress with an Emphasis on an Animal Model of Trovafloxacin Hepatotoxicity

机译:特异药引起的肝损伤和炎症应激的作用重点是托伐沙星肝毒性动物模型

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摘要

Idiosyncratic adverse drug reactions (IADRs) occur in a minority of patients yet account for the majority of postmarketing use restrictions by the Food and Drug Administration. Despite the impact of these toxicities, the underlying mechanisms are still poorly understood. Animal models of IADRs would be beneficial in understanding mechanisms and in developing assays with predictive potential. Recent work exploring the interactions between inflammatory stress and drugs associated with human idiosyncratic drug-induced liver injury (IDILI) has led to the development of the first animal models that apply to a range of drugs. Here, we discuss hypotheses for the mechanisms of IDILI and focus on a murine model of trovafloxacin-induced hepatotoxicity as an example related to the inflammatory stress hypothesis.
机译:少数患者发生特异药物不良反应(IADR),但占美国食品药品监督管理局售后使用限制的大部分。尽管有这些毒性的影响,但对潜在的机制仍知之甚少。 IADR的动物模型将有助于理解机制和开发具有预测潜力的分析方法。探索炎性应激与与人特异药物性肝损伤相关的药物之间相互作用的最新工作已导致开发出适用于多种药物的首批动物模型。在这里,我们讨论IDILI机制的假设,并以曲妥沙星诱导的肝毒性小鼠模型为例,与炎症应激假设相关。

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