Literature DB >> 12915914

Hepatic regeneration: If it ain't broke, don't fix it.

G Y Minuk1.   

Abstract

The capacity for the liver to regenerate after injury or resection has long been recognized, as implied by the legend of Prometheus. Resections of up to 70% of the liver are followed by a sequence of events that generally result in complete restitution of hepatic mass and function. Hypertrophy of hepatocytes begins within hours, with accumulation of amino acids and triglycerides and activation of enzymes that are associated with proliferative activity. Increased DNA synthesis is associated initially with hyperplasia of hepatocytes, and then other cells, which begins in the periportal region and spreads in a wave-like fashion to the pericentral region of the lobule. Quiescent hepatocytes are primed to enter the cell cycle and then proceed through the G1/S and G2/M restriction points, under the influence of a variety of proteins, growth factors (especially hepatocyte growth factor) and cycle dependent kinases. At each stage there is interplay between growth promoters and inhibitors, including transforming growth factor-beta and GABA. Factors that initiate hepatic regeneration are unknown, and might include hepatic depolarization, increases in blood flow, destruction of liver matrix (with release of growth factors), and increased production or expression of growth promoters compared to inhibitors. Regenerative activity increases with the amount of resection to a point, and then relatively declines. Uncontrolled proliferation of liver tissue after resection or injury is not necessarily beneficial, because it could lead to a diversion of resources from the maintenance of hepatic function and to an increased risk of neoplasia. Therefore, it is unclear whether clinicians should attempt to enhance hepatocyte regeneration. Since both hepatic regeneration and metabolic function require energy from high-energy nucleotide triphosphates, especially adenosine triphosphate (ATP), a reasonable strategy might be to augment energy delivery and ATP production. Mortality rates after limited (fewer than 70%) resections and mild or moderate injuries of previously normal livers are low, and supportive care is often sufficient. The prognosis is unclear; however, in cases of more massive resection, resections in the setting of underlying liver disease or cirrhosis, and fulminant hepatic failure, and liver transplantation is still an important option.

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Year:  2003        PMID: 12915914     DOI: 10.1155/2003/615403

Source DB:  PubMed          Journal:  Can J Gastroenterol        ISSN: 0835-7900            Impact factor:   3.522


  5 in total

Review 1.  ALR and liver regeneration.

Authors:  Rafał Pawlowski; Jolanta Jura
Journal:  Mol Cell Biochem       Date:  2006-05-12       Impact factor: 3.396

2.  The identification of stem cells in human liver diseases and hepatocellular carcinoma.

Authors:  Joan Oliva; Barbara A French; X Qing; Samuel W French
Journal:  Exp Mol Pathol       Date:  2010-01-18       Impact factor: 3.362

3.  Reduced antioxidant level and increased oxidative damage in intact liver lobes during ischaemia-reperfusion.

Authors:  László Váli; Gabriella Taba; Klára Szentmihályi; Hedvig Fébel; Tímea Kurucz; Zsolt Pallai; Péter Kupcsulik; Anna Blázovics
Journal:  World J Gastroenterol       Date:  2006-02-21       Impact factor: 5.742

4.  Smad3 signaling in the regenerating liver: implications for the regulation of IL-6 expression.

Authors:  Michael Kremer; Gakuhei Son; Kun Zhang; Sherri M Moore; Amber Norris; Giulia Manzini; Michael D Wheeler; Ian N Hines
Journal:  Transpl Int       Date:  2014-05-22       Impact factor: 3.782

5.  Homeostatic response under carcinogen withdrawal, heme oxygenase 1 expression and cell cycle association.

Authors:  Cynthia C Castronuovo; Paula A Sacca; Roberto Meiss; Fabiana A Caballero; Alcira Batlle; Elba S Vazquez
Journal:  BMC Cancer       Date:  2006-12-14       Impact factor: 4.430

  5 in total

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