Analyze Diet
PloS one2019; 14(3); e0207568; doi: 10.1371/journal.pone.0207568

Lipid classes in adipose tissues and liver differ between Shetland ponies and Warmblood horses.

Abstract: Fatty acids, as key components of cellular membranes and complex lipids, may play a central role in endocrine signalling and the function of adipose tissue and liver. Thus, the lipid fatty acid composition may play a role in health status in the equine. This study aimed to investigate the fatty acid composition of different tissues and liver lipid classes by comparing Warmblood horses and Shetland ponies under defined conditions. We hypothesized that ponies show different lipid patterns than horses in adipose tissue, liver and plasma. Six Warmblood horses and six Shetland ponies were housed and fed under identical conditions. Tissue and blood sampling were performed following a standardized protocol. A one-step lipid extraction, methylation and trans-esterification method with subsequent gas chromatography was used to analyse the total lipid content and fatty acid profile of retroperitoneal, mesocolon and subcutaneous adipose tissue, liver and plasma. Fatty acids were grouped according to their degree of saturation and their conjugated double bond into the respective lipid classes. In the adipose tissues, saturated fatty acids (SFAs) and n-9 monounsaturated fatty acids (n-9 MUFAs) were most present in ponies and horses. N-6 polyunsaturated fatty acids (n-6 PUFAs), followed by SFAs, were most frequently found in liver tissue and plasma in all animals. Horses, in comparison to ponies, had significantly higher n-6 PUFA levels in all tissues and plasma. In liver tissue, horses had significantly lower hepatic iso-branched-chain fatty acids (iso-BCFAs) than ponies. The hepatic fatty acid composition of selected lipid classes was different between horses and ponies. In the polar PL fraction, horses had low n-9 MUFA and n-3 PUFA contents but higher n-6 PUFA contents than ponies. Furthermore, iso-BCFAs are absent in several hepatic lipid fractions of horses but not ponies. The differences in fatty acid lipid classes between horses and ponies provide key information on the species- and location-specific regulation of FA metabolism, thus affecting health status such as inflammatory responses.
Publication Date: 2019-03-21 PubMed ID: 30897169PubMed Central: PMC6428305DOI: 10.1371/journal.pone.0207568Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research compared the fatty acid composition in different tissues and liver lipid classes in Warmblood horses and Shetland ponies. The findings indicated notable differences in lipid patterns between the two breeds, which may influence aspects like endocrine signaling and tissue functionality.

Objective and Hypothesis

  • The study aimed to examine the fatty acid composition in different tissues and liver lipid classes in two different equine breeds: Warmblood horses and Shetland ponies. With fatty acids playing an integral role in cellular membrane composition, endocrine signaling, and tissue functions, this comparison aimed to shed light on their differential impact on the health status of the two breeds.
  • The researchers hypothesized that ponies and horses would exhibit significantly different lipid patterns in their adipose tissue, liver, and plasma under identical housing and feeding conditions.

Methods and Procedures

  • Twelve animals, consisting of six Warmblood horses and six Shetland ponies, were put under identical conditions of feeding and housing.
  • Researchers then collected tissue and blood samples following a standardised protocol.
  • To analyze the total lipid content and the fatty acid profile, the researchers used a unified process combining lipid extraction, methylation, and transesterification, followed by gas chromatography analysis.
  • The tested tissues included retroperitoneal, mesocolon and subcutaneous adipose tissue along with liver and plasma.
  • The fatty acids were classified according to their saturation degree and their conjugated double bond into respective lipid classes.

Findings and Interpretations

  • In both ponies and horses, the most prevalent fatty acids in adipose tissues were saturated fatty acids (SFAs) and n-9 monounsaturated fatty acids (n-9 MUFAs).
  • Furthermore, n-6 polyunsaturated fatty acids (n-6 PUFAs) were found to be the most common in liver tissue and plasma across all tested animals, followed by SFAs.
  • Comparatively, horses exhibited significantly higher n-6 PUFA levels in all analyzed tissues and plasma as compared to ponies.
  • On the other hand, the ponies’ liver tissue contained significantly more hepatic iso-branched-chain fatty acids (iso-BCFAs) than those of the horses.
  • When looking at the fatty acid composition of specific lipid classes in the liver, differences between horses and ponies were apparent. Horses had lower n-9 MUFA and n-3 PUFA contents in the polar PL fraction, but a higher content of n-6 PUFA than ponies.
  • In several of the horses’ hepatic lipid fractions, iso-BCFAs were absent, contrasting with the ponies.

