Lombardi B, Estes L W, Longnecker D S
Am J Pathol. 1975 Jun;79(3):465-80.
Female, albino mice were fed a choline-deficient diet containing 0.5% DL-ethionine. All animals died within 5 days due to the development of an acute hemorrhagic pancreatis with fat necrosis throughout the peritoneal cavity. The apancreatitis was characterized by a massive necrosis of the exocrine parenchyma with intense hemorrhage and inflammatory reaction of the stroma. The sequence of histologic and ultrastructural alterations occurring in the acinar cells of the pancreas were studied in mice fed the diet for 1, 2, and 3 days. Major findings consited of accumulation of zymogen granules, vacuolation due to foci of cytoplasmic degradation, and alterations in the morphology of the zymogen granules. The pancreatitis appears to be due to intraparenchymal activation of zymogens, resulting from a synergistic action of choline deficiency with the basic toxicity of ethionine toward the acinar cells of the pancreas. The experimental model simulates closely the acute hemorrhagic pancreatitis with fat necrosis occurring in humans and may prove useful for exploring the pathogenesis of this condition.
雌性白化小鼠被喂食含0.5% DL-乙硫氨酸的胆碱缺乏饮食。所有动物在5天内死亡,原因是发生急性出血性胰腺炎并伴有整个腹腔的脂肪坏死。胰腺炎的特征是外分泌实质大量坏死,伴有强烈出血和间质炎症反应。对喂食该饮食1天、2天和3天的小鼠胰腺腺泡细胞中发生的组织学和超微结构改变序列进行了研究。主要发现包括酶原颗粒的积累、由于细胞质降解灶导致的空泡化以及酶原颗粒形态的改变。胰腺炎似乎是由于酶原在实质内激活,这是胆碱缺乏与乙硫氨酸对胰腺腺泡细胞的基本毒性协同作用的结果。该实验模型与人类发生的伴有脂肪坏死的急性出血性胰腺炎非常相似,可能对探索这种疾病的发病机制有用。