Literature DB >> 31312996

Ontogenesis and Modulation of Intestinal Unesterified Cholesterol Sequestration in a Mouse Model of Niemann-Pick C1 Disease.

Adam M Lopez1, Charina M Ramirez2, Anna M Taylor3,4, Ryan D Jones3,5, Joyce J Repa1,3, Stephen D Turley6.   

Abstract

BACKGROUND: Mutations in the NPC1 gene result in sequestration of unesterified cholesterol (UC) and glycosphingolipids in most tissues leading to multi-organ disease, especially in the brain, liver, lungs, and spleen. Various data from NPC1-deficient mice suggest the small intestine (SI) is comparatively less affected, even in late stage disease.
METHODS: Using the Npc1nih mouse model, we measured SI weights and total cholesterol (TC) levels in Npc1-/- versus Npc1+/+ mice as a function of age, and then after prolonged ezetimibe-induced inhibition of cholesterol absorption. Next, we determined intestinal levels of UC and esterified cholesterol (EC), and cholesterol synthesis rates in Npc1-/- and Npc1+/+ mice, with and without the cholesterol-esterifying enzyme SOAT2, following a once-only subcutaneous injection with 2-hydroxypropyl-β-cyclodextrin (2HPβCD).
RESULTS: By ~ 42 days of age, intestinal TC levels averaged ~ 2.1-fold more (mostly UC) in the Npc1-/- versus Npc1+/+ mice with no further increase thereafter. Chronic ezetimibe treatment lowered intestinal TC levels in the Npc1-/- mice by only ~ 16%. In Npc1-/- mice given 2HPβCD 24 h earlier, UC levels fell, EC levels increased (although less so in mice lacking SOAT2), and cholesterol synthesis was suppressed equally in the Npc1-/-:Soat2+/+ and Npc1-/-:Soat2-/- mice.
CONCLUSIONS: The low and static levels of intestinal UC sequestration in Npc1-/- mice likely reflect the continual sloughing of cells from the mucosa. This sequestration is blunted by about the same extent following a single acute treatment with 2HPβCD as it is by a prolonged ezetimibe-induced block of cholesterol absorption.

Entities:  

Keywords:  2-Hydroxypropyl-β-cyclodextrin; Biliary cholesterol; Ezetimibe; Fecal sterol excretion; Lysosomal cholesterol storage disease; Small intestine

Year:  2019        PMID: 31312996     DOI: 10.1007/s10620-019-05736-x

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  69 in total

Review 1.  From blood to gut: direct secretion of cholesterol via transintestinal cholesterol efflux.

Authors:  Carlos L J Vrins
Journal:  World J Gastroenterol       Date:  2010-12-21       Impact factor: 5.742

2.  Lysosome lipid storage disorder in NCTR-BALB/c mice. I. Description of the disease and genetics.

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Journal:  Am J Pathol       Date:  1982-08       Impact factor: 4.307

3.  Cholesterol esters (CE) derived from hepatic sterol O-acyltransferase 2 (SOAT2) are associated with more atherosclerosis than CE from intestinal SOAT2.

Authors:  Jun Zhang; Janet K Sawyer; Stephanie M Marshall; Kathryn L Kelley; Matthew A Davis; Martha D Wilson; J Mark Brown; Lawrence L Rudel
Journal:  Circ Res       Date:  2014-09-19       Impact factor: 17.367

4.  Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann-Pick type C disease.

Authors:  Charina M Ramirez; Adam M Lopez; Lam Q Le; Kenneth S Posey; Arthur G Weinberg; Stephen D Turley
Journal:  Biochim Biophys Acta       Date:  2013-09-26

Review 5.  Hepatic uptake of chylomicron remnants.

Authors:  A D Cooper
Journal:  J Lipid Res       Date:  1997-11       Impact factor: 5.922

6.  Extra-hepatic metabolism of 7-ketocholesterol occurs by esterification to fatty acids via cPLA2α and SOAT1 followed by selective efflux to HDL.

Authors:  Jung Wha Lee; Jiahn-Dar Huang; Ignacio R Rodriguez
Journal:  Biochim Biophys Acta       Date:  2015-01-22

7.  Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acid.

Authors:  Benny Liu; Charina M Ramirez; Anna M Miller; Joyce J Repa; Stephen D Turley; John M Dietschy
Journal:  J Lipid Res       Date:  2009-11-18       Impact factor: 5.922

8.  Biochemical studies in Niemann-Pick disease. I. Major sphingolipids of liver and spleen.

Authors:  M T Vanier
Journal:  Biochim Biophys Acta       Date:  1983-01-07

9.  Cholesterol balance and metabolism in mice with loss of function of Niemann-Pick C protein.

Authors:  C Xie; S D Turley; P G Pentchev; J M Dietschy
Journal:  Am J Physiol       Date:  1999-02

10.  Neurochemical alterations in the cerebellum of a murine model of Niemann-Pick type C disease.

Authors:  G Yadid; I Sotnik-Barkai; C Tornatore; B Baker-Cairns; J Harvey-White; P G Pentchev; E Goldin
Journal:  Brain Res       Date:  1998-07-20       Impact factor: 3.252

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  1 in total

1.  Delineation of metabolic responses of Npc1-/-nih mice lacking the cholesterol-esterifying enzyme SOAT2 to acute treatment with 2-hydroxypropyl-β-cyclodextrin.

Authors:  Charina M Ramirez; Anna M Taylor; Adam M Lopez; Joyce J Repa; Stephen D Turley
Journal:  Steroids       Date:  2020-09-02       Impact factor: 2.668

  1 in total

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