1First Department of Medicine, University of Szeged, Szeged, Hungary. 2Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany. 3Department of Pathology, University of Szeged, Szeged, Hungary. 4Department of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary. 5Department of Microbiology, University of Szeged, Szeged, Hungary. 6Institute of Surgical Research, University of Szeged, Szeged, Hungary. 7Department of Surgery, Tufts Medical Center, Boston, MA. 8Department of Pharmacology and Pharmacotherapy, University of Szeged, Szeged, Hungary. 9Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Crit Care Med. 2014 Mar;42(3):e177-88. doi: 10.1097/CCM.0000000000000101.
A common potentially fatal disease of the pancreas is acute pancreatitis, for which there is no treatment. Most studies of this disorder focus on the damage to acinar cells since they are assumed to be the primary target of multiple stressors affecting the pancreas. However, increasing evidence suggests that the ducts may also have a crucial role in induction of the disease. To test this hypothesis, we sought to determine the specific role of the duct in the induction of acute pancreatitis using well-established disease models and mice with deletion of the Na/H exchanger regulatory factor-1 that have selectively impaired ductal function.
Randomized animal study.
Animal research laboratory.
Wild-type and Na/H exchanger regulatory factor-1 knockout mice.
Acute necrotizing pancreatitis was induced by i.p. administration of cerulein or by intraductal administration of sodium taurocholate. The pancreatic expression of Na/H exchanger regulatory factor-1 and cystic fibrosis transmembrane conductance regulator (a key player in the control of ductal secretion) was analyzed by immunohistochemistry. In vivo pancreatic ductal secretion was studied in anesthetized mice. Functions of pancreatic acinar and ductal cells as well as inflammatory cells were analyzed in vitro.
Deletion of Na/H exchanger regulatory factor-1 resulted in gross mislocalization of cystic fibrosis transmembrane conductance regulator, causing marked reduction in pancreatic ductal fluid and bicarbonate secretion. Importantly, deletion of Na/H exchanger regulatory factor-1 had no deleterious effect on functions of acinar and inflammatory cells. Deletion of Na/H exchanger regulatory factor-1, which specifically impaired ductal function, increased the severity of acute pancreatitis in the two mouse models tested.
Our findings provide the first direct evidence for the crucial role of ductal secretion in protecting the pancreas from acute pancreatitis and strongly suggest that improved ductal function should be an important modality in prevention and treatment of the disease.
胰腺的一种常见潜在致命疾病是急性胰腺炎,目前尚无治疗方法。大多数关于这种疾病的研究都集中在腺泡细胞的损伤上,因为腺泡细胞被认为是影响胰腺的多种应激源的主要靶标。然而,越来越多的证据表明,胆管在疾病的诱导中也可能具有关键作用。为了验证这一假说,我们试图使用已建立的疾病模型和选择性损害胆管功能的 Na/H 交换调节剂-1 缺失小鼠来确定胆管在急性胰腺炎诱导中的特定作用。
随机动物研究。
动物研究实验室。
野生型和 Na/H 交换调节剂-1 缺失小鼠。
通过腹腔内给予 Cerulein 或通过胆管内给予牛磺胆酸钠诱导急性坏死性胰腺炎。通过免疫组织化学分析胰腺中 Na/H 交换调节剂-1 和囊性纤维化跨膜电导调节剂(控制胆管分泌的关键因子)的表达。在麻醉小鼠中研究体内胰腺胆管分泌。在体外分析胰腺腺泡和胆管细胞以及炎症细胞的功能。
Na/H 交换调节剂-1 的缺失导致囊性纤维化跨膜电导调节剂的严重定位错误,导致胰腺胆管液和碳酸氢盐分泌明显减少。重要的是,Na/H 交换调节剂-1 的缺失对腺泡和炎症细胞的功能没有不良影响。特异性损害胆管功能的 Na/H 交换调节剂-1 的缺失增加了两种模型中急性胰腺炎的严重程度。
我们的发现为胆管分泌在保护胰腺免受急性胰腺炎方面的关键作用提供了首个直接证据,并强烈表明改善胆管功能应该是预防和治疗这种疾病的重要手段。