Literature DB >> 12023622

A novel inhibitor of inducible nitric oxide synthase (ONO-1714) prevents critical warm ischemia-reperfusion injury in the pig liver.

Makoto Meguro1, Tadashi Katsuramaki, Minoru Nagayama, Hitoshi Kimura, Masato Isobe, Yasutoshi Kimura, Takashi Matsuno, Akihiro Nui, Koichi Hirata.   

Abstract

BACKGROUND: Recently, a novel inhibitor of inducible nitric oxide synthase, ONO-1714, was developed. We evaluated the effect of ONO-1714 on a critical warm I/R model of the pig liver.
METHODS: Pigs were subjected to 180 min of hepatic warm I/R under the extracorporeal circulation. We investigated the time course of changes in the serum NO2- + NO3- (NOx), the cellular distribution of endothelial and inducible nitric oxide synthase, thrombocyte-thrombi, and nitrotyrosine by immunohistochemistry. The hepatic tissue blood flow (HTBF) was measured continuously using a laser-Doppler blood flowmeter.
RESULTS: ONO-1714 at 0.05 mg/kg improved the survival rate from 54 (control group) to 100%. The serum NOx levels in the ONO-1714 group were significantly lower than those in the control group at 1, 1.5, 2, 3, and 6 hr after reperfusion. The serum aspartate aminotransferase (AST) and lactate dehydrogenase (LDH) levels of the ONO-1714 group were significantly lower than the control group, and the HTBF of the ONO-1714 group was significantly higher than the control group. The formation of thrombocyte-thrombi and nitrotyrosine after reperfusion was significantly lower in the ONO-1714 group.
CONCLUSIONS: These results indicated that ONO-1714 improved the survival rates and attenuated I/R injury in a critical hepatic warm I/R model of the pig. ONO-1714 will be beneficial for hepatectomy or liver transplantation in the clinical field.

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Year:  2002        PMID: 12023622     DOI: 10.1097/00007890-200205150-00013

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  7 in total

1.  Beneficial effects of green tea catechin on massive hepatectomy model in rats.

Authors:  Yu Saito; Hiroki Mori; Chie Takasu; Masato Komatsu; Jun Hanaoka; Shinichiro Yamada; Michihito Asanoma; Tetsuya Ikemoto; Satoru Imura; Yuji Morine; Tohru Utsunomiya; Mitsuo Shimada
Journal:  J Gastroenterol       Date:  2013-03-30       Impact factor: 7.527

2.  Inhibition of inducible nitric oxide synthase prevents hepatic, but not pulmonary, injury following ischemia-reperfusion of rat liver.

Authors:  Yuji Takamatsu; Kazuo Shimada; Koji Yamaguchi; Syoji Kuroki; Kazuo Chijiiwa; Masao Tanaka
Journal:  Dig Dis Sci       Date:  2006-03       Impact factor: 3.199

Review 3.  Molecular mediators of liver ischemia and reperfusion injury: a brief review.

Authors:  Andrew J Vardanian; Ronald W Busuttil; Jerzy W Kupiec-Weglinski
Journal:  Mol Med       Date:  2008 May-Jun       Impact factor: 6.354

Review 4.  Molecular mechanisms of liver ischemia reperfusion injury: insights from transgenic knockout models.

Authors:  Gourab Datta; Barry J Fuller; Brian R Davidson
Journal:  World J Gastroenterol       Date:  2013-03-21       Impact factor: 5.742

Review 5.  Effects of iNOS in Hepatic Warm Ischaemia and Reperfusion Models in Mice and Rats: A Systematic Review and Meta-Analysis.

Authors:  Richi Nakatake; Mareike Schulz; Christina Kalvelage; Carina Benstoem; René H Tolba
Journal:  Int J Mol Sci       Date:  2022-10-07       Impact factor: 6.208

6.  Selective gene expression profiling contributes to a better understanding of the molecular pathways underlying the histological changes observed after RHMVL.

Authors:  Janine Arlt; Sebastian Vlaic; Ronny Feuer; Maria Thomas; Utz Settmacher; Uta Dahmen; Olaf Dirsch
Journal:  BMC Med Genomics       Date:  2022-10-07       Impact factor: 3.622

7.  Adenovirus-mediated eNOS expression augments liver injury after ischemia/reperfusion in mice.

Authors:  Arun P Palanisamy; Gang Cheng; Alton G Sutter; John Liu; David N Lewin; Julie Chao; Kenneth Chavin
Journal:  PLoS One       Date:  2014-03-25       Impact factor: 3.240

  7 in total

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