Does Grass Fed Beef Have Amoega 3

  • Journal List
  • Nutr J
  • v.ix; 2010
  • PMC2846864

A review of fatty acid profiles and antioxidant content in grass-fed and grain-fed beefiness

Cynthia A Daley

1Higher of Agriculture, California Land Academy, Chico, CA, USA

Amber Abbott

oneCollege of Agriculture, California State University, Chico, CA, USA

Patrick S Doyle

iHigher of Agriculture, California Country University, Chico, CA, Usa

Glenn A Nader

2University of California Cooperative Extension Service, Davis, CA, United states of america

Stephanie Larson

2University of California Cooperative Extension Service, Davis, CA, U.s.a.

Received 2009 Jul 29; Accepted 2010 Mar ten.

Abstract

Growing consumer interest in grass-fed beef products has raised a number of questions with regard to the perceived differences in nutritional quality between grass-fed and grain-fed cattle. Enquiry spanning three decades suggests that grass-based diets can significantly better the fat acid (FA) composition and antioxidant content of beef, admitting with variable impacts on overall palatability. Grass-based diets have been shown to raise full conjugated linoleic acid (CLA) (C18:ii) isomers, trans vaccenic acid (TVA) (C18:1 t11), a precursor to CLA, and omega-iii (due north-3) FAs on a m/k fat basis. While the overall concentration of total SFAs is non different between feeding regimens, grass-finished beefiness tends toward a higher proportion of cholesterol neutral stearic FA (C18:0), and less cholesterol-elevating SFAs such equally myristic (C14:0) and palmitic (C16:0) FAs. Several studies suggest that grass-based diets elevate precursors for Vitamin A and E, besides as cancer fighting antioxidants such as glutathione (GT) and superoxide dismutase (SOD) activity as compared to grain-fed contemporaries. Fatty conscious consumers will also prefer the overall lower fat content of a grass-fed beef product. All the same, consumers should exist aware that the differences in FA content volition also give grass-fed beef a distinct grass flavor and unique cooking qualities that should exist considered when making the transition from grain-fed beef. In improver, the fatty from grass-finished beef may have a yellow advent from the elevated carotenoid content (precursor to Vitamin A). It is also noted that grain-fed beef consumers may attain similar intakes of both n-3 and CLA through the consumption of higher fat grain-fed portions.

Review Contents

1. Introduction

2. Fatty acid contour in grass-fed beef

three. Impact of grass-finishing on omega-3 fatty acids

four. Touch on of grass-finishing on conjugated linoleic acid (CLA) and trans-vaccenic acid (TVA)

five. Bear upon of grass-finishing on β-carotenes/carotenoids

half dozen. Touch of grass-finishing on α-tocopherol

vii. Impact of grass-finishing on GT & SOD activeness

8. Touch of grass-finishing on flavor and palatability

9. Conclusion

10. References

Introduction

In that location is considerable back up among the nutritional communities for the diet-heart (lipid) hypothesis, the idea that an imbalance of dietary cholesterol and fats are the master crusade of atherosclerosis and cardiovascular affliction (CVD) [ane]. Wellness professionals earth-wide recommend a reduction in the overall consumption of SFAs, trans-fatty acids (TAs) and cholesterol, while emphasizing the need to increase intake of north-3 polyunsaturated fats [1,2]. Such wide sweeping nutritional recommendations with regard to fat consumption are largely due to epidemiologic studies showing stiff positive correlations between intake of SFA and the incidence of CVD, a status believed to result from the concomitant ascension in serum low-density-lipoprotein (LDL) cholesterol as SFA intake increases [iii,iv]. For example, it is generally accepted that for every ane% increment in free energy from SFA, LDL cholesterol levels reportedly increase past i.three to one.7 mg/dL (0.034 to 0.044 mmol/L) [five-7].

Broad promotion of this correlative data spurred an anti-SFA campaign that reduced consumption of dietary fats, including about animal proteins such as meat, dairy products and eggs over the last 3 decades [8], indicted on their relatively high SFA and cholesterol content. Even so, more than recent lipid research would suggest that not all SFAs have the same impact on serum cholesterol. For instance, lauric acrid (C12:0) and myristic acrid (C14:0), accept a greater total cholesterol raising effect than palmitic acid (C16:0), whereas stearic acrid (C18:0) has a neutral effect on the concentration of full serum cholesterol, including no apparent affect on either LDL or HDL. Lauric acrid increases total serum cholesterol, although it also decreases the ratio of total cholesterol:HDL because of a preferential increase in HDL cholesterol [5,7,nine]. Thus, the individual fatty acid profiles tend to be more than instructive than broad lipid classifications with respect to subsequent impacts on serum cholesterol, and should therefore be considered when making dietary recommendations for the prevention of CVD.

Conspicuously the lipid hypothesis has had broad sweeping impacts; non only on the way we eat, but also on the way food is produced on-farm. Indeed, changes in animal breeding and genetics have resulted in an overall leaner beef product[10]. Preliminary examination of diets containing today's leaner beefiness has shown a reduction in serum cholesterol, provided that beef consumption is limited to a 3 ounce portion devoid of all external fat [11]. O'Dea's piece of work was the first of several studies to show today'due south leaner beef products can reduce plasma LDL concentrations in both normal and hyper-cholesterolemic subjects, theoretically reducing risk of CVD [12-xv].

Beyond changes in genetics, some producers have also altered their feeding practices whereby reducing or eliminating grain from the ruminant diet, producing a production referred to as "grass-fed" or "grass-finished". Historically, most of the beef produced until the 1940's was from cattle finished on grass. During the 1950's, considerable enquiry was done to improve the efficiency of beefiness production, giving nativity to the feedlot manufacture where loftier energy grains are fed to cattle as means to subtract days on feed and meliorate marbling (intramuscular fatty: International monetary fund). In improver, U.S. consumers have grown accustomed to the taste of grain-fed beef, generally preferring the flavor and overall palatability afforded by the higher energy grain ration[16]. However, changes in consumer demand, coupled with new research on the issue of feed on nutrient content, take a number of producers returning to the pastoral arroyo to beef production despite the inherent inefficiencies.

Research spanning three decades suggests that grass-only diets can significantly modify the fatty acid limerick and improve the overall antioxidant content of beef. It is the intent of this review, to synthesize and summarize the information currently bachelor to substantiate an enhanced nutrient merits for grass-fed beef products as well as to discuss the furnishings these specific nutrients have on man health.

Review of fatty acid profiles in grass-fed beef

Red meat, regardless of feeding regimen, is nutrient dumbo and regarded every bit an important source of essential amino acids, vitamins A, B6, B12, D, East, and minerals, including fe, zinc and selenium [17,18]. Along with these important nutrients, meat consumers also ingest a number of fats which are an important source of energy and facilitate the absorption of fat-soluble vitamins including A, D, East and Thousand. According to the ADA, creature fats contribute approximately 60% of the SFA in the American diet, virtually of which are palmitic acid (C16:0) and stearic acid (C18:0). Stearic acid has been shown to have no net impact on serum cholesterol concentrations in humans[17,xix]. In addition, xxx% of the FA content in conventionally produced beef is composed of oleic acid (C18:1) [20], a monounsaturated FA (MUFA) that elicits a cholesterol-lowering effect among other healthful attributes including a reduced adventure of stroke and a significant decrease in both systolic and diastolic blood pressure in susceptible populations [21].

Be that as it may, changes in finishing diets of conventional cattle can alter the lipid profile in such a way every bit to amend upon this nutritional bundle. Although there are genetic, historic period related and gender differences among the various meat producing species with respect to lipid profiles and ratios, the effect of animal nutrition is quite significant [22]. Regardless of the genetic makeup, gender, age, species or geographic location, direct contrasts between grass and grain rations consistently demonstrate significant differences in the overall fatty acid profile and antioxidant content found in the lipid depots and body tissues [22-24].

Table 1 summarizes the saturated fat acid assay for a number of studies whose objectives were to contrast the lipid profiles of cattle fed either a grain or grass diets [25-31]. This tabular array is express to those studies utilizing the longissimus dorsi (loin eye), thereby standardizing the contrasts to similar cuts within the carcass and limits the comparisons to cattle between 20 and xxx months of age. Unfortunately, not all studies study data in similar units of measure out (i.e., k/thousand of fatty acid), so direct comparisons between studies are non possible.

Tabular array 1

Comparison of hateful saturated fatty acid composition (expressed as mg/1000 of fat acrid or equally a % of total lipid) between grass-fed and grain-fed cattle.

Fatty Acrid

Writer, publication year, breed, treatment C12:0 lauric C14:0 myristic C16:0 palmitic C18:0 stearic C20:0 arachidic Total SFA (units equally specified) Total lipid (units every bit specified)
Alfaia, et al., 2009, Crossbred steers grand/100 g lipid
 Grass 0.05 1.24* 18.42* 17.54* 0.25* 38.76 9.76* mg/thousand muscle
 Grain 0.06 i.84* 20.79* 14.96* 0.19* 39.27 13.03* mg/k muscle
Leheska, et al., 2008, Mixed cattle 1000/100 g lipid
 Grass 0.05 2.84* 26.9 17.0* 0.13* 48.8* two.8* % of muscle
 Grain 0.07 iii.45* 26.3 xiii.two* 0.08* 45.1* four.four* % of muscle
Garcia et al., 2008, Angus X-bred steers % of total FA
 Grass na two.19 23.ane 13.1* na 38.4* two.86* %International monetary fund
 Grain na 2.44 22.1 10.8* na 35.iii* 3.85* %IMF
Ponnampalam, et al., 2006, Angus steers mg/100 g muscle tissue
 Grass na 56.9* 508* 272.8 na 900* 2.12%* % of muscle
 Grain na 103.7* 899* 463.3 na 1568* three.61%* % of musculus
Nuernberg, et al., 2005, Simmental bulls % of total intramuscular fat reported equally LSM
 Grass 0.04 i.82 22.56* 17.64* na 43.91 i.51* % of muscle
 Grain 0.05 1.96 24.26* 16.80* na 44.49 2.61* % of muscle
Descalzo, et al., 2005 Crossbred Steers % of full FA
 Grass na ii.2 22.0 19.1 na 42.8 two.vii* %IMF
 Grain na 2.0 25.0 eighteen.ii na 45.5 4.7* %IMF
Realini, et al., 2004, Hereford steers % fat acid within intramuscular fat
 Grass na i.64* 21.61* 17.74* na 49.08 1.68* % of muscle
 Grain na two.17* 24.26* 15.77* na 47.62 three.eighteen* % of muscle

*Indicates a significant difference (at least P < 0.05) between feeding regimens was reported within each respective written report. "na" indicates that the value was non reported in the original report.

