Dear Label_Name,

Greetings! I hope you are well.

I am writing on behalf of an international publishing house, Science and Education Publishing, USA (http://www.sciepub.com).

Science and Education Publishing (SciEP) is a multidisciplinary open access publisher of Journals covering the fields of Science, Technology and Medicine. All SciEP publications are subject to high-quality peer review, editorial and production processes and are freely available online.

Welcome to the April, 2013 edition of SciEP newsletter, providing monthly summaries of articles on science & education related topics of interest to scientist and professionals. The mission of our journals is to provide an open access forum for publishing new findings on issues pertinent to scientific and academic field. We also invite you to submit original research papers, review articles, short reports, or case studies are considered for publication in our Multidisciplinary Journals.

American Journal of Public Health Research
DOI: 10.12691/ajphr-1-1-3

The Implementation of a Tele-Homecare System with Service Oriented Architecture and HL7 Message Transmission Standard
Ching-Sung Wang

American Journal of Medical and Biological Research
DOI: 10.12691/ajmbr-1-1-2

The Influence of Ethanol on Pyruvate Kinases Activity in Vivo, in Vitro, in Silico
Lelevich Sergey Vladimirovich, Khrustalev Vladislav Victorovich, Barkovsky Eugene Victorovich, Shedogubova Tatyana Aleksandrovna

American Journal of Medical Sciences and Medicine
DOI: 10.12691/ajmsm-1-1-1

Clinical and Histological Features in Wegener Granulomatosis
Li Cavoli Gioacchino, Passantino Rita, Bono Luisa, Tortorici Calogera, Ferrantelli Angelo, Giammarresi Carlo, Rotolo Ugo

American Journal of Infectious Diseases and Microbiology
DOI: 10.12691/ajidm-1-1-2

The Curse of Lymphatic Filariasis: Would the Continual Use of Diethylcarbamazine Eliminate this Scourge in Papua New Guinea?
Anne Lanham, Lillian Mwanri

We have released issues of some journals on February 2013.
American Journal of Public Health Research
American Journal of Medical Sciences and Medicine
American Journal of Medical and Biological Research
American Journal of Pharmacological Sciences
American Journal of Clinical Medicine Research
American Journal of Nursing Research
American Journal of Cancer Prevention
American Journal of Medicine Studies
American Journal of Infectious Diseases and Microbiology
American Journal of Cardiovascular Disease Research
American Journal of Biomedical Research
American Journal of Mechanical Engineering
American Journal of Microbiological Research
Journal of Preventive Medicine
American Journal of Food and Nutrition
American Journal of Hypertension Research
American Journal of Sports Science and Medicine
Journal of Cancer Research and Treatment
American Journal of Zoological Research
Journal of Biomedical Engineering and Technology
American Journal of Microbiological Research
Biomedical Science and Engineering

We are pleased to announce that submissions are now being accepted for peer review for all the journals across all our subject areas in SciEP.

Please submit your manuscript via our online submission system:
http://www.sciepub.com/author/signin

To unsubscribe from our mailing list, please click on the following link: unsubscribe

I am looking forward to hearing from you.

Kind regards,

David Rain
Email:join@sciepub.com
Science and Education Publishing (http://www.sciepub.com)

Fatty Acid Profile Differences Among the Muscle Tissue of Three Rodents (Hydroahoerus hidrochaeris, Cuniculus paca and Cavia porcellus) and one Lagomorph (Oryctolagus cuniculus)

Liliana Betancourt*, Gonzalo JairDiaz

Universidad de La Salle, Facultad de Ciencias Agropecuarias, Departamento de Producción Animal, Bogotá, Colombia

