Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8336446 | The Journal of Nutritional Biochemistry | 2018 | 31 Pages |
Abstract
Altogether, MCA and CDCA synthesis is selectively induced in ApoE-deficient mice. These hydrophilic BAs alter micellar size and structure to lower intestinal cholesterol solubilization. Furthermore, CDCA and MCA are potent FXR agonist and antagonist, respectively, and function in a regulatory loop to mitigate impaired ApoE function.
Keywords
MCASOAT1LRHSREBP1CDCAMRMSHPESI-MS/MSAsbtApoeapolipoprotein EApolipoprotein E (APOE)Chenodeoxycholic acidBile acidmuricholic acidapical sodium-dependent bile acid transporterGoIchylomicron remnantsLipid transportBile acid synthesissmall heterodimer partnerMass spectrometryElectrospray ionization tandem mass spectrometryTranscription factorsCholesterol metabolismTMCAmultiple reaction monitoringSterol regulatory element-binding proteingene of interestCholesterol esterfree cholesterol
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Authors
Sandra von Hardenberg, Carsten Gnewuch, Gerd Schmitz, Jürgen Borlak,