Table 1 reports that grass finished cattle are typically lower in total fat as compared to grain-fed contemporaries. Interestingly, there is no consistent divergence in total SFA content between these two feeding regimens. Those SFA's considered to exist more detrimental to serum cholesterol levels, i.due east., myristic (C14:0) and palmitic (C16:0), were higher in grain-fed beef as compared to grass-fed contemporaries in sixty% of the studies reviewed. Grass finished meat contains elevated concentrations of stearic acrid (C18:0), the only saturated fat acrid with a internet neutral impact on serum cholesterol. Thus, grass finished beef tends to produce a more favorable SFA composition although little is known of how grass-finished beefiness would ultimately touch serum cholesterol levels in hyper-cholesterolemic patients as compared to a grain-fed beef.

Like SFA intake, dietary cholesterol consumption has also become an important issue to consumers. Interestingly, beef's cholesterol content is similar to other meats (beef 73; pork 79; lamb 85; chicken 76; and turkey 83 mg/100 one thousand) [32], and can therefore be used interchangeably with white meats to reduce serum cholesterol levels in hyper-cholesterolemic individuals[11,33]. Studies have shown that breed, diet and sex exercise non bear upon the cholesterol concentration of bovine skeletal musculus, rather cholesterol content is highly correlated to IMF concentrations[34]. Equally IMF levels rise, so goes cholesterol concentrations per gram of tissue [35]. Because pasture raised beef is lower in overall fatty [24-27,30], peculiarly with respect to marbling or IMF [26,36], information technology would seem to follow that grass-finished beef would be lower in overall cholesterol content although the data is very limited. Garcia et al (2008) study 40.3 and 45.eight grams of cholesterol/100 grams of tissue in pastured and grain-fed steers, respectively (P < 0.001) [24].

Interestingly, grain-fed beef consistently produces higher concentrations of MUFAs as compared to grass-fed beef, which include FAs such every bit oleic acid (C18:i cis-9), the main MUFA in beefiness. A number of epidemiological studies comparison affliction rates in different countries accept suggested an inverse association between MUFA intake and mortality rates to CVD [3,21]. Withal, grass-fed beef provides a higher concentration of TVA (C18:1 t11), an important MUFA for de novo synthesis of conjugated linoleic acid (CLA: C18:ii c-9, t-11), a potent anti-carcinogen that is synthesized within the body tissues [37]. Specific data relative to the health benefits of CLA and its biochemistry volition be detailed subsequently.

The important polyunsaturated fatty acids (PUFAs) in conventional beef are linoleic acrid (C18:2), blastoff-linolenic acid (C18:3), described as the essential FAs, and the long-concatenation fatty acids including arachidonic acid (C20:4), eicosapentaenoic acrid (C20:5), docosanpetaenoic acid (C22:5) and docosahexaenoic acid (C22:6) [38]. The significance of nutrition on fatty acid composition is conspicuously demonstrated when profiles are examined by omega half dozen (n-6) and omega 3 (n-three) families. Tabular array 2 shows no meaning change to the overall concentration of north-6 FAs betwixt feeding regimens, although grass-fed beef consistently shows a college concentrations of n-iii FAs as compared to grain-fed contemporaries, creating a more than favorable n-6:north-3 ratio. There are a number of studies that report positive effects of improved n-3 intake on CVD and other wellness related bug discussed in more detail in the next department.

Table 2

Comparison of hateful polyunsatured fatty acid composition (expressed equally mg/1000 of fatty acid or as a % of total lipid) betwixt grass-fed and grain-fed cattle.

Fatty Acrid

Author, publication year, breed, treatment C18:1 t11 Vaccenic Acid C18:2 n-half dozen Linoleic Total CLA C18:3 north-three Linolenic C20:5n-three EPA C22:5n-iii DPA C22:6n-three DHA Full PUFA Total MUFA Full northward-6 Total n-iii n-6/n-3 ratio
Alfaia, et al., 2009, Crossbred steers g/100 g lipid
 Grass 1.35 12.55 5.14* v.53* 2.13* two.56* 0.xx* 28.99* 24.69* 17.97* 10.41* 1.77*
 Grain 0.92 11.95 2.65* 0.48* 0.47* 0.91* 0.11* 19.06* 34.99* 17.08 1.97* eight.99*
Leheska, et al., 2008, Mixed cattle g/100 g lipid
 Grass 2.95* 2.01 0.85* 0.71* 0.31 0.24* na 3.41 42.five* ii.xxx one.07* two.78*
 Grain 0.51* 2.38 0.48* 0.13* 0.19 0.06* na 2.77 46.2* 2.58 0.19* 13.6*
Garcia, et al., 2008, Angus steers % of total FAs
 Grass iii.22* 3.41 0.72* 1.30* 0.52* 0.seventy* 0.43* vii.95 37.7* five.00* 2.95* 1.72*
 Grain ii.25* 3.93 0.58* 0.74* 0.12* 0.30* 0.14* 9.31 forty.8* 8.05* 0.86* 10.38*
Ponnampalam, et al., 2006, Angus steers mg/100 g muscle tissue
 Grass na 108.8* xiv.3 32.4* 24.5* 36.v* 4.2 na 930* 191.six 97.6* 1.96*
 Grain na 167.iv* sixteen.1 fourteen.9* 13.one* 31.half dozen* 3.7 na 1729* 253.8 63.three* iii.57*
Nuernberg, et al., 2005, Simmental bulls % of total fat acids
 Grass na 6.56 0.87* two.22* 0.94* ane.32* 0.17* 14.29* 56.09 9.80 four.70* 2.04*
 Grain na five.22 0.72* 0.46* 0.08* 0.29* 0.05* 9.07* 55.51 7.73 0.xc* eight.34*
Descalzo, et al., 2005, Crossbred steers % of total FAs
 Grass 4.2* five.4 na i.4* tr 0.half dozen tr 10.31* 34.17* seven.4 ii.0 three.72*
 Grain two.8* 4.7 na 0.seven* tr 0.4 tr 7.29* 37.83* half dozen.3 ane.1 5.73*
Realini, et al., 2004, Hereford steers % fatty acid inside intramuscular fat
 Grass na 3.29* 0.53* one.34* 0.69* 1.04* 0.09 nine.96* xl.96* na na one.44*
 Grain na 2.84* 0.25* 0.35* 0.30* 0.56* 0.09 6.02* 46.36* na na 3.00*

* Indicates a meaning difference (at to the lowest degree P < 0.05) between feeding regimens within each respective study reported. "na" indicates that the value was not reported in the original written report. "tr" indicates trace amounts detected.

Review of Omega-iii: Omega-half dozen fatty acrid content in grass-fed beefiness

In that location are ii essential fat acids (EFAs) in homo diet: α-linolenic acid (αLA), an omega-3 fatty acid; and linoleic acid (LA), an omega-6 fatty acrid. The human being body cannot synthesize essential fat acids, still they are disquisitional to human health; for this reason, EFAs must be obtained from nutrient. Both αLA and LA are polyunsaturated and serve equally precursors of other important compounds. For instance, αLA is the precursor for the omega-iii pathway. Also, LA is the parent fat acrid in the omega-6 pathway. Omega-3 (northward-iii) and omega-6 (n-6) fatty acids are 2 divide distinct families, even so they are synthesized by some of the same enzymes; specifically, delta-v-desaturase and delta-6-desaturase. Excess of 1 family unit of FAs can interfere with the metabolism of the other, reducing its incorporation into tissue lipids and altering their overall biological furnishings [39]. Figure ane depicts a schematic of northward-6 and n-3 metabolism and elongation within the body [forty].

An external file that holds a picture, illustration, etc.  Object name is 1475-2891-9-10-1.jpg

Linoleic (C18:2n-6) and α-Linolenic (C18:3n-3) Acid metabolism and elongation. (Adapted from Simopoulos et al., 1991)

A salubrious diet should consist of roughly ane to four times more omega-6 fatty acids than omega-three fatty acids. The typical American nutrition tends to contain 11 to xxx times more omega -6 fatty acids than omega -3, a miracle that has been hypothesized as a pregnant factor in the ascension rate of inflammatory disorders in the U.s.[40]. Table 2 shows significant differences in n-half-dozen:due north-3 ratios between grass-fed and grain-fed beef, with and overall average of 1.53 and 7.65 for grass-fed and grain-fed, respectively, for all studies reported in this review.