Abstract: The consumer demand for functional food with nutraceutical properties has increased in recent years, and the food’s fatty acid profile is one of the factors that define its potential value asa functional food. The aim of the present study was to compare fatty acids composition of semitendinosus muscle in two native rodents, the capybara (Hydroahoerus hidrochaeris) and lowland paca (Cuniculus paca) and two domesticated species, one rodent, the guinea pig (Cavia porcellus) and one lagomorph, the common rabbit (Oryctolagus cuniculus). The animals were fed with forage-based diet. The fatty acid composition in lyophilized tissue was determined by gas chromatography. The capybara, lowland paca and guinea pig had the highest levels of omega-3 (n-3) fatty acids, predominantly α-linolenic acid (p<0.05). The guinea pig and common rabbit showed a higher content of linoleic acid (18:2 n-6) (p<0.05). The n-6: n-3 fatty acids ratio was higher to the common rabbit (p<0.05) with 8.9, in contrast, capybara and lowland paca had the lowest ratio, with lower than zero values indicating a predominance of n-3 fatty acids. These results were presented without any diet manipulation. The guinea pig meat contained an adequate balance of n-6 to n-3 fatty acids (< 4) whereas in rabbit meat there was an excess of n-6 fatty acids. The capybara and lowland paca can be considered as sources of n-3 fatty acids, represented by α-linolenic acid (18:3 n-3). These results confirm that native species not subjected to genetic selection and intensive feeding, showed higher content of n-3 fatty acids.

Keywords: Omega-3 fatty acids, small herbivores, fatty acid profile, α-linolenic acid

Received September 09, 2014; Revised September 30, 2014; Accepted October 09, 2014

Citation: Liliana Betancourt, Gonzalo JairDiaz, Fatty Acid Profile Differences Among the Muscle Tissue of Three Rodents (Hydroahoerus hidrochaeris, Cuniculus paca and Cavia porcellus) and one Lagomorph (Oryctolagus cuniculus). Journal of Food and Nutrition Research, 2 (10). 744-748. January 2014. doi:10.12691/jfnr-2-10-14

1. Introduction

In recent years, numerous studies have been focused on increase the n-3 fatty acid content in meat, eggs or milk through modifications of animal diets [1,2]. This increased focus is a result of the increased demand for functional foods that can prevent or control diseases. The functional food market value can attain twice the commercial value of ordinary food [3], and foods enriched with n-3 fatty acids can be considered functional foods because n-3 fatty acids are essential for health and can prevent and control diseases such as arthritis, inflammation, autoimmune disorders, cardiovascular disease and cancer [4,5]. Currently, it is known that an interaction occurs between nutrition and genetic material, mainly between n-6: n-3 fatty acids ratio, specific genetic variants and disease phenotypes [6,7]. Many of the chronic conditions of cardiovascular disease, diabetes, cancer, obesity, autoimmune diseases, rheumatoid arthritis, asthma and depression are associated with increased production of thromboxane A2 (TXA2), leukotriene B4 (LTB4), suppress interleukin 1β (IL-1β), tumor necrosis factor-α (TNFα) and interleukin-6 (IL-6), and C-reactive protein (CRP). All these factors are increased by increases in omega-6 fatty acid intake and decreased by increases in omega-3 fatty acid intake [8]. Furthermore, the balance of omega-6 and omega-3 fatty acids is very important for homeostasis and normal development.

However, few studies have addressed to native foods fatty acid composition, which were staple foods for our ancestors, compared to the food that are produced under commercial conditions and had been subject to selection and breeding. The muscular fibre type composition and fatty acid profile has been showed that changes for intensively produced species respect to natives species [9].

The capybara, lowland paca, guinea pig and rabbit are predominantly herbivorous species that are cecal fermenters and practice caecotrophy. The capybara is considered the largest rodent in the world (50 kg of body weight) and is the most abundant in the flooded savannas of South America. It is distributed from Panama to Uruguay and north of Argentina, and it mainly inhabits the edge of the Atlantic coast of South America [10]. However, the capybara as a species has not yet undergone programs of genetic improvement and intensive production. The lowland paca or spotted paca has a similar past to the capybara and guinea pig as a food source for the natives who inhabited the Andean region of South America. The lowland paca is one of the largest rodents in the world (12 kg of body weight). It lives in Andean forests, inhabits flooded savannas, and its diet is based on vegetables and aquatic animals. The lowland paca is a species that can adapt to living in intensively cultivated areas [11]. The guinea pig is a species native to the Andes, breeding commercially to human intake; there are approximately 35,000,000 of animals in countries such as Peru, Bolivia, Ecuador and Colombia and is appreciated for the high quality of its meat and linked to the local gastronomic traditions. The guinea pig reaches a body weight of 900 g in seven weeks of age, and it is fed a diet based on forage, with protein and energy supplementation [12]. The breeding of rabbit is globally standardized, and similar to the guinea pig, they have been subjected to genetic selection and breeding. Traditionally, the rabbit has been recognized as a suitable meat source for human feeding because of its high protein and low fat content compared to poultry, beef or pork [13].

