Expression and nutritional regulation of lipogenic genes in mammary gland and adipose tissues of lactating goats

2005 ◽  
Vol 72 (2) ◽  
pp. 250-255 ◽  
Author(s):  
Laurence Bernard ◽  
Christine Leroux ◽  
Muriel Bonnet ◽  
Jacques Rouel ◽  
Patrice Martin ◽  
...  

While the effect of long-chain fatty acids on adipose tissue (AT) lipogenic activities has been described in non-lactating ruminants (Vernon, 1977), little is known about their effects on the mammary gland and the AT in lactating animals. However, in cows in mid lactation, duodenal rapeseed oil infusion decreased the rate of fatty acid (FA) synthesis in AT and increased milk yield of long-chain FA (18[ratio ]1, 18[ratio ]2 and 18[ratio ]3) and decreased medium-chain FA (14[ratio ]0 and 16[ratio ]0), suggesting a depressive effect of fat feeding on mammary lipid synthesis de novo (Chilliard et al. 1991). On the other hand, in goat species, the addition of vegetable lipids to the diet led to an increase in the milk fat content and yield (Chilliard et al. 2003) suggesting that the possible negative effect of long-chain FA on FA synthesis in the lactating mammary gland could be more than compensated by increasing the supply of FA brought to the mammary gland for milk synthesis. Elsewhere, AT from various anatomical sites are characterized by different FA composition in goat (Bas et al. 1987) together with different patterns of lipogenic gene expression in sheep (Barber et al. 2000). These results suggest that each AT site is characterized by a specific metabolism. However, in lactating ruminants, few data are available on the extent of expression and regulation of genes coding for lipogenic enzymes in AT. Therefore, the current study was performed in three lipogenic tissues of lactating goats, namely the mammary gland, an internal AT site (perirenal AT) and an external AT site (subcutaneous AT).

2013 ◽  
Vol 5 (3) ◽  
pp. 270-274 ◽  
Author(s):  
Anamaria COZMA ◽  
Doina MIERE ◽  
Lorena FILIP ◽  
Sanda ANDREI ◽  
Roxana BANC ◽  
...  

Milk fat and its fatty acid profile are important determinants of the technological, sensorial, and nutritional properties of milk and dairy products. The two major processes contributing to the presence of fatty acids in ruminant milk are the mammary lipogenesis and the lipid metabolism in the rumen. Among fatty acids, 4:0 to 12:0, almost all 14:0 and about a half of 16:0 in milk fat derive from de novo synthesis within the mammary gland. De novo synthesis utilizes as precursors acetate and butyrate produced through carbohydrates ruminal fermentation and involves acetyl-CoA carboxylase and fatty acid synthetase as key enzymes. The rest of 16:0 and all of the long-chain fatty acids derive from mammary uptake of circulating lipoproteins and nonesterified fatty acids that originate from digestive absorption of lipids and body fat mobilization. Further, long-chain fatty acids as well as medium-chain fatty acids entering the mammary gland can be desaturated via Δ-9 desaturase, an enzyme that acts by adding a cis-9-double bond on the fatty acid chain. Moreover, ruminal biohydrogenation of dietary unsaturated fatty acids results in the formation of numerous fatty acids available for incorporation into milk fat. Ruminal biohydrogenation is performed by rumen microbial population as a means of protection against the toxic effects of polyunsaturated fatty acids. Within the rumen microorganisms, bacteria are principally responsible for ruminal biohydrogenation when compared to protozoa and anaerobic fungi.


Genes ◽  
2020 ◽  
Vol 11 (11) ◽  
pp. 1357
Author(s):  
Yongliang Fan ◽  
Ziyin Han ◽  
Xubin Lu ◽  
Huimin Zhang ◽  
Abdelaziz Adam Idriss Arbab ◽  
...  

