Literature DB >> 1323148

Evidence that free radicals are involved in graft failure following orthotopic liver transplantation in the rat--an electron paramagnetic resonance spin trapping study.

H D Connor1, W Gao, S Nukina, J J Lemasters, R P Mason, R G Thurman.   

Abstract

The purpose of these studies was to determine whether free radicals were formed as a consequence of reperfusion during orthotopic liver transplantation and whether their formation was related to graft failure. Grafts were stored for 18 hr in Euro-Collins solution or for 48 hr in University of Wisconsin solution (nonsurvival conditions) and reperfused with blood containing the spin trap alpha-phenyl N-tert-butylnitrone (PBN). Venous blood samples (4-5 ml) were collected, and serum was extracted with chloroform and methanol (2:1) and analyzed for radical adducts by electron paramagnetic resonance (EPR) spectroscopy. In samples from livers stored under nonsurvival conditions, EPR spectra were detected indicating the presence of PBN radical adducts. In contrast, radical adduct formation was 3- to 4-fold lower in similar experiments performed with untransplanted livers or with livers stored under survival conditions (1 hr in Ringer's solution or 24 hr in UW solution). Oxygen radicals are more likely involved in the production of radical adducts because formation was nearly completely prevented by superoxide dismutase plus catalase or Carolina rinse, which contains glutathione, desferrioxamine mesylate, and allopurinol. Radical adduct formation was much greater in a blood-free perfusion system where oxygen delivery was high, suggesting that blood elements are not necessary for radical adduct formation. An inverse correlation between survival of livers stored in UW solution and radical adduct signal was observed in this study. Thus, it is concluded that free radicals formed during reperfusion are involved in the mechanism of graft failure following liver transplantation in the rat.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1323148     DOI: 10.1097/00007890-199208000-00002

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


  8 in total

1.  C-Jun N-terminal kinase 2 promotes graft injury via the mitochondrial permeability transition after mouse liver transplantation.

Authors:  T P Theruvath; C Czerny; V K Ramshesh; Z Zhong; K D Chavin; J J Lemasters
Journal:  Am J Transplant       Date:  2008-07-28       Impact factor: 8.086

2.  CD47 blockade reduces ischemia/reperfusion injury and improves survival in a rat liver transplantation model.

Authors:  Zhen-Yu Xiao; Babak Banan; Jianluo Jia; Pamela T Manning; Ronald R Hiebsch; Muthukumar Gunasekaran; Gundumi A Upadhya; William A Frazier; Thalachallour Mohanakumar; Yiing Lin; William C Chapman
Journal:  Liver Transpl       Date:  2015-01-29       Impact factor: 5.799

Review 3.  Therapeutic modulation of free radical-mediated reperfusion injury of the liver and its surgical implications.

Authors:  S Marubayashi; K Dohi
Journal:  Surg Today       Date:  1996       Impact factor: 2.549

4.  The protective mechanism of Yisheng Injection against hepatic ischemia reperfusion injury in mice.

Authors:  Feng Cheng; You-Ping Li; Jing-Qiu Cheng; Li Feng; Sheng-Fu Li
Journal:  World J Gastroenterol       Date:  2004-04-15       Impact factor: 5.742

5.  Thiram inhibits angiogenesis and slows the development of experimental tumours in mice.

Authors:  M Marikovsky
Journal:  Br J Cancer       Date:  2002-03-04       Impact factor: 7.640

6.  Protection of rat liver against hepatic ischemia-reperfusion injury by a novel selenocysteine-containing 7-mer peptide.

Authors:  Qianqian Jiang; Yu Pan; Yupeng Cheng; Huiling Li; Hui Li
Journal:  Mol Med Rep       Date:  2016-07-01       Impact factor: 2.952

7.  Para-Substituted α-Phenyl-N-tert-butyl Nitrones: Spin-Trapping, Redox and Neuroprotective Properties.

Authors:  Anaïs Deletraz; Béatrice Tuccio; Julien Roussel; Maud Combes; Catherine Cohen-Solal; Paul-Louis Fabre; Patrick Trouillas; Michel Vignes; Noelle Callizot; Grégory Durand
Journal:  ACS Omega       Date:  2020-11-20

8.  Role of EC-SOD overexpression in preserving pulmonary angiogenesis inhibited by oxidative stress.

Authors:  Shahana Perveen; Hardik Patel; Arslan Arif; Sharif Younis; Champa N Codipilly; Mohamed Ahmed
Journal:  PLoS One       Date:  2012-12-20       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.