Abstract
When administered to rats, mogroside V (a pentaglucose-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 monoand diglucosides. However, trace amounts of mogrol and its monoglucoside were found in the portal blood as sulfates and/or glucuronide conjugates.
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Murata, Y., Ogawa, T., Suzuki, Y. A., Yoshikawa, S., Inui, H., Sugiura, M., & Nakano, Y. (2010). Digestion and absorption of siraitia grosvenori triterpenoids in the rat. Bioscience, Biotechnology and Biochemistry, 74(3), 673–676. https://doi.org/10.1271/bbb.90832
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