The major types of omega-3 fatty acids used past the body include: α-linolenic acid (C18:3n-3, αLA), eicosapentaenoic acid (C20:5n-3, EPA), docosapentaenoic acid (C22:5n-iii, DPA), and docosahexaenoic acid (C22:6n-3, DHA). Once eaten, the body converts αLA to EPA, DPA and DHA, albeit at depression efficiency. Studies generally hold that whole torso conversion of αLA to DHA is below 5% in humans, the majority of these long-chain FAs are consumed in the diet [41].

The omega-3 fatty acids were first discovered in the early 1970's when Danish physicians observed that Greenland Eskimos had an exceptionally low incidence of heart illness and arthritis despite the fact that they consumed a nutrition loftier in fat. These early studies established fish as a rich source of due north-3 fatty acids. More recent enquiry has established that EPA and DHA play a crucial role in the prevention of atherosclerosis, heart attack, low and cancer [40,42]. In addition, omega-3 consumption reduced the inflammation acquired by rheumatoid arthritis [43,44].

The human brain has a loftier requirement for DHA; low DHA levels take been linked to low brain serotonin levels, which are connected to an increased tendency for depression and suicide. Several studies have established a correlation between low levels of omega -3 fatty acids and depression. High consumption of omega-3 FAs is typically associated with a lower incidence of depression, a decreased prevalence of historic period-related memory loss and a lower risk of developing Alzheimer'southward disease [45-51].

The National Institutes of Health has published recommended daily intakes of FAs; specific recommendations include 650 mg of EPA and DHA, 2.22 g/solar day of αLA and 4.44 g/day of LA. However, the Institute of Medicine has recommended DRI (dietary reference intake) for LA (omega-half dozen) at 12 to 17 g and αLA (omega-3) at i.1 to ane.6 g for developed women and men, respectively. Although seafood is the major dietary source of north-3 fat acids, a recent fat acrid intake survey indicated that crimson meat also serves equally a meaning source of northward-3 fatty acids for some populations [52].

Sinclair and co-workers were the first to bear witness that beefiness consumption increased serum concentrations of a number of north-iii fatty acids including, EPA, DPA and DHA in humans [forty]. Likewise, there are a number of studies that have been conducted with livestock which written report similar findings, i.e., animals that consume rations loftier in precursor lipids produce a meat product higher in the essential fatty acids [53,54]. For instance, cattle fed primarily grass significantly increased the omega-3 content of the meat and also produced a more favorable omega-vi to omega-iii ratio than grain-fed beef [46,55-57].

Table ii shows the effect of ration on polyunsaturated fat acrid limerick from a number of contempo studies that dissimilarity grass-based rations to conventional grain feeding regimens [24-28,30,31]. Grass-based diets resulted in significantly higher levels of omega-three inside the lipid fraction of the meat, while omega-6 levels were left unchanged. In fact, every bit the concentration of grain is increased in the grass-based nutrition, the concentration of n-3 FAs decreases in a linear fashion. Grass-finished beef consistently produces a higher concentration of n-3 FAs (without effecting due north-6 FA content), resulting in a more favorable n-6:n-3 ratio.

The amount of total lipid (fat) found in a serving of meat is highly dependent upon the feeding regimen as demonstrated in Tables i and 2. Fat will as well vary by cut, as not all locations of the carcass will deposit fatty to the same degree. Genetics also play a part in lipid metabolism creating significant breed effects. All the same, the issue of feeding regimen is a very powerful determinant of fatty acrid composition.

Review of conjugated linoleic acid (CLA) and trans vaccenic acrid (TVA) in grass-fed beef

Conjugated linoleic acids make up a grouping of polyunsaturated FAs found in meat and milk from ruminant animals and exist every bit a general mixture of conjugated isomers of LA. Of the many isomers identified, the cis-9, trans-11 CLA isomer (likewise referred to as rumenic acid or RA) accounts for up to 80-ninety% of the total CLA in ruminant products [58]. Naturally occurring CLAs originate from two sources: bacterial isomerization and/or biohydrogenation of polyunsaturated fatty acids (PUFA) in the rumen and the desaturation of trans-fatty acids in the adipose tissue and mammary gland [59,60].

Microbial biohydrogenation of LA and αLA by an anaerobic rumen bacterium Butyrivibrio fibrisolvens is highly dependent on rumen pH [61]. Grain consumption decreases rumen pH, reducing B. fibrisolven action, conversely grass-based diets provide for a more favorable rumen environs for subsequent bacterial synthesis [62]. Rumen pH may assistance to explain the apparent differences in CLA content between grain and grass-finished meat products (see Table ii). De novo synthesis of CLA from 11t-C18:1 TVA has been documented in rodents, dairy cows and humans. Studies suggest a linear increase in CLA synthesis every bit the TVA content of the nutrition increased in human subjects [63]. The rate of conversion of TVA to CLA has been estimated to range from five to 12% in rodents to nineteen to 30% in humans[64]. True dietary intake of CLA should therefore consider native ninecxit-C18:2 (actual CLA) besides every bit the 11t-C18:1 (potential CLA) content of foods [65,66]. Effigy 2 portrays de novo synthesis pathways of CLA from TVA [37].

An external file that holds a picture, illustration, etc.  Object name is 1475-2891-9-10-2.jpg

De novo synthesis of CLA from 11t-C18:1 vaccenic acid. (Adapted from Bauman et al., 1999)

Natural augmentation of CLA c9t11 and TVA inside the lipid fraction of beef products can exist accomplished through diets rich in grass and lush green forages. While precursors can be plant in both grains and lush green forages, grass-fed ruminant species have been shown to produce ii to 3 times more CLA than ruminants fed in confinement on high grain diets, largely due to a more favorable rumen pH [34,56,57,67] (see Table 2).

The impact of feeding practices becomes fifty-fifty more evident in light of recent reports from Canada which suggests a shift in the predominate trans C18:1 isomer in grain-fed beef. Dugan et al (2007) reported that the major trans isomer in beef produced from a 73% barley grain diet is 10t-18:ane (ii.13% of total lipid) rather than elevent-18:ane (TVA) (0.77% of total lipid), a finding that is not particularly favorable because the data that would support a negative bear upon of 10t-18:1 on LDL cholesterol and CVD [68,69].

Over the past two decades numerous studies have shown meaning health benefits attributable to the actions of CLA, as demonstrated past experimental animal models, including deportment to reduce carcinogenesis, atherosclerosis, and onset of diabetes [lxx-72]. Conjugated linoleic acid has as well been reported to modulate trunk composition by reducing the accumulation of adipose tissue in a variety of species including mice, rats, pigs, and now humans [73-76]. These changes in body composition occur at ultra high doses of CLA, dosages that tin but be attained through synthetic supplementation that may besides produce ill side-effects, such every bit gastrointestinal upset, agin changes to glucose/insulin metabolism and compromised liver role [77-81]. A number of fantabulous reviews on CLA and human health can exist found in the literature [61,82-84].

Optimal dietary intake remains to be established for CLA. It has been hypothesized that 95 mg CLA/day is enough to show positive effects in the reduction of chest cancer in women utilizing epidemiological data linking increased milk consumption with reduced breast cancer[85]. Ha et al. (1989) published a much more than conservative estimate stating that iii thousand/day CLA is required to promote homo wellness benefits[86]. Ritzenthaler et al. (2001) estimated CLA intakes of 620 mg/mean solar day for men and 441 mg/day for women are necessary for cancer prevention[87]. Obviously, all these values represent crude estimates and are mainly based on extrapolated creature information. What is clear is that nosotros as a population do not swallow enough CLA in our diets to have a pregnant impact on cancer prevention or suppression. Reports indicate that Americans consume between 150 to 200 mg/twenty-four hour period, Germans consumer slightly more between 300 to 400 mg/day[87], and the Australians seem to be closer to the optimum concentration at 500 to m mg/day according to Parodi (1994) [88].

Review of pro-Vitamin A/β-carotene in grass-fed meat

Carotenoids are a family of compounds that are synthesized by higher plants every bit natural plant pigments. Xanthophylls, carotene and lycopene are responsible for yellow, orangish and red coloring, respectively. Ruminants on high forage rations pass a portion of the ingested carotenoids into the milk and trunk fatty in a fashion that has yet to exist fully elucidated. Cattle produced nether extensive grass-based production systems generally accept carcass fat which is more yellow than their concentrate-fed counterparts acquired by carotenoids from the lush green forages. Although yellow carcass fat is negatively regarded in many countries around the world, it is also associated with a healthier fat acid profile and a college antioxidant content [89].

Plant species, harvest methods, and flavour, all accept significant impacts on the carotenoid content of fodder. In the process of making silage, haylage or hay, equally much as 80% of the carotenoid content is destroyed [90]. Further, significant seasonal shifts occur in carotenoid content owing to the seasonal nature of found growth.

Carotenes (mainly β-carotene) are precursors of retinol (Vitamin A), a critical fat-soluble vitamin that is important for normal vision, bone growth, reproduction, cell partitioning, and cell differentiation [91]. Specifically, it is responsible for maintaining the surface lining of the eyes and also the lining of the respiratory, urinary, and intestinal tracts. The overall integrity of skin and mucous membranes is maintained by vitamin A, creating a bulwark to bacterial and viral infection [fifteen,92]. In addition, vitamin A is involved in the regulation of immune function by supporting the product and part of white blood cells [12,xiii].

The electric current recommended intake of vitamin A is 3,000 to five,000 IU for men and 2,300 to 4,000 IU for women [93], respectively, which is equivalent to 900 to 1500 μg (micrograms) (Note: DRI equally reported by the Found of Medicine for not-pregnant/not-lactating adult females is 700 μg/solar day and males is 900 μg/day or 2,300 - iii,000 I U (assuming conversion of 3.33 IU/μg). While there is no RDA (Required Daily Allowance) for β-carotene or other pro-vitamin A carotenoids, the Institute of Medicine suggests consuming iii mg of β-carotene daily to maintain plasma β-carotene in the range associated with normal part and a lowered run a risk of chronic diseases (NIH: Role of Dietary Supplements).

