| Project/Area Number |
03670611
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Digestive surgery
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| Research Institution | FUKUI MEDICAL SCHOOL (1992-1993)
Kanazawa University (1991) |
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Principal Investigator |
YAMAGUCHI Akio Faculity of Medicine, Fukui Medical School, Associate Professor, 医学部, 助教授 (10174608)
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| Co-Investigator(Kenkyū-buntansha) |
米村 豊 金沢大学, 医学部附属病院, 講師 (20167042)
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| Project Period (FY) |
1991 – 1993
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| Project Status |
Completed (Fiscal Year 1993)
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| Budget Amount *help |
¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 1993: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1992: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1991: ¥600,000 (Direct Cost: ¥600,000)
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| Keywords | Carcinogenesis / Xanthine oxidase / Migration time / 粘膜脱落時間 / Xanthine Xidase |
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| Research Abstract |
To clarify the organ specificity of the carcinogenresistance of the small bowel, a segment of the ileum was interposed in the distal colon in male wister rats. The rats were administered MNNG at a dose of 2.5 mg/day via the rectum for 2 weeks from the second postoperative week. Cell kinetic analysis of intestinal epithelium was performed by the double labeling method. Also xanthine oxidase activity of ileal and colon mucosa was measured by spectrophotometric assay in crude tissue homegenate.
1. The carcinogenic rate in the interposed ileum was 3.3%, significantly lower than the 38.3% in the distal colon. Also the number of cancers per rat was 0.03 in the interposed ileum, significantly lower than 0.07 in the distal colon.
2. The migration time of the MNNG-treated group was 91.4(〕SY.+-.〔)21.1 hours in the distal colon and 40.6(〕SY.+-.〔)8.2 hours in the interposed ileum.
3. The epithelial cell migration time from the bottom of the crypt to the surface in the interposed ileum was significantly shorter than that in the distal colon.
4. Xanthine oxidase activity for interposed ileum was sinificantly higer than that for distal colon.
From these results, it was suspected that the rapid renewal rates and high xanthine oxidase activity were the principal carcinogen-resistance mechanism of the small bowel.
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