Health Implications and Insights for Future Research

  • The differences in lipid patterns between horses and ponies may impact cellular functions, endocrine signaling, and, consequently, the overall health status in these equine species. It potentially influences inflammatory responses associated with different fatty acid metabolisms.
  • The findings provide critical insights on the species-specific regulation of fatty acid metabolism, particularly in relation to their physiological environments.
  • These results may inform future research and nutritional approaches for both ponies and horses, potentially leading to improvements in their health status and longevity.

Cite This Article

APA
Adolph S, Schedlbauer C, Blaue D, Schöniger A, Gittel C, Brehm W, Fuhrmann H, Vervuert I. (2019). Lipid classes in adipose tissues and liver differ between Shetland ponies and Warmblood horses. PLoS One, 14(3), e0207568. https://doi.org/10.1371/journal.pone.0207568

Publication

ISSN: 1932-6203
NlmUniqueID: 101285081
Country: United States
Language: English
Volume: 14
Issue: 3
Pages: e0207568

Researcher Affiliations

Adolph, Stephanie
  • Institute of Animal Nutrition, Nutrition Diseases and Dietetics, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Schedlbauer, Carola
  • Institute of Animal Nutrition, Nutrition Diseases and Dietetics, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Blaue, Dominique
  • Institute of Animal Nutrition, Nutrition Diseases and Dietetics, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Schöniger, Axel
  • Institute of Biochemistry, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Gittel, Claudia
  • University Equine Hospital, formerly Large Animal Clinic for Surgery, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Brehm, Walter
  • University Equine Hospital, formerly Large Animal Clinic for Surgery, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Fuhrmann, Herbert
  • Institute of Biochemistry, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.
Vervuert, Ingrid
  • Institute of Animal Nutrition, Nutrition Diseases and Dietetics, Faculty of Veterinary Medicine, University of Leipzig, Leipzig, Germany.

MeSH Terms

  • Adipose Tissue / chemistry
  • Age Factors
  • Animals
  • Chromatography, Gas
  • Esterification
  • Fatty Acids / analysis
  • Fatty Acids / blood
  • Fatty Acids / classification
  • Horses
  • Liver / chemistry
  • Methylation

Conflict of Interest Statement

The authors have declared that no competing interests exist.

