Literature DB >> 26270074

Comparative Effects of Ischemic Preconditioning and Iron Chelation in Hepatectomy.

Georgios Trogadas1, Aikaterini Mastoraki1, Constantinos Nastos1, Agathi Kondi-Pafiti2, Georgia Kostopanagiotou3, Vassilios Smyrniotis1, Nikolaos Arkadopoulos1.   

Abstract

PURPOSE/AIM: Major hepatectomies can result in severe ischemia/reperfusion (I/R) injury of the liver. The aim of this survey is to comparatively evaluate the effects of a surgical and a pharmacological hepatoprotective modality on the liver remnant in a porcine model of hepatectomy.
MATERIAL AND METHODS: Twenty-one Landrace pigs were randomly divided into three groups: a control group (CON) (n = 7), an Ischemic Preconditioning (PRE) group (n = 7) and a Desferoxamine (DFX) treated one (n = 7). Animals were subjected to 120 min of liver ischemia with subsequent 75% hepatectomy followed by 24-hr reperfusion. In all animals, continuous intracranial pressure (ICP) monitoring was employed. Blood samples were collected at t0, t6, t12, and t24 hrs after reperfusion. Liver remnant specimens were excised for histological examination.
RESULTS: In the PRE group, ICP was statistically lower at t6 time point compared to CON group and in comparison with t0. In addition, ICP was significantly lower at all-time points after reperfusion in the DFX group. Finally, with regard to DFX and PRE group correlation, ICP was significantly lower at t0, t12, and t24 time points after reperfusion in the DFX group. In the PRE group, NH3 levels were significantly lower at t12 after reperfusion compared to CON and DFX groups. Histological evaluation elucidated significantly less hepatocellular necrosis, apoptosis, and degeneration in the PRE and DFX groups correlated to CON group.
CONCLUSIONS: Both hepatoprotective modalities including PRE and DFX administration are associated with lower ICP levels and correlated with attenuated liver remnant injury.

Entities:  

Keywords:  desferoxamine; hepatectomy; hepatoprotective modalities; intracranial pressure; iron chelation; ischemic preconditioning; swine

Mesh:

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Year:  2015        PMID: 26270074     DOI: 10.3109/08941939.2015.1024803

Source DB:  PubMed          Journal:  J Invest Surg        ISSN: 0894-1939            Impact factor:   2.533


  3 in total

1.  GADD45β induction by S-adenosylmethionine inhibits hepatocellular carcinoma cell proliferation during acute ischemia-hypoxia.

Authors:  Ding Ma; Baiyong Shen; Varun Seewoo; Hui Tong; Weiping Yang; Xi Cheng; Zhijian Jin; Chenghong Peng; Weihua Qiu
Journal:  Oncotarget       Date:  2016-06-14

Review 2.  SIRT3 a Major Player in Attenuation of Hepatic Ischemia-Reperfusion Injury by Reducing ROS via Its Downstream Mediators: SOD2, CYP-D, and HIF-1α.

Authors:  Gaurav Katwal; Dilip Baral; Xiaoli Fan; He Weiyang; Xinjiang Zhang; Li Ling; Yan Xiong; Qifa Ye; Yanfeng Wang
Journal:  Oxid Med Cell Longev       Date:  2018-11-13       Impact factor: 6.543

3.  Combined Pharmacotherapy with Alendronate and Desferoxamine Regulate the Bone Resorption and Bone Regeneration for Preventing Glucocorticoids-Induced Osteonecrosis of the Femoral Head.

Authors:  Hongfeng Sheng; Yangjun Lao; Shuliang Zhang; Weiguo Ding; Di Lu; Bin Xu
Journal:  Biomed Res Int       Date:  2020-09-21       Impact factor: 3.411

  3 in total

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