Literature DB >> 20207439

Reperfusion stress induced during intermittent selective clamping accelerates rat liver regeneration through JNK pathway.

Hélène Duval1, Sasse-Fanie Mbatchi, Stéphane Grandadam, Claire Legendre, Pascal Loyer, Catherine Ribault, Claire Piquet-Pellorce, Christiane Guguen-Guillouzo, Karim Boudjema, Anne Corlu.   

Abstract

BACKGROUND & AIMS: Liver resection includes temporal vascular inflow occlusion resulting in ischemia/reperfusion injury in the remnant liver. Here, we developed a rat model of selective lobe occlusion to isolate reperfusion stress from ischemia and to analyze its effect on liver regeneration.
METHODS: Left lateral and median lobes of liver were either mobilized or subjected twice for 10min to ischemia followed by 5min reperfusion prior to resection while the regenerative lobes were only subjected to reperfusion.
RESULTS: Although intermittent reperfusion stress induced higher levels of serum transaminases, analysis of cell cycle regulators revealed accelerated regenerative response compared to standard partial hepatectomy. The G0/G1 transition occurred before tissue resection, as evidenced by c-fos, junB, and IL-6 induction. Following hepatectomy, Cyclin D1 up-regulation, G1/S transition, and cell division occurred earlier than normal. Unexpectedly, liver mobilization, a component of the clamping procedure, also resulted in earlier G1/S transition. The shortened G1-phase was driven by the c-Jun N-terminal Kinase pathway and was associated with an oxidative stress response as evidenced by the expression of inducible nitric oxide synthase.
CONCLUSION: Intermittent selective clamping of lobes to be resected induced reperfusion stress on remnant liver that was beneficial for liver regeneration, suggesting this procedure could be applied in clinical practice.

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Year:  2010        PMID: 20207439     DOI: 10.1016/j.jhep.2010.01.013

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  6 in total

1.  Activation of different neuronal phenotypes in the rat brain induced by liver ischemia–reperfusion injury: dual Fos/neuropeptide immunohistochemistry.

Authors:  J Bundzikova; Z Pirnik; L Lackovicova; B Mravec; A Kiss
Journal:  Cell Mol Neurobiol       Date:  2011-03       Impact factor: 5.046

2.  Intermittent selective clamping improves rat liver regeneration by attenuating oxidative and endoplasmic reticulum stress.

Authors:  I Ben Mosbah; H Duval; S-F Mbatchi; C Ribault; S Grandadam; J Pajaud; F Morel; K Boudjema; P Compagnon; A Corlu
Journal:  Cell Death Dis       Date:  2014-03-06       Impact factor: 8.469

3.  Glutathione transferases P1/P2 regulate the timing of signaling pathway activations and cell cycle progression during mouse liver regeneration.

Authors:  J Pajaud; C Ribault; I Ben Mosbah; C Rauch; C Henderson; P Bellaud; C Aninat; P Loyer; F Morel; A Corlu
Journal:  Cell Death Dis       Date:  2015-01-15       Impact factor: 8.469

Review 4.  Effects of iNOS in Hepatic Warm Ischaemia and Reperfusion Models in Mice and Rats: A Systematic Review and Meta-Analysis.

Authors:  Richi Nakatake; Mareike Schulz; Christina Kalvelage; Carina Benstoem; René H Tolba
Journal:  Int J Mol Sci       Date:  2022-10-07       Impact factor: 6.208

5.  Combined Stimulation with the Tumor Necrosis Factor α and the Epidermal Growth Factor Promotes the Proliferation of Hepatocytes in Rat Liver Cultured Slices.

Authors:  Francis Finot; Régis Masson; Fabienne Desmots; Catherine Ribault; Nicole Bichet; Joan A Vericat; Patricia Lafouge; Christiane Guguen-Guillouzo; Pascal Loyer
Journal:  Int J Hepatol       Date:  2012-10-16

6.  Yiqi Huoxue Recipe Improves Liver Regeneration in Rats after Partial Hepatectomy via JNK Pathway.

Authors:  Wen-Cong Li; Su-Xian Zhao; Wei-Guang Ren; Hui-Juan Du; Yu-Guo Zhang; Yue-Min Nan
Journal:  Evid Based Complement Alternat Med       Date:  2020-04-26       Impact factor: 2.629

  6 in total

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