References

This article includes 74 references
  1. Bauer JE, Ransone WD. Fatty acid composition of serum lipids in fasting ponies. Lipids 1983;18: 397–401.
    pubmed: 6877044
  2. Watson TDG, Burns L, Love S, Packard CJ, Shepherd J. The isolation, characterisation and quantification of the equine plasma lipoproteins. Equine Vet J 1991;23: 353–359.
    pubmed: 1959526
  3. Asadi F, Asadian P, Shahriari A, Pourkabir M, Kazemi A. Serum lipid and lipoprotein patterns of Iranian horses. Rev Sci Tech 2011;30: 955–960.
    pubmed: 22435206
  4. Nazifi S, Saeb M, Rategh S, Khojandi A. Serum lipids and lipoproteins in clinically healthy Caspian miniature horses. Veterinarski Arhiv 2005;75: 175–182.
  5. Straub R, Petitjean J, Tschudi P. Serumlipide und lipoproteide bei gesunden Equiden. Schweizer Archiv fur Tierheilkunde 1977;119: 92–101.
    pubmed: 867021
  6. Jeffcott L, Field J. Current concepts of hyperlipaemia in horses and ponies. Vet Rec 1985;116: 461–466.
    pubmed: 3890349
  7. Calder PC. Functional roles of fatty acids and their effects on human health. J Parenter Enteral Nutr 2015;39: 18S–32S.
    pubmed: 26177664
  8. Juárez-Hernández E, Chávez-Tapia NC, Uribe M, Barbero-Becerra VJ. Role of bioactive fatty acids in nonalcoholic fatty liver disease. Nutr J 2016;15: 72.
    doi: 10.1186/s12937-016-0191-8pmc: PMC4970250pubmed: 27485440google scholar: lookup
  9. Rodrigues HG, Sato FT, Curi R, Vinolo MAR. Fatty acids as modulators of neutrophil recruitment, function and survival. Eur J Pharmacol 2016;785: 50–58.
    doi: 10.1016/j.ejphar.2015.03.098pubmed: 25987417google scholar: lookup
  10. Michalak A, Mosińska P, Fichna J. Polyunsaturated fatty acids and their derivatives: therapeutic value for inflammatory, functional gastrointestinal disorders, and colorectal cancer. Front Pharmacol 2016;7: 459.
    doi: 10.3389/fphar.2016.00459pmc: PMC5131004pubmed: 27990120google scholar: lookup
  11. Serhan CN. Pro-resolving lipid mediators are leads for resolution physiology. Nature 2014;510: 92–101.
    doi: 10.1038/nature13479pmc: PMC4263681pubmed: 24899309google scholar: lookup
  12. Choe SS, Huh JY, Hwang IJ, Kim JI, Kim JB. Adipose tissue remodeling: its role in energy metabolism and metabolic disorders. Front Endocrinol 2016;7: 30.
    pmc: PMC4829583pubmed: 27148161
  13. Blüher M. Clinical relevance of adipokines. Diabetes Metab J 2012;36: 317–327.
    doi: 10.4093/dmj.2012.36.5.317pmc: PMC3486977pubmed: 23130315google scholar: lookup
  14. Frank N, Geor RJ, Bailey SR, Durham AE, Johnson PJ. Equine metabolic syndrome. J Vet Intern Med 2010;24: 467–475.
  15. Ertelt A, Barton A-K, Schmitz RR, Gehlen H. Metabolic syndrome: is equine disease comparable to what we know in humans?. Endocr Connect 2014;3: R81–R93.
    doi: 10.1530/EC-14-0038pmc: PMC4068110pubmed: 24894908google scholar: lookup
  16. Burns TA, Geor RJ, Mudge MC, McCutcheon LJ, Hinchcliff KW, Belknap JK. Proinflammatory cytokine and chemokine gene expression profiles in subcutaneous and visceral adipose tissue depots of insulin-resistant and insulin-sensitive light breed horses. J Vet Intern Med 2010;24: 932–939.
  17. Bruynsteen L, Erkens T, Peelman LJ, Ducatelle R, Janssens GPJ, Harris PA. Expression of inflammation-related genes is associated with adipose tissue location in horses. BMC Vet Res 2013;9: 240.
    doi: 10.1186/1746-6148-9-240pmc: PMC4220830pubmed: 24295090google scholar: lookup
  18. Carroll CL, Huntington PJ. Body condition scoring and weight estimation of horses. Equine Vet J 1988;20: 41–45.
    pubmed: 3366105
  19. Eiler H, Frank N, Andrews FM, Oliver JW, Fecteau KA. Physiologic assessment of blood glucose homeostasis via combined intravenous glucose and insulin testing in horses. Am J Vet Res 2005;66: 1598–1604.
    pubmed: 16261835
  20. Raabo BE, Terkildsen TC. On the enzymatic determination of blood glucose. Scand J Clin Lab Invest 1960;12: 402–407.
    doi: 10.3109/00365516009065404pubmed: 13738785google scholar: lookup
  21. Bligh EG, Dyer WJ. A rapid method of total lipid extraction and purification. Can J Biochem Physiol 1959;37: 911–917.
