Small intestinal transit and digestibility of lactitol in Wistar rats.

S Soontornchai, D Krüger, R Grossklaus
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引用次数: 5

Abstract

The study was conducted to evaluate if the recovery of lactitol and its cleavage products varied when different doses of this disaccharide sugar alcohol (150 and 1,200 mg/kg body weight, respectively) were given by gastric gavage to unadapted male rats. Phenol red added to the test solution as marker dye served to determine the intestinal transit and distribution areas. Marker transit revealed that the test substance did not reach the cecum in all series. Gastric emptying was more retarded after the high dose. Administration of low doses did not alter intestinal transit and luminal volume as compared to control animals. But a much larger luminal volume was found in the third intestinal quarter after the high doses, although the marker transit through this segment was equal under all experimental conditions. The total gastrointestinal recovery of lactitol at 63.2 (+/- 3.9) and 75.5 (+/- 4.5)% was significantly different (p < 0.001) 1 hour after administration of 150 mg and 1200 mg/kg body weight, respectively. Only free sorbitol was detected in the gastrointestinal contents in both dosage groups. Based on these results and correcting the values for marker recovery (85% in both groups), it is reasonable to assume that the maximum amount of lactitol that can be hydrolyzed and absorbed by the small intestine is 11.2 and 25.2%, respectively, and not zero. In conclusion, the caloric availability of lactitol is dose-dependent and should be determined under normal conditions in which the laxative threshold is not exceeded.

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Wistar大鼠乳糖醇小肠转运及消化率。
本研究旨在评估未适应的雄性大鼠胃灌胃给予不同剂量(分别为150和1200 mg/kg体重)的乳醇及其裂解产物的回收率是否不同。在测试溶液中加入酚红作为标记染料,用于确定肠道运输和分布区域。标记运输显示试验物质在所有系列中均未到达盲肠。大剂量后胃排空更迟缓。与对照动物相比,低剂量给药没有改变肠道运输和肠道容积。尽管在所有实验条件下,通过该段的标记物传输量都是相等的,但高剂量后,在第三肠区发现了更大的管腔容积。给药150 mg/kg和1200 mg/kg后1 h乳醇的胃肠道总恢复率分别为63.2(+/- 3.9)%和75.5(+/- 4.5)%,差异有统计学意义(p < 0.001)。在两个给药组的胃肠道内容物中均检测到游离山梨醇。根据这些结果并校正标记回收率(两组均为85%),可以合理地假设小肠可水解和吸收的最大乳醇量分别为11.2和25.2%,而不是零。总之,乳酸醇的热量利用率是剂量依赖性的,应在正常情况下测定,即不超过通便阈值。
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