Is hepatic lipid metabolism of beef cattle influenced by breed and dietary silage level?
da Costa et al. BMC Veterinary Research 2014, 10:65
http://www.biomedcentral.com/1746-6148/10/65
RESEARCH ARTICLE
Open Access
Is hepatic lipid metabolism of beef cattle
influenced by breed and dietary silage level?
Ana Sofia Henriques da Costa1, Rui José Branquinho Bessa1, Virgínia Maria Rico Pires1, Eva Alves Rolo1,
Rui Manuel Amaro Pinto2, Carlos Mendes Godinho Andrade Fontes1 and José António Mestre Prates1*
Abstract
Background: In ruminants, unsaturated dietary fatty acids are biohydrogenated in the rumen and are further
metabolised in various tissues, including liver, which has an important role in lipid and lipoprotein
metabolism. Therefore, manipulation of muscle fatty acid composition should take into account liver
metabolism. In the present study, the influence of breed and diet on liver lipid composition and gene
expression was investigated in order to clarify the role of this organ in the lipid metabolism of ruminants.
Forty purebred young bulls from two phylogenetically distant autochthonous cattle breeds, Alentejana and
Barrosã, were assigned to two different diets (low vs. high silage) and slaughtered at 18 months of age. Liver
fatty acid composition, mRNA levels of enzymes and transcription factors involved in lipid metabolism, as well
as the plasma lipid profile, were assessed.
Results: In spite of similar plasma non-esterified fatty acids levels, liver triacylglycerols content was higher in
Barrosã than in Alentejana bulls. Moreover, the fatty acid composition of liver was clearly distinct from the
remaining tissues involved in fatty acid metabolism of ruminants, as shown by Principal Components Analysis.
The hepatic tissue is particularly rich in α-linolenic acid and their products of desaturation and elongation.
Results indicate that DGAT1, ELOVL2, FADS1 and FADS2 genes influence the fatty acid composition of the liver
the most. Moreover, genes such as DGAT1 and ELOVL2 appear to be more sensitive to genetic background
than to dietary manipulation, whereas genes encoding for desaturases, such as FADS1, appear to be
modulated by dietary silage level.
Conclusions: Our results indicate that liver plays an important role in the biosynthesis of n-3 LC-PUFA. It is
also suggested that dietary silage level influences the hepatic fatty acid metabolism in a breed-dependent
manner, through changes in the expression of genes encoding for enzymes associated with the desaturation
and elongation pathway. The importance of devising custom-made feeding strategies taking into account the
genetic background is, therefore, stressed by the results from this experiment.
Keywords: Liver, Beef cattle, Fatty acids, Gene expression
Background
Despite the predominant role of adipose tissue in ruminant’s de novo fatty acid synthesis, the liver also plays an
important role in ruminant lipid metabolism [1]. This
organ carries out central metabolic functions in various
aspects of lipid and lipoprotein metabolism, such as uptake, oxidation and metabolic conversion of non-esterified
* Correspondence:
1
CIISA, Faculdade de Medicina Veterinária, Universidade de Lisboa, Av. da
Universidade Técnica, Pólo Universitário do Alto da Ajuda, 1300-477 Lisboa,
Portugal
Full list of author information is available at the end of the article
fatty acids (NEFA), synthesis of cholesterol and phospholipids, and formation and secretion of specific classes of lipoproteins [1]. The ruminants’ liver removes little or no
triacylglycerols from blood lipoproteins [2]. Uptake of
NEFA is the predominant route by which fatty acids are
supplied to the liver [3] and, thus, plasma lipid fatty acid
composition should influence the liver fatty acid metabolism and composition [2]. Consequently, the regulation of
these liver metabolic pathways may affect fatty acid deposition into lipids of ruminant products [4].
Interest in n-3 long-chain polyunsaturated fatty acids
(n-3 LC-PUFA) has increased since it was found that
© 2014 da Costa et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative
Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and
reproduction in any medium, provided the original work is properly credited.
da Costa et al. BMC Veterinary Research 2014, 10:65
http://www.biomedcentral.com/1746-6148/10/65
their consumption in most Western populations, particularly those of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), is sub-optimal for protection
against the most prevalent chronic diseases [5]. In grazing ruminants, α-linolenic acid content of muscles increases with the concomitant increase in n-3 LC-PUFA
contents [6]. In contrast, although the addition of linseed
to ruminant diets [7,8] increases the α-linolenic acid content of muscles, the n-3 LC-PUFA levels stay unchanged
or increase only slightly. In fact, Bessa et al. [9] reported
that lucerne supplementation with linseed oil promoted an
increase in ALA coupled with a decrease in n-3 LC-PUFA
in lambs, when compared to the control diet (lucerne
only). According to the authors, these results suggest the
inhibition of α-linolenic acid metabolism by vegetable oils
rich in n-3 PUFA. Therefore, the abundance of n-3 LCPUFA in ruminants’ tissues appears to depend not only on
dietary n-3 PUFA but also on their endogenous synthesis
via elongation and desaturation of dietary n-3 PUFA.
The biosynthesis of DHA from α-linolenic acid is performed through alternating steps of desaturation and
elongation, followed by a final step of peroxisomal βoxidation. This metabolic pathway involves two desaturases (Δ5 and Δ6 desaturases), two elongases (elongases
2 and 5) and enzymes of the peroxisomal β-oxidation [10].
The activity of these enzymes is currently regarded as
potential limiting steps in this biosynthesis, possibly in a
tissue dependent manner. However, recent studies addressed the role of the liver in ruminants’ lipid metabolism, either using in vitro experiments [4] or in vivo assays
[11]. These experiments raised some interesting clues on
hepatic lipid metabolism, namely the extensive catabolism
of α-linolenic acid [4] and the low or negligible expression
level of genes encoding for enzymes of fatty acid desaturation and elongation [11]. Therefore, the role of bovine
liver, as a central metabolic organ, on lipid metabolism remains to be elucidated.
An experiment with 40 young bulls from two genetically
diverse beef cattle breeds, Alentejana and Barrosã, fed
either high (70% silage/30% concentrate) or low (30% silage/70% concentrate) silage diets was carried out by our
group to study the breed and diet effects on lipid metabolism. Previous reports from this experiment [12,13] showed
that these breeds have a distinct response to the variation
in dietary silage level, as assessed by the fatty acid composition and the mRNA levels of key lipogenic factors of
the main fat depots and muscle. Bearing this in mind, as
well as (...truncated)