    doi: 10.1139/o59-099pubmed: 13671378google scholar: lookup
  22. Seidel A, Gueck T, Fuhrmann H. The influence of long-chain polyunsaturated fatty acids on total lipid fatty acid composition of a canine mastocytoma cell line. J Vet Med Ser A 2005;52: 219–224.
    pubmed: 15943605
  23. Carter RA, Geor RJ, Staniar WB, Cubitt TA, Harris PA. Apparent adiposity assessed by standardised scoring systems and morphometric measurements in horses and ponies. Vet J 2009;179: 204–210.
    doi: 10.1016/j.tvjl.2008.02.029pubmed: 18440844google scholar: lookup
  24. Breidenbach A, Fuhrmann H, Deegen E, Lindholm A, Sallmann HP. Studies on equine lipid metabolism—2. Lipolytic activities of plasma and tissue lipases in large horses and ponies. J Vet Med Ser A 1999;46: 39–48.
    pubmed: 10085766
  25. Adolph S, Fuhrmann H, Schumann J. Unsaturated fatty acids promote the phagocytosis of Pseudomonas aeruginosa and Rhodococcus equi by RAW264.7 macrophages. Curr Microbiol 2012;65: 649–655.
    doi: 10.1007/s00284-012-0207-3pubmed: 22903555google scholar: lookup
  26. Belaunzaran X, Bessa RJB, Lavín P, Mantecón AR, Kramer JKG, Aldai N. Horse-meat for human consumption—Current research and future opportunities. Meat Sci 2015;108: 74–81.
    doi: 10.1016/j.meatsci.2015.05.006pubmed: 26047980google scholar: lookup
  27. Juárez M, Polvillo O, Gómez MD, Alcalde MJ, Romero F, Valera M. Breed effect on carcass and meat quality of foals slaughtered at 24months of age. Meat Sci 2009;83: 224–228.
    doi: 10.1016/j.meatsci.2009.04.022pubmed: 20416753google scholar: lookup
  28. He ML, Ishikawa S, Hidari H. Fatty acid profiles of various muscles and adipose tissues from fattening horses in comparison with beef cattle and pigs. Asian-Australas J Anim Sci 2005;18: 1655–1661.
  29. Sarriés MV, Murray BE, Troy D, Beriain MJ. Intramuscular and subcutaneous lipid fatty acid profile composition in male and female foals. Meat Sci 2006;72: 475–485.
    doi: 10.1016/j.meatsci.2005.08.014pubmed: 22061731google scholar: lookup
  30. Shorland FB, Bruce LW, Jessop AS. Studies on the composition of horse oil. 2. The component fatty acids of lipids from fatty tissues, muscle and liver. Biochem J 1952;52: 400–407.
    pmc: PMC1198011pubmed: 13018246
  31. Summers LKM, Barnes SC, Fielding BA, Beysen C, Ilic V, Humphreys SM. Uptake of individual fatty acids into adipose tissue in relation to their presence in the diet. Am J Clin Nutr 2000;71: 1470–1477.
    doi: 10.1093/ajcn/71.6.1470pubmed: 10837287google scholar: lookup
  32. Wood JD, Enser M, Fisher AV, Nute GR, Sheard PR, Richardson RI. Fat deposition, fatty acid composition and meat quality: a review. Meat Sci 2008;78: 343–358.
    doi: 10.1016/j.meatsci.2007.07.019pubmed: 22062452google scholar: lookup
  33. Clauss M, Grum C, Hatt J-M. Polyunsaturated fatty acid content in adipose tissue in foregut and hindgut fermenting mammalian herbivores: a literature survey. Mamm Biol 2009;74: 153–158.
  34. Allard JP, Aghdassi E, Mohammed S, Raman M, Avand G, Arendt BM. Nutritional assessment and hepatic fatty acid composition in non-alcoholic fatty liver disease (NAFLD): a cross-sectional study. J Hepatol 2008;48: 300–307.
    doi: 10.1016/j.jhep.2007.09.009pubmed: 18086506google scholar: lookup
  35. Ahmadian M, Duncan RE, Jaworski K, Sarkadi-Nagy E, Sul HS. Triacylglycerol metabolism in adipose tissue. Future Lipidol 2007;2: 229–237.
    doi: 10.2217/17460875.2.2.229pmc: PMC2633634pubmed: 19194515google scholar: lookup
  36. Suagee JK, Corl BA, Crisman MV, Wearn JG, McCutcheon LJ, Geor RJ. De novo fatty acid synthesis and NADPH generation in equine adipose and liver tissue. Comp Biochem Physiol B Biochem Mol Biol 2010;155: 322–326.
    doi: 10.1016/j.cbpb.2009.11.019pubmed: 19962447google scholar: lookup
  37. Nakamura MT, Nara TY. Structure, function, and dietary regulation of δ6, δ5, and δ9 desaturases. Annu Rev Nutr 2004;24: 345–376.
  38. Calder PC. Mechanisms of action of (n-3) fatty acids. J Nutr 2012;142: 592S–599S.
    doi: 10.3945/jn.111.155259pubmed: 22279140google scholar: lookup
