IFISE   05411
INSTITUTO DE FISIOLOGIA EXPERIMENTAL
Unidad Ejecutora - UE
artículos
Título:
Participation of 5-lipoxygenase and LTB4 in liver regeneration after partial hepatectomy
Autor/es:
VERA, MARINA CECILIA; PISANI, GERARDO BRUNO; COMANZO, CARLA GABRIELA; QUIROGA, ARIEL DARÍO; VERA, MARINA CECILIA; PISANI, GERARDO BRUNO; COMANZO, CARLA GABRIELA; QUIROGA, ARIEL DARÍO; CEBALLOS, MARÍA PAULA; MONTI, JUAN ALBERTO; TORDJMANN, THIERRY; ALVAREZ, MARÍA DE LUJÁN; CEBALLOS, MARÍA PAULA; MONTI, JUAN ALBERTO; TORDJMANN, THIERRY; ALVAREZ, MARÍA DE LUJÁN; LORENZETTI, FLORENCIA; RONCO, MARÍA TERESA; LUCCI, ALVARO; CARRILLO, MARÍA CRISTINA; LORENZETTI, FLORENCIA; RONCO, MARÍA TERESA; LUCCI, ALVARO; CARRILLO, MARÍA CRISTINA
Revista:
Scientific Reports
Editorial:
Nature Research
Referencias:
Año: 2019 vol. 9 p. 1 - 14
Resumen:
Regeneration is the unmatched liver ability for recovering its functional mass after tissue lost. Leukotrienes (LT) are a family of eicosanoids with the capacity of signaling to promote proliferation. We analyzed the impact of blocking LT synthesis during liver regeneration after partial hepatectomy (PH). Male Wistar rats were subjected to two-third PH and treated with zileuton, a specific inhibitor of 5-lipoxygenase (5-LOX). Our first find was a significant increment of intrahepatic LTB4 during the first hour after PH together with an increase in 5-LOX expression. Zileuton reduced hepatic LTB4 levels at the moment of hepatectomy and also inhibited the increase in hepatic LTB4. This inhibition produced a delay in liver proliferation as seen by decreased PCNA and cyclin D1 nuclear expression 24 h post-PH. Results also showed that hepatic LTB4 diminution by zileuton was associated with a decrease in NF-ĸB activity. Additionally, decreased hepatic LTB4 levels by zileuton affected the recruitment of neutrophils and macrophages. Non-parenchymal cells (NPCs) from zileuton-treated PH-rats displayed higher apoptosis than NPCs from PH control rats. In conclusion, the present work provides evidences that 5-LOX activation and its product LTB4 are involved in the initial signaling events for liver regeneration after PH and the pharmacological inhibition of this enzyme can delay the initial time course of the phenomenon.