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Effect of ONO-4057 and tacrolimus on ischemia-reperfusion injury of the liver

查看全文 作  者:Takayuki [1,2,3]Takeichi;Shinji [1]Uemoto;Sachiko [4]Minamiguchi;Izumi [2]Takeyoshi;Yukihiro [3]Inomata;Koichi [1]Tanaka;Eiji [5]Kobayashi 高影响力作者 机构地区:[1]Department of Transplantation and Immunology, Kyoto University Hospital, 54 Kawara-cho, Shogoin,Sakyo-ku, Kyoto 606-8507, Japan;[2]Second Department of Surgery, Gunma University School of Medicine, 3-39-15 Showa-machi, Maebashi, Gunma 371-8511, Japan;[3]Department of Trans-plantation and Pediatric Surgery, Postgraduate School of Medical Science, Kumamoto University, Kumamoto, 1-1-1 Honjyo, Ku-mamoto 860-8556, Japan;[4]Laboratory of Anatomic Pathology, Kyoto University Hospital, 54 Kawara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan;[5]Division of Organ Replacement Research, Center for Molecular Medicine, Jichi Medical School, Minami-kawachi-machi, Kawachi-gun, Tochigi 329-0498, Japan高影响力机构 出  处:《World Journal of Gastroenterology》索引2009年第15卷第45期,共4页高影响力期刊 摘  要:AIM: To investigate the effects of a novel Leukotriene B4 receptor antagonist and/or tacrolimus on ischemia-reperfusion in a rat liver model. METHODS: Male Lewis rats were pretreated with ONO-4057 (100 mg/kg) and/or tacrolimus (1 mg/kg) orally, and divided into four experimental groups; group 1 (control), group 2 (ONO-4057), group 3 (tacrolimus), group 4 (ONO-4057 + tacrolimus). RESULTS: There was a tendency for long survival in the groups treated with tacrolimus alone and ONO-4057 plus tacrolimus. Post-reperfusion serum aspartate aminotransferase levels decreased more signif icantly in ONO-4057 plus tacrolimus group (P < 0.01), than in the tacrolimus alone group (P < 0.05), compared to controls. CONCLUSION: This study demonstrated that pretreat-ment with ONO-4057 in combination with tacrolimus produced additive effects in a rat model of liver isch-emia-reperfusion injury. 关 键 词:再灌注损伤 缺血再灌注 肝损伤 大鼠模型 受体拮抗剂 谷草转氨酶 联合生产 加性效应
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