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Postnatal development of phospholipids and their fatty acid profile in rat heart

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The aim of this study was to determine the concentration of phospholipids (PL), plasmalogen components of choline (PC) and ethanolamine (PE) phosphoglycerides (PLPC, PLPE) and fatty acid profile of PL and triacylglycerols (TAG) in developing rat left ventricular myocardium between postnatal day (d) 2 and 100. The steepest increase of total PL (TPL) concentration occurs between d2 and d5, followed by a further slower increase between d20 and d40. Similar developmental changes were observed in PC and PE. The PLPE concentration rises by d10, whereas PLPC does not change during the whole period investigated, except for the transient decline on d5. The concentration of diphosphatidylglycerol (DPG) increases by d60; the steepest rise occurs between d20 and d40. Phosphatidylinositol (PI) concentration rises only by d5. The concentration of phosphatidylserine (PS) decreases between d5 and d10 and then it does not change. Sphingomyelin (SM) concentration is maintained till d10, it declines on d20 and does not change thereafter. The proportion of saturated fatty acids (SFA) increases by d5 in PC, PE, PS and TAG, and by d10 in DPG and PI. After d20 the SFA proportion gradually decline in all lipids. Monounsaturated FA (MUFA) proportion decreases in PC, PE, PI and PS from d2 till d10, and in the weaning period it tends to rise again. In contrast, in DPG and TAG the proportion of MUFA declines during the whole postnatal period. N-6 polyunsaturated FA (PUFA) decrease in all PL by d20 and rise again thereafter; in TAG they decline between d2 and d10 and return to the initial level by d100. N-3 PUFA increase in all PL during the suckling period and decline after weaning; in TAG they increase only by d5 and then they decline. This remodeling of myocardial PL and TAG composition during postnatal development may affect membrane properties and contribute to developmental changes in the function of membrane proteins and cell signaling.

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References

  1. Girard J, Pascal F, Pégorier JP, Duée PH: Adaptation of glucose and fatty acid metabolism during perinatal period and suckling-weaning transition. Physiol Rev 72: 507–562, 1992

    PubMed  CAS  Google Scholar 

  2. Li F, Wang X, Capasso JM, Gerdes AM: Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development. J Mol Cell Cardiol 28: 1737–1746, 1996

    Article  PubMed  CAS  Google Scholar 

  3. Wibo M, Bravo G, Godfraind T: Postnatal maturation of excitation-contraction coupling in rat ventricle in relation to the subcellular localization and surface density of 1,4-dihydropyridine and ryanodine receptors. Circ Res 68: 662–673, 1991

    PubMed  CAS  Google Scholar 

  4. Gudmundsdottir A, Gudbjarnason S: Neonatal changes in fatty acid profile of phospholipids in rat heart muscle. Biochim Biophys Acta 752: 284–290, 1983

    PubMed  CAS  Google Scholar 

  5. Rogers CG: Fatty acids and phospholipids of adult and newborn rat hearts and of cultured, beating neonatal rat myocardial cells. Lipids 9: 541–547, 1974

    Article  Google Scholar 

  6. Folch J, Lees M, Sloan-Stanley GH: A simple method for the isolation and purification of total lipids from animal tissue. J Biol Chem 226: 497–509, 1957

    Google Scholar 

  7. Rouser G, Fleischer S, Yamamoto A: Two dimensional thin layer chromatographic separation of polar lipids and determination of phospholipids by phosphorus analysis of spots. Lipids 5: 494–496, 1970

    Google Scholar 

  8. Horrocks LA: The alk-1-enyl group content of mammalian myelin phosphoglycerides by quantitative two-dimensional thin-layer chromatography. J Lipid Res 9: 469–472, 1968

    PubMed  CAS  Google Scholar 

  9. Tvrzicka E, Vecka M, Stankova B, Zak A: Analysis of fatty acids in plasma lipoproteins by gas chromatography-flame ionisation detection. Quantitative aspects. Anal Chim Acta 465: 337–350, 2002.

