Literature DB >> 8806465

Ischemia/reperfusion alters uric acid and ascorbic acid levels in liver.

M E Layton1, J G Wood, Z Y Yan, J Forster.   

Abstract

Tissue damage in ischemia/reperfusion injury may be mediated by oxidative stress caused by reactive oxidant species. Since such reactive species are difficult to measure directly, changes in antioxidant concentrations are often used as an indication of oxidative stress. In this study, microdialysis membranes were inserted into the livers of anesthetized rats to determine the effects of ischemia/reperfusion on the extra-cellular concentrations of two antioxidants, uric acid and ascorbic acid. Total hepatic ischemia was induced for 30 min by clamping the portal triad and was followed by 60 min of reperfusion. Uric acid and ascorbic acid concentrations were measured in microdialysis perfusates by high-performance liquid chromatography with electrochemical detection. Initial uric acid and ascorbic acid concentrations were high after insertion of membranes into the liver and decreased rapidly within 90 min (P < 0.001; ANOVA with repeated measures). Uric acid concentrations increased over 300% after ischemia and by 600% during the first 30 min of reperfusion (n = 8; P < 0.05). Ascorbic acid concentrations were 60% higher than controls after ischemia and 90% higher during the first 30 min of reperfusion (n = 8; P < 0.05). Alterations in concentrations of these redox-active molecules may be associated with oxidative stress in liver extracellular fluid during ischemia/reperfusion.

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Year:  1996        PMID: 8806465     DOI: 10.1006/jsre.1996.0297

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  5 in total

Review 1.  Pharmacokinetic and metabolism studies using microdialysis sampling.

Authors:  D K Hansen; M I Davies; S M Lunte; C E Lunte
Journal:  J Pharm Sci       Date:  1999-01       Impact factor: 3.534

2.  Increase in post-reperfusion sensitivity to tissue plasminogen activator-mediated fibrinolysis during liver transplantation is associated with abnormal metabolic changes and increased blood product utilisation.

Authors:  Hunter B Moore; Angelo D'Alessandro; Ernest E Moore; Matthew Wither; Peter J Lawson; Benjamin R Huebner; Kirk Hansen; Rashikh Choudhury; Trevor L Nydam
Journal:  Blood Transfus       Date:  2019-02-04       Impact factor: 3.443

3.  Redox changes in perfusates following intracerebral penetration of microdialysis probes.

Authors:  M E Layton; J K Wagner; F E Samson; T L Pazdernik
Journal:  Neurochem Res       Date:  1997-06       Impact factor: 3.996

4.  Warm ischemia time and elevated serum uric acid are associated with metabolic syndrome after liver transplantation with donation after cardiac death.

Authors:  Liang-Shuo Hu; Yi-Chao Chai; Jie Zheng; Jian-Hua Shi; Chun Zhang; Min Tian; Yi Lv; Bo Wang; Ai Jia
Journal:  World J Gastroenterol       Date:  2018-11-21       Impact factor: 5.742

5.  Deregulation of the Purine Pathway in Pre-Transplant Liver Biopsies Is Associated with Graft Function and Survival after Transplantation.

Authors:  Jin Xu; Mohammad Hassan-Ally; Ana María Casas-Ferreira; Tommi Suvitaival; Yun Ma; Hector Vilca-Melendez; Mohamed Rela; Nigel Heaton; Jassem Wayel; Cristina Legido-Quigley
Journal:  J Clin Med       Date:  2020-03-05       Impact factor: 4.241

  5 in total

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