The furnishings of grass feeding on beta-carotene content of beefiness was described by Descalzo et al. (2005) who found pasture-fed steers incorporated significantly higher amounts of beta-carotene into muscle tissues every bit compared to grain-fed animals [94]. Concentrations were 0.45 μg/g and 0.06 μg/one thousand for beef from pasture and grain-fed cattle respectively, demonstrating a 7 fold increase in β-carotene levels for grass-fed beefiness over the grain-fed contemporaries. Similar data has been reported previously, presumably due to the high β-carotene content of fresh grasses as compared to cereal grains[38,55,95-97]. (see Table 3)

Table 3

Comparison of mean β-carotene vitamin content in fresh beef from grass-fed and grain-fed cattle.

β-carotene

Author, year, animal course Grass-fed (ug/g tissue) Grain-fed (ug/k tissue)
Insani et al., 2007, Crossbred steers 0.74* 0.17*
Descalzo et al., 2005 Crossbred steers 0.45* 0.06*
Yang et al., 2002, Crossbred steers 0.xvi* 0.01*

* Indicates a significant departure (at least P < 0.05) between feeding regimens was reported inside each respective report.

Review of Vitamin East/α-tocopherol in grass-fed beefiness

Vitamin Eastward is likewise a fat-soluble vitamin that exists in viii different isoforms with powerful antioxidant action, the nearly active being α-tocopherol [98]. Numerous studies have shown that cattle finished on pasture produce higher levels of α-tocopherol in the final meat product than cattle fed high concentrate diets[23,28,94,97,99-101] (meet Tabular array 4).

Table four

Comparing of hateful α-tocopherol vitamin content in fresh beef from grass-fed and grain-fed cattle.

α-tocopherol

Writer, year, animal class Grass-fed (ug/g tissue) Grain-fed (ug/g tissue)
De la Fuente et al., 2009, Mixed cattle 4.07* 0.75*
Descalzo, et al., 2008, Crossbred steers 3.08* 1.50*
Insani et al., 2007, Crossbred steers two.1* 0.viii*
Descalzo, et al., 2005, Crosbred steers iv.6* ii.2*
Realini et al., 2004, Hereford steers 3.91* 2.92*
Yang et al., 2002, Crossbred steers 4.5* 1.8*

* Indicates a pregnant difference (at least P < 0.05) between feeding regimens was reported inside each respective study.

Antioxidants such as vitamin E protect cells confronting the furnishings of costless radicals. Free radicals are potentially dissentious by-products of metabolism that may contribute to the development of chronic diseases such as cancer and cardiovascular disease.

Preliminary research shows vitamin E supplementation may help prevent or delay coronary middle affliction [102-105]. Vitamin Due east may also block the formation of nitrosamines, which are carcinogens formed in the stomach from nitrates consumed in the diet. Information technology may also protect against the development of cancers past enhancing immune function [106]. In addition to the cancer fighting effects, there are some observational studies that found lens clarity (a diagnostic tool for cataracts) was better in patients who regularly used vitamin E [107,108]. The current recommended intake of vitamin East is 22 IU (natural source) or 33 IU (synthetic source) for men and women [93,109], respectively, which is equivalent to 15 milligrams by weight.

The concentration of natural α-tocopherol (vitamin E) found in grain-fed beef ranged between 0.75 to 2.92 μg/g of musculus whereas pasture-fed beef ranges from 2.i to 7.73 μg/g of tissue depending on the type of fodder fabricated available to the animals (Tabular array 4). Grass finishing increases α-tocopherol levels three-fold over grain-fed beef and places grass-fed beefiness well within range of the muscle α-tocopherol levels needed to extend the shelf-life of retail beef (3 to 4 μg α-tocopherol/gram tissue) [110]. Vitamin Eastward (α-tocopherol) acts mail service-mortem to delay oxidative deterioration of the meat; a process by which myoglobin is converted into brown metmyoglobin, producing a darkened, brownish appearance to the meat. In a study where grass-fed and grain-fed beefiness were straight compared, the bright red colour associated with oxymyoglobin was retained longer in the retail display in the grass-fed grouping, even idea the grass-fed meat contains a higher concentration of more oxidizable n-iii PUFA. The authors concluded that the antioxidants in grass probably caused college tissue levels of vitamin E in grazed animals with benefits of lower lipid oxidation and better color retentiveness despite the greater potential for lipid oxidation[111].

Review of antioxidant enzyme content in grass-fed beef

Glutathione (GT), is a relatively new protein identified in foods. It is a tripeptide composed of cysteine, glutamic acid and glycine and functions as an antioxidant primarily every bit a component of the enzyme system containing GT oxidase and reductase. Within the jail cell, GT has the capability of quenching complimentary radicals (like hydrogen peroxide), thus protecting the prison cell from oxidized lipids or proteins and prevent damage to Dna. GT and its associated enzymes are establish in virtually all plant and animate being tissue and is readily absorbed in the minor intestine[112].

Although our knowledge of GT content in foods is yet somewhat limited, dairy products, eggs, apples, beans, and rice contain very little GT (< 3.3 mg/100 one thousand). In contrast, fresh vegetables (e.g., asparagus 28.3 mg/100 g) and freshly cooked meats, such every bit ham and beef (23.three mg/100 g and 17.5 mg/100 yard, respectively), are high in GT [113].

Because GT compounds are elevated in lush dark-green forages, grass-fed beef is particularly high in GT every bit compared to grain-fed contemporaries. Descalzo et al. (2007) reported a significant increase in GT molar concentrations in grass-fed beef [114]. In add-on, grass-fed samples were as well higher in superoxide dismutase (SOD) and catalase (CAT) activity than beef from grain-fed animals[115]. Superoxide dismutase and catalase are coupled enzymes that work together as powerful antioxidants, SOD scavenges superoxide anions by forming hydrogen peroxide and CAT then decomposes the hydrogen peroxide to HtwoO and Otwo. Grass merely diets amend the oxidative enzyme concentration in beef, protecting the muscle lipids confronting oxidation equally well every bit providing the beef consumer with an additional source of antioxidant compounds.

Issues related to season and palatability of grass-fed beef

Maintaining the more favorable lipid contour in grass-fed beefiness requires a high percentage of lush fresh fodder or grass in the ration. The higher the concentration of fresh green forages, the higher the αLA forerunner that volition be bachelor for CLA and north-three synthesis [53,54]. Fresh pasture forages have x to 12 times more than C18:three than cereal grains [116]. Dried or cured forages, such every bit hay, will accept a slightly lower amount of forerunner for CLA and north-3 synthesis. Shifting diets to cereal grains will crusade a significant change in the FA profile and antioxidant content within thirty days of transition [57].

Because grass-finishing alters the biochemistry of the beefiness, odor and flavor volition also exist affected. These attributes are directly linked to the chemical makeup of the final production. In a study comparing the flavor compounds between cooked grass-fed and grain-fed beef, the grass-fed beefiness contained higher concentrations of diterpenoids, derivatives of chlorophyll call phyt-ane-ene and phyt-2-ene, that changed both the flavor and olfactory property of the cooked production [117]. Others have identified a "light-green" odor from cooked grass-fed meat associated with hexanals derived from oleic and αLA FAs. In contrast to the "green" aroma, grain-fed beef was described as possessing a "soapy" odor, presumably from the octanals formed from LA that is constitute in high concentration in grains [118]. Grass-fed beef consumers can expect a different flavour and aroma to their steaks as they cook on the grill. Too, considering of the lower lipid content and high concentration of PUFAs, cooking time will be reduced. For an exhaustive look at the outcome of meat compounds on season, see Calkins and Hodgen (2007) [119].

With respect to palatability, grass-fed beefiness has historically been less well accepted in markets where grain-fed products predominant. For example, in a study where British lambs fed grass and Spanish lambs fed milk and concentrates were assessed past British and Spanish taste panels, both found the British lamb to accept a college odor and flavour intensity. Yet, the British panel preferred the flavor and overall eating quality of the grass-fed lamb, the Spanish panel much preferred the Castilian fed lamb [120]. Also, the U.S. is well known for producing corn-fed beef, gustation panels and consumers who are more familiar with the sense of taste of corn-fed beefiness seem to prefer it as well [16]. An individual unremarkably comes to adopt the foods they grew up eating, making consumer sensory panels more of an fine art than scientific discipline [36]. Trained taste panels, i.e., persons specifically trained to evaluate sensory characteristics in beef, found grass-fed beefiness less palatable than grain-fed beef in flavor and tenderness [119,121].

Conclusion

Enquiry spanning three decades supports the argument that grass-fed beef (on a g/one thousand fat basis), has a more desirable SFA lipid profile (more C18:0 cholesterol neutral SFA and less C14:0 & C16:0 cholesterol elevating SFAs) every bit compared to grain-fed beef. Grass-finished beef is also college in total CLA (C18:ii) isomers, TVA (C18:i t11) and n-3 FAs on a one thousand/g fatty basis. This results in a better due north-6:northward-3 ratio that is preferred past the nutritional community. Grass-fed beefiness is too higher in precursors for Vitamin A and E and cancer fighting antioxidants such as GT and SOD activity as compared to grain-fed contemporaries.