The concentration of bovine milk fat changes regularly with lactation stages. In particular, milk fat percentage is higher in late lactation than mid lactation. Furthermore, milk fat composition is highly subject to a few genes. Thus, transcriptome sequencing was performed to explore the expression patterns of differentially-expressed genes (DEGs) in the parenchymal mammary gland of Holstein dairy cows between mid and late lactation. The 725 DEGs were screened (fold change > 2 and p-value < 0.05), and the peroxisome proliferator-activated receptor (PPAR) signaling pathway associated with lipid synthesis had a significant variation between the two periods (p-value < 0.05). The activation of the PPAR signal pathway may a key factor in the increasing of milk fat content in late lactation compared to mid lactation. Acyl-CoA synthetase long-chain family member 4 (ACSL4), a member of the PPAR signaling pathway, was upregulated in late lactation compared to mid lactation (p < 0.05). ACSL4 catalyzes the activation of long-chain fatty acids for cellular lipid synthesis. However, it remains uncertain that the molecular mechanism of milk fat synthesis is regulated by ACSL4 in dairy cows. Subsequently, the function verification of ACSL4 was performed in bovine mammary epithelial cells (BMECs). The upregulated expression of ACSL4 was accompanied by the increase of the concentration of intracellular triglycerides, whereas knockdown of ACSL4 decreased the concentration of intracellular triglycerides, which demonstrated that ACSL4 plays an important role in modulating milk fat synthesis. In conclusion, the results displayed that ACSL4 expression regulates triglyceride metabolism in ruminant mammary cells.


