Cho So Yean, Sim Joon-Soo, Kang Sam Sik, Jeong Choon-Sik, Linhardt Robert J, Kim Yeong Shik
Natural Products Research Institute, College of Pharmacy Seoul National University, Seoul 110-460, Korea.
Arch Pharm Res. 2003 Dec;26(12):1102-8. doi: 10.1007/BF02994765.
We studied the effects of phytolaccosides, saponins from Phytolacca americana, on the intestinal absorption of heparin in vitro and in vivo. The absorption enhancing activity of these compounds (phytolaccosides B, D2, E, F, G and I) was determined by changes in transepithelial electrical resistance (TEER) and the transport amount of heparin disaccharide, the major repeating unit of heparin, across Caco-2 cell monolayers. With the exception of phytolaccoside G, all of them decreased TEER values and increased the permeability in a dose-dependent and time-dependent manner. In vitro, phytolaccosides B, D2, and E showed significant absorption enhancing activities, while effects by phytolaccoside F and I were mild. In vivo, phytolaccoside E increased the activated partial thromboplastin time (APTT) and thrombin time, indicating that phytolaccoside E modulated the transport of heparin in intestinal route. Our results suggest that a series of phytolaccosides from Phytolacca americana can be applied as pharmaceutical excipients to improve the permeability of macromolecules and hydrophilic drugs having difficulty in absorption across the intestinal epithelium.
我们研究了美洲商陆中的皂苷类化合物商陆皂苷对肝素在体外和体内肠道吸收的影响。通过跨上皮电阻(TEER)的变化以及肝素的主要重复单元肝素二糖跨Caco-2细胞单层的转运量来测定这些化合物(商陆皂苷B、D2、E、F、G和I)的吸收增强活性。除商陆皂苷G外,其他所有化合物均以剂量和时间依赖性方式降低TEER值并增加通透性。在体外,商陆皂苷B、D2和E表现出显著的吸收增强活性,而商陆皂苷F和I的作用较为温和。在体内,商陆皂苷E延长了活化部分凝血活酶时间(APTT)和凝血酶时间,表明商陆皂苷E调节了肝素在肠道途径中的转运。我们的结果表明,美洲商陆中的一系列商陆皂苷可作为药物辅料,以提高大分子和亲水性药物在肠道上皮的吸收通透性,这些药物难以吸收。