The mutagenic potential of steviol has been tested sufficiently only in vitro 甜菊醇的致畸能力，只在动物体外作过充分的测试。
Furthermore , no studies of metabolism of stevioside and steviol in humans were available 此外，现时并没有研究探讨甜菊糖或甜菊醇在人体的新陈代谢。
It weakly inhibited oxidative phosphorylation ; steviol was about 30 times more potent in this respect 甜菊糖轻微抑制氧化磷酸化而甜菊醇的抑制能力则大约强三十倍。
It weakly inhibited oxidative phosphorylation ; steviol was about 30 times more potent in this respect 甜菊糖?轻微抑制氧化磷酸化；而甜菊醇的抑制能力则大约强三十倍。
Preliminary data indicate that steviol may be activated to a mutagenic metabloite by human liver microsomes 初步数据显示，甜菊醇可能经人体的肝脏微粒体活化成引致基因突变的代谢物。
Steviol also inhibited glucose absorption from rat gut by reducing the atp content of the intestinal mucosa 此外，甜菊醇亦透过减低肠黏膜的三磷酸腺含量，抑制大鼠肠道吸收葡萄糖的能力。
Steviol also inhibited glucose absorption from rat gut by reducing the atp content of the intestinal mucosa 此外，甜菊醇亦透过减低肠黏膜的三磷酸腺?含量，抑制大鼠肠道吸收葡萄糖的能力。
Steviol is completely absorbed and is excreted in the bile as conjugates ; only a very small fraction is detectable in urine 甜菊醇被完全吸收后，成为轭合物在汁中排出，只有极微的份量在尿液中检出。
Steviol is completely absorbed and is excreted in the bile as conjugates ; only a very small fraction is detectable in urine 甜菊醇被完全吸收后，成为轭合物在?汁中排出，只有极微的份量在尿液中检出。
Steviol is the only feacal metabolite of stevioside that has been identified , and excretion in the faeces is the major route 到目前为止，甜菊醇是唯一在粪便中能检出的甜菊糖代谢物，粪便是主要的排出途径。
