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Apoptosis and necrosis in liver disease.

机译:肝脏疾病中的细胞凋亡和坏死。

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摘要

Liver cell injury and cell death is a prominent feature in all liver disease processes. During the last 5-10 years, most research activities focused almost exclusively on evaluating apoptotic cell death and the corresponding intracellular signaling pathways. Although this effort led to substantial progress in our understanding of the mechanisms of apoptosis, it also created substantial confusion regarding the predominant mode of cell death and the relevance of apoptosis in a variety of liver disease models, as discussed in this review for acetaminophen and troglitazone hepatotoxicity, obstructive cholestasis and viral hepatitis. Part of the problem is related to the fact that there is no specific assay or parameter, with the exception of morphological changes in vivo, which allows the unequivocal distinction between apoptosis and oncotic necrosis. In addition, some aspects of the signaling pathways are similar. Therefore, to make progress in identifying relevant pharmacological intervention strategies to prevent or attenuate human liver disease processes, it is of critical importance to apply several different experimental approaches and analyze as many parameters as possible. In addition, positive controls for the assumed process should be used whenever possible and mechanisms of cell injury should only be investigated in model systems relevant for the human pathophysiology.
机译:肝细胞损伤和细胞死亡是所有肝脏疾病过程中的突出特征。在过去的5-10年中,大多数研究活动几乎都集中在评估凋亡性细胞死亡和相应的细胞内信号传导途径上。尽管这项工作导致我们对凋亡机制的理解取得了实质性进展,但也引起了人们对各种肝病模型中主要的细胞死亡模式和凋亡相关性的巨大困惑,如本综述中对乙酰氨基酚和曲格列酮所讨论的那样。肝毒性,阻塞性胆汁淤积和病毒性肝炎。问题的一部分与以下事实有关:除了体内的形态变化外,没有特定的测定方法或参数,这可以明确区分凋亡和肿瘤坏死。另外,信号传导途径的一些方面是相似的。因此,为了在确定相关的预防或减轻人类肝脏疾病过程的药理干预策略方面取得进展,应用几种不同的实验方法并分析尽可能多的参数至关重要。此外,应尽可能使用假定过程的阳性对照,并且仅在与人类病理生理相关的模型系统中研究细胞损伤的机制。

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