Thus far, the studies performed on the capybara and lowland paca have focused on the biology, geographic distribution and breeding [14]. However, little is known of their meat composition, in particular the fatty acid profile. The knowledge of meat fatty acid profile and their comparing between wild and domesticated species could help to define changes in the profile and metabolism of fatty acids as a result of domestication. Also, it is important to characterize these meats from the human food quality perspective. This study characterized the fatty acid profile in four small herbivorous species, rabbit and guinea pig bred commercially, capybara and lowland lapa were produced under not conventionally breeding.

2. Materials and Methods

Twelve samples of each species were collected from commercial farms (guinea pig and rabbits) or wild animals breeding (capybara and lowland paca). The animals were fed with forage-based diet. Three hundred grams of semitendinosus muscle to analysis were taken. The tissue was lyophilized and conserved at -10°C until analysis. Lipids were extracted by a chloroform/methanol 2 to 1 solution [15] using a mechanical homogenizer. The homogenized product was filtered, and 5 ml of distilled water was added to 20 ml of this filtrate. The mix was centrifuged at 3000 rpm for 20 minutes, the supernatant was discarded, 1 ml of the lower organic phase was placed in a previously weighed test tube, and the solvent was evaporated under a gentle stream of nitrogen. The dry lipids were dissolved in a chloroform/methanol 1 to 1 solution (1 ml for each 100 mg of lipids). A 50 µl aliquot of the lipid solution was esterified by the methyl esterification Meth-Prep II reagent (Alltech Associates Inc., Deerfield, IL, USA) to produce fatty acid methyl esters.

The fatty acid methyl esters were analyzed by a Shimadzu GC-2014 (Kyoto, Japan) gas chromatograph equipped with a flame ionization detector (260°C). Separation was performed on a 30 m x 0.32 mm Supelco® Omegawax 320 column with 0.25 µm film thickness. Separation was achieved by a temperature ramp program (initial temperature of 80°C, then increased by 10°C/min until attaining 190°C, held for 20 min at 190°C, then increased by 2°C/min until attaining 220°C and held for 10 min at 220°C). Helium was the transporter gas, and the injection was performed in “split” mode (ratio 1 to 50). The fatty acid methyl esters were identified by comparing their retention time to a standard mix of fatty acids (Supelco 37 component FAME Mix, Supelco, Inc., Bellefonte, PA, USA). The fatty acid composition was expressed as a percentage of each fatty acid to the total of the identified fatty acids.

The statistical analysis was performed using an analysis of variance at one way to evaluate the results and compare the fatty acid content between the four species under study. The differences were tested Tukey’s test [16].

3. Results

The muscle fatty acid profile of the four species under study and lists the content of saturated fatty acids (SFAs), monounsaturated fatty acids (MUFAs), polyunsaturated fatty acids (PUFAs), n-3 and n-6 fatty acid concentrations and ratio of n-6 to n-3 fatty acids are presented in the Table 1.

