Document Detail


Regular exercise reduces colon tumorigenesis associated with suppression of iNOS.
MedLine Citation:
PMID:  20633535     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Several epidemiological studies have shown that regular exercise can prevent the onset of colon cancer, although the mechanism involved is unclear. Expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) is often elevated in an initial step of tumorigenesis and promotes colorectal cancer. We investigated the effect of exercise on colon tumorigenesis associated with iNOS and COX-2 in azoxymethan (AOM)-injected mice. Balb/c mice (8 weeks old) were divided into three groups of 20 animals each, consisting of a sedentary control group, an AOM group, and an exercise plus AOM group. Mice in the groups receiving AOM were injected intraperitoneally with AOM weekly for 2 weeks. Six weeks of regular exercise suppressed the generation of aberrant crypt foci (ACF) in the colon by AOM. Expression of iNOS was decreased by exercise compared with that in sedentary mice along with lower nitrotyrosine level while COX-2 was not changed by either AOM or exercise. Additionally, tumor necrosis factor alpha (TNFalpha) was decreased by exercise in the colon and plasma. There was no effect of exercise on the expression of antioxidant enzymes and chaperon protein in the colon. Our results suggest that regular exercise prevents colon tumorigenesis, at least partly via the suppression of iNOS expression associated with anti-inflammation.
Authors:
Wataru Aoi; Yuji Naito; Tomohisa Takagi; Satoshi Kokura; Katsura Mizushima; Yoshikazu Takanami; Yukari Kawai; Yuko Tanimura; Liu Po Hung; Ryota Koyama; Hiroshi Ichikawa; Toshikazu Yoshikawa
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-07-13
Journal Detail:
Title:  Biochemical and biophysical research communications     Volume:  399     ISSN:  1090-2104     ISO Abbreviation:  Biochem. Biophys. Res. Commun.     Publication Date:  2010 Aug 
Date Detail:
Created Date:  2010-08-16     Completed Date:  2010-09-02     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0372516     Medline TA:  Biochem Biophys Res Commun     Country:  United States    
Other Details:
Languages:  eng     Pagination:  14-9     Citation Subset:  IM    
Copyright Information:
2010 Elsevier Inc. All rights reserved.
Affiliation:
Kyoto Prefectural University, Japan. waoi@koto.kpu-m.ac.jp
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MeSH Terms
Descriptor/Qualifier:
Animals
Azoxymethane / toxicity
Body Weight
Cell Transformation, Neoplastic / metabolism*
Citrate (si)-Synthase / metabolism
Colonic Neoplasms / chemically induced,  enzymology,  prevention & control*
Cyclooxygenase 2 / metabolism
Male
Mice
Mice, Inbred BALB C
Nitric Oxide Synthase Type II / antagonists & inhibitors*
Physical Conditioning, Animal*
Tumor Necrosis Factor-alpha / blood
Chemical
Reg. No./Substance:
0/Tumor Necrosis Factor-alpha; 25843-45-2/Azoxymethane; EC 1.14.13.39/Nitric Oxide Synthase Type II; EC 1.14.13.39/Nos2 protein, mouse; EC 1.14.99.-/Ptgs2 protein, mouse; EC 1.14.99.1/Cyclooxygenase 2; EC 2.3.3.1/Citrate (si)-Synthase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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