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A reduced protein diet modulates enzymes of vitamin D and cholesterol metabolism in young ruminants.

Authors :
Wilkens MR
Firmenich CS
Schnepel N
Muscher-Banse AS
Source :
The Journal of steroid biochemistry and molecular biology [J Steroid Biochem Mol Biol] 2019 Feb; Vol. 186, pp. 196-202. Date of Electronic Publication: 2018 Oct 28.
Publication Year :
2019

Abstract

Besides other adverse effects, a low protein diet has been shown to modulate cholesterol and vitamin D metabolism in monogastric species like rats and humans. As ruminants can increase the efficiency of the rumino-hepatic circulation of urea, it is assumed that goats should be able to compensate for a low dietary protein intake better. After a dietary protein restriction (9% vs. 20%) for six weeks, plasma concentrations of urea, albumin, 1,25-dihydroxyvitamin D <subscript>3</subscript> and calcium were decreased, while plasma 25-hydroxyvitamin D <subscript>3</subscript> (25-OHD <subscript>3</subscript> ), and total cholesterol were significantly increased in young goats. Because this was not accompanied by any decrease in expression of CYP24A1 mRNA, we investigated mRNA expression of additional enzymes with known 24- and/or 25-hydroxylase activities (CYP2R1, CYP2J2, CYP3 A24, CYP27A1), receptors involved in their regulation (VDR, PXR, RXRα) and vitamin D binding protein (VDBP). CYP2R1expression was stimulated with the low dietary protein intake, negatively correlated with plasma urea and positively associated with serum 25-OHD <subscript>3</subscript> . The greater plasma concentrations of total cholesterol could be explained with the reduction of CYP2J2 and CYP27A1 expression. None of the receptors investigated were affected by the dietary protein restriction but mRNA expression of VDBP was slightly reduced. Taken together our results show that dietary protein restriction has an impact on vitamin D and cholesterol metabolism in ruminants, too. Therefore, further investigations are needed before dietary interventions aiming at diminishing nitrogen excretion can be implemented.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1879-1220
Volume :
186
Database :
MEDLINE
Journal :
The Journal of steroid biochemistry and molecular biology
Publication Type :
Academic Journal
Accession number :
30394334
Full Text :
https://doi.org/10.1016/j.jsbmb.2018.10.014