Induction of intestinal damage by rofecoxib, the selective COX-2 inhibitor, under inhibition of nitric oxide production in rats

被引:2
|
作者
Ohno R. [1 ]
Miyazawa T. [1 ]
Hayashi Y. [1 ]
Kanatsu K. [1 ]
Tanaka A. [1 ]
Takeuchi K. [1 ]
机构
[1] Department of Pharmacology, Kyoto Pharmaceutical University, Yamashina
关键词
COX-2; inhibitor; Intestinal damage; L-NAME; Rat;
D O I
10.1163/156856002321544909
中图分类号
学科分类号
摘要
We examined whether intestinal damage is provoked in rats under inhibition of both cNOS and COX-2. SC-560, rofecoxib or L-NAME was given either alone or in combination, and the animals were killed 24 h later. Neither SC-560 nor rofecoxib alone provoked damage in the small intestinal mucosa. However, SC-560 produced gross lesions when administered together with rofecoxib. Likewise, L-NAME alone did not cause damage, but this agent provoked gross lesions when administered together with rofecoxib. Mucosal PGE2 content was decreased by SC-560 but not by rofecoxib and L-NAME. The expression of COX-2 was upregulated by L-NAME as well as by SC-560. Both L-NAME and SC-560 enhanced intestinal motility, decreased mucus secretion, and increased the enterobacterial number in the mucosa. We conclude that inhibition of both cNOS and COX-2 provokes intestinal damage. Inhibition of cNOS up-regulates COX-2 expression, and this may be a key to occurrence of intestinal damage associated with COX-2 inhibition.
引用
收藏
页码:435 / 447
页数:12
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