English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/85454
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

Dietary marine algae and its influence on tissue gene network expression during milk fat depression in dairy ewes

AuthorsBichi, Elena ; Frutos, Pilar ; Toral, Pablo G. ; Keisler, Duane; Hervás, Gonzalo ; Loor, Juan J.
KeywordsMarine lipids
Gene expression
Lipid metabolism
Sheep
Issue Date2013
PublisherElsevier
CitationAnimal Feed Science and Technology, 186: 36-44 (2013)
AbstractSupplementation of a linoleic acid-rich diet with marine algae reduces milk fat content while impacting milk fatty acid profile in dairy sheep. Unlike other ruminant species, in ovine there are limited data on the molecular mechanisms that may regulate adipose, liver, and mammary responses to dietary marine lipids. This study was conducted to investigate changes in mRNA expression and relative mRNA abundance of key enzymes involved in lipid metabolism in mammary, subcutaneous adipose and liver tissue in response to long-term milk fat depression induced by marine algae. Eleven Assaf ewes were randomly assigned to 2 experimental diets consisting of a TMR based on alfalfa hay and concentrate (40:60) supplemented with 25 g of sunflower oil/kg DM plus 0 (SO; control diet) or 8 g of marine algae/kg of DM (SOMA diet) for 54 d. Quantitative reverse transcription-PCR was used to study expression of target genes in tissues harvested at slaughter at the end of the feeding period (54 d). There was no effect of SOMA on mammary and adipose tissue expression of genes encoding proteins required for fatty acid uptake and activation (ACSS2, LPL), intracellular fatty acid transport (FABP3, FABP4), de novo fatty acid synthesis (ACACA, FASN), esterification (DGAT1, DGAT2, LPIN1), desaturation (SCD), elongation (ELOVL6), trans-criptional regulation (INSIG1, MED1, PPARG, RXRA, SCAP, SREBF1, THRSP) and lipid droplet formation (ADFP, BTN1A1, XDH). Abundance of PPARG (0.04%) and INSIG1 (2.22%) in mammary tissue was markedly greater than that of SREBF1 (0.002%), suggesting that they may play a more important role in milk fat synthesis regulation. Addition of marine algae did not affect the expression of-hydroxybutyrate, NEFA, glucose,triacylglycerol, growth hormone, insulin-like growth factor 1, insulin, and leptin was not different between groups at d 54. Taken together with the milk fat responses and previous data from bovine fed similar diets, results suggest that transcriptional control mechanisms regulating fat synthesis in mammary secretory tissue were likely established during earlier stages of the feeding period.
Description9 páginas, 3 tablas, 1 figura.
Publisher version (URL)http://dx.doi.org/10.1016/j.anifeedsci.2013.09.010
URIhttp://hdl.handle.net/10261/85454
DOI10.1016/j.anifeedsci.2013.09.010
ISSN0377-8401
Appears in Collections:(IGM) Artículos
Files in This Item:
File Description SizeFormat 
Bichi et al 2013_ANIFEE (post-print).pdf203,13 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.