Grass-fed beefiness tends to be lower in overall fat content, an important consideration for those consumers interested in decreasing overall fat consumption. Because of these differences in FA content, grass-fed beef also possesses a distinct grass flavour and unique cooking qualities that should be considered when making the transition from grain-fed beefiness. To maximize the favorable lipid contour and to guarantee the elevated antioxidant content, animals should be finished on 100% grass or pasture-based diets.

Grain-fed beef consumers may attain similar intakes of both n-3 and CLA through consumption of college fat portions with college overall palatability scores. A number of clinical studies have shown that today'south lean beef, regardless of feeding strategy, tin be used interchangeably with fish or skinless chicken to reduce serum cholesterol levels in hypercholesterolemic patients.

Abbreviations

c: cis; t: trans; FA: fatty acid; SFA: saturated fatty acid; PUFA: polyunsaturated fatty acid; MUFA: monounsaturated fatty acid; CLA: conjugated linoleic acid; TVA: trans-vaccenic acrid; EPA: eicosapentaenoic acid; DPA: docosapentaenoic acid; DHA: docosahexaenoic acid; GT: glutathione; SOD: superoxide dismutase; CAT: catalase.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

CAD was responsible for the literature review, completed virtually of the main writing, created the manuscript and worked through the submission process; AA conducted the literature search, organized the articles co-ordinate to category, completed some of the chief writing and served as editor; SPD conducted a portion of the literature review and served as editor for the manuscript; GAN conducted a portion of the literature review and served equally editor for the manuscript; SL conducted a portion o the literature review and served equally editor for the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors would similar to acknowledge Grace Berryhill for her aid with the figures, tables and editorial contributions to this manuscript.