    Google Scholar 

  10. Ostadal B, Ostadalova I, Dhalla NS: Development of cardiac sensitivity to oxygen deficiency: Comparative and ontogenetic aspects. Physiol Rev 79: 635–659, 1999

    Google Scholar 

  11. Page E: Quantitative ultrastructural analysis in cardiac membrane physiology. Am J Physiol 235: C147–C158, 1978

    PubMed  CAS  Google Scholar 

  12. Smith HE, Page E: Ultrastructural changes in rabbit heart mitochondria during the perinatal period. J Ultrastruct Res 55: 31–41, 1976

    Article  PubMed  CAS  Google Scholar 

  13. Hoch FL: Cardiolipins and biomembrane function. Biochim Biophys Acta 1113: 71–133, 1992

    PubMed  CAS  Google Scholar 

  14. Paradies G, Fuggiero FN, Petrosillo G, Quagliariello El: Peroxidative damage to cardiac mitochondria: cytochrome oxidase and cardiolipin alterations. FEBS Lett 424: 155–158, 1998

    Google Scholar 

  15. Skarka L, Bardova K, Brauner P, Flachs P, Jarkovska D, Kopecky J, Ostadal B: Expression of mitochondrial uncoupling protein 3 and adenine nucleotide translocase 1 genes in developing rat heart: putative involvement in control of mitochondrial membrane potential. J Mol Cell Cardiol 35: 321–330, 2003

    Google Scholar 

  16. Bass A, Stejskalova M, Stieglerova A, Ostadal B, Samanek M: Ontogenetic development of energy-supplying enzymes in rat and guinea-pig heart. Physiol Res 50: 237–245, 2001

    PubMed  CAS  Google Scholar 

  17. Kako KJ, Zaror-Behrens G, Peckett SD: Phosphatidic acid synthesis in the heart. Effect of age and species differences in the mitochondrial and microsomal synthesis. Can J Biochem 55: 308–314, 1977

    Google Scholar 

  18. Parkers JG, Thompson W: Phosphatidylethanolamine in liver mitochondria and endoplasmic reticulum: molecular species distribution and turnover. Can J Biochem 53: 698–705, 1975

    Article  Google Scholar 

  19. Stanacev NZ, Stuhne-Sekalec L, Brooks KB, Davidson JB: Intermediary metabolism of phospholipids. The biosynthesis of phosphatidylglycerophosphate and phosphatidyl-glycerol in heart mitochondria. Biochim Biophys Acta 176: 650–653, 1969

    Google Scholar 

  20. Stuhne-Sekalec L, Wassenaar M, Jackowski G, Stanacev NZ: Comparison of the biosynthesis and composition of polyglycerophosphatides and phosphatidylinositols in mitochondria and microsomes isolated from neonatal and adult rat heart and liver. Membr Biochem 9: 29–45, 1990

    Google Scholar 

  21. Skerjans I: Mitochondrial import: Properties of precursor proteins. Cell Biol 68: 9–16, 1990

    Google Scholar 

  22. Berridge MJ: Inositol triphosphate and diacylglycerol: two interacting second messengers. Ann Rev Biochem 56: 159–193, 1995

    Google Scholar 

  23. Hamplova B, Novakova O, Kolar F, Tvrzicka E, Novak F: Protein kinase C activity and isoform expression during early postnatal development of rat myocardium. Cell Biochem Biophys 43: 105–118, 2005

    Google Scholar 

  24. Hack MH, Helmy FM: On the plasmalogenation of myocardial choline glycerophospholipid during maturation of various vertebrates. Comp Biochem Physiol 89B: 111–118, 1988

    Article  CAS  Google Scholar 

  25. Lee T, Qian Ch, Snyder F: Biosynthesis of choline plasmalogens in neonatal rat myocytes. Arch Biochem Biophys 286: 498–503, 1991

