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L-arginine-induced experimental pancreatitis

机译:L-精氨酸诱导的实验性胰腺炎

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摘要

Despite medical treatment, the lethality of severe acute pancreatitis is still high (20-30%). Therefore, it is very important to find good animal models to characterise the events of this severe disease. In 1984, Mizunuma et al. developed a new type of experimental necrotizing pancreatitis by intraperitoneal administration of a high dose of L-arginine in rats. This non-invasive model is highly reproducible and produces selective, dose-dependent acinar cell necrosis. Not only is this a good model to study the pathomechanisms of acute necrotizing pancreatitis, but it is also excellent to observe and influence the time course changes of the disease. By writing this review we iluminate some new aspects of cell physiology and pathology of acute necrotizing pancreatitis. Unfortunately, the reviews about acute experimental pancreatitis usually did not discuss this model. Therefore, the aim of this manuscript was to summarise the observations and address some challenges for the future in L-arginine-induced pancreatitis.
机译:尽管有药物治疗,重症急性胰腺炎的致死率仍然很高(20-30%)。因此,找到良好的动物模型来表征这种严重疾病的事件非常重要。 1984年,Mizunuma等人。通过在大鼠腹腔内施用高剂量的L-精氨酸,开发了一种新型的实验性坏死性胰腺炎。这种非侵入性模型可高度重现,并产生选择性的,剂量依赖性的腺泡细胞坏死。这不仅是研究急性坏死性胰腺炎的发病机制的良好模型,而且观察和影响疾病的时程变化也非常有用。通过撰写此评论,我们阐明了急性坏死性胰腺炎的细胞生理学和病理学的一些新方面。不幸的是,有关急性实验性胰腺炎的评论通常没有讨论该模型。因此,本手稿的目的是总结观察结果,并应对L-精氨酸诱导的胰腺炎的未来挑战。

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