Cavuoti O P, Moody F G, Martinez G
Department of Surgery, University of Texas Medical School, Houston, TX 77030.
Surgery. 1988 Mar;103(3):361-6.
There is evidence that the pancreatic duct plays an important role in the evolution of necrotizing pancreatitis. We hypothesized that occlusion of the pancreatic duct and its smaller ductules with prolamine (Ethibloc) in opossums at risk of severe necrotizing pancreatitis would have a beneficial effect on the progression of the disease. Sixteen opossums underwent bile duct ligation below the entrance of the pancreatic duct. They were divided into four groups at 6 days. Group I (control, n = 5) opossums were killed for histologic observation of the degree of necrosis of the pancreas; group II (n = 5) underwent external drainage of the pancreatic biliary duct; group III (n = 4) had external biliary drainage and ligation of the pancreatic duct; group IV (n = 7) was treated with external biliary drainage and ligation of the main pancreatic duct after instillation of prolamine. Serum amylase, lipase, and calcium values were determined. The pancreas was examined by inspection and histologically at the time of death, and the severity of the disease was determined by quantitation of pancreatic tissue necrosis. All animals in groups II and III died 8 to 14 days after bile duct ligation, and all had severe necrotizing pancreatitis. All animals in group IV survived and were killed at 2 to 10 weeks after prolamine (Ethibloc) injection into the pancreatic duct. A mild edematous pancreatitis was observed in all seven animals. Prolamine (Ethibloc) provided dramatic protection from progressive necrosis. This study does not provide an explanation, but it allows for speculation that ductal injection interrupted the deleterious effect of proteolytic enzymes and their leakage into the interstitial space of the pancreas.
有证据表明胰管在坏死性胰腺炎的发展过程中起重要作用。我们推测,对有发生严重坏死性胰腺炎风险的负鼠,用醇溶蛋白(Ethibloc)阻塞胰管及其较小的分支胰管,可能对疾病进展产生有益影响。16只负鼠在胰管入口下方进行胆管结扎。6天后将它们分为四组。第一组(对照组,n = 5)负鼠处死,用于胰腺坏死程度的组织学观察;第二组(n = 5)进行胰胆管外引流;第三组(n = 4)进行胆管外引流并结扎胰管;第四组(n = 7)在注入醇溶蛋白后进行胆管外引流并结扎主胰管。测定血清淀粉酶、脂肪酶和钙值。在处死时通过检查和组织学检查胰腺,并通过胰腺组织坏死定量确定疾病的严重程度。第二组和第三组的所有动物在胆管结扎后8至14天死亡,均患有严重的坏死性胰腺炎。第四组的所有动物均存活,并在向胰管注射醇溶蛋白(Ethibloc)后2至10周处死。所有7只动物均观察到轻度水肿性胰腺炎。醇溶蛋白(Ethibloc)显著防止了坏死的进展。本研究未提供解释,但推测导管注射中断了蛋白水解酶的有害作用及其向胰腺间质间隙的渗漏。