Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice

Cattle bile (CB) has long been used in Japan as an ingredient of digestive medicines. Bile acids are major chemical constituents of CB, and CB ingestion is assumed to affect small intestinal injury induced by nonsteroidal anti-inflammatory drugs (NSAIDs). Mice were fed a diet supplemented with or wi...

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Main Authors: Hironori Ishikawa, Shiro Watanabe
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:Evidence-Based Complementary and Alternative Medicine
Online Access:http://dx.doi.org/10.1155/2011/315858
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spelling doaj-cac2bd3f4f004bed9218d5bf9a6429a52020-11-24T21:45:01ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882011-01-01201110.1155/2011/315858315858Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in MiceHironori Ishikawa0Shiro Watanabe1Division of Clinical Application, Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, JapanDivision of Clinical Application, Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, JapanCattle bile (CB) has long been used in Japan as an ingredient of digestive medicines. Bile acids are major chemical constituents of CB, and CB ingestion is assumed to affect small intestinal injury induced by nonsteroidal anti-inflammatory drugs (NSAIDs). Mice were fed a diet supplemented with or without CB for 7 days and treated with diclofenac sodium (DIF) to induce small intestinal injury. Lesion formation was enhanced, and PGE2 content and COX expression levels were elevated in the small intestine of DIF-treated mice fed the CB diet compared with those fed the control diet. The administration of a reconstituted mixture of bile acids found in CB enhanced lesion formation in DIF-treated mice. CB administration elevated the contents of CB-derived bile acids in the small intestine, some of which exhibited a high cytotoxicity to cultured intestinal epithelial cells. These results suggest that the elevated levels of CB-derived cytotoxic bile acids in the small intestine contribute to the aggravation of DIF-induced small intestinal injury. The use of CB may be limited during the therapy of inflammatory diseases with NSAIDs.http://dx.doi.org/10.1155/2011/315858
collection DOAJ
language English
format Article
sources DOAJ
author Hironori Ishikawa
Shiro Watanabe
spellingShingle Hironori Ishikawa
Shiro Watanabe
Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice
Evidence-Based Complementary and Alternative Medicine
author_facet Hironori Ishikawa
Shiro Watanabe
author_sort Hironori Ishikawa
title Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice
title_short Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice
title_full Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice
title_fullStr Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice
title_full_unstemmed Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice
title_sort cattle bile aggravates diclofenac sodium-induced small intestinal injury in mice
publisher Hindawi Limited
series Evidence-Based Complementary and Alternative Medicine
issn 1741-427X
1741-4288
publishDate 2011-01-01
description Cattle bile (CB) has long been used in Japan as an ingredient of digestive medicines. Bile acids are major chemical constituents of CB, and CB ingestion is assumed to affect small intestinal injury induced by nonsteroidal anti-inflammatory drugs (NSAIDs). Mice were fed a diet supplemented with or without CB for 7 days and treated with diclofenac sodium (DIF) to induce small intestinal injury. Lesion formation was enhanced, and PGE2 content and COX expression levels were elevated in the small intestine of DIF-treated mice fed the CB diet compared with those fed the control diet. The administration of a reconstituted mixture of bile acids found in CB enhanced lesion formation in DIF-treated mice. CB administration elevated the contents of CB-derived bile acids in the small intestine, some of which exhibited a high cytotoxicity to cultured intestinal epithelial cells. These results suggest that the elevated levels of CB-derived cytotoxic bile acids in the small intestine contribute to the aggravation of DIF-induced small intestinal injury. The use of CB may be limited during the therapy of inflammatory diseases with NSAIDs.
url http://dx.doi.org/10.1155/2011/315858
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