References

  • Griel AE, Kris-Etherton PM. Beyond saturated fat: The importance of the dietary fatty acrid profile on cardiovascular disease. Diet Reviews. 2006;64(v):257–62. doi: x.1111/j.1753-4887.2006.tb00208.x. [PubMed] [CrossRef] [Google Scholar]
  • Kris-Etherton PM, Innis S. Dietary Fat Acids -- Position of the American Dietetic Association and Dietitians of Canada. American Dietetic Association Position Study. Journal of the American Dietetic Association. 2007;107(nine):1599–1611. Ref Blazon: Report. [PubMed] [Google Scholar]
  • Hu FB, Stampfer MJ, Manson JE, Rimm East, Colditz GA, Rosner BA, Hennekins CH, Willett WC. Dietary fat intake and the risk of coronary center disease in women. New England Journal of Medicine. 1997;337:1491–ix. doi: 10.1056/NEJM199711203372102. [PubMed] [CrossRef] [Google Scholar]
  • Posner BM, Cobb JL, Belanger AJ, Cupples LA, D'Agostino RB, Stokes J. Dietary lipid predictors of coronary heart affliction in men. The Framingham Written report. Archives of Internal Medicine. 1991;151:1181–vii. doi: 10.1001/archinte.151.6.1181. [PubMed] [CrossRef] [Google Scholar]
  • Mensink RP, Katan MB. Effect of dietary fatty acids on serum lipids and lipoproteins. Arteriosclerosis Thrombosis Vascular Biology. 1992;12:911–9. [PubMed] [Google Scholar]
  • Keys A. Coronary heart illness in seven countries. Apportionment. 1970;41(1):211. [Google Scholar]
  • Mensink RP, Zock PL, Kester AD, Katan MB. Effects of dietary fatty acids and carbohydrates on the ratio of serum total HDL cholesterol and on serum lipids and apolipoproteins: A meta-assay of 60 controlled trials. American Journal of Clinical Nutrition. 2003;77:1146–55. [PubMed] [Google Scholar]
  • Putnam J, Allshouse J, Scott-Kantor L. U.S. per capita nutrient supply trends: More than calories, refined carbohydrates, and fats. Food Review. 2002;25(3):2–15. [Google Scholar]
  • Kris-Etherton PMYS. Private fatty acid effects on plasma lipids and lipoproteins. Man studies. American Journal of Clinical Nutrition. 1997;65(suppl.5):1628S–44S. [PubMed] [Google Scholar]
  • Higgs JD. The changing nature of ruby meat: xx years improving nutritional quality. Trends in Food Scientific discipline and Technology. 2000;xi:85–95. doi: ten.1016/S0924-2244(00)00055-8. [CrossRef] [Google Scholar]
  • O'Dea K, Traianedes K, Chisholm 1000, Leyden H, Sinclair AJ. Cholesterol-lowering consequence of a depression-fat diet containing lean beef is reversed past the addition of beef fat. American Journal of Clinical Diet. 1990;52:491–4. [PubMed] [Google Scholar]
  • Beauchesne-Rondeau E, Gascon A, Bergeron J, Jacques H. Plasma lipids and lipoproteins in hypercholesterolemic men fed a lipid-lowering diet containing lean beef, lean fish, or poultry. American Journal of Clinical Nutrition. 2003;77(3):587–93. [PubMed] [Google Scholar]
  • Melanson K, Gootman J, Myrdal A, Kline K, Rippe JM. Weight loss and total lipid contour changes in overweight women consuming beefiness or chicken as the primary protein source. Diet. 2003;19:409–xiv. doi: 10.1016/S0899-9007(02)01080-viii. [PubMed] [CrossRef] [Google Scholar]
  • Denke MA. Role of beefiness and beef tallow, an enriched source of stearic acid, in a cholesterol-lowering diet. American Journal of Clinical Nutrition. 1994;60:1044S–9S. [PubMed] [Google Scholar]
  • Smith DR, Wood R, Tseng Southward, Smith SB. Increased beefiness consumption increases lipoprotein A-I only not serum cholesterol of mildly hypercholesterolemic men with different levels of habitual beef intake. Experimental Biological Medicine. 2002;227(4):266–75. [PubMed] [Google Scholar]
  • Wood JD, Richardson RI, Nute GR, Fisher AV, Campo MM, Kasapidou Due east, Sheard PR, Enser Grand. Effects of fat acids on meat quality: review. Meat Science. 2003;66:21–32. doi: 10.1016/S0309-1740(03)00022-half-dozen. [PubMed] [CrossRef] [Google Scholar]
  • Williamson CS, Foster RK, Stanner SA, Buttriss JL. Red meat in the diet. British Nutrition Foundation. Nutrition Bulletin. 2005;30:323–335. doi: 10.1111/j.1467-3010.2005.00525.x. Ref Blazon: Written report. [CrossRef] [Google Scholar]
  • Biesalski HK. Meat as a component of a salubrious diet - are there any risks or benefits if meat is avoided? Meat Science. 2005;70(iii):509–24. doi: ten.1016/j.meatsci.2004.07.017. [PubMed] [CrossRef] [Google Scholar]
  • Yu S, Derr J, Etherton TD, Kris-Etherton PM. Plasma cholesterol-predictive equations demonstrate that stearic acid is neutral and monosaturated fat acids are hypocholesterolemic. American Journal of Clinical Diet. 1995;61:1129–39. [PubMed] [Google Scholar]
  • Whetsell MS, Rayburn EB, Lozier JD. Human Health Furnishings of Fatty Acids in Beef. Fact Sheet: West Virgina Academy & U.S.D.A. Agronomics Research Service. Extension Service W Virginia University; 2003. Ref Type: Electronic Citation. [Google Scholar]
  • Kris-Etherton PM. Monounsaturated fat acids and risk of cardiovascular disease. Circulation. 1999;100:1253. [PubMed] [Google Scholar]
  • DeSmet S, Raes K, Demeyer D. Meat fatty acrid composition every bit affected past fatness and genetic factors: a review. Brute Research. 2004;53:81–98. doi: 10.1051/animres:2004003. [CrossRef] [Google Scholar]
  • De la Fuente J, Diaz MT, Alvarez I, Oliver MA, Font i Furnols Thousand, Sanudo C, Campo MM, Montossi F, Nute GR, Caneque V. Fatty acid and vitamin E limerick of intramuscular fat in cattle reared in different product systems. Meat Science. 2009;82:331–7. doi: 10.1016/j.meatsci.2009.02.002. [PubMed] [CrossRef] [Google Scholar]
  • Garcia PT, Pensel NA, Sancho AM, Latimori NJ, Kloster AM, Amigone MA, Casal JJ. Beef lipids in relation to animal breed and diet in Argentina. Meat Scientific discipline. 2008;79:500–8. doi: 10.1016/j.meatsci.2007.10.019. [PubMed] [CrossRef] [Google Scholar]
  • Alfaia CPM, Alves SP, Martins SIV, Costa ASH, Fontes CMGA, Lemos JPC, Bessa RJB, Prates JAM. Effect of feeding arrangement on intramuscular fatty acids and conjugated linoleic acid isomers of beefiness cattle, with accent on their nutritional value and discriminatory ability. Nutrient Chemical science. 2009;114:939–46. doi: 10.1016/j.foodchem.2008.10.041. [CrossRef] [Google Scholar]
  • Leheska JM, Thompson LD, Howe JC, Hentges Eastward, Boyce J, Brooks JC, Shriver B, Hoover L, Miller MF. Effects of conventional and grass-feeding systems on the nutrient composition of beef. Journal Creature Science. 2008;86:3575–85. doi: 10.2527/jas.2007-0565. [PubMed] [CrossRef] [Google Scholar]
  • Nuernberg 1000, Dannenberger D, Nuernberg Thousand, Ender G, Voigt J, Scollan ND, Wood JD, Nute GR, Richardson RI. Event of a grass-based and a concentrate feeding system on meat quality characteristics and fat acid composition of longissimus muscle in different cattle breeds. Livestock Production Science. 2005;94:137–47. doi: 10.1016/j.livprodsci.2004.xi.036. [CrossRef] [Google Scholar]
  • Realini CE, Duckett SK, Brito GW, Rizza MD, De Mattos D. Effect of pasture vs. concentrate feeding with or without antioxidants on carcass characteristics, fatty acid composition, and quality of Uruguayan beef. Meat Science. 2004;66:567–77. doi: 10.1016/S0309-1740(03)00160-8. [PubMed] [CrossRef] [Google Scholar]
  • Warren HE, Enser Thousand, Richardson I, Forest JD, Scollan ND. Consequence of breed and nutrition on total lipid and selected shelf-life parameters in beef muscle. Proceedings of British Social club of animate being science. 2003. p. 23.
  • Ponnampalam EN, Mann NJ, Sinclair AJ. Upshot of feeding systems on omega-3 fatty acids, conjugated linoleic acid and trans fatty acids in Australian beefiness cuts, potential impact on human wellness. Asia Pacific Journal of Clinical Nutrition. 2006;15(ane):21–9. [PubMed] [Google Scholar]
  • Descalzo A, Insani EM, Biolatto A, Sancho AM, Garcia PT, Pensel NA. Influence of pasture or grain-based diets supplemented with vitamin Due east on antioxidant/oxidative balance of Argentine beefiness. Meat Science. 2005;70:35–44. doi: ten.1016/j.meatsci.2004.11.018. [PubMed] [CrossRef] [Google Scholar]
  • Wheeler TL, Davis GW, Stoecker BJ, Harmon CJ. Cholesterol concentrations of longissimus muscle, subcutaneous fatty and serum of two beef cattle breed types. Periodical of Beast Science. 1987;65:1531–7. [PubMed] [Google Scholar]
  • Smith DR, Forest R, Tseng Due south, Smith SB. Increased beef consumption increases apolipoprotein A-ane but not serum cholesterol of mildly hypercholesterolemic men with different levels of habitual beefiness intake. Experimental Biological Medicine. 2002;227(4):266–75. [PubMed] [Google Scholar]
  • Rule DC, Broughton KS, Shellito SM, Maiorano Thousand. Comparison of musculus fat acid profiles and cholesterol concentrations of bison, cattle, elk and chicken. Journal Animal Science. 2002;eighty:1202–11. [PubMed] [Google Scholar]
  • Alfaia CPM, Castro MLF, Martins SIV, Portugal APV, Alves SPA, Fontes CMGA. Influence of slaughter season and muscle type on faty acid limerick, conjugated linoleic acid isomeric distribution and nutritional quality of intramuscular fat in Arouquesa-PDO veal. Meat Science. 2007;76:787–95. doi: 10.1016/j.meatsci.2007.02.023. [PubMed] [CrossRef] [Google Scholar]
  • Sitz BM, Calkins CR, Feuz DM, Umberger WJ, Eskridge KM. Consumer sensory acceptance and value of domestic, Canadian, and Australian grass-fed beef steaks. Journal of Animate being Science. 2005;83:2863–8. [PubMed] [Google Scholar]
  • Bauman DE, Lock AL. Advanced Dairy Chemical science. 3. 2. Springer, New York; 2006. Conjugated linoleic acid: biosynthesis and nutritional significance. Fox and McSweeney; pp. 93–136. Ref Blazon: Serial (Volume, Monograph) [Google Scholar]
  • Enser Chiliad, Hallett KG, Hewett B, Fursey GAJ, Wood JD, Harrington Thousand. Fatty acid content and composition of UK beef and lamb muscle in relation to product organisation and implications for homo nutrition. Meat Science. 1998;49(three):329–41. doi: 10.1016/S0309-1740(97)00144-7. [PubMed] [CrossRef] [Google Scholar]
  • Ruxton CHS, Reed SC, Simpson JA, Millington KJ. The wellness benefits of omega-three polyunsaturated fatty acids: a review of the evidence. The Journal of Man Nutrition and Dietetics. 2004;17:449–59. doi: 10.1111/j.1365-277X.2004.00552.ten. [PubMed] [CrossRef] [Google Scholar]
  • Simopoulos A. Omega-three fat acids in health and illness and in growth and development. American Journal of Clinical Nutrition. 1991;54:438–63. [PubMed] [Google Scholar]