  39. Lattka E, Klopp N, Demmelmair H, Klingler M, Heinrich J, Koletzko B. Genetic variations in polyunsaturated fatty acid metabolism—implications for child health?. Ann Nutr Metab 2012;60: 8–17.
    pubmed: 22614814
  40. Xie L, Innis SM. Genetic variants of the FADS1 FADS2 gene cluster are associated with altered (n-6) and (n-3) essential fatty acids in plasma and erythrocyte phospholipids in women during pregnancy and in breast milk during lactation. J Nutr 2008;138: 2222–2228.
    doi: 10.3945/jn.108.096156pubmed: 18936223google scholar: lookup
  41. Sergeant S, Hugenschmidt CE, Rudock ME, Ziegler JT, Ivester P, Ainsworth HC. Differences in arachidonic acid levels and fatty acid desaturase (FADS) gene variants in African Americans and European Americans with diabetes or the metabolic syndrome. Br J Nutr 2012;107: 547–555.
    doi: 10.1017/S0007114511003230pmc: PMC3494092pubmed: 21733300google scholar: lookup
  42. Lemaitre RN, Tanaka T, Tang W, Manichaikul A, Foy M, Kabagambe EK. Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE consortium. PLoS Genet 2011;7: e1002193.
  43. Schaeffer L, Gohlke H, Müller M, Heid IM, Palmer LJ, Kompauer I. Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. Hum Mol Genet 2006;15: 1745–1756.
    doi: 10.1093/hmg/ddl117pubmed: 16670158google scholar: lookup
  44. Birsoy K, Festuccia WT, Laplante M. A comparative perspective on lipid storage in animals. J Cell Sci 2013;126: 1541–1552.
    doi: 10.1242/jcs.104992pubmed: 23658371google scholar: lookup
  45. Goldberg IJ, Eckel RH, Abumrad NA. Regulation of fatty acid uptake into tissues: lipoprotein lipase- and CD36-mediated pathways. J Lipid Res 2009;50: S86–S90.
    doi: 10.1194/jlr.R800085-JLR200pmc: PMC2674753pubmed: 19033209google scholar: lookup
  46. Raclot T, Oudart H. Selectivity of fatty acids on lipid metabolism and gene expression. Proc Nutr Soc 1999;58: 633–646.
    pubmed: 10604197
  47. Hansen IA. Selective incorporation of fatty acids into lipids of lamb and rat intestinal mucosa. Comp Biochem Physiol 1965;15: 27–31.
    pubmed: 14348000
  48. Raclot T. Selective mobilization of fatty acids from adipose tissue triacylglycerols. Prog Lipid Res 2003;42: 257–288.
    pubmed: 12689620
  49. Raclot T, Groscolas R. Individual fish-oil n−3 polyunsaturated fatty acid deposition and mobilization rates for adipose tissue of rats in a nutritional steady state. Am J Clin Nutr 1994;60: 72–78.
    doi: 10.1093/ajcn/60.1.72pubmed: 8017341google scholar: lookup
  50. Simopoulos A. An increase in the omega-6/omega-3 fatty acid ratio increases the risk for obesity. Nutrients 2016;8: 128.
    doi: 10.3390/n耰128pmc: PMC4808858pubmed: 26950145google scholar: lookup
  51. Calder PC. Omega-3 fatty acids and inflammatory processes. Nutrients 2010;2: 355–374.
    doi: 10.3390/n‰355pmc: PMC3257651pubmed: 22254027google scholar: lookup
  52. Camandola S, Leonarduzzi G, Musso T, Varesio L, Carini R, Scavazza A. Nuclear factor kB Is activated by arachidonic acid but not by eicosapentaenoic acid. Biochem Biophys Res Commun 1996;229: 643–647.
    doi: 10.1006/bbrc.1996.1857pubmed: 8954951google scholar: lookup
  53. Rabionet M, Gorgas K, Sandhoff R. Ceramide synthesis in the epidermis. Biochim Biophys Acta (BBA)—Mol Cell Biol Lipids 2014;1841: 422–434.
    pubmed: 23988654
  54. Pischon T, Hankinson SE, Hotamisligil GKS, Rifai N, Willett WC, Rimm EB. Habitual dietary intake of n-3 and n-6 fatty acids in relation to inflammatory markers among US men and women. Circulation 2003;108: 155–160.
  55. Schoeniger A, Adolph S, Fuhrmann H, Schumann J. The impact of membrane lipid composition on macrophage activation in the immune defense against Rhodococcus equi and Pseudomonas aeruginosa. Int J Mol Sci 2011;12: 7510–7528.
    doi: 10.3390/ijms12117510pmc: PMC3233420pubmed: 22174614google scholar: lookup
  56. Leat W, Baker J. Plasma polyunsaturated fatty acids of herbivores grazing pasture. Proc Nutr Soc 1969;28: 37A–38A.
    pubmed: 5353330
  57. Watson TDG, Burns L, Love S, Packard CJ, Shepherd J. Plasma lipids, lipoproteins and post-heparin lipases in ponies with hyperlipaemia. Equine Vet J 1992;24: 341–346.
