Literature DB >> 9645798

A new and simple technique of total hepatic ischemia in the mouse.

S S Yadav1, W Gao, R C Harland, P A Clavien.   

Abstract

BACKGROUND: A model of total hepatic ischemia is currently not available in mice. Models described in rats using portosystemic shunts to achieve total ischemia have been notoriously difficult. In mice, the problem is compounded further when using this type of technique because of the small size of the animal. A new technique is described combining partial hepatectomy with clamping of the remnant liver.
METHODS: A partial (30%) hepatectomy is performed with resection of the caudate, right lateral, and quadrate lobes, and papillary process. Vascular microclamps are placed across the pedicles of the median and left lateral lobe at the level of the hilum to achieve total ischemia. Spontaneous portocaval shunts through caudate branches and collateral vessels prevent mesenteric congestion. Animals were studied for survival.
RESULTS: The procedure consistently took less than 30 min (25+/-2 min), and no bleeding of the resected tissue was observed. Evidence for total hepatic ischemia and spontaneous shunts was demonstrated by the use of an intraportal dye. All animals survived 60 min of ischemia, whereas all died after 90 min of ischemia.
CONCLUSION: This is a technically simple and rapid procedure to perform. In the current environment of multiple knockout mice and bioreagents that are available, a model of this type is essential.

Entities:  

Mesh:

Year:  1998        PMID: 9645798     DOI: 10.1097/00007890-199806150-00004

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


  7 in total

1.  Hydrogen sulfide augments survival signals in warm ischemia and reperfusion of the mouse liver.

Authors:  Shingo Shimada; Moto Fukai; Kenji Wakayama; Takahisa Ishikawa; Nozomi Kobayashi; Taichi Kimura; Kenichiro Yamashita; Toshiya Kamiyama; Tsuyoshi Shimamura; Akinobu Taketomi; Satoru Todo
Journal:  Surg Today       Date:  2014-11-02       Impact factor: 2.549

2.  Comparison of ischemic preconditioning and intermittent and continuous inflow occlusion in the murine liver.

Authors:  Hannes A Rüdiger; Koo J Kang; David Sindram; Hans M Riehle; Pierre A Clavien
Journal:  Ann Surg       Date:  2002-03       Impact factor: 12.969

3.  Liver damage and systemic inflammatory responses are exacerbated by the genetic deletion of CD39 in total hepatic ischemia.

Authors:  Xiaofeng Sun; Masato Imai; Martina Nowak-Machen; Olaf Guckelberger; Keiichi Enjyoji; Yan Wu; Zain Khalpey; Pascal Berberat; Jeeva Munasinghe; Simon Christopher Robson
Journal:  Purinergic Signal       Date:  2011-06-09       Impact factor: 3.765

4.  Wnt agonist attenuates liver injury and improves survival after hepatic ischemia/reperfusion.

Authors:  Michael Kuncewitch; Weng-Lang Yang; Ernesto Molmenti; Jeffrey Nicastro; Gene F Coppa; Ping Wang
Journal:  Shock       Date:  2013-01       Impact factor: 3.454

5.  Glutathione protects the rat liver against reperfusion injury after prolonged warm ischemia.

Authors:  Rolf J Schauer; Alexander L Gerbes; Daniel Vonier; Herbert Meissner; Patrick Michl; Rosemarie Leiderer; Friedrich W Schildberg; Konrad Messmer; Manfred Bilzer
Journal:  Ann Surg       Date:  2004-02       Impact factor: 12.969

6.  Bone marrow-derived mesenchymal stem cells ameliorate hepatic ischemia reperfusion injury in a rat model.

Authors:  Hiroyuki Kanazawa; Yasuhiro Fujimoto; Takumi Teratani; Junji Iwasaki; Naoya Kasahara; Kouji Negishi; Tatsuaki Tsuruyama; Shinji Uemoto; Eiji Kobayashi
Journal:  PLoS One       Date:  2011-04-29       Impact factor: 3.240

7.  Mangafodipir protects against hepatic ischemia-reperfusion injury in mice.

Authors:  Romain Coriat; Mahaut Leconte; Niloufar Kavian; Sassia Bedda; Carole Nicco; Christiane Chereau; Claire Goulvestre; Bernard Weill; Alexis Laurent; Frédéric Batteux
Journal:  PLoS One       Date:  2011-11-02       Impact factor: 3.240

  7 in total

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