2000 ◽  
Vol 25 ◽  
pp. 201-223 ◽  
Author(s):  
J.J. Murphy

AbstractMilk fat consists of approximately 960-980 g of triacylglycerol, 20-25 g of 1,2-diacylglycerol, 10 g of phospholipid, 5g of cholesterol and very small quantities of free fatty acids and monoacylglycerol per kg. There are three stages in milk fat biosynthesis: the accumulation of fatty acids in the mammary cells through de-novo synthesis or absorption from the blood stream, triacylglycerol construction and fat globule assembly and secretion. Fatty acids in mammary secretory cells arise from two sources. Those having between 4 and 14 carbon atoms are synthesised de-novo in the mammary gland whereas those with 18 carbon atoms are of dietary origin and are absorbed from the blood stream. Palmitic acid (16 carbon atoms) is supplied almost equally from the diet and de-novo synthesis. In ruminants the principal sources of carbon for fatty acid synthesis are acetic acid and b-hydroxybutyrate.Alteration of milk fat concentration is achieved by changimore spreadable butter. Monounsaturated fatty acids in the diet have been shown to have beneficial effects on the plasma lipoprotein indicators of coronary heart disease risk. From a human nutrition point of view it could be beneficial to incorporate the long chain omega-3 fatty acids, eicosapentanoic (EPA, C20:5) and docosahexanoic (C22:6) acids, into milk fat. The principal source of these fatty acids is fish oil but research to date indicates that their transfer into milk fat is inefficient. Conjugated linoleic acid (CLA) is a collective term describing one or more positional and geometric isomers of linoleic acid (cis-9, cis-12 C18:2). CLA has been shown to have anticarcinogenic activity, antiatherogenic activity, an ability to reduce the catabolic effects of immune stimulation and an ability to enhance growth promotion and reduce body fat. It is present in ruminant milk and meat as a result of biohydrogenation in the rumen where it is an intermediate. Its concentration in bovine milk fat is influenced by dietary factors such as pasture feeding and supplementation with full fat oilseeds. Two other components of bovine milk fat which have been shown to have anticarcinogenic properties are butyric acid and sphingomyelin and their concentration warrants further study. It is likely that research will continue into means of manipulating both the content and composition of milk fat but ultimately the adoption of any of the strategies in practice is likely to depend on strong economic or consumer imperatives.ng either the level of de-novo synthesis in the mammary gland or the supply of long chain fatty acids in the diet. Dietary factors that affect the supply of acetic acid from the rumen for de-novo synthesis include fibre quantity and quality, forage to concentrate ratio, buffer inclusion, concentrate composition and concentrate feeding frequency. The effects of fat supplements on fat concentration are variable. In general, feeding rumen protected fat increases milk fat concentration whereas moderate amounts of unprotected unsaturated fat tend to decrease it.Most nutritional manipulation has been directed at increasing the proportion of unsaturated fatty acids in milk fat in order to enhance its appeal to the consumer and to produce a softer fat. A more spreadable butter could be produced from such fat thus overcoming a major criticism of conventional butter.If unsaturated fatty acids are fed to ruminants in an unprotected form rumen microbial digestion can be impaired and the unsaturated fatty acids are extensively saturated in the rumen. One strategy to overcome this is to include unsaturated fatty acids in a form protected from microbial digestion in the rumen. This resulted in the production of polyunsaturated milk fat from which a low melting point butter was produced. This product was predisposed to oxidative deterioration. More recently whole oilseeds have been fed to dairy cows. The unsaturated 18-carbon fatty acids in these seeds are hydrogenated in the rumen but the activity of a D-9 desaturase in the mammary gland and to a lesser extent the intestine converts the stearic acid (C18:0) to the monounsaturated fatty acid, oleic acid (C18:1). Milk fat rich in oleic acid is softer than conventional milk fat allowing the manufacture of a more spreadable butter. Monounsaturated fatty acids in the diet have been shown to have beneficial effects on the plasma lipoprotein indicators of coronary heart disease risk.From a human nutrition point of view it could be beneficial to incorporate the long chain omega-3 fatty acids, eicosapentanoic (EPA, C20:5) and docosahexanoic (C22:6) acids, into milk fat. The principal source of these fatty acids is fish oil but research to date indicates that their transfer into milk fat is inefficient. Conjugated linoleic acid (CLA) is a collective term describing one or more positional and geometric isomers of linoleic acid (cis-9, cis-12 C18:2). CLA has been shown to have anticarcinogenic activity, antiatherogenic activity, an ability to reduce the catabolic effects of immune stimulation and an ability to enhance growth promotion and reduce body fat. It is present in ruminant milk and meat as a result of biohydrogenation in the rumen where it is an intermediate. Its concentration in bovine milk fat is influenced by dietary factors such as pasture feeding and supplementation with full fat oilseeds. Two other components of bovine milk fat which have been shown to have anticarcinogenic properties are butyric acid and sphingomyelin and their concentration warrants further study.It is likely that research will continue into means of manipulating both the content and composition of milk fat but ultimately the adoption of any of the strategies in practice is likely to depend on strong economic or consumer imperative.


Endocrinology ◽  
2006 ◽  
Vol 147 (9) ◽  
pp. 4048-4055 ◽  
Author(s):  
William B. Kinlaw ◽  
Jennifer L. Quinn ◽  
Wendy A. Wells ◽  
Christopher Roser-Jones ◽  
Joel T. Moncur

Spot 14 (S14) is a nuclear protein that communicates the status of dietary fuels and fuel-related hormones to genes required for long-chain fatty acid synthesis. In mammary gland, S14 is important for both epithelial proliferation and milk fat production. The S14 gene is amplified in some breast cancers and is strongly expressed in most. High expression of S14 in primary invasive breast cancer is conspicuously predictive of recurrence. S14 mediates the induction of lipogenesis by progestin in breast cancer cells and accelerates their growth. Conversely, S14 knockdown impairs de novo lipid synthesis and causes apoptosis. We found that breast cancer cells do not express lipoprotein lipase (LPL) and hypothesize that they do not have access to circulating lipids unless the local environment supplies it. This may explain why primary breast cancers with low S14 do not survive transit from the LPL-rich mammary fat pad to areas devoid of LPL, such as lymph nodes, and thus do not appear as distant metastases. Thus, S14 is a marker for aggressive breast cancer and a potential target as well. Future effort will center on validation of S14 as a therapeutic target and producing antagonists of its action.