  • Thomas BJ. Efficiency of conversion of blastoff-linolenic acid to long chain n-three fatty acids in man. Current Opinion in Clincal Nutrition and Metabolic Care. 2002;5(2):127–32. doi: 10.1097/00075197-200203000-00002. [PubMed] [CrossRef] [Google Scholar]
  • Connor WE. Importance of n-3 fatty acids in health and disease. American Journal of Clinical Nutrition. 2000;71:171S–5S. [PubMed] [Google Scholar]
  • Kremer JM, Lawrence DA, Jubiz W, Galli C, Simopoulos AP. Dietary Omega-three and Omega-6 fat acids: biological furnishings and nutritional essentiality. New York: Plenum Press; 1989. Different doses of fish -oil fatty acid ingestion in agile rheumatoid arthritis: a prospective study of clinical and immunological parameters. [Google Scholar]
  • DiGiacomo RA, Kremer JM, Shah DM. Fish-oil dietary supplementation in patients with Raynaud'southward Phenomenon: A double-blind, controlled, prospective study. The American Periodical of Medicine. 1989;86:158–64. doi: 10.1016/0002-9343(89)90261-1. [PubMed] [CrossRef] [Google Scholar]
  • Kalmijn Due south. Dietary fat intake and the hazard of incident dementia in the Rotterdam Written report. Annals of Neurology. 1997;42(5):776–82. doi: 10.1002/ana.410420514. [PubMed] [CrossRef] [Google Scholar]
  • Yehuda Southward, Rabinovtz South, Carasso RL, Mostofsky DI. Essential fat acids training (SR-3) improves Alzheimer's patient's quality of life. International Journal of Neuroscience. 1996;87(iii-4):141–nine. doi: 10.3109/00207459609070833. [PubMed] [CrossRef] [Google Scholar]
  • Hibbeln JR. Fish oil consumption and major depression. The Lancet. 1998;351:1213. doi: ten.1016/S0140-6736(05)79168-6. (Apr 18 1998) [PubMed] [CrossRef] [Google Scholar]
  • Hibbeln JR, Salem N. Dietary polyunsaturated fatty acids and depression: when cholesterol does not satisfy. American Journal of Clinical Nutrition. 1995;62:1–9. [PubMed] [Google Scholar]
  • Stoll AL. Omega 3 fatty acids in bipolar disorder. Archives of General Psychiatry. 1999;56 407-12-415-16. [PubMed] [Google Scholar]
  • Calabrese JR, Rapport DJ, Shleton MD. Fish oils and bipolar disorder. Archives of General Psychiatry. 1999;56:413–iv. doi: ten.1001/archpsyc.56.5.413. [PubMed] [CrossRef] [Google Scholar]
  • Laugharne JDE. Fat acids and schizophrenia. Lipids. 1996;31:S163–S165. doi: x.1007/BF02637070. [PubMed] [CrossRef] [Google Scholar]
  • Sinclair AJ, Johnson L, O'Dea K, Holman RT. Diets rich in lean beef increase arachidonic acid and long-chain omega 3 polyunsaturated fatty acid levels in plasma phospholipids. Lipids. 1994;29(5):337–43. doi: x.1007/BF02537187. [PubMed] [CrossRef] [Google Scholar]
  • Raes One thousand, DeSmet S, Demeyer D. Effect of dietary fat acids on incorporation of long chain polyunsaturated fat acids and conjugated linoleic acrid in lamb, beef and pork meat: a review. Animal Feed Scientific discipline and Engineering. 2004;113:199–221. doi: x.1016/j.anifeedsci.2003.09.001. [CrossRef] [Google Scholar]
  • Marmer WN, Maxwell RJ, Williams JE. Effects of dietary regimen and tissue site on bovine fat acid profiles. Journal Brute Science. 1984;59:109–21. [Google Scholar]
  • Wood JD, Enser Chiliad. Factors influencing fatty acids in meat and the function of antioxidants in improving meat quality. British Periodical of Nutrition. 1997;78:S49–S60. doi: ten.1079/BJN19970134. [PubMed] [CrossRef] [Google Scholar]
  • French P, Stanton C, Lawless F, O'Riordan EG, Monahan FJ, Caffery PJ, Moloney AP. Fat acid composition, including conjugated linoleic acid of intramuscular fat from steers offered grazed grass, grass silage or concentrate-based diets. Journal Fauna Science. 2000;78:2849–55. [PubMed] [Google Scholar]
  • Duckett SK, Wagner DG, Yates LD, Dolezal HG, May SG. Furnishings of time on feed on beef nutrient composition. Periodical Fauna Science. 1993;71:2079–88. [PubMed] [Google Scholar]
  • Nuernberg Grand, Nuernberg K, Ender K, Lorenz Due south, Winkler Grand, Rickert R, Steinhart H. Omega-3 fatty acids and conjugated linoleic acids of longissimus muscle in beef cattle. European Journal of Lipid Science Technology. 2002;104:463–71. doi: 10.1002/1438-9312(200208)104:8<463::Assist-EJLT463>3.0.CO;two-U. [CrossRef] [Google Scholar]
  • Griinari JM, Corl BA, Lacy SH, Chouinard PY, Nurmela KV, Bauman DE. Conjugated linoleic acid is synthesized endogenoulsy in lactating dairy cows past delta-nine desaturase. Journal of Diet. 2000;130:2285–91. [PubMed] [Google Scholar]
  • Sehat N, Rickert RR, Mossoba MM, Dramer JKG, Yurawecz MP, Roach JAG, Adlof RO, Morehouse KM, Fritsche J, Eulitz KD, Steinhart H, Ku M. Improved separation of conjugated fatty acrid methyl esters by silver ion-high-performance liquid chromatography. Lipids. 1999;34:407–thirteen. doi: 10.1007/s11745-999-0379-three. [PubMed] [CrossRef] [Google Scholar]
  • Pariza MW, Park Y, Cook ME. Mechanisms of action of conjugated linoleic acid: evidence and speculation. Proceedings for the Guild of Experimental Biology and Medicine. 2000;32:853–eight. [PubMed] [Google Scholar]
  • Bessa RJB, Santos-Silva J, Ribeiro JMR, Portugal AV. Reticulo-rumen biohydrogenation and the enrichment of ruminant edible products with linoleic acid conjugated isomers. Livestock Production Science. 2000;63:201–eleven. doi: 10.1016/S0301-6226(99)00117-seven. [CrossRef] [Google Scholar]
  • Turpeinen AM, Mutanen M, Aro ASI, Basu SPD, Griinar JM. Bioconversion of vaccenic acid to conjugated linoleic acid in humans. American Journal of Clinical Diet. 2002;76:504–10. [PubMed] [Google Scholar]
  • Turpeinen AM, Mautanen M, Aro A, Salminen I, Basu S, Palmquist DL. Bioconversion of vaccenic acid to conjugated linoleic acid in humans. American Periodical of Clinical Nutrition. 2002;76:504–ten. [PubMed] [Google Scholar]
  • Turpeinen AM, Mautanen M, Aro A, Salminen I, Basu S, Palmquist DL. Bioconversion of vaccenic acid to conjugated linoleic acid in humans. American Journal of Clinical Nutrition. 2002;76:504–10. [PubMed] [Google Scholar]
  • Adlof RO, Duval South, Emken EA. Biosynthesis of conjugated linoleic acrid in humans. Lipids. 2000;35:131–5. doi: 10.1007/BF02664761. [PubMed] [CrossRef] [Google Scholar]
  • Mandell IB, Gullett JG, Buchanan-Smith JG, Campbell CP. Effects of diet and slaughter endpoint on carcass limerick and beef quality in Charolais cross steers fed alfalfa silage and (or) high concentrate diets. Canadian Journal of Animal Science. 1997;77:403–14. [Google Scholar]
  • Dugan MER, Rollan DC, Aalhus JL, Aldai N, Kramer JKG. Subcutaneous fatty composition of youthful and mature Canadian beefiness: emphasis on individual conjugated linoleic acid and trans-xviii:1 isomers. Canadian Journal of Animal Science. 2008;88:591–nine. [Google Scholar]
  • Hodgson JM, Wahlqvist ML, Boxall JA, Balazs ND. Platelet trans fatty acids in relation to angiographically assessed coronary artery disease. Atherosclerosis. 1996;120:147–54. doi: 10.1016/0021-9150(95)05696-three. [PubMed] [CrossRef] [Google Scholar]
  • IP C, Scimeca JA, Thompson HJ. Conjugated linoleic acid. Cancer Supplement. 1994;74(3):1050–4. [PubMed] [Google Scholar]
  • Kritchevsky D, Tepper SA, Wright S, Tso P, Czarnecki SK. Influence of conjugated linoleic acid (CLA) on establishment and progression of atherosclerosis in rabbits. Journal American Collection of Nutrition. 2000;19(four):472S–7S. [PubMed] [Google Scholar]
  • Steinhart H, Rickert R, Winkler K. Identification and analysis of conjugated linoleic acrid isomers (CLA) European Journal of Medicine. 1996;20(8):370–2. [PubMed] [Google Scholar]
  • Dugan MER, Aalhus JL, Jeremiah LE, Kramer JKG, Schaefer AL. The effects of feeding conjugated linoleic acrid on subsequent port quality. Canadian Journal of Fauna Scientific discipline. 1999;79:45–51. [Google Scholar]
  • Park Y, Albright KJ, Liu W, Storkson JM, Cook ME, Pariza MW. Effect of conjugated linoleic acrid on body composition in mice. Lipids. 1997;32:853–viii. doi: 10.1007/s11745-997-0109-x. [PubMed] [CrossRef] [Google Scholar]
  • Sisk K, Hausman D, Martin R, Azain M. Dietary conjugated linoleic acid reduces adiposity in lean but not obese Zucker rats. Journal of Nutrition. 2001;131:1668–74. [PubMed] [Google Scholar]
  • Smedman A, Vessby B. Conjugated linoleic acid supplementation in humans - Metabolic effects. Journal of Diet. 2001;36:773–81. [PubMed] [Google Scholar]
  • Tsuboyama-Kasaoka Due north, Takahashi M, Tanemura Chiliad, Kim HJ, Tange T, Okuyama H, Kasai M, Ikemoto SS, Ezaki O. Conjugated linoleic acrid supplementation reduces adipose tissue by apoptosis and develops lipodystrophy in mice. Diabetes. 2000;49:1534–42. doi: x.2337/diabetes.49.9.1534. [PubMed] [CrossRef] [Google Scholar]
  • Clement 50, Poirier H, Niot I, Bocher Five, Guerre-Millo Chiliad, Krief B, Staels B, Besnard P. Dietary trans-ten, cis-12 conjugated linoleic acid induces hyperinsulemia and fat liver in the mouse. Journal of Lipid Research. 2002;43:1400–9. doi: 10.1194/jlr.M20008-JLR200. [PubMed] [CrossRef] [Google Scholar]
  • Roche HM, Noone E, Sewter C, McBennett S, Barbarous D, Gibney MJ, O'Rahilly South, Vidal-Plug AJ. Isomer-dependent metabolic effects of conjugated linoleic acid: insights from molecular markers sterol regulatory element-binding protein 1c and LXR alpha. Diabetes. 2002;51:2037–44. doi: 10.2337/diabetes.51.7.2037. [PubMed] [CrossRef] [Google Scholar]
  • Riserus U, Arner P, Brismar K, Vessby B. Treatment with dietary trans 10 cis 12 conjugated linoleic acid causes isomer specific insulin resistance in obese men with the metabolic syndrome. Diabetes Care. 2002;25:1516–21. doi: 10.2337/diacare.25.nine.1516. [PubMed] [CrossRef] [Google Scholar]
  • Delany JP, Blohm F, Truett AA, Scimeca JA, West DB. Conjugated linoleic acrid quickly reduces body fatty content in mice without affecting energy intake. American Journal of Physiology. 1999;276(4 pt 2):R1172–R1179. [PubMed] [Google Scholar]
  • Kelley DS, Simon VA, Taylor PC, Rudolph IL, Benito P. Dietary supplementation with conjugated linoleic acid increased its concentration in homo peripheral claret mononuclear cells, but did non alter their function. Lipids. 2001;36:669–74. doi: 10.1007/s11745-001-0771-z. [PubMed] [CrossRef] [Google Scholar]
  • Whigham LD, Cook ME, Atkinson RL. Conjugated linoleic acid: Implications for human wellness. Pharmacological Research. 2000;42(6):503–10. doi: 10.1006/phrs.2000.0735. [PubMed] [CrossRef] [Google Scholar]