    Article  PubMed  CAS  Google Scholar 

  26. Diagne A, Fauvel J, Record M, Chap H, Douste-Blazy L: Studies on ether phospholipids II. Comparative composition of various tissues from human, rat and guinea pig. Biochim Biophys Acta 793: 221–231, 1984

    Google Scholar 

  27. Van der Vusse GJ, Glatz JFC, Stam HCG, Reneman RS: Fatty acid homeostasis in the normoxic and ischemic heart. Physiol Rev 72: 881–940, 1992

    Google Scholar 

  28. Ford DA, Gross RW: Activation of myocardial protein kinase C by plasmalogenic diglycerides. Am J Physiol 258: C30–C36, 1990

    PubMed  CAS  Google Scholar 

  29. Arthur G, Mock T, Zaborniac Ch, Choy PC: The distribution and acyl composition of plasmalogens in guinea pig heart. Lipids 20: 693–698, 1985

  30. Gross RW: High plasmalogen and arachidonic acid content of canine myocardial sarcolemma: a fast atom bombardment mass spectroscopic and gas chromatography-mass spectroscopic characterisation. Biochemistry 23: 158–165, 1984

    Article  PubMed  CAS  Google Scholar 

  31. Huang YS, Wainwright PE, Rodden PR, Mills DE, Bulman-Fleming B, Horrobin DF: Effect of maternal dietary fats with variable n-3/n-6 ratios on tissue fatty acid composition in suckling mice. Lipids 27: 104–110, 1992

    Google Scholar 

  32. Berger A, Gershwin ME, German JB: Effects of various dietary fats on cardiolipin acyl composition during ontogeny of mice. Lipids 27: 605–612, 1992

    Google Scholar 

  33. Ghosal J, Whitworth T, Coniglio JG: Biosynthesis of fatty acids from [1-14C] acetate in the perfused rat heart. Biochim Biophys Acta 187: 576–578, 1969

    Google Scholar 

  34. Brenner RR: The desaturation step in the animal biosynthesis of polyunsaturated fatty acids. Lipids 6: 567–575, 1971

    Article  PubMed  CAS  Google Scholar 

  35. Cunnane SC, Chen ZY: Triacylglycerol: an important pool of essential fatty acids during early postnatal development in rats. Am J Physiol 262: R8–R13, 1992

  36. Cunnane SC, Chen ZY: Quantitative changes in long-chain fatty acids during fetal and early postnatal development in rats. Am J Physiol 262: R14–R19, 1992

    PubMed  CAS  Google Scholar 

  37. Chen ZY, Cunnane SC: Early postnatal development is characterized by accumulation of highly unsaturated triacylglycerols. Pediatr Res 31: 47–51, 1992

    Google Scholar 

  38. Schroedl NA, Hartzell ChR: Preferential distribution of non-esterified fatty acids to phosphatidylcholine in the neonatal mammalian myocardium. Biochem J 224: 651–659, 1984

    PubMed  CAS  Google Scholar 

  39. Apstein CS, Gmeiner R, Brachfeld N: Effect of palmitate on hypoxic myocardial metabolism and contractility. Recent Adv Stud Cardiac Struct Metab 1: 136–146, 1972

    Google Scholar 

  40. Vasdev CS, Kako KJ: Incorporation of fatty acids into rat heart lipids. In vivo and in vitro studies. J Mol Cell Cardiol 9: 617–631, 1977

    PubMed  Google Scholar 

  41. Gloster J, Achillea M, Harris P: Subcellular distribution of [1-14C]palmitate and [1-14C]oleate incorporated into lipids in the perfused rat heart: a comparison under isothermal and hypothermic conditions. J Mol Cell Cardiol 10: 439–448, 1978

    Google Scholar 

  42. Ghebremeskel K, Bitsanis D, Koukkou E, Lovy C, Poston L, Crawford MA: Post-natal modulation of heart and liver phosphoglyceride fatty acids in pups. Ann Nutr Metab 43: 365–373, 1999

    Google Scholar 

  43. Gudbjarnason S: Dynamics of n-3 and n-6 fatty acids in phospholipids of heart muscle. J Int Med 225: Supl 1, 117–128, 1989

