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Niacin inhibits the synthesis of milk fat in BMECs through the GPR109A-mediated downstream signalling pathway.
- Source :
-
Life sciences [Life Sci] 2020 Nov 01; Vol. 260, pp. 118415. Date of Electronic Publication: 2020 Sep 09. - Publication Year :
- 2020
-
Abstract
- Aims: Previous studies have shown the effect of niacin on dairy cow production, but no study on the role of niacin in milk fat synthesis has been performed. Therefore, the purpose of this study was to examine the effect of niacin on milk fat synthesis and its specific mechanism in BMECs.<br />Main Methods: In this study, 0.5 mM niacin, a GPR109A-inhibiting plasmid, and an AMPK inhibitor were added to BMECs. Milk fat was measured by a triglyceride kit and BODIPY staining. The protein expression of GPR109A, FASN, SREBP1, AMPK, ACC, mTOR and S6K was measured by Western blotting. The gene expression of GPR109A, FASN, and SREBP1 was analysed by RT-PCR.<br />Key Findings: Our results showed that 0.5 mM niacin could significantly reduce milk fat synthesis in BMECs and activate the AMPK/ACC signalling pathway by stimulating GPR109A, reducing the protein expression of p-mTOR and p-S6K, and reducing the expression of SREBP1 and FASN in BMECs.<br />Significance: The present study clarified the effect of niacin on milk fat synthesis. The results show that niacin inhibits the synthesis of milk fat in BMECs through the downstream signalling pathway mediated by GPR109A. The function of niacin has been expanded, and knowledge of the new mechanism and signalling pathway will help improve the biosynthesis of milk fat.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cattle
Epithelial Cells drug effects
Female
Hypolipidemic Agents pharmacology
Mammary Glands, Animal drug effects
Milk drug effects
Receptors, G-Protein-Coupled genetics
Dietary Fats metabolism
Epithelial Cells metabolism
Mammary Glands, Animal metabolism
Milk metabolism
Niacin pharmacology
Receptors, G-Protein-Coupled metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0631
- Volume :
- 260
- Database :
- MEDLINE
- Journal :
- Life sciences
- Publication Type :
- Academic Journal
- Accession number :
- 32918974
- Full Text :
- https://doi.org/10.1016/j.lfs.2020.118415