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低脂高纤维饮食对Apc(delta716)基因敲除小鼠肠道息肉发育的抑制作用

Suppression of intestinal polyp development by low-fat and high-fiber diet in Apc(delta716) knockout mice.

作者信息

Hioki K, Shivapurkar N, Oshima H, Alabaster O, Oshima M, Taketo M M

机构信息

Central Institute for Experimental Animals, Kawasaki, Japan.

出版信息

Carcinogenesis. 1997 Oct;18(10):1863-5. doi: 10.1093/carcin/18.10.1863.

Abstract

Most epidemiological and animal studies show a positive correlation of the dietary intake of fat with the incidence of colon cancer, whereas an inverse correlation of the dietary intake of fiber. In rats fed a diet low in fat and high in wheat bran fiber and calcium, a significant decrease was reported in the number of azoxymethane-induced aberrant crypt foci compared with those fed a high-fat, low-fiber and low-calcium diet. Mutations in the human APC gene play a key role, not only in familial adenomatous polyposis, but also in many sporadic cancers of the entire digestive tract. We previously constructed a mouse strain Apc(delta716), carrying a truncation mutation at codon 716 of the Apc gene, the homolog of human APC (10). The heterozygous mice developed numerous intestinal polyps, and all microadenomas dissected from the earliest polyps had already lost the wild-type allele, indicating the loss of heterozygosity. Using these Apc(delta716) knockout mice, we have investigated the effect of a low-fat and high-fiber diet (LRD for 'low-risk' diet) on intestinal polyposis, and compared it with that of a high-fat and low-fiber diet (HRD for 'high-risk' diet). The mice were fed either diet for 7 weeks, and the number and size of intestinal polyps were scored. The LRD-fed mice had fewer polyps than the HRD-fed mice, by 36% in the small intestine and by 64% in the colon. As for the polyp size distribution, there was no significant difference between the HRD- and LRD-fed mice. These results indicate that LRD can suppress intestinal polyposis compared with HRD which does not, and suggest that its suppression is at the initiation of polyp formation. This is likely to be due to a decreased frequency of loss of heterozygosity, rather than a retarded growth of the polyp adenomas.

摘要

大多数流行病学和动物研究表明,脂肪的饮食摄入量与结肠癌的发病率呈正相关,而膳食纤维的饮食摄入量则呈负相关。在喂食低脂、高麦麸纤维和钙的饮食的大鼠中,与喂食高脂肪、低纤维和低钙饮食的大鼠相比,据报道偶氮甲烷诱导的异常隐窝病灶数量显著减少。人类APC基因的突变不仅在家族性腺瘤性息肉病中起关键作用,而且在整个消化道的许多散发性癌症中也起关键作用。我们之前构建了一种小鼠品系Apc(delta716),其Apc基因(人类APC的同源基因)的第716密码子处存在截断突变。杂合小鼠长出了许多肠道息肉,并且从最早的息肉中解剖出的所有微腺瘤都已经失去了野生型等位基因,表明杂合性丧失。利用这些Apc(delta716)基因敲除小鼠,我们研究了低脂高纤维饮食(“低风险”饮食,简称LRD)对肠道息肉病的影响,并将其与高脂肪低纤维饮食(“高风险”饮食,简称HRD)进行了比较。给小鼠喂食这两种饮食7周,然后对肠道息肉的数量和大小进行评分。喂食LRD的小鼠息肉比喂食HRD的小鼠少,小肠中少36%,结肠中少64%。至于息肉大小分布,喂食HRD和LRD的小鼠之间没有显著差异。这些结果表明,与不具有抑制作用的HRD相比,LRD可以抑制肠道息肉病,并表明其抑制作用发生在息肉形成的起始阶段。这可能是由于杂合性丧失频率降低,而不是息肉腺瘤生长迟缓所致。

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