Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 1, 2004; 10(19): 2814-2817
Published online Oct 1, 2004. doi: 10.3748/wjg.v10.i19.2814
Lansoprazole ameliorates intestinal mucosal damage induced by ischemia-reperfusion in rats
Hiroshi Ichikawa, Norimasa Yoshida, Tomohisa Takagi, Naoya Tomatsuri, Kazuhiro Katada, Yutaka Isozaki, Kazuhiko Uchiyama, Yuji Naito, Takeshi Okanoue, Toshikazu Yoshikawa
Hiroshi Ichikawa, Department of Food Sciences and Nutritional Health, Faculty of Human Environment, Kyoto Prefectural University, 606-8522, Japan
Norimasa Yoshida, Yuji Naito, Takeshi Okanoue, Department of Molecular Gastroenterology and Hepatology, Graduate School of Medical Sciences, Kyoto Prefectural University of Medicine, 606-8522, Japan
Tomohisa Takagi, Naoya Tomatsuri, Kazuhiro Katada, Yutaka Isozaki, Kazuhiko Uchiyama, Toshikazu Yoshikawa, Department of Inflammation and Immunology, Graduate School of Medical Sciences, Kyoto Prefectural University of Medicine, 606-8522, Japan
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Norimasa Yoshida, Department of Molecular Gastroenterology and Hepatology, Graduate School of Medical Sciences, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan. nyoshida@koto.kpu-m.ac.jp
Telephone: +81-75-251-5508 Fax: +81-75-252-3721
Received: March 18, 2004
Revised: April 22, 2004
Accepted: April 29, 2004
Published online: October 1, 2004
Abstract

AIM: To investigate the protective effect of lansoprazole on ischemia and reperfusion (I/R)-induced rat intestinal mucosal injury in vivo.

METHODS: Intestinal damage was induced by clamping both the superior mesenteric artery and the celiac trunk for 30 min followed by reperfusion in male Sprague-Dawley rats. Lansoprazole was given to rats intraperitoneally 1 h before vascular clamping.

RESULTS: Both the intraluminal hemoglobin and protein levels, as indices of mucosal damage, significantly increased in I/R-groups comparion with those of sham-operation groups. These increases in intraluminal hemoglobin and protein levels were significantly inhibited by the treatment with lansoprazole at a dose of 1 mg/kg. Small intestine exposed to I/R resulted in mucosal inflammation that was characterized by significant increases in thiobarbituric acid-reactive substances (TBARS), tissue-associated myeloperoxidase activity (MPO), and mucosal content of rat cytokine-induced neutrophil chemoattractant-1 (CINC-1). These increases in TBARS, MPO activities and CINC-1 content in the intestinal mucosa after I/R were all inhibited by pretreatment with lansoprazole at a dose of 1 mg/kg. Furthermore, the CINC-1 mRNA expression was increased during intestinal I/R, and this increase in mRNA expression was inhibited by treatment with lansoprazole.

CONCLUSION: Lansoprazole inhibits lipid peroxidation and reduces development of intestinal mucosal inflammation induced by I/R in rats, suggesting that lansoprazole may have a therapeutic potential for I/R injury.

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