    pubmed: 1396507
  58. Spector AA, Hoak JC, Fry GL, Denning GM, Stoll LL, Smith JB. Effect of fatty acid modification on prostacyclin production by cultured human endothelial cells. J Clin Invest 1980;65: 1003–1012.
    doi: 10.1172/JCI109752pmc: PMC371430pubmed: 6767738google scholar: lookup
  59. Spector AA, Kiser RE, Denning GM, Koh S-W, DeBault L. Modification of the fatty acid composition of cultured human fibroblasts. J Lipid Res 1979;20: 536–547.
    pubmed: 458270
  60. Schroit A, Gallily R. Macrophage fatty acid composition and phagocytosis: effect of unsaturation on cellular phagocytic activity. Immunology 1979;36: 199–205.
    pmc: PMC1457479pubmed: 374248
  61. Lands B, Bibus D, Stark KD. Dynamic interactions of n-3 and n-6 fatty acid nutrients. Prostaglandins Leukot Essent Fatty Acids (PLEFA) 2017.
    doi: 10.1016/j.plefa.2017.01.012pubmed: 28189338google scholar: lookup
  62. Liu H-Q, Qiu Y, Mu Y, Zhang X-J, Liu L, Hou X-H. A high ratio of dietary n-3/n-6 polyunsaturated fatty acids improves obesity-linked inflammation and insulin resistance through suppressing activation of TLR4 in SD rats. Nutr Res 2013;33: 849–858.
    doi: 10.1016/j.nutres.2013.07.004pubmed: 24074743google scholar: lookup
  63. Mika A, Stepnowski P, Kaska L, Proczko M, Wisniewski P, Sledzinski M. A comprehensive study of serum odd- and branched-chain fatty acids in patients with excess weight. Obesity 2016;24: 1669–1676.
    doi: 10.1002/oby.21560pubmed: 27355152google scholar: lookup
  64. Kniazeva M, Crawford QT, Seiber M, Wang C-Y, Han M. Monomethyl branched-chain fatty acids play an essential role in caenorhabditis elegans development. PLoS Biol 2004;2: e257.
    doi: 10.1371/journal.pbio.0020257pmc: PMC514883pubmed: 15340492google scholar: lookup
  65. Wongtangtintharn S, Oku H, Iwasaki H, Toda T. Effect of branched-chain fatty acids on fatty acid biosynthesis of human breast cancer cells. J Nutr Sci Vitaminol 2004;50: 137–143.
    pubmed: 15242018
  66. Yang Z, Liu S, Chen X, Chen H, Huang M, Zheng J. Induction of apoptotic cell death and in vivo growth inhibition of human cancer cells by a saturated branched-chain fatty acid, 13-methyltetradecanoic acid. Cancer Res 2000;60: 505–509.
    pubmed: 10676625
  67. Alves SP, Raundrup K, Cabo Â, Bessa RJB, Almeida AM. Fatty acid composition of muscle, adipose tissue and liver from muskoxen (Ovibos moschatus) living in West Greenland. PLoS One 2015;10: e0145241.
  68. Horning MG, Martin DB, Karmen A, Vagelos PR. Fatty acid synthesis in adipose tissue. II. Enzymatic synthesis of branched chain and odd-numbered fatty acids. J Biol Chem 1961;236: 669–672.
    pubmed: 13715907
  69. Aungst BJ. Structure/effect studies of fatty acid isomers as skin penetration enhancers and skin irritants. Pharm Res 1989;06: 244–247.
    pubmed: 2726682
  70. Santos AS, Rodrigues MAM, Bessa RJB, Ferreira LM, Martin-Rosset W. Understanding the equine cecum-colon ecosystem: current knowledge and future perspectives. Animal 2011;5: 48–56.
    doi: 10.1017/S1751731110001588pubmed: 22440701google scholar: lookup
  71. Belaunzaran X, Lavín P, Barron LJR, Mantecón AR, Kramer JKG, Aldai N. An assessment of the fatty acid composition of horse-meat available at the retail level in northern Spain. Meat Sci 2017;124: 39–47.
    doi: 10.1016/j.meatsci.2016.10.014pubmed: 27835833google scholar: lookup
  72. Still GG, Davis DG, Zander GL. Plant epicuticular lipids: alteration by herbicidal carbamates. Plant Physiol 1970;46: 307–314.
    pmc: PMC396584pubmed: 16657455
  73. Yamamoto M, Tanaka Y, Sugano M. Serum and liver lipid composition and lecithin: cholesterol acyltransferase in horses, Equus caballus. Comp Biochem Physiol B 1979;62: 185–193.
    pubmed: 318442
  74. Ma DWL, Arendt BM, Hillyer LM, Fung SK, McGilvray I, Guindi M. Plasma phospholipids and fatty acid composition differ between liver biopsy-proven nonalcoholic fatty liver disease and healthy subjects. Nutr Diabetes 2016;6: e220.
    doi: 10.1038/nutd.2016.27pmc: PMC4973140pubmed: 27428872google scholar: lookup

