Browsing by Author "Pimentel Muller, Fernando Ernesto"

Now showing 1 - 2 of 2
  • Thumbnail Image
    Item
    Actitudes disruptivas en el ambiente de pabellón
    (Elsevier, 2017) Campos Daziano, Mauricio Andrés; Lira Salas, María Jesús; Mery Illanes, Pamela Pía; Pimentel Muller, Fernando Ernesto; Zuñiga Parada, Denisse Alejandra; Roman, Javier
  • No Thumbnail Available
    Item
    Ezetimibe prevents cholesterol gallstone formation in mice
    (2008) Zuñiga, Silvia Eugenia; Molina, Héctor; Azócar, Lorena; Amigo Boker, Ludwig Peter; Nervi Oddone, Flavio; Pimentel Muller, Fernando Ernesto; Jarufe Cassis, Nicolas Patricio; Arrese Jimenez, Marco Antonio; Lammert, Frank; Miquel Poblete, Juan Francisco
    Background: Intestinal cholesterol absorption may influence gallstone formation and its modulation could be a useful therapeutic strategy for gallstone disease (GSD). Ezetimibe (EZET) is a cholesterol-lowering agent that specifically inhibits intestinal cholesterol absorption. Aims: To test whether EZET can prevent gallstone formation in mice. Methods/Results: Gallstone-susceptible C57BL/6 inbred mice were fed control and lithogenic diets with or without simultaneous EZET administration. Lithogenic diet increased biliary cholesterol content and secretion, and induced sludge or gallstone formation in 100% of the animals. EZET administration reduced intestinal cholesterol absorption by 90% in control animals and by 35% in mice receiving the lithogenic diet. EZET prevented the appearance of cholesterol crystals and gallstones. In addition, mice fed the lithogenic diet plus EZET exhibited a 60% reduction in biliary cholesterol saturation index. Of note, EZET treatment caused a significant increase in bile flow (+50%, P < 0.01) as well as bile salt, phospholipid and glutathione secretion rates (+60%, +44% and +100%, respectively, P < 0.01), which was associated with a moderately increased expression of hepatic bile salt transporters. In addition, relative expression levels of Nieman-Pick C1 like 1 (NPC1L1) in the enterohepatic axis in humans were assessed. Expression levels of NPC1L1 were 15-to 30-fold higher in the duodenum compared with the liver at transcript and protein levels, respectively, suggesting preferential action of EZET on intestinal cholesterol absorption in humans. Conclusions: In a murine model of GSD, EZET prevented gallstone formation by reducing intestinal cholesterol absorption and increasing bile salt-dependent and -independent bile flow. EZET could be useful in preventing GSD disease in susceptible patients.