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Duodenal toxicity of dietary Phaseolus vulgaris lectins in the rat: an integrative assay.

作者信息

Lafont J, Rouanet J M, Gabrion J, Assouad J L, Zambonino Infante J L, Besançon P

机构信息

Laboratoires de Physiologie de la Nutrition, Université de Montpellier II, France.

出版信息

Digestion. 1988;41(2):83-93. doi: 10.1159/000199736.

DOI:10.1159/000199736
PMID:3220180
Abstract

It is now generally admitted that phytohemagglutinin (PHA) constitutes the main factor responsible for the dietary toxicity of raw kidney beans. In the growing rat, an impairment of growth is the unique expression of a malnutrition syndrome. The aim of this work was to precise to what extent the intestinal injuries may account for this malnutrition. PHA was administered for 9 days to growing rats at levels ranging from 0.0025 to 0.25% of food dry matter. One group of controls was fed ad libitum and other groups were restrained. In such conditions, PHA reduced the food intake when offered at a level higher than 0.04% as a linear function of the logarithm of lectin rate. Intestinal injuries were also dose-dependent: blebbing of microvilli and loss of alkaline phosphatase occurred at the smallest dose of PHA, cell loss occurred at higher doses. A compensatory hyperplasia was observed as a consequence of both intestinal injury and reduced food intake. Our main results are that, whatever may be the damages caused to the duodenal mucosa, the observed growth impairment was quasi-totally imputable to the reduction of food intake.

摘要

相似文献

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引用本文的文献

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Gut. 1995 Sep;37(3):353-60. doi: 10.1136/gut.37.3.353.
2
Intestinal sphingolipid excretion associated with feeding of phytohemagglutinin lectin (Phaseolus vulgaris) to germ-free and conventional rats.与向无菌和普通大鼠喂食植物血凝素凝集素(菜豆)相关的肠道鞘脂排泄
Glycoconj J. 1989;6(4):539-50. doi: 10.1007/BF01053776.
3
Binding of kidney bean (Phaseolus vulgaris) isolectins to differentiated human colon carcinoma Caco-2 cells and their effect on cellular metabolism.
菜豆(Phaseolus vulgaris)同工凝集素与分化的人结肠癌Caco-2细胞的结合及其对细胞代谢的影响。
Gut. 1991 Feb;32(2):196-201. doi: 10.1136/gut.32.2.196.