Literature DB >> 19399926

Histological and biochemical alterations in early-stage lobar ischemia-reperfusion in rat liver.

Hossein-Ali Arab1, Farhang Sasani, Mohammad-Hossein Rafiee, Ahmad Fatemi, Abbas Javaheri.   

Abstract

AIM: To investigate the structural and biochemical changes in the early stage of reperfusion in the rat livers exposed to lobar ischemia-reperfusion (IR).
METHODS: The median and left lobes of the liver were subjected to 60 min ischemia followed by 5, 10, 30, 45, 60 and 120 min reperfusion. Blood samples were taken at different time intervals to test enzyme activities and biochemical alterations induced by reperfusion. At the end of each reperfusion period, the animals were killed by euthanasia and tissue samples were taken for histological examination and immunohistochemistry.
RESULTS: Cell vacuolation, bleb formation and focal hepatitis were the most important changes occur during ischemia. While some changes including bleb formation were removed during reperfusion, other alterations including portal hepatitis, inflammation and the induction of apoptosis were seen during this stage. The occurrence of apoptosis, as demonstrated by apoptotic cells and bodies, was the most important histological change during reperfusion. The severity of apoptosis was dependent on the time of reperfusion, and by increasing the time of reperfusion, the numbers of apoptotic bodies was significantly enhanced. The amounts of lactate dehydrogenase, alanine aminotransferase, aspartate aminotransferase, creatinine and urea were significantly increased in serum obtained from animals exposed to hepatic IR.
CONCLUSION: Inflammation and subsequent apoptotic cell death were the most important changes in early-stage hepatic reperfusion injury, and the number of apoptotic bodies increased with time of reperfusion.

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Mesh:

Year:  2009        PMID: 19399926      PMCID: PMC2675084          DOI: 10.3748/wjg.15.1951

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  37 in total

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  8 in total

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2.  The effects of low-intensity laser therapy on hepatic ischemia-reperfusion injury in a rat model.

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3.  The protection of hepatocyte cells from the effects of oxidative stress by treatment with vitamin E in conjunction with DTT.

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Authors:  D Degli Esposti; M Sebagh; P Pham; M Reffas; C Poüs; C Brenner; D Azoulay; A Lemoine
Journal:  Cell Death Dis       Date:  2011-01-13       Impact factor: 8.469

5.  Inhalation of molecular hydrogen prevents ischemia-reperfusion liver damage during major liver resection.

Authors:  Ondřej Malý; Ján Zajak; Radomír Hyšpler; Zdeněk Turek; David Astapenko; Daniel Jun; Nela Váňová; Aleš Kohout; Věra Radochová; Jiří Kotek; Jiří Páral
Journal:  Ann Transl Med       Date:  2019-12

6.  Sustained Isoprostane E2 Elevation, Inflammation and Fibrosis after Acute Ischaemia-Reperfusion Injury Are Reduced by Pregnane X Receptor Activation.

Authors:  Aimen O Amer; Philip M Probert; Michael Dunn; Margaret Knight; Abigail E Vallance; Paul A Flecknell; Fiona Oakley; Iain Cameron; Steven A White; Peter G Blain; Matthew C Wright
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7.  Sildenafil attenuates hepatocellular injury after liver ischemia reperfusion in rats: a preliminary study.

Authors:  Spyridon Savvanis; Constantinos Nastos; Marios-Konstantinos Tasoulis; Nikolaos Papoutsidakis; Maria Demonakou; Iosifina Karmaniolou; Nikolaos Arkadopoulos; Vassilios Smyrniotis; Kassiani Theodoraki
Journal:  Oxid Med Cell Longev       Date:  2014-06-04       Impact factor: 6.543

8.  The role of N-acetyltransferase 8 in mesenchymal stem cell-based therapy for liver ischemia/reperfusion injury in rats.

Authors:  Jinqiu Fu; Haiyan Zhang; Yong Zhuang; Huan Liu; Qing Shi; Dong Li; Xiuli Ju
Journal:  PLoS One       Date:  2014-07-24       Impact factor: 3.240

  8 in total

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