Steviol glycosides in purified stevia leaf extract sharing the same metabolic fate

甜菊醇 糖苷 甜叶菊 甜菊苷 代谢物 化学 甜菊 生物化学 雷巴迪甙A 食品科学 生物 立体化学 医学 病理 替代医学
作者
Sidd Purkayastha,A. A. Markosyan,Indra Prakash,Sachin Bhusari,George Pugh,Barry Lynch,Ashley Roberts
出处
期刊:Regulatory Toxicology and Pharmacology [Elsevier]
卷期号:77: 125-133 被引量:38
标识
DOI:10.1016/j.yrtph.2016.02.015
摘要

The safety of steviol glycosides is based on data available on several individual steviol glycosides and on the terminal absorbed metabolite, steviol. Many more steviol glycosides have been identified, but are not yet included in regulatory assessments. Demonstration that these glycosides share the same metabolic fate would indicate applicability of the same regulatory paradigm. In vitro incubation assays with pooled human fecal homogenates, using rebaudiosides A, B, C, D, E, F and M, as well as steviolbioside and dulcoside A, at two concentrations over 24–48 h, were conducted to assess the metabolic fate of various steviol glycoside classes and to demonstrate that likely all steviol glycosides are metabolized to steviol. The data show that glycosidic side chains containing glucose, rhamnose, xylose, fructose and deoxy-glucose, including combinations of α(1–2), β-1, β(1–2), β(1–3), and β(1–6) linkages, were degraded to steviol mostly within 24 h. Given a common metabolite structure and a shared metabolic fate, safety data available for individual steviol glycosides can be used to support safety of purified steviol glycosides in general. Therefore, steviol glycosides specifications adopted by the regulatory authorities should include all steviol glycosides belonging to the five groups of steviol glycosides and a group acceptable daily intake established.
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