5-氟尿嘧啶处理大鼠肠道吸收的变化。

K Hirata, T Horie
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引用次数: 20

摘要

5-氟尿嘧啶化疗常伴有胃肠道毒性。在这项研究中,我们研究了5-氟尿嘧啶对大鼠小肠上皮屏障功能的影响,通过检测一种难以吸收的标记物——异硫氰酸荧光素标记的葡聚糖(分子量4400)的吸收。我们进一步评估了5-氟尿嘧啶口服大鼠肠道吸收,每天1次,连续4天。采用原位封闭肠法和体外翻肠法分别检测异硫氰酸荧光素标记葡聚糖和5-氟尿嘧啶的小肠吸收。5-氟尿嘧啶给药4天后,与单独给药的对照组相比,大鼠体重明显下降,血浆中异硫氰酸荧光素标记的葡聚糖浓度明显升高。此外,与对照组相比,5-氟尿嘧啶治疗大鼠肠道对5-氟尿嘧啶的吸收明显增强。给大鼠施用5-氟尿嘧啶导致大鼠体重减轻和小肠上皮屏障功能障碍,这可以从高分子量化合物——异硫氰酸荧光素标记的葡聚糖的渗透增加中看出。5-氟尿嘧啶的吸收增加表明5-氟尿嘧啶的毒性可能因其处理而被放大。
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Changes in intestinal absorption of 5-fluorouracil-treated rats.

5-Fluorouracil chemotherapy is often accompanied by gastrointestinal toxicity. In this study, we investigated the effect of 5-fluorouracil on the epithelial barrier function of rat small intestine by examining the absorption of a poorly absorbable marker, fluorescein isothiocyanate-labelled dextran (molecular weight 4,400). We further evaluated the intestinal absorption of 5-fluorouracil in rats treated orally with 5-fluorouracil once daily for 4 days. The small intestinal absorption of fluorescein isothiocyanate-labelled dextran and 5-fluorouracil was tested using in situ closed loop intestine technique and in vitro everted intestine technique, respectively. After administration of 5-fluorouracil to rats for 4 days, the body weight of rats decreased significantly and the fluorescein isothiocyanate-labelled dextran concentration in plasma increased significantly, compared with that of control rats to which the saline solution alone was administered. Moreover, the intestinal absorption of 5-fluorouracil in the 5-fluorouracil-treated rats was enhanced significantly, compared with that of control rats. The administration of 5-fluorouracil to rats caused body weight loss and epithelial barrier dysfunction of the small intestine in rats as shown by the increased permeation of the high molecular weight compound, fluorescein isothiocyanate-labelled dextran. The increased absorption of 5-fluorouracil after this treatment suggest that the 5-fluorouracil toxicity might be amplified by its treatment.

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