Skip to main content
Log in

Varying incorporation of fatty acids into phospholipids from muscle, adipose and pancreatic exocrine tissues and thymocytes in adult rats fed with diets rich in different fatty acids

  • Published:
European Journal of Epidemiology Aims and scope Submit manuscript

Abstract

Despite numerous studies, the importance which the tissue or the composition of the diet may have in the biological distribution of each fatty acid is not well known. To determine the importance of tissue origin and dietary fatty acids in the fatty acid composition of cell phospholipids, 54 male adult rats were fed isocaloric diets for one month varying only in their fatty acid compositions. The fat component of the six experimental groups was derived from olive oil, sunflower oil, fish oil, soybean oil, palmitic acid, or 82% palmitic acid plus 18% soybean oil, supplying the essential fatty acid. The fatty acid composition of phospholipids from thymocytes, pancreatic exocrine, muscle and adipose tissues was studied by gas-chromatography. The tissue of origin was a more important source of variation than diet in the fatty acid content of the cell phospholipids except for palmitic acid (16:0), eicosapentaenoic acid (20:5 n-3), and docosahexaenoic acid (22:6 n-3). This study points out the complexity of the interrelations between different families of fatty acids and of the specificity of each tissue to changes in the composition of dietary fatty acids, as well as the inconvenience of speaking from the dietary point of view of groups of fatty acid families based on the position of the double bond, since their individual behaviour, including saturated fatty acids, is very different in the face of dietary manipulation. The study also highlights the different behaviour of each of the fatty acids in relation to the others in the diet in each of the tissues, a circumstance which should be taken into account when evaluating the biological effects in both epidemiological and experimental studies.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hunter EJ, Applewithe TH. Reassesment of trans-fatty acids availability in the US diet. Am J Clin Nutr 1991; 54: 363–365.

    Google Scholar 

  2. Hirsch J. Fatty acid patterns in human adipose tissue. In: Renold AE, Cahill GF (eds), Handbook of Physiology. Washington, DC: Amer Phys Soc, 1965.

    Google Scholar 

  3. Field CJ, Angel A, Clandenin MT. Relationship of diet to the fatty acid composition of human adipose tissue structural and stored lipids. Am J Clin Nutr 1985; 42: 1206–1220.

    Google Scholar 

  4. Melero Bellido M, Yañez Polo MA, Soriguer F. Composición del tejido adiposo en el arteriosclerótico, obeso y diabético sometidos a la dieta de la población de Sevilla. I Rev Clin Esp 1974; 133: 503–510.

    Google Scholar 

  5. Ayre KJ, Hulbert A. Dietary fatty acid profile influences the composition of skeletal muscle phospholipids in rats. J Nutr 1996; 126: 653–662.

    Google Scholar 

  6. Black SC, McNeill JH. Influence of w-3–fatty acid treatment on cardiac phospholipid composition and coronary flow of streptotozin-diabetic rats. Metabolism 1993; 42: 320–326.

    Google Scholar 

  7. Jones PHE, Toy BR, Cha MC. Differential fatty acid accretion in heart, liver and adipose tissues of rats fed tallow, fish oil, olive oil and sa.ower oils at three levels of energy intake. J Nutr 1992; 125: 1175–1182.

    Google Scholar 

  8. Ruiz Gutierrez V, Molina MT, Vazquez CM. Comparative effects of feeding different fats on fatty acid composition of major individual phospholipids of rat hearts. Ann Nutr Metab 1990; 34: 350–358.

    Google Scholar 

  9. Valette L, Croset M, Prigent AF, Meskini N, Lagard M. Dietary polyunsaturated fatty acids modulate fatty acid composition and early activation steps of concavalin A-stimulated rat thymocytes. J Nutr 1991; 121: 1844–1859.

    Google Scholar 

  10. Malaisse WJ, Mallaisse-Lagae F, Sener A, Hellerstrom C. Participation of endogenous fatty acids in the secretory activity of the exocrine α-cell. Biochem J 1985; 227: 95–102.

    Google Scholar 

  11. Ballabriga A. Essential fatty acids and human tissue composition. An overview. Acta Paediatr Suppl. 1994; 402: 63–68.

    Google Scholar 

  12. Moussa M, Barcía J, Ghisolfi J, Periquet B, Thouvenot JP. Dietary essential fatty acid deficiency differentially affects tissue of rats. J Nutr 1996; 126: 3040–3045.

    Google Scholar 

  13. Soriguer-Escofet FJ, Esteva I, Tinahones FJ, Pareja A. Adipose tissue fatty acids and size and number of fat cells from birth to 9 years of age. A cross-sectional study in 96 boys. Metabolism 1996; 45: 1–8.

    Google Scholar 

  14. Esteva de Antonio I, Soriguer-Escofet FJ, Vicioso I. La célula beta pancreática en los primeros 5 dias de la pancreatitis aguda. Endocrinología 1982; 29: 164–170.

    Google Scholar 

  15. Tinahones FJ, Pareja A, Esteva de Antonio I, Olveira G, Soriguer FJ. Unsaturated fatty acids change insulin secretion in Langerhans islets in vitro. Diabetologia 1995; 38(Suppl. 1): 106.

