Literature DB >> 15951943

Ischemic preconditioning versus intermittent vascular inflow control during major liver resection in pigs.

Vassilios Smyrniotis1, Georgia Kostopanagiotou, Kassiani Theodoraki, Charalampos Farantos, Nikolaos Arkadopoulos, Evangelos Gamaletsos, Agathi Condi-Paphitis, Alexis Fotopoulos, Panagiotis Dimakakos.   

Abstract

Ischemic preconditioning (IPC) and intermittent vascular control (IVC) have been shown to reduce the number of ischemia/reperfusion injuries during liver resections with the Pringle maneuver. Our study aimed to compare the beneficial effect of these two modalities in relation to the duration of normothermic liver ischemia. A group of 24 Landrace pigs with a mean body weight of 25 to 30 kg were subjected to extended liver resection of more than 65%. Although, 12 animals underwent IPC (10 minutes of ischemia and 10 minutes of reperfusion), and subsequently the Pringle maneuver was applied for 90 minutes (n= 6) or 120 minutes (n= 6). Another 12 animals underwent liver resection by IVC (20 minutes of ischemia alternated with 5 minutes of reperfusion) for 60 minutes (n = 6) or 120 minutes (n = 6) of inflow vascular control. At 90 minutes of liver ischemia, the IPC group demonstrated lower levels of asportate aminotransferase (AST) (173 +/- 53 vs. 265 +/- 106 IU; p =0.089) and malondialdehyde (MDA) (2.60 +/- 1.03 vs. 5.33 +/- 2.25 micromol/L; p =0.022) and higher liver tissue cAMP (200 +/- 42 vs. 146 +/- 40 pmol/g wet wt, p = 0.04) compared to the IVC group. However, no pathologic differences were observed between the two groups. By contrast, at 120 minutes of liver ischemia, IVC proved to be more beneficial, reflected by lower levels of AST (448 +/- 135 vs. 857 +/- 268 IU; p = 0.006) and MDA (8.33 +/- 1.75 vs. 12.7 +/- 4.31 micromol/L; (p = 0.045), a higher cAMP level (127 +/- 10 vs. 97 +/- 31 pmol/g wet wt p = 0.045), and eventually less cellular necrosis (necrosis score 1.66 +/- 0.51 vs. 2.85 +/- 1.16; p = 0.04) compared to the IPC group. It appears that IPC should be employed when liver ischemia is anticipated to last less than 90 minutes, followed by IVC when the liver ischemia is expected to last 120 minutes.

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Year:  2005        PMID: 15951943     DOI: 10.1007/s00268-005-7591-9

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


  26 in total

1.  Platelets induce sinusoidal endothelial cell apoptosis upon reperfusion of the cold ischemic rat liver.

Authors:  D Sindram; R J Porte; M R Hoffman; R C Bentley; P A Clavien
Journal:  Gastroenterology       Date:  2000-01       Impact factor: 22.682

2.  Intermittent vascular exclusion of the liver (without vena cava clamping) during major hepatectomy.

Authors:  D Elias; P Lasser; B Debaene; L Doidy; V Billard; A Spencer; B Leclercq
Journal:  Br J Surg       Date:  1995-11       Impact factor: 6.939

3.  Endothelial cell and hepatocyte deaths occur by apoptosis after ischemia-reperfusion injury in the rat liver.

Authors:  V Kohli; M Selzner; J F Madden; R C Bentley; P A Clavien
Journal:  Transplantation       Date:  1999-04-27       Impact factor: 4.939

4.  Continuous versus intermittent portal triad clamping for liver resection: a controlled study.

Authors:  J Belghiti; R Noun; R Malafosse; P Jagot; A Sauvanet; F Pierangeli; J Marty; O Farges
Journal:  Ann Surg       Date:  1999-03       Impact factor: 12.969

5.  Preconditioning protects against systemic disorders associated with hepatic ischemia-reperfusion through blockade of tumor necrosis factor-induced P-selectin up-regulation in the rat.

Authors:  C Peralta; L Fernández; J Panés; N Prats; M Sans; J M Piqué; E Gelpí; J Roselló-Catafau
Journal:  Hepatology       Date:  2001-01       Impact factor: 17.425

6.  Liver ischemic preconditioning is mediated by the inhibitory action of nitric oxide on endothelin.

Authors:  C Peralta; D Closa; G Hotter; E Gelpí; N Prats; J Roselló-Catafau
Journal:  Biochem Biophys Res Commun       Date:  1996-12-04       Impact factor: 3.575

7.  An experimental study of survival after two hours of normothermic hepatic ischemia.

Authors:  B Nordlinger; D Douvin; L Javaudin; P Bloch; A Aranda; M Boschat; C Huguet
Journal:  Surg Gynecol Obstet       Date:  1980-06

8.  Effects of amrinone on hepatic ischemia-reperfusion injury in rats.

Authors:  Takashi Kobayashi; Yasuhiko Sugawara; Takao Ohkubo; Hiroshi Imamura; Masatoshi Makuuchi
Journal:  J Hepatol       Date:  2002-07       Impact factor: 25.083

9.  Amelioration of liver injury by ischaemic preconditioning.

Authors:  T Yoshizumi; K Yanaga; Y Soejima; T Maeda; H Uchiyama; K Sugimachi
Journal:  Br J Surg       Date:  1998-12       Impact factor: 6.939

10.  Sub-lethal oxidative stress triggers the protective effects of ischemic preconditioning in the mouse liver.

Authors:  Hannes A Rüdiger; Rolf Graf; Pierre-Alain Clavien
Journal:  J Hepatol       Date:  2003-12       Impact factor: 25.083

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  3 in total

Review 1.  Role of ischaemic preconditioning in liver regeneration following major liver resection and transplantation.

Authors:  D Gomez; S Homer-Vanniasinkam; A M Graham; K R Prasad
Journal:  World J Gastroenterol       Date:  2007-02-07       Impact factor: 5.742

Review 2.  How much ischemia can the liver tolerate during resection?

Authors:  Wouter G van Riel; Rowan F van Golen; Megan J Reiniers; Michal Heger; Thomas M van Gulik
Journal:  Hepatobiliary Surg Nutr       Date:  2016-02       Impact factor: 7.293

3.  Ischemic preconditioning confers antiapoptotic protection during major hepatectomies performed under combined inflow and outflow exclusion of the liver. A randomized clinical trial.

Authors:  Nikolaos Arkadopoulos; Georgia Kostopanagiotou; Kassiani Theodoraki; Charalambos Farantos; Theodosios Theodosopoulos; Vaia Stafyla; John Vassiliou; Dionyssios Voros; Agathi Pafiti; Vassilios Smyrniotis
Journal:  World J Surg       Date:  2009-09       Impact factor: 3.352

  3 in total

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