Irritant-induced cyclooxygenase-2 is involved in the defense mechanism of the gastric mucosa in mice

被引:8
作者
Miyake, K [1 ]
Tsukui, T [1 ]
Wada, K [1 ]
Tatsuguchi, A [1 ]
Futagami, S [1 ]
Hiratsuka, T [1 ]
Shinoki, K [1 ]
Iizumi, T [1 ]
Akamatsu, T [1 ]
Sakamoto, C [1 ]
Kobayashi, M [1 ]
机构
[1] Nippon Med Coll, Dept Internal Med 3, Bunkyo Ku, Tokyo 1138603, Japan
关键词
COX-2; cytoprotection; adaptive cytoprotection; gastric damage; selective COX-2 inhibitor; ethanol;
D O I
10.1007/s005350200016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background. Endogenous and exogenous prostaglandins (PGs) have been shown to contribute to reducing the gastric injury caused by irritants given subsequently. The aim of this study was to clarify whether cyclooxygenase-2 (COX-2) protein induced by pretreatment was involved in the prevention of subsequent ethanol-caused gastric injury in mice. Methods. Mice were pretreated with acidified ethanol or saline and then COX-2 protein expression in the stomach was immunohistochemically determined every 8h. Mice were administered 95% ethanol 24h after the acidified ethanol pretreatment, and gastric mucosal damage was evaluated macroscopically and histologically. The effects of NS-398 or indomethacin on the 95% ethanol-caused damage were also examined. Results. Acidified ethanol pretreatment induced COX-2 protein expression in lamina propria macrophages of the gastric mucosa, with a peak level 24h after the pretreatment. The 95% ethanol treatment caused gastric mucosal damage. The degree of the damage was not different between mice pretreated with acidified ethanol and those pretreated with saline. However, NS-398 aggravated the ethanol-caused damage only in mice pretreated with acidified ethanol, while indomethacin aggravated the damage, evaluated histologically, irrespective of the pretreatment. Conclusions. Pretreatment-induced COX-2, in addition to COX-1, seemed to be involved in the defense mechanism through minimizing the damage caused by a subsequent irritant.
引用
收藏
页码:164 / 171
页数:8
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