The guinea pig presented the greatest content of PUFAs (P<0.05) at more than 40% compared to the paca, capybara and rabbit. The capybara and lowland paca showed higher levels of n-3 fatty acids (P<0.05) with 20.0 and 22.5%, respectively; whereas guinea pig and rabbit had 9.0 and 3.5%, respectively. The α-linolenicfatty acid (C18:3 n-3) was prevalent among the n-3 fatty acids. However, a large content of eicosatetraenoic acid (C20:3 n-3) was found in the lowland paca with a 9.0%, also docosapentaenoic acid (C20:5 n-3) at 1.0%. The guinea pig and rabbit showed the highest content of n-6 fatty acids (P<0.05), with more than 30% of linoleic acid (C18:2n-6), where astocapybara and lowland paca, the contents were 12 and 13%, respectively. The rabbit showed the highest n-6 to n-3 ratio (P<0.05) with a value of 8.9, when is compared with another studied species. Remarkably, the capybara and lowland paca showed n-6: n-3 ratio lower than 1, which implies that n-3 fatty acids predominated in these species.

The capybara and rabbit showed the highest levels of total MUFAs respect to lowland paca. The predominant fatty acid of this group in all species under study was the oleic acid (C18:1n-9), and there were no differences among the species. The second-most prevalent MUFA was palmitoleic acid, which was higher in the rabbit compared to the guinea pig (P<0.05). Heptadecenoic acid (C17:1) was only detected in the capybara and lowland paca, at levels ≤1%.

Capybara showed higher saturated fatty acids than guinea pig (P<0.05). Palmitic acid (C16:0) was the predominant saturated fatty acid to all of the species. Palmitic acid levels ranged from 25.6 to 27.8% and there were no significant differences among species. Stearic acid (C18:0), another saturated fatty acid, was the second-most prevalent fatty acid, and it was higher in the lowland paca meat (P<0.05) compared to rabbit with 8.4 and 6.0%, respectively.

Table 1. Fatty acid composition in the capybara (Hydroahoerus hidrochaeris), lowland paca (Cuniculus paca), guinea pig (Cavia porcellus) and common rabbit (Oryctolagus cuniculus) muscle¹

4. Discussion

The present study is the first to compare the fatty acid profiles of three rodent and one lagomorph species, with two domesticated herbivores species (guinea pig and common rabbit) and two wild species (capybara and lowland paca) included to assess their animal breeding potential.

Although dietary fatty acid composition is a determinant factor of the animal tissue fatty acid content [17], such profiles in herbivorous species also depend on factors other than diet. These factors include fatty acid microbial metabolism and hydrogenation in the digestive tract [18], enzymatic activity in the digestive tract, oxidation status [19] and genetic aspects in the specific case of rabbits [20], novo synthesis and beta-oxidation in the mitochondria lead to accumulation of fatty acids in tissues and depend of genes expression such as acetyl-CoA carboxylase (ACC) 1, ACC2, and fatty acid synthase (FAS). A decrease in the n-3 fatty acid content may occur in animal tissue because of animal domestication and intensive breeding. In general, n-3 fatty acid levels found in the capybara, lowland paca and guinea pig were equal to or greater than the levels found in studies where the animal diet was manipulated with n-3 fatty acids sources. This enrichment was performed to increase the n-3 fatty acid levels in the consequent animal products, such as the meat or eggs, in different species. For example, Crespo and Esteve-García [21] obtained contents of 24.4% to α-linolenic acid in broiler chickens fed with a diet supplemented with 10% of linseed oil, whereas Galobart et al. [22] obtained contents of 10.3% to α-linolenic acid in the egg yolk of hens fed a 5% of linseed oil in diet. The herbivorous rodent species studied were under natural feeding conditions based on forage, the levels of n-3 fatty acids were higher in these species than other herbivorous species, including lamb, beef and buffalo meat [23].

The percentage of n-3 fatty acids in the meat of capybara was less than reported by Delfinoand Sarno [24]. They found levels of 25% to α-linolenic acid, 0.3% eicosapentaenoic acid (C20:5n-3, EPA) and 2.5% to docosahexaenoic acid (C22:6n-3, DHA). In the present study, a 20% of α-linolenic acid level was found and neither EPA nor DHA was detected. These differences might be attributed to different environments and diets since the data from Delfino and Sarno [24] were from Argentina´s capybaras, whereas the present study was conducted with Colombia´s capybaras.

