Inokuchi Hitoshi, Takei Takuto, Aikawa Katsuyoshi, Shimizu Makoto
Oral Liquid Formulation R&D Laboratories, Self Medication Business, Taisho Pharmaceutical Co., Ltd., Saitama-shi, Japan.
Biosci Biotechnol Biochem. 2009 Feb;73(2):328-34. doi: 10.1271/bbb.80538. Epub 2009 Feb 7.
The intestinal epithelium is a significant barrier to oral absorption of hydrophilic compounds, and their passage through the intercellular space is restricted by the tight junctions. In this study we found that hyperosmosis is a significant factor altering paracellular transport in Caco-2 cell monolayers. Osmotic regulators, such as sodium chloride, mannitol, and raffinose, decreased transepithelial electrical resistance and enhanced lucifer yellow permeability. The effect of these osmotic regulators on Caco-2 cell monolayers was not likely to be caused by gross cytotoxicity. Although certain amino acids and oligosaccharides have been reported to have specific tight junction-modulating activity, we found that the increased paracellular permeability of Caco-2 monolayers induced by these compounds was at least partly due to the increased osmotic pressure of the test solutions. These findings provide a new potential precaution in the evaluation of paracellular permeability-modulating substances using the Caco-2 cell monolayer system.
肠上皮是亲水性化合物口服吸收的重要屏障,它们通过细胞间隙的过程受到紧密连接的限制。在本研究中,我们发现高渗是改变Caco-2细胞单层细胞旁转运的一个重要因素。渗透压调节剂,如氯化钠、甘露醇和棉子糖,可降低跨上皮电阻并增强荧光素黄通透性。这些渗透压调节剂对Caco-2细胞单层的作用不太可能是由严重的细胞毒性引起的。虽然已有报道某些氨基酸和寡糖具有特定的紧密连接调节活性,但我们发现这些化合物诱导的Caco-2单层细胞旁通透性增加至少部分是由于测试溶液渗透压的升高。这些发现为使用Caco-2细胞单层系统评估细胞旁通透性调节物质提供了一个新的潜在预防措施。