Guarini S, Fano R A, Rompianesi E, Martinelli A M, Ferrari W
J Pharm Pharmacol. 1986 Dec;38(12):922-4. doi: 10.1111/j.2042-7158.1986.tb03385.x.
To gain direct insight into the mechanism of sodium deoxycholate (DOC)-induced enhancement of gastroenteral heparin absorption in rats, we performed light and electron microscopic examination of the mucosa of the small intestine of animals treated orally with DOC, heparin or DOC plus heparin. The sole morphological change observed after DOC and DOC plus heparin administration was a marked reduction in the length and distribution of glycocalyx filaments on the microvilli of epithelial cells. The morphological picture had reverted to normal after 24 h, when the promotion of enteral heparin absorption by DOC is greatly reduced. Thus, we suggest that DOC may promote the enteral absorption of heparin in rats by affecting some as yet unidentified barrier mechanism requiring glycocalyx integrity.
为了直接深入了解脱氧胆酸钠(DOC)诱导大鼠胃肠肝素吸收增强的机制,我们对口服DOC、肝素或DOC加肝素处理的动物小肠黏膜进行了光镜和电镜检查。给予DOC和DOC加肝素后观察到的唯一形态学变化是上皮细胞微绒毛上糖萼丝长度和分布的显著减少。24小时后形态恢复正常,此时DOC对肠内肝素吸收的促进作用大大降低。因此,我们认为DOC可能通过影响某种尚未明确的需要糖萼完整性的屏障机制来促进大鼠肠内肝素的吸收。