Leibowitz M J, Merker P C
Gut. 1971 Feb;12(2):123-5. doi: 10.1136/gut.12.2.123.
Methyl bis (beta-chlorethyl) amine (HN(2)) was administered as a single intraperitoneal dose to male Sprague-Dawley rats. Animals were given either a median lethal dose and perfused one day after treatment or were given a larger dose and perfused two days after treatment. Intestinal segments were perfused in vivo and samples of effluent were collected and measured for glucose using the glucose oxidase method. Animals treated with the larger dose of HN(2) displayed significant reduction in intestinal dry weight. The average water content of intestinal segments derived from treated animals did not differ significantly from that in controls.Steady-state glucose absorption, obtained from data collected during the last 40 minutes of the perfusion period, was found to be significantly reduced in animals treated with drugs when intestinal absorption for control and treated animals was adjusted for water movement but not for dry intestinal weight and length. However, when glucose absorption was adjusted for dry tissue mass and length as well as for water movement, no significant differences in intestinal glucose absorption between control and treated rats were observed. Alterations can therefore be attributed to loss of intestinal tissue rather than to loss in the ability of the intestinal mass to absorb glucose.
将甲基双(β-氯乙基)胺(HN(2))以单次腹腔注射剂量给予雄性斯普拉格-道利大鼠。动物接受中位致死剂量并在治疗后一天进行灌注,或者接受更大剂量并在治疗后两天进行灌注。对肠段进行体内灌注,收集流出液样本并使用葡萄糖氧化酶法测量葡萄糖含量。用较大剂量HN(2)处理的动物肠道干重显著降低。来自处理动物的肠段平均含水量与对照组相比无显著差异。当根据水的移动情况对对照组和处理组动物的肠道吸收进行调整,但不根据肠道干重和长度进行调整时,发现在灌注期最后40分钟收集的数据中,用药处理的动物稳态葡萄糖吸收显著降低。然而,当根据干组织质量、长度以及水的移动情况对葡萄糖吸收进行调整时,未观察到对照组和处理组大鼠在肠道葡萄糖吸收方面有显著差异。因此,变化可归因于肠道组织的损失,而非肠道组织吸收葡萄糖能力的丧失。