Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1986 Jun 1;236(2):475–480. doi: 10.1042/bj2360475

The catabolism of plasmenylcholine in the guinea pig heart.

G Arthur, L Page, T Mock, P C Choy
PMCID: PMC1146864  PMID: 3753461

Abstract

The hydrolysis of the alkenyl bonds of plasmenylcholine and plasmenylethanolamine by plasmalogenase, followed by hydrolysis of the resultant lysophospholipid by lysophospholipase, has been postulated as the major pathway for the catabolism of these plasmalogens. However, the postulation was based solely on the presence of plasmalogenase activity towards plasmenylethanolamine and plasmenylcholine in the brain. In this study we have demonstrated the absence of plasmalogenase activity for plasmenylcholine in the guinea pig heart under a wide range of experimental conditions. Plasmