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糖苷类甜味剂甜菊糖苷和莱鲍迪苷A的肠道降解与吸收。

Intestinal degradation and absorption of the glycosidic sweeteners stevioside and rebaudioside A.

作者信息

Wingard R E, Brown J P, Enderlin F E, Dale J A, Hale R L, Seitz C T

出版信息

Experientia. 1980 May 15;36(5):519-20. doi: 10.1007/BF01965774.

DOI:10.1007/BF01965774
PMID:7379936
Abstract

Contrary to prior indications, the glycosidic sweeteners stevioside and rebaudioside A are degraded to the diterpenoid aglycone steviol by rat intestinal microflora in vitro. Additional studies with steviol-17-[14C] show almost total absorption from the rat lower bowel following intracecal administration.

摘要

与之前的研究结果相反，在体外实验中，糖苷类甜味剂甜菊糖苷和莱鲍迪苷A可被大鼠肠道微生物群降解为二萜类苷元甜菊醇。用甜菊醇-17-[14C]进行的进一步研究表明，经盲肠内给药后，大鼠下肠道对其吸收几乎完全。

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