2019 ◽  
Vol 123 (6) ◽  
pp. 610-618 ◽  
Author(s):  
E. C. Sandri ◽  
K. J. Harvatine ◽  
D. E. Oliveira

AbstractTrans-10, cis-12 conjugated linoleic acid (CLA) decreases milk fat synthesis in lactating sows and involves, at least in part, the down-regulation of lipogenic genes. The objective was to evaluate the effect of CLA on milk composition and lipogenic gene expression. Twenty multiparous sows were randomly assigned to one of the two treatments for 18 d (from day 7 to day 25 of lactation): (1) control (no CLA added) and (2) 1 % of CLA mixed into the ration. CLA treatment decreased milk fat and protein content by 20 % (P = 0·004) and 11 % (P = 0·0001), respectively. However, piglet weight did not differ between treatments (P = 0·60). Dietary CLA increased the concentration of SFA in milk fat by 16 % (P < 0·0001) and decreased MUFA by 17·6 % (P < 0·0001). In the mammary gland, CLA reduced gene expression of acetyl-CoA carboxylase-α by 37 % (P = 0·003), fatty acid synthase by 64 % (P = 0·002), stearoyl-CoA desaturase 1 by 52 % (P = 0·003), lipoprotein lipase by 26 % (P = 0·03), acyl glycerol phosphate acyltransferase 6 by 15 % (P = 0·02) and diacylglycerol acyltransferase 1 by 27 % (P = 0·02), whereas the expression of fatty acid binding protein 3 was not altered by CLA treatment (P = 0·09). Mammary expression of casein-β and α-lactalbumin was reduced by CLA by 68 % (P = 0·0004) and 62 % (P = 0·005), respectively. Additionally, CLA had no effect on the expression of lipogenic genes evaluated in adipose tissue. In summary, CLA reduced milk fat content without negatively affecting litter performance and it affected mammary expression of genes involved in all lipogenic pathways studied.


2002 ◽  
Vol 69 (4) ◽  
pp. 511-520 ◽  
Author(s):  
PIERRE LACASSE ◽  
JOHN J. KENNELLY ◽  
LOUIS DELBECCHI ◽  
CHARAF E. AHNADI

Thirty Holstein cows in mid-lactation (158±20 DIM) were given a total mixed ration based on grass silage, maize silage and rolled barley. After a preliminary period of 1 week, this diet was supplemented with nothing (control), unprotected fish oil (3.7% of dry matter, DM), or two levels of glutaraldehyde-protected microcapsules of fish oil (1.5% and 3.0% of DM, respectively). Unprotected and protected supplements contained, respectively, 74% and 58% of DM as lipids. Cows given the unprotected supplement reduced their feed intake by >25%. Consequently, these cows lost body weight and produced less milk. DM intake, body weight, and milk yield were unaffected by protected fish oil. Fish oil reduced both milk fat and protein percentages, and decreased the proportion of short-chain fatty acids, stearic, and oleic acids in milk fat. Milk trans C18[ratio ]1 fatty acids increased in cows given both unprotected and protected fish oil. Milk fat content of very-long-chain n3 polyunsaturated fatty acids, including C20[ratio ]5 and C22[ratio ]6, increased with fish oil in the diet. Accordingly, the peroxide index increased and a taste panel was able to detect unusual taste in milk from cows consuming the higher level of protected fish oil and disliked the milk from cows given unprotected fish oil. In conclusion, when lactating cows consumed fish oil, milk concentration of long-chain n3 fatty acids increased and mammary de novo synthesis of fatty acids decreased, but milk yield and milk protein content were reduced, and the milk was more susceptible to oxidation and its taste was adversely affected.


Endocrinology ◽  
2005 ◽  
Vol 146 (8) ◽  
pp. 3343-3350 ◽  
Author(s):  
Qihong Zhu ◽  
Grant W. Anderson ◽  
Gregory T. Mucha ◽  
Elizabeth J. Parks ◽  
Jennifer K. Metkowski ◽  
...  