The main dietary fatty acid for monogastric animals, particularly for rabbit, is linoleic acid (C18:2 n-6) [25]. The levels of linoleic acid were high in the guinea pig (31.3%) and rabbit (22.1%), with similar value to the reported in previous studies [13,26]. In contrast, the lowest levels of linoleic acid were found in the wild species of lowland paca and capybara. These results confirm that the foods commonly consumed from commercial production system are usually deficient in n-3 and rich in n-6 fatty acids, caused by intensification of agriculture [19,27] which promotes the disequilibrium of the n-6 to n-3 ratio in the modern human diet.

The meat of capybara, lowland paca and guinea pig showed a suitablen-6 to n-3 fatty acids ratio (less than 4) for human nutrition [5]. However, the values for rabbit meat did not fall within these levels. In previous studies with rabbit meat, a decreased n-6 to n-3 fatty acids ratio to less than 4 values of has been reached by diet modifications and the inclusion of linseed oil [24,28] or Chia seed (Salvia hispanica L.) [2]. However, the same authors confirmed a reduced oxidative stability of the fat samples through a thiobarbituric acid reactive substance (TBARS) assay when the diet was enriched with n-3 fatty acids. Other studies with different domesticated species have also reported higher levels to n-6 to n-3 fatty acids ratio, with 11.3, 10.7 34.9 ratio in rabbit meat, chicken breast and beef longissimus, respectively [26,29]. Maintain the equilibrium between n-6 and n-3 fatty acids is essential. Eicosanoids of great physiological significance are generated from these two fatty acids groups and show antagonistic functions. Therefore, the n-6 and n-3 fatty acids must be maintained within a balance [19]. Thus, the ratio of n-6 to n-3 requires values within the physiological range of 4:1 to 2:1 [7]. An excess of omega-6 fatty acids and a deficiency of omega-3 fatty acids are frequently found to the most of foods. This tendency has been attributed to the intensification of agriculture [5,7] and has been confirmed by the present study. Native species such as capybara and lowland paca have not been subjected to genetic selection pressure and maintain suitable levels of n-3 and n-6 fatty acids.

Another important factor related to fatty acid profilesis the PUFAs and SFAs ratio because this determines the fluidity and physical properties of the cell membranes. Low values have been associated with diabetes, obesity, hypertension, cancer and cardiovascular disease [30]. The meat of the guinea pig and lowland paca showed a PUFAs and SFA sratio of 1.2, whereas the capybara and rabbit meat had a ratio of 0.8. All species of the present study showed a better (higher) ratio between polyunsaturated and saturated fatty acids compared to other domesticated species. Chicken meat had a value of 0.3 [1], beef had a value of 0.23 [23] and pork had a value of 0.54 [31].

The SFA content was relatively low to the species studied when they were compared to other herbivorous animals, such as bovine or moose [23]. DalleZote [26] reported a 38.3% of SFA content in rabbit leg and 38.9% to beef. Enser et al. [32] reported a 36.9% of SFA content in pork meat. Low levels of stearic acid with high levels of oleic acid (18:1n-9) and the presence of monounsaturated fatty acids C16:1 and C17:1 indicate a proper enzymatic activity of stearoyl-CoA desaturases [31], mainly of delta-9-desaturase enzyme in the liver or the possible bacterial isomerization of 18:1n-9 [33] in the species under this study. The muscular fiber type composition and fatty acid profile has been showed that changes for intensively produced species respect to natives species [9].

5. Conclusions

The results of the present study suggest that the meat of the capybara, and lowland paca could be considered as differentiated food because their high content of omega-3 fatty acids and low (<1) n-6: n-3 fatty acids ratio. These meats also have a higher PUFA to SFA ratio when they are compared with chicken, beef and pork. There are contrasting differences in the fatty acid composition in the species under study compared to another herbivorous species, such as bovine or lamb. It is possible that different fatty acid metabolism exists among these species that is associated with the ruminant digestive system. Thus, would be interesting to investigate the differences in fatty acid metabolism and deposition between herbivorous monogastric and polygastric species, as well as the genes that regulate the metabolism of fatty acids through different animal species.