    Google Scholar 

  44. Decrock F, Groscolas R, Speake BK: FA composition of heart and skeletal muscle during embryonic development of the king penguin. Lipids 37: 407–415, 2002

    Google Scholar 

  45. Cunnane SC, Armstrong JK: Long chain fatty acid composition of maternal liver lipids during pregnancy and lactation in the rat comparison of triglyceride to phospholipid. J Nutr 120: 338–345, 1990

    PubMed  CAS  Google Scholar 

  46. Chen ZY, Cunnane SC: Short-term energy deficit causes net accumulation of linoleoyl-enriched triacylglycerols in rat liver. FEBS Lett 280: 393–396, 1991

    Article  PubMed  CAS  Google Scholar 

  47. Guesnet P, Alasnier C, Alessandri JM, Durand G: Modifying the n-3 fatty acid content of the maternal diet to determine the requirements of the fetal and suckling rat. Lipids 32: 527–534, 1997

    Google Scholar 

  48. Gibson RA, Kneebone GM: Fatty acid composition of human colostrum and mature breast milk. Am J Clin Nutr 34: 252–257, 1981

    Google Scholar 

  49. Vigouroux E: Dynamic study of post-natal thyroid function in the rat. Acta Endocrinol (Copenh) 83: 752–762, 1976

    CAS  Google Scholar 

  50. Hamplova B, Novakova O, Tvrzicka E, Pelouch V, Novak F: Effect of hypo- and hyperthyroid states on phospholipid composition in developing rat heart. Mol Cell Biochem 252: 295–303, 2003

    Google Scholar 

  51. Novotny J, Bourova L, Malkova O, Svoboda P, Kolar F: G proteins, beta-adrenoreceptors and beta-adrenergic responsiveness in immature and adult rat ventricular myocardium: influence of neonatal hypo- and hyperthyroidism. J Mol Cell Cardiol 31: 761–772, 1999

    Google Scholar 

  52. Emilsson A, Gudbjarnason S: Reversible alterations in fatty acid profile of glycerophospholipids in rat heart muscle induced by repeated norepinephrine administration. Biochim Biophys Acta 750: 1–6, 1983

    PubMed  CAS  Google Scholar 

  53. Novak F, Tvrzicka E, Pelouch V, Jezkova J, Smik D, Novakova O: Phospholipid composition of immature rat myocardium exposed to chronic hypoxia and the effect of normoxic recovery. Collect Czech Chem Commun 69: 674–688, 2004

    Google Scholar 

  54. Jezkova J, Novakova O, Kolar F, Tvrzicka E, Neckar J, Novak F: Chronic hypoxia alters fatty acid composition of phospholipids in right and left ventricular myocardium. Mol Cell Biochem 232: 49–56, 2002

    Google Scholar 

  55. Novakova O, Pelouch V, Mrnka L, Tvrzicka E, Novak F: Phospholipid composition in mitochondria of pressure overloaded maturating rat heart. J Mol Cell Cardiol 34: A87, 2002

    Google Scholar 

  56. Gudbjarnason S, Doell B, Oskardottier G, Hallgrimsson J: Modification of cardiac phospholipids and catecholamine stress tolerance. In: C. deDuve, O. Hayaishi (eds). Tocoferol, Oxygen and Biomembranes. Elsevier, Amsterdam, 1978, pp. 297–310

  57. Stillwell W, Wassall SR: Docosahexaenoic acid: membrane properties of a unique fatty acid. Chem Phys Lipids 126: 1–27, 2003

    Article  PubMed  CAS  Google Scholar 

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Novák, F., Tvrzická, E., Hamplová, B. et al. Postnatal development of phospholipids and their fatty acid profile in rat heart. Mol Cell Biochem 293, 23–33 (2006). https://doi.org/10.1007/s11010-006-2215-8

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  • DOI: https://doi.org/10.1007/s11010-006-2215-8

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