Digestion and Absorption of Siraitia grosvenori Triterpenoids in the Rat

Digestion and Absorption of Siraitia grosvenori Triterpenoids in the Rat
复制标题

DOI:
10.1271/bbb.90832
复制
发表时间:
2010-03-01
影响因子:
1.6
通讯作者:
Nakano, Yoshihisa
Nakano, Yoshihisa
中科院分区:
工程技术4区
文献类型:
--
作者:
Murata, Yuji;Ogawa, Takahisa;Nakano, Yoshihisa

文献摘要

被引文献

相似文献

当给予大鼠时,罗汉果苷V(一种五葡萄糖缀合的罗汉果苷),罗汉果的主要甜味成分,主要被消化酶和肠道微生物降解,并以罗汉果醇(糖苷配基)及其单和二葡萄糖苷的形式在粪便中排泄。然而,在门静脉血中发现痕量的罗汉果醇及其单葡萄糖苷作为硫酸盐和/或葡糖苷酸结合物。
When administered to rats, mogroside V (a penta-glucose-conjugated mogroside), the main sweetening component of Siraitia grosvenori, was mostly degraded by digestive enzymes and intestinal microflora, and was excreted in the feces as mogrol (aglycone) and its mono- and diglucosides. However, trace amounts of mogrol and its monoglucoside were found in the portal blood as sulfates and/or glucuronide conjugates.