Citations

This article has been cited 6 times.
  1. Wermer K, Korbacska-Kutasi O, Berkecz R, Csupor D, Ágh N, Sztojkov-Ivanov A, Cserhalmi D. Pharmacokinetics of cannabidiol and its two main phase I metabolites in Connemara ponies. Front Vet Sci 2025;12:1599934.
    doi: 10.3389/fvets.2025.1599934pubmed: 40654508google scholar: lookup
  2. Dosi M, Scott L, Payne H, Poldy J, Keen J, McGorum B, Malbon A, Morgan R. Markers of Hepatic Insulin Clearance and Their Association With Steatosis in Hyperinsulinaemic Horses. J Vet Intern Med 2025 Jul-Aug;39(4):e70143.
    doi: 10.1111/jvim.70143pubmed: 40476757google scholar: lookup
  3. Theinert KB, Snedec T, Pietsch F, Theile S, Leonhardt AS, Spilke J, Pichelmann S, Bannert E, Reichelt K, Dobeleit G, Fuhrmann H, Baumgartner W, Schären-Bannert M, Starke A. Qualitative and Quantitative Changes in Total Lipid Concentration and Lipid Fractions in Liver Tissue of Periparturient German Holstein Dairy Cows of Two Age Groups. Front Vet Sci 2022;9:814808.
    doi: 10.3389/fvets.2022.814808pubmed: 35372546google scholar: lookup
  4. Reichelt K, Niebisch AM, Kacza J, Schoeniger A, Fuhrmann H. The Bovine Hepatic Cell Line BFH12 as a Possible Model for Hepatosteatosis in Dairy Cows. Front Vet Sci 2022;9:840202.
    doi: 10.3389/fvets.2022.840202pubmed: 35359674google scholar: lookup
  5. Theelen MJP, Luiken REC, Wagenaar JA, Sloet van Oldruitenborgh-Oosterbaan MM, Rossen JWA, Zomer AL. The Equine Faecal Microbiota of Healthy Horses and Ponies in The Netherlands: Impact of Host and Environmental Factors. Animals (Basel) 2021 Jun 12;11(6).
    doi: 10.3390/ani11061762pubmed: 34204691google scholar: lookup
  6. Petrov KA, Dudareva LV, Nokhsorov VV, Stoyanov KN, Makhutova ON. Fatty Acid Content and Composition of the Yakutian Horses and Their Main Food Source: Living in Extreme Winter Conditions. Biomolecules 2020 Feb 17;10(2).
    doi: 10.3390/biom10020315pubmed: 32079257google scholar: lookup