Literature DB >> 7766302

Reperfusion injury to endothelial cells after cold storage of rat livers: protection by mildly acidic pH and lack of protection by antioxidants.

J C Caldwell-Kenkel1, R T Currin, A Coote, R G Thurman, J J Lemasters.   

Abstract

Lethal reperfusion injury to sinusoidal endothelial cells occurs after cold ischemic storage of livers and may be responsible for liver graft failure from storage injury. Here, we evaluated potential mechanisms underlying this reperfusion injury. In rat livers stored in Euro-Collins solution for 24 h and reperfused with Krebs-Henseleit bicarbonate buffer, nonparenchymal cell killing showed periportal predominance as assessed by nuclear staining with trypan blue. In livers reperfused in the retrograde direction, the lobular distribution of cell killing was reversed, indicating that cell killing was more rapid in oxygen-rich upstream regions. However, antioxidants, including allopurinol, desferrioxamine, catalase, superoxide dismutase, superoxide dismutase plus catalase, and U74006F, did not reduce cell killing. Similarly, reperfusion with anoxic buffer did not prevent lethal injury. Antioxidants and anoxic reperfusion also did not improve cell viability in livers stored in UW solution. Nevertheless, superoxide generation, as identified by formazan formation from nitroblue tetrazolium, was increased in Kupffer cells after lives storage and reperfusion as compared to unstored livers. Acidification of the reperfusion buffer from pH 7.4 to pH 7.15 reduced overall nonparenchymal cell killing from about 40% to 10%. Moreover, a pH gradient developed across the liver lobule during reperfusion with the effluent 0.2-0.4 pH units more acidic than the influent. This intralobular pH gradient appears to account for the relative sparing of cells in more acidic downstream regions of the lobule. Lower temperatures of reperfusion also reduced lethal injury. In conclusion, Kupffer cells generated superoxide after perfusion of stored rat livers, but formation of oxygen free radicals did not appear to contribute to lethal reperfusion injury to endothelial cells.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7766302     DOI: 10.1007/BF00344415

Source DB:  PubMed          Journal:  Transpl Int        ISSN: 0934-0874            Impact factor:   3.782


  5 in total

1.  Serum acidosis prior to reperfusion facilitates hemodynamic recovery following liver transplantation.

Authors:  Kyota Fukazawa; Alexander A Vitin; Ernesto A Pretto
Journal:  J Anesth       Date:  2015-10-08       Impact factor: 2.078

Review 2.  The mitochondrial permeability transition in toxic, hypoxic and reperfusion injury.

Authors:  J J Lemasters; A L Nieminen; T Qian; L C Trost; B Herman
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

3.  Polyethylene glycol-superoxide dismutase inhibits lipid peroxidation in hepatic ischemia/reperfusion injury.

Authors:  W D Nguyen; D H Kim; H B Alam; H S Provido; J R Kirkpatrick
Journal:  Crit Care       Date:  1999-09-23       Impact factor: 9.097

4.  Inhibition of Na+/H+ exchange preserves viability, restores mechanical function, and prevents the pH paradox in reperfusion injury to rat neonatal myocytes.

Authors:  I S Harper; J M Bond; E Chacon; J M Reece; B Herman; J J Lemasters
Journal:  Basic Res Cardiol       Date:  1993 Sep-Oct       Impact factor: 17.165

Review 5.  Ischemic preconditioning modulates ROS to confer protection in liver ischemia and reperfusion.

Authors:  Phillip Bystrom; Nicole Foley; Luis Toledo-Pereyra; Kelly Quesnelle
Journal:  EXCLI J       Date:  2017-04-07       Impact factor: 4.068

  5 in total

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