Karlqvist P A, Franzén L, Sjödahl R, Tagesson C
Acta Chir Scand. 1986 Apr;152:279-84.
The influence of lysophosphatidylcholine (LPC) on the permeability to different sized molecules in the stomach has been studied. Using a rat experimental model, we determined the gastric permeability to sodium fluorescein (molecular weight 376 dalton) and to fluorescein-labeled dextran 3000 (molecular weight 3000 dalton) in the absence or presence of LPC. We also examined the influence of LPC on the morphology of the gastric mucosa using light microscopy, scanning electron microscopy and transmission electron microscopy. We found that 10 mM LPC increased the gastric permeability to both sodium fluorescein and to dextran 3000. Moreover, by transmission electron microscopy, damaged microvillous structures could be seen after LPC treatment. Light microscopy and scanning electron microscopy showed no difference between LPC-treated rats and controls. These findings indicate that LPC, a naturally occurring component in duodenal juice, may damage the gastric mucosa and increase the stomach permeability to larger, potentially pathogenic molecules.
已研究溶血磷脂酰胆碱(LPC)对胃中不同大小分子通透性的影响。使用大鼠实验模型,我们测定了在不存在或存在LPC的情况下,胃对荧光素钠(分子量376道尔顿)和荧光素标记的葡聚糖3000(分子量3000道尔顿)的通透性。我们还使用光学显微镜、扫描电子显微镜和透射电子显微镜检查了LPC对胃黏膜形态的影响。我们发现,10 mM的LPC增加了胃对荧光素钠和葡聚糖3000的通透性。此外,通过透射电子显微镜观察,LPC处理后可见微绒毛结构受损。光学显微镜和扫描电子显微镜显示,LPC处理的大鼠与对照组之间无差异。这些发现表明,LPC作为十二指肠液中的一种天然成分,可能会损害胃黏膜,并增加胃对更大的潜在致病分子的通透性。