Farnbacher Michael J, Voll Reinhard E, Faissner Ralf, Wehler Markus, Hahn Eckhart G, Löhr Matthias, Schneider H Thomas
Medizinische Klinik 2, Klinikum Fürth, Germany.
Gastrointest Endosc. 2005 Jun;61(7):862-6. doi: 10.1016/s0016-5107(05)00316-0.
Endoscopic management of chronic pancreatitis (CP), especially pancreatic stent placement, has made tremendous advances. However, good clinical results are hampered by rapid occlusion. The objective of this study was to understand mechanisms and materials that cause stent occlusion.
The clogging material of 50 lyophilized pancreatic endoprostheses (length 8.5 cm, range 5-14 cm, diameter 7-11F) from patients with CP was completely removed and weighed. Protein solubilization was achieved at pH 8.0 by using sodium dodecyl sulfate (SDS) and 2-mercaptoethanol in the presence of proteasome inhibitors. Proteins were separated by using a SDS-polyacrylamide gel electrophoresis. Protein identification was performed by the Western blot technique, as well as by mass spectrometry. Insoluble components were examined by polarized light microscopy and after staining (periodic acid-Schiff [PAS]).
Clogging material was found in 49 prostheses, mainly at the duodenal flap (80%). More than a third of the prostheses contained visible calcium carbonate calculi. Light microscopy and PAS staining showed plant debris (80%), crystals (73.5%), and mucopolysaccharides (100%). The dry weight of clogging material (18 +/- 13 mg, range 3-72 mg) correlated significantly with the stent diameter ( p = 0.029) but not with any other stent- or patient-related criteria. Albumin, its degradation products, and lithostathine were identified as the main proteinaceous components.
Almost all pancreatic stents had clogging material, predominantly located at the duodenal flap, which contained plant material, mucopolysaccharides, and crystals, as well as visible calcium carbonate calculi. Albumin and lithostathine may play an important role in the development of stent occlusion.
慢性胰腺炎(CP)的内镜治疗,尤其是胰管支架置入术,已经取得了巨大进展。然而,支架快速堵塞阻碍了良好的临床效果。本研究的目的是了解导致支架堵塞的机制和物质。
从CP患者中获取50个冻干的胰管内支架(长度8.5 cm,范围5 - 14 cm,直径7 - 11F),将堵塞物完全清除并称重。在蛋白酶体抑制剂存在的情况下,使用十二烷基硫酸钠(SDS)和2 - 巯基乙醇在pH 8.0条件下实现蛋白质溶解。通过SDS - 聚丙烯酰胺凝胶电泳分离蛋白质。采用蛋白质印迹技术和质谱法进行蛋白质鉴定。通过偏振光显微镜和染色(过碘酸 - 希夫染色[PAS])检查不溶性成分。
在49个支架中发现堵塞物,主要位于十二指肠瓣(80%)。超过三分之一的支架含有可见的碳酸钙结石。光学显微镜和PAS染色显示植物碎片(80%)、晶体(73.5%)和粘多糖(100%)。堵塞物的干重(18±13 mg,范围3 - 72 mg)与支架直径显著相关(p = 0.029),但与任何其他支架或患者相关标准无关。白蛋白、其降解产物和抑石素被鉴定为主要蛋白质成分。
几乎所有胰管支架都有堵塞物,主要位于十二指肠瓣,其中包含植物物质、粘多糖、晶体以及可见的碳酸钙结石。白蛋白和抑石素可能在支架堵塞的发生中起重要作用。