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甜蜜素在人类及其他物种体内的代谢情况。

The fate of cyclamate in man and other species.

作者信息

Renwick A G, Williams R T

出版信息

Biochem J. 1972 Oct;129(4):869-79. doi: 10.1042/bj1290869.

Abstract
  1. (14)C-labelled cyclamate has been administered to guinea pigs, rabbits, rats and humans. When given orally to these species on a cyclamate-free diet, cyclamate is excreted unchanged. In guinea pigs some 65% of a single dose is excreted in the urine and 30% in the faeces, the corresponding values for rats being 40 and 50%, for man, 30-50% and 40-60%, and for rabbits, 90 and 5%, the excretion being over a period of 2-3 days. 2. Cyclamate appears to be readily absorbed by rabbits but less readily by guinea pigs, rats and humans. 3. If these animals, including man, are placed on a diet containing cyclamate they develop the ability to convert orally administered cyclamate into cyclohexylamine and consequently into the metabolites of the latter. The extent to which this ability develops is variable, the development occurring more readily in rats than in rabbits or guinea pigs. In three human subjects, one developed the ability quite markedly in 10 days whereas two others did not in 30 days. Removal of the cyclamate from the diet caused a diminution in the ability to convert cyclamate into the amine. 4. In rats that had developed the ability to metabolize orally administered cyclamate, intraperitoneally injected cyclamate was not metabolized and was excreted unchanged in the urine. The biliary excretion of injected cyclamate in rats was very small, i.e. about 0.3% of the dose. 5. The ability of animals to convert cyclamate into cyclohexylamine appears to depend upon a continuous intake of cyclamate and on some factor in the gastrointestinal tract, probably the gut flora.
摘要
  1. 已将用(14)C标记的甜蜜素给予豚鼠、兔子、大鼠和人类。当在不含甜蜜素的饮食条件下经口给予这些物种时,甜蜜素原样排出。在豚鼠中,单次剂量的约65%经尿液排出,30%经粪便排出;大鼠的相应数值分别为40%和50%;人类为30 - 50%和40 - 60%;兔子为90%和5%,排泄过程持续2 - 3天。2. 甜蜜素似乎很容易被兔子吸收,但被豚鼠、大鼠和人类吸收的程度较低。3. 如果将这些动物(包括人类)置于含有甜蜜素的饮食中,它们会产生将经口摄入的甜蜜素转化为环己胺并进而转化为环己胺代谢产物的能力。这种能力发展的程度各不相同,在大鼠中比在兔子或豚鼠中更容易发展。在三名人类受试者中,一名在10天内这种能力显著发展,而另外两名在30天内未发展。从饮食中去除甜蜜素会导致将甜蜜素转化为胺的能力降低。4. 在已经产生代谢经口给予甜蜜素能力的大鼠中,腹腔注射的甜蜜素未被代谢,原样经尿液排出。大鼠中注射的甜蜜素经胆汁排泄量非常少,即约为剂量的0.3%。5. 动物将甜蜜素转化为环己胺的能力似乎取决于持续摄入甜蜜素以及胃肠道中的某些因素,可能是肠道菌群。

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