Hardin J A, Kimm M H, Wirasinghe M, Gall D G
Gastrointestinal Research Group, University of Calgary, Alberta, Canada.
Gut. 1999 Feb;44(2):218-25. doi: 10.1136/gut.44.2.218.
Although many studies have investigated macromolecular uptake in the stomach and small intestine, little is known about macromolecular uptake in the colon.
To investigate the mechanisms involved in the transport of large antigenically intact macromolecules across the proximal and distal colonic epithelium in the rabbit.
The mucosal to serosal movement of bovine serum albumin (BSA) was examined in modified Ussing chambers under short circuited conditions. The mucosal surface was exposed to varying concentrations of BSA, and after a 50 minute equilibration period, the mucosal to serosal flux of immunologically intact BSA was determined by ELISA. Total BSA flux was determined by the transport of radiolabelled 125I-BSA.
Intact BSA transport in proximal and distal colonic tissue showed saturable kinetics. Intact BSA transport in the proximal and distal segment was 7% and 2% of the total 125I-BSA flux respectively. Immunologically intact BSA transport in the distal segment was significantly less than that in the proximal segment. Intact BSA transport in the proximal colon was significantly reduced following treatment with sodium fluoride, colchicine, and tetrodotoxin. Cholinergic blockade had no effect on the uptake of intact BSA.
The findings indicate that the transport of intact macromolecules across the proximal and distal large intestine is a saturable process. Further, intact BSA transport in the proximal colon is an energy dependent process that utilises microtubules and is regulated by the enteric nervous system.
尽管许多研究已经调查了胃和小肠中的大分子摄取情况,但对于结肠中的大分子摄取了解甚少。
研究完整抗原性大分子在兔近端和远端结肠上皮细胞跨膜转运的机制。
在改良的尤斯灌流室中,于短路条件下检测牛血清白蛋白(BSA)从黏膜向浆膜的转运。将黏膜表面暴露于不同浓度的BSA中,经过50分钟的平衡期后,通过酶联免疫吸附测定法(ELISA)测定免疫完整的BSA从黏膜到浆膜的通量。通过放射性标记的125I - BSA的转运来测定总BSA通量。
近端和远端结肠组织中完整BSA的转运呈现出饱和动力学。近端和远端节段中完整BSA的转运分别占总125I - BSA通量的7%和2%。远端节段中免疫完整的BSA转运显著低于近端节段。用氟化钠、秋水仙碱和河豚毒素处理后,近端结肠中完整BSA的转运显著减少。胆碱能阻断对完整BSA的摄取没有影响。
这些发现表明完整大分子在近端和远端大肠的转运是一个饱和过程。此外,近端结肠中完整BSA的转运是一个能量依赖过程,利用微管并受肠神经系统调节。