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急性胰腺炎中的细胞凋亡与坏死

Apoptosis versus necrosis in acute pancreatitis.

作者信息

Bhatia Madhav

机构信息

Department of Pharmacology, National University of Singapore, Faculty of Medicine, Singapore 117597, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2004 Feb;286(2):G189-96. doi: 10.1152/ajpgi.00304.2003.

Abstract

Acute pancreatitis is a disease of variable severity in which some patients experience mild, self-limited attacks, whereas others manifest a severe, highly morbid, and frequently lethal attack. The events that regulate the severity of acute pancreatitis are, for the most part, unknown. It is generally believed that the earliest events in acute pancreatitis occur within acinar cells and result in acinar cell injury. Other processes, such as recruitment of inflammatory cells and generation of inflammatory mediators, are believed to occur subsequent to acinar cell injury, and these "downstream" events are believed to influence the severity of the disease. Several recently reported studies, however, have suggested that the acinar cell response to injury may, itself, be an important determinant of disease severity. In these studies, mild acute pancreatitis was found to be associated with extensive apoptotic acinar cell death, whereas severe acute pancreatitis was found to involve extensive acinar cell necrosis but very little acinar cell apoptosis. These observations led to the hypothesis that apoptosis could be a favorable response to acinar cells and that interventions that favor induction of apoptotic, as opposed to necrotic, acinar cell death might reduce the severity of an attack of acute pancreatitis. Indeed, in an experimental setting, the induction of pancreatic acinar cell apoptosis protects mice against acute pancreatitis. Little is known about the mechanism of apoptosis in the pancreatic acinar cell, although some early attempts have been made in that direction. Also, clinical relevance of these experimental studies remains to be investigated.

摘要

急性胰腺炎是一种严重程度不一的疾病,一些患者经历轻度、自限性发作,而另一些患者则表现为严重、高致残性且常致命的发作。调节急性胰腺炎严重程度的事件在很大程度上尚不清楚。一般认为,急性胰腺炎最早的事件发生在腺泡细胞内,导致腺泡细胞损伤。其他过程,如炎症细胞的募集和炎症介质的产生,被认为发生在腺泡细胞损伤之后,并且这些“下游”事件被认为会影响疾病的严重程度。然而,最近的几项报道研究表明,腺泡细胞对损伤的反应本身可能是疾病严重程度的一个重要决定因素。在这些研究中,发现轻度急性胰腺炎与广泛凋亡的腺泡细胞死亡有关,而重度急性胰腺炎则涉及广泛的腺泡细胞坏死但很少有腺泡细胞凋亡。这些观察结果导致了这样一种假设,即凋亡可能是腺泡细胞的一种有利反应,并且有利于诱导凋亡而非坏死的腺泡细胞死亡的干预措施可能会降低急性胰腺炎发作的严重程度。事实上,在实验环境中,诱导胰腺腺泡细胞凋亡可保护小鼠免受急性胰腺炎的影响。尽管已经在这方面进行了一些早期尝试,但关于胰腺腺泡细胞凋亡的机制知之甚少。此外,这些实验研究的临床相关性仍有待研究。

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