Abstract We generated a Spot 14 null mouse to assess the role of Spot 14 in de novo lipid synthesis and report the Spot 14 null mouse exhibits a phenotype in the lactating mammary gland. Spot 14 null pups nursed by Spot 14 null dams gain significantly less weight than wild-type pups nursed by wild-type dams. In contrast, Spot 14 null pups nursed by heterozygous dams show similar weight gain to wild-type littermates. We found the triglyceride content in Spot 14 null milk is significantly reduced. We demonstrate this reduction is the direct result of decreased de novo lipid synthesis in lactating mammary glands, corroborated by a marked reduction of medium-chain fatty acids in the triglyceride pool. Importantly, the reduced lipogenic rate is not associated with significant changes in the activities or mRNA of key lipogenic enzymes. Finally, we report the expression of a Spot 14-related gene in liver and adipose tissue, which is absent in the lactating mammary gland. We suggest that expression of both the Spot 14 and Spot 14-related proteins is required for maximum efficiency of de novo lipid synthesis in vivo and that these proteins impart a novel mechanism regulating de novo lipogenesis.


1974 ◽  
Vol 41 (2) ◽  
pp. 175-191 ◽  
Author(s):  
G. H. Smith ◽  
S. McCarthy ◽  
J. A. F. Rook

SummaryThe relative importance of β-hydroxybutyric acid (BHBA) and acetate as precursors for milk-fat synthesis was studied in lactating goats by infusing separately tracer quantities of [3−14C]DL-BHBA and [1−14C]acetate into the jugular vein, and [1−14C]butyrate into the portal vein. The concentrations and specific radioactivities of blood plasma constituents, the yields and specific radioactivities of individual milk fatty acids and the relative radioactivities of individual carbon atoms of milk fatty acids were determined.The infusion of [1−14C]butyrate resulted in the appearance of labelled BHBA in the blood plasma which behaved almost identically with infused [14C]BHBA as a precursor for milk fatty acids.The relative radioactivity of carbon atoms of the fatty acids of milk fat following the infusions provided direct evidence that BHBA had provided an intact 4-carbon unit at the methyl end of each fatty-acid chain. Acetate provided 2-carbon units both for the elongation of the 4-carbon units and for complete de novo synthesis. BHBA also provided 2-carbon units which behaved in a similar fashion to those from acetate.Acetate and BHBA together accounted for all of the C4–C12 acids of milk fat, about 75% of the C14, 45% of the C16 and 10% of the C18.The total contributions of the various precursors to the fatty acids of milk fat were: acetate 42%, BHBA 9·4% and other plasma precursors (by difference) 48·6%.


2007 ◽  
Vol 74 (2) ◽  
pp. 160-166 ◽  
Author(s):  
Amanda Aparecida Hayashi ◽  
Sérgio Raposo de Medeiros ◽  
Marina Hojaij Carvalho ◽  
Dante Pazzanese Duarte Lanna

Conjugated linoleic acid (CLA) has a range of biological properties, including effects on lipid metabolism, milk and body composition in animals. This study investigated the effects of dietary CLA on lactating rats and development of the suckling pups. Dams were fed either a control diet or the same diet supplemented with 25 g/kg of a fat supplement containing 540 g CLA/kg (final concentration of 13·5 g CLA/kg diet) from parturition to the 15th day post-partum. The CLA mixture used in this study contained the following isomers (per 100 g): cis-9, trans-11 (24 g); cis-10, trans-12 (35 g); cis-8, trans-10 (15 g); cis-11, trans-13 (17 g) and others (9 g). On d 15 post partum, CLA supplementation reduced milk fat content by 33% and pup growth by 21%. The milk fatty acid profile, with decreased content of short and medium chain acids, suggests CLA inhibition was more pronounced for de novo lipid synthesis. Consistent with these results, activities of fatty acid synthase, glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase were reduced by CLA treatment in the mammary gland and liver. In contrast, the activity of NADP-malate dehydrogenase was unchanged.


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