References

[1]   | López-Ferrer, S.,Baucells,M. D., Barroeta,A. C., and Grashorn, M. A. “n-3 enrichment of chicken meat. 1. Use of very long chain fatty acids in chicken diets and their influence on meat quality: fish oil”. Poultry Science 80, 741-752, 2001.
[2]   | Meineri, G., Cornale, P., Tassone, S., and Peiretti, P. G. “Effects of Chia (Salvia hispanicaL.) seed supplementation on rabbit meat quality, oxidative stability and sensory traits”. Italian Journal of Animal Science 9, e10. 2010.
[3]   | Patterson P. H., Koelkebeck, K. W., Bell, D. D., Carey, J. B., Anderson, K. E., and Darre, M. J. “Egg marketing in national supermarkets: specialty eggs - Part 2”. Poultry. Science. 80, 390-395, 2001.
[4]   | Lewis, N. M.,Schalch,K., and Scheideler, S. E. “Serum lipid response to n-3 fatty acid enriched eggs in persons with hypercholesterolemia”. Journal of the American Dietetic Association 100, 365-367, 2000.
[5]   | Simopoulos A. P. “Human requirement for n-3 polyunsaturated fatty acids”. Poultry Science 79, 961-970, 2000.
[6]   | Corella, D., and Ordovás, J. M. “Interactions between dietary n-3 fatty acids and genetic variants and risk of disease”. British Journal of Nutrition 107, S271-S283, 2012.
[7]   | Simopoulos, A. P. “Genetic variants in the metabolism of omega-6 and omega-3 fatty acids: their role in the determination of nutritional requirements and chronic disease risk”. Experimental Biology and Medicine 235, 785-795, 2010.
[8]   | Simopoulos, A. Evolutionary aspects of diet, the omega-6/omega-3 ratio and genetic variation: nutritional implications for chronic diseases. Biomedicine & Pharmacotherapy 60, 502–507, 2006.
[9]   | Velotto, S., Vitale, C., Crasto, A. Muscle fibre types, fat deposition and fatty acid profile of Casertana versus Large White pig. Animal Science Papers and Reports 30, 35-44, 2012.
[10]   | Alho, C.J.R., Campos, Z.M., and Gonçalves, H. C.Ecology, social behavior and management of the capybara in the Pantanal of Brazil. pp 163-194. In: Redford, K. H, and Eisemberg, J. F, editors, Advances in Neotropical Mammalogy. Sandhill Crane Press, Gainesville, FL. 1989, 163-194.
[11]   | Rincón F.Y., Tinjacá, J. K., and Murillo, R. “Experiences in animal breeding Barnacle (Cuniculuspaca) as a contribution to their conservation and sustainable use in the department of Meta”. Revista Sistemas de Producción Agroecológicos 4, 174-201, 2013.
[12]   | Chauca, L. 1997. Producción de cuyes (Cavia porcellus) [Guinea pigs (Cavia porcellus) production]. Instituto Nacional de Investigación Agraria [NationalInstitute of AgriculturalResearch], La Molina, Perú. Departamento de Agricultura, FAO [Agriculture Department, FAO].
[13]   | Lazzaroni, C., Biagini,D., and Lussiana, C. “Fatty acid composition of meat and perirenal fat in rabbits from two different rearing systems”. Meat Science 83, 135-139, 2009.
[14]   | Bonilla, M. M., Rodríguez, J., Murillo, R. “ Biology of agouti (Cuniculus paca Brisson): a breedingperspective”. Revista CES Medicina Zootecnia 8, 83-96, 2013.
[15]   | Folch, J.,Lees,M., and Sloane-Stanley, G. H. “A simple method for the isolation and purification of total lipids from animal tissues”. Journal Biological Chemistry 226, 497-509, 1957.
[16]   | Kaps, M., and W. Lamberson. 2004. Biostatistics for Animal Science. CABI Publishing, Cambridge.
[17]   | Dal Bosco, A.,Castellini,C., Bianchi,L., and Mugnai, C. “Effect of dietary α-linolenic acid and vitamin E on the fatty acid composition, storage stability and sensory traits of rabbit meat”. Meat Science 66, 407-413, 2004.