  • Schmid A, Collomb 1000, Sieber R, Bee 1000. Conjugated linoleic acid in meat and meat products. A review Meat Scientific discipline. 2006;73:29–41. doi: x.1016/j.meatsci.2005.10.010. [PubMed] [CrossRef] [Google Scholar]
  • Knekt P, Jarvinen R, Seppanen R, Pukkala E, Aromaa A. Intake of dairy products and the risk of breast cancer. British Periodical of Cancer. 1996;73:687–91. [PMC free article] [PubMed] [Google Scholar]
  • Ha YL, Grimm NK, Pariza MW. Newly recognized anticarcinogenic fat acids: identification and quantification in natural and processed cheese. Periodical of Agricultural and Food Chemistry. 1989;37:75–81. doi: x.1021/jf00085a018. [CrossRef] [Google Scholar]
  • Ritzenthaler KL, McGuire MK, Falen R, Shultz TD, Dasgupta Northward, McGuire MA. Interpretation of conjugated linoleic acid intake past written dietary assessment methodologies underestimates actual intake evaluated by food duplicate methodology. Journal of Nutrition. 2001;131:1548–54. [PubMed] [Google Scholar]
  • Parodi Prisoner of war. Conjugated linoleic acid: an anticarcinogenic fatty acid nowadays in milk fat (review) Australian Journal of Dairy Technology. 1994;49(2):93–7. [Google Scholar]
  • Dunne PG, Monahan FJ, O'Mara FP, Moloney AP. Colour of bovine subcutaneous adipose tissue: A review of contributory factors, associations with carcass and meat quality and its potential utility in hallmark of dietary history. Meat Science. 2009;81(1):28–45. doi: 10.1016/j.meatsci.2008.06.013. [PubMed] [CrossRef] [Google Scholar]
  • Chauveau-Duriot B, Thomas D, Portelli J, Doreau M. Carotenoids content in forages: variation during conservation. Renc Rech Ruminants. 2005;12:117. [Google Scholar]
  • Scott LW, Dunn JK, Pownell HJ, Brauchi DJ, McMann MC, Herd JA, Harris KB, Savell JW, Cross 60 minutes, Gotto AM Jr. Effects of beef and chicken consumption on plasma lipid levels in hypercholesterolemic men. Archives of Internal Medicine. 1994;154(xi):1261–seven. doi: ten.1001/archinte.154.11.1261. [PubMed] [CrossRef] [Google Scholar]
  • Hunninghake DB, Maki KC, Kwiterovick PO Jr, Davidson MH, Dicklin MR, Kafonek SD. Incorporation of lean carmine meat National Cholesterol Education Program Pace I diet: a long-term, randomized clinical trial in free-living persons with hypercholesterolemic. Periodical of American Colleges of Nutrition. 2000;19(iii):351–60. [PubMed] [Google Scholar]
  • National Constitute of Health Clinical Nutrition Middle. Facts almost dietary supplements: Vitamin A and Carotenoids. 2002. Ref Blazon: Pamphlet.
  • Descalzo AM, Insani EM, Biolatto A, Sancho AM, Garcia PT, Pensel NA, Josifovich JA. Influence of pasture or grain-based diets supplemented with vitamin E on antioxidant/oxidative balance of Argentine beefiness. Journal of Meat Science. 2005;70:35–44. doi: x.1016/j.meatsci.2004.xi.018. [PubMed] [CrossRef] [Google Scholar]
  • Simonne AH, Green NR, Bransby DI. Consumer acceptability and beta-carotene content of beef as related to cattle finishing diets. Periodical of Nutrient Science. 1996;61:1254–6. doi: ten.1111/j.1365-2621.1996.tb10973.x. [CrossRef] [Google Scholar]
  • Duckett SK, Pratt SL, Pavan E. Corn oil or corn grain supplementation to stters grazing endophyte-gratuitous tall fescue. II. Furnishings on subcutaneous fatty acid content and lipogenic gene expression. Periodical of Fauna Science. 2009;87:1120–8. doi: 10.2527/jas.2008-1420. [PubMed] [CrossRef] [Google Scholar]
  • Yang A, Brewster MJ, Lanari MC, Tume RK. Issue of vitamin Due east supplementation on alpha-tocopherol and beta-carotene concentrations in tissues from pasture and grain-fed cattle. Meat Science. 2002;sixty(1):35–40. doi: x.1016/S0309-1740(01)00102-iv. [PubMed] [CrossRef] [Google Scholar]
  • Pryor WA. Vitamin E and Carotenoid Abstracts- 1994 Studies of Lipid-Soluble Antioxidants. Vitamin E Inquiry and Information Services. 1996.
  • Arnold RN, Scheller North, Arp KK, Williams SC, Beuge DR, Schaefer DM. Effect of long or short-term feeding of alfa-tocopherol acetate to Holstein and crossbred beefiness steers on performance, carcass characteristics, and beefiness colour stability. Journal Animal Science. 1992;70:3055–65. [PubMed] [Google Scholar]
  • Descalzo AM, Sancho AM. A review of natural antioxidants and their effects on oxidative condition, olfactory property and quality of fresh beef in Argentine republic. Meat Science. 2008;79:423–36. doi: 10.1016/j.meatsci.2007.12.006. [PubMed] [CrossRef] [Google Scholar]
  • Insani EM, Eyherabide A, Grigioni M, Sancho AM, Pensel NA, Descalzo AM. Oxidative stability and its relationship with natural antioxidants during refrigerated retail brandish of beef produced in Argentine republic. Meat Science. 2008;79:444–52. doi: 10.1016/j.meatsci.2007.x.017. [PubMed] [CrossRef] [Google Scholar]
  • Lonn EM, Yusuf S. Is in that location a office for antioxidant vitamins in the prevention of cardiovascular diseases? An update on epidemiological and clinical trials data. Cancer Journal of Cardiology. 1997;13:957–65. [PubMed] [Google Scholar]
  • Jialal I, Fuller CJ. Effect of vitamin E, vitamin C and beta-carotene on LDL oxidation and atherosclerosis. Canadian Journal of Cardiology. 1995;11(supplemental G):97G–103G. [PubMed] [Google Scholar]
  • Stampfer MJ, Hennekens CH, Manson JE, Colditz GA, Rosner B, Willett WC. Vitamin E consumption and the risk of coronary affliction in women. New England Journal of Medicine. 1993;328(1444):1449. [PubMed] [Google Scholar]
  • Knekt P, Reunanen A, Jarvinen R, Seppanen R, Heliovaara M, Aromaa A. Antioxidant vitamin intake and coronary bloodshed in a longitudinal population study. American Journal of Epidemiology. 1994;139:1180–9. [PubMed] [Google Scholar]
  • Weitberg AB, Corvese D. Effects of vitamin Eastward and beta-carotene on Deoxyribonucleic acid strand breakage induced by tobacco-specific nitrosamines and stimulated human phagocytes. Journal of Experimental Cancer Research. 1997;16:eleven–four. [PubMed] [Google Scholar]
  • Leske MC, Chylack LT Jr, He Q, Wu SY, Schoenfeld E, Friend J, Wolfe J. Antioxidant vitamins and nuclear opacities: The longitudinal study of cataract. Ophthalmology. 1998;105:831–six. doi: 10.1016/S0161-6420(98)95021-7. [PubMed] [CrossRef] [Google Scholar]
  • Teikari JM, Virtamo J, Rautalahi M, Palmgren J, Liestro K, Heinonen OP. Long-term supplementation with blastoff-tocopherol and beta-carotene and historic period-related cataract. Acta Ophthalmologica Scandinavica. 1997;75:634–40. doi: 10.1111/j.1600-0420.1997.tb00620.x. [PubMed] [CrossRef] [Google Scholar]
  • Dietary guidelines Advisory Committee, Agricultural Research Service The states Department of Agriculture USDA. Report of the dietary guidelines informational committee on the dietary guidelines for Americans. Dietary guidelines Advisory Committee. 2000. Ref Type: Hearing.
  • McClure EK, Belk KE, Scanga JA, Smith GC. Determination of advisable Vitamin E supplementation levels and administration times to ensure adequate muscle tissue alpha-tocopherol concentration in cattle destined for the Nolan Ryan tender-aged beef programme. Animal Sciences Research Study. The Department of Animal Sciences, Colorado State Academy; 2002. Ref Type: Study. [Google Scholar]
  • Yang A, Lanari MC, Brewster MJ, Tume RK. Lipid stability and meat color of beef from pasture and grain-fed cattle with or without vitamin E supplement. Meat Science. 2002;threescore:41–fifty. doi: 10.1016/S0309-1740(01)00103-6. [PubMed] [CrossRef] [Google Scholar]
  • Valencia Due east, Marin A, Hardy G. Glutathione - Nutritional and Pharmacological Viewpoints: Part II. Nutraceuticals. 2001;17:485–6. [PubMed] [Google Scholar]
  • Valencia E, Marin A, Hardy Thou. Glutathione - Nutritional and Pharmacologic Viewpoints: Function IV. Nutraceuticals. 2001;17:783–four. [PubMed] [Google Scholar]
  • Descalzo AM, Rossetti L, Grigioni G, Irurueta M, Sancho AM, Carrete J, Pensel NA. Antioxidant status and odor profile in fresh beef from pasture or grain-fed cattle. Meat Science. 2007;75:299–307. doi: 10.1016/j.meatsci.2006.07.015. [PubMed] [CrossRef] [Google Scholar]
  • Gatellier P, Mercier Y, Renerre M. Effect of diet finishing mode (pasture or mixed diet) on antioxidant status of Charolais bovine meat. Meat Science. 2004;67:385–94. doi: 10.1016/j.meatsci.2003.11.009. [PubMed] [CrossRef] [Google Scholar]
  • French P, O'Riordan EG, Monahan FJ, Caffery PJ, Moloney AP. Fatty acid composition of intra-muscular tricylglycerols of steers fed autumn grass and concentrates. Livestock Production Science. 2003;81:307–17. doi: 10.1016/S0301-6226(02)00253-1. [CrossRef] [Google Scholar]
  • Elmore JS, Warren HE, Mottram DS, Scollan ND, Enser Chiliad, Richardson RI. A comparison of the olfactory property volatiles and fatty acid compositions of grilled beef muscle from Aberdeen Angus and Holstein-Friesian steers fed deits based on silage or concentrates. Meat Science. 2006;68:27–33. doi: 10.1016/j.meatsci.2004.01.010. [PubMed] [CrossRef] [Google Scholar]
  • Lorenz S, Buettner A, Ender Grand, Nuernberg One thousand, Papstein HJ, Schieberle P. Influence of keeping organization on the fatty acrid limerick in the longissimus muscle of bulls and odorants formed after pressure level-cooking. European Nutrient Research and Applied science. 2002;214:112–8. doi: 10.1007/s00217-001-0427-4. [CrossRef] [Google Scholar]
  • Calkins CR, Hodgen JM. A fresh look at meat flavor. Meat Scientific discipline. 2007;77:63–fourscore. doi: 10.1016/j.meatsci.2007.04.016. [PubMed] [CrossRef] [Google Scholar]
  • Sanudo C, Enser ME, Campo MM, Nute GR, Maria G, Sierra I, Wood JD. Fatty acid composition and sensory characteristics of lamb carcasses from U.k. and Spain. Meat Science. 2000;54:339–46. doi: 10.1016/S0309-1740(99)00108-iv. [PubMed] [CrossRef] [Google Scholar]
  • Killinger KM, Calkins CR, Umberger WJ, Feuz DM, Eskridge KM. A comparison of consumer sensory credence and value of domestic beef steaks and steaks form a branded, Argentine beefiness programme. Journal Animal Scientific discipline. 2004;82:3302–7. [PubMed] [Google Scholar]

Articles from Nutrition Journal are provided hither courtesy of BioMed Central


gasparsumate.blogspot.com

Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846864/

0 Response to "Does Grass Fed Beef Have Amoega 3"

Post a Comment

Iklan Atas Artikel

Iklan Tengah Artikel 1

Iklan Tengah Artikel 2

Iklan Bawah Artikel