    Google Scholar 

  16. Borkman M, Storlien LH, Pan DA, Jenkins AB, Chisholm DJ, Cambell LV. The relation between insulin sensitivity and the fatty-acid composition of skeletal-muscle phospholipids. N Eng J Med 1993; 328: 238–244.

    Google Scholar 

  17. Morlion BJ, Torwesten E, Lessire H, et al. The effect of parenteral fish oil on leukocyte membrane fatty acid composition and leukotriene-synthesizing capacity in patients with postoperative trauma. Metabolism 1996; 45: 1208–1213.

    Google Scholar 

  18. Lindsey S, Benattar J, Pronczuk A, Hayes KC. Dietary palmitic (16:0) enhances high density lipoprotein cholesterol and low density lipoprotein receptor mRNA abundance in hamster. Proc Soc Exp Biol Med 1990; 195: 261–268.

    Google Scholar 

  19. Suarez A, Ramirez MC, Faus MJ, Gil A. Dietary long-chain polyunsaturated fatty acids influence tissue fatty acid composition in rats at weaning. J Nutr 1996; 126: 887–897.

    Google Scholar 

  20. Chen ZY, Cunnane SC. Preferential retention of linoleic acid-enriched triacylglycerols in liver and serum during fasting. Am J Physiol 1992; 263: R233–R239.

    Google Scholar 

  21. Kholmeier L. Biomarkers of fatty acids exposure and breast cancer risk. Am J Clin Nutr 1997; 66(suppl. 6): 1548s-1565s.

    Google Scholar 

  22. Hamilton S, Hamilton RJ, Sewell PA. Extraction of lipids and derivative formation, en Lipid analysis. A practical approach. Eds. Hamilton y Hamilton. Oxford: Oxford University Press, 1992.

    Google Scholar 

  23. Hughes TA, Eimberg M, Wang X, et al. Comparative lipoprotein metabolism of myristate, palmitate and stearate in normolipemic men. Metabolism 1996; 45: 1108–1118.

    Google Scholar 

  24. Woolet LA, Spady DK, Dietschy JM. Mechanism by which saturated triacylglycerols elevate the plasma low density lipoprotein-cholesterol concentrations in hamster. Differential effects of fatty acids chain length. J Clin Invest 1980; 84: 119–128.

    Google Scholar 

  25. Morris CM, Manson JE, Rosner B, Buring JE, Willet WC, Hennekens CH. Fish consumption and cardiovascular disease in the physicians’ health study: A prospective study. Am J Epidemiol 1995; 142: 166–175.

    Google Scholar 

  26. Katan MB, Zock PL, Mensink RP. Dietary oils, serum lipoproteins, and coronary heart disease. Am J Clin Nutr 1995; 61(suppl. 6): 1368S-1373S.

    Google Scholar 

  27. Soriguer F, Serna S, Valverde E, et al. Lipid, protein and caloric content of different Atlantic and Mediterranean fish, shellfish and molluscs commonly eaten in the South of Spain. Eur J Epidemiol 1997; 13: 1–13.

    Google Scholar 

  28. De Schriver R, Privet OS. Effects of dietary longchain fatty acids on the biosynthesis of unsaturated fatty acids in the rat. J Nutr 1982; 112: 619–626.

    Google Scholar 

  29. Brenner RR, Peluffo RO. Inhibitory effects of 22:6 n-3 upon oxidative desaturation of linoleic into α-linolenic acid and a-linolenic into 18:4 n-3. Biochim Biophys Acta 1967; 137: 184–186.

    Google Scholar 

  30. Brenner RR, Peluffo RO. Effect of saturated and unsaturated fatty acids on the desaturation in vivo of palmitic, stearic, oleic, linoleic and linolenic acids. J Biol Chem 1966; 241: 5213–5216.

    Google Scholar 

  31. Innis SM, Rioux FM, Auestad N, Ackman RG. Marine and freshwater fish oil varying in arachidonic, eicosapentaenoic and docosahexaenoic acids differ in their effects on organ lipids and fatty acids in growing rats. J Nutr 1995; 125: 2286–2293.

    Google Scholar 

  32. Innis SM. Essential fatty acids in growth and development. Prog Lipid Res 1991; 30: 39–103.

    Google Scholar 

  33. Herzberg GR. The influence of dietary fatty acid composition on lipogenesis. Adv Nutr Res 1983; 5: 221–253.

    Google Scholar 

  34. Su W, Jones PJH. Dietary fatty acid composition influences energy accretion in rats. J Nutr 1993; 123: 2109–2144.

    Google Scholar 

  35. Garcia MC, Sprecher H, Rosenthal MD. Chain elongation of polyunsaturated fatty acids by vascular endothelial cells: studies with arachidonate analogues. Lipids 1990; 25: 211–215.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Soriguer, F., Tinahones, F., Monzón, A. et al. Varying incorporation of fatty acids into phospholipids from muscle, adipose and pancreatic exocrine tissues and thymocytes in adult rats fed with diets rich in different fatty acids. Eur J Epidemiol 16, 585–594 (2000). https://doi.org/10.1023/A:1007684808188

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1007684808188

Navigation