[18]  
French, P.,Stanton,C., Lawless,F., O’Riordan,E. G., Monahan,F. J., Caffrey,P. J., and Moloney, A. P. “Fatty acid composition, including conjugated linoleic acid, of intramuscular fat from steers offered grazed grass, grass silage, or concentrate-based diets”. Journal of Animal Science 78, 2849-2855, 2000.

[19]   | Palmquist, D.L. “Omega-3 fatty acids in metabolism, health, and nutrition and for modified animal product foods”. Professional Animal Scientist 25, 207-249, 2009.
[20]   | Hernández, P.,Cesari,V., and Blasco, A. “Effect of genetic rabbit lines on lipid content, lipolytic activities and fatty acid composition of hind leg meat and perirenal fat”. Meat Science 78, 485-491, 2008.
[21]   | Crespo, N., and Esteve-García, E. “Dietary polyunsaturated fatty acids decrease fat deposition in separable fat depots but not in the remainder carcass”. Poultry Science 81, 512-518, 2002.
[22]   | Galobart, J.,Barroeta, A. C., Baucells, M. D., Codony, R., and Ternes, W. “Effect of dietary supplementation with rosemary extract and α-tocopheryl acetate on lipid oxidation in eggs enriched with ω3-fatty acid”. Poultry Science 80, 460-467, 2001.
[23]   | Felton, E. E. D., and Kerley, M. S. “Performance of carcass quality of steers fed different source of dietary fat”. Journal of Animal Science 82, 1794-1805, 2004.
[24]   | Delfino, M., y Sarno, M. Perfil de ácidos grasos de algunos alimentos autóctonos de origen animal. Cátedra de Análisis Instrumental, Facultad de Ciencias Exactas y Naturales, UNNE, Corrientes, Argentina. 2003. 4 p.
[25]   | Kouba, M.,Benatmane,F., Blochet,J. E., and Mourot, J. “Effect of a linseed diet on lipid oxidation, fatty acid composition of muscle, perirenal fat, and raw and cooked rabbit meat”. Meat Science 80, 829-834, 2008.
[26]   | DalleZotte, A. “Perception of rabbit meat quality and major factors influencing the rabbit carcass and meat quality”. Livestock Production Science 75, 11-32, 2002.
[27]   | Eaton, S. B., and Konner, M. “Paleolithic nutrition: a consideration of its nature and current implications”. New England Journal of Medicine 312, 283-289, 1985.
[28]   | Peiretti, P. G. “Effects of dietary fatty acids on lipid traits in the muscle and perirenal fat of growing rabbits fed mixed diets”. Animals 2, 55-67, 2012.
[29]   | Wattanachant, S.,Benjakul, S., and Ledward, D. A. “Composition, color, and texture of Thai indigenous and broiler chicken muscles”. Poultry Science 83, 123-128, 2004.
[30]   | Kim, Y.C., and Ntambi, J. M. “Regulation of stearoyl-CoA desaturase genes: role in cellular metabolism and preadipocyte differentiation”. Biochemical and Biophysical Research Communications 266, 1-4, 1999.
[31]   | Kouba, M.,Enser,M., Whittington, F. M., Nute, G. R., and Wood, J. D. “Effect of high-linolenic acid on lipogenic enzyme activities, fatty acid composition, and meat quality in the growing pig”. Journal of Animal Science 81, 1967-1975, 2003.
[32]   | Enser, M.,Hallet,K., Hewitt,B., Fursey,G. A. J., and Wood.J. D. “Fatty acid content and composition of English beef, lamb and pig at retail”. Meat Science 42, 443-456, 1996.
[33]   | Cordain, L., Watkins, B. A., Florant, G. L., Kelher, M., Rogers, L., and Li, Y. “Fatty acid analysis of wild ruminant tissues: evolutionary implications for reducing diet-related chronic disease”. European Journal of Clinical Nutrition 56, 181-191, 2002.