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从离体灌注大鼠肠道管腔中摄取雌酮。

The uptake of oestrone from the lumen of the isolated perfused rat gut.

作者信息

Roy A B, Curtis C G, Hughes H

机构信息

Protein Chemistry Group, John Curtin School of Medical Research, Canberra, ACT, Australia.

出版信息

Xenobiotica. 1991 Apr;21(4):491-8. doi: 10.3109/00498259109039489.

Abstract
  1. In the isolated perfused rat gut oestrone was not taken up from the perfusate but was rapidly taken up from the gut lumen when administered in dimethyl sulphoxide or in 10% acetone in water. 2. Uptake from corn oil was much slower and the rate was concentration-dependent. 3. When given in dimethyl sulphoxide or in aqueous acetone, the residual oestrone in the gut lumen was largely unchanged, with only about 10% being present as the glucuronide. Of the oestrone in the gut perfusate, some 40% was glucuronidated. 4. No evidence was obtained for any reduction or hydroxylation, or for any sulphation, during uptake of oestrone by the gut. 5. No secretion of oestrone or its metabolites into lymph could be detected.
摘要
  1. 在离体灌注的大鼠肠道中,雌酮不会从灌注液中被摄取,但当以二甲基亚砜或10%丙酮水溶液给药时,会迅速从肠腔中被摄取。2. 从玉米油中摄取的速度要慢得多,且摄取速率呈浓度依赖性。3. 当以二甲基亚砜或丙酮水溶液给药时,肠腔中残留的雌酮基本未发生变化,只有约10%以葡糖醛酸苷的形式存在。在肠道灌注液中的雌酮,约40%被葡糖醛酸化。4. 在肠道摄取雌酮的过程中,未获得任何还原、羟基化或硫酸化的证据。5. 未检测到雌酮或其代谢产物分泌到淋巴中。

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