Olofsson P, Nylander G, Olsson P
Acta Chir Scand. 1985;151(7):635-9.
A rat model representing segmental intestinal ischemia was used to study the absorption and transport of endotoxin from the ischemic gut. Serial quantitative analyses were made on peritoneal fluid, thoracic duct lymph and arterial and portal vein blood. Significantly increased endotoxin concentrations were found in thoracic duct lymph before transmural leakage took place. After leaking through the devitalized intestinal wall, endotoxin was transported by both lymphatic and portal routes. Kinetic analysis revealed that systemic endotoxemia paralleled the appearance of endotoxins in thoracic duct lymph, preceding a significant increase in the portal vein. The amount transported by the portal vein never exceeded the proposed endotoxin-filtrating capacity of the liver. In intestinal ischemia, consequently, systemic endotoxemia appears to be mediated mainly by lymphatic transport.
采用一种代表节段性肠缺血的大鼠模型来研究内毒素从缺血肠段的吸收和转运。对腹腔液、胸导管淋巴液以及动脉血和门静脉血进行了系列定量分析。在透壁渗漏发生之前,胸导管淋巴液中的内毒素浓度显著升高。内毒素通过失活的肠壁渗漏后,通过淋巴和门静脉途径进行转运。动力学分析显示,全身内毒素血症与胸导管淋巴液中内毒素的出现平行,先于门静脉内毒素显著增加。门静脉转运的内毒素量从未超过肝脏假定的内毒素滤过能力。因此,在肠缺血时,全身内毒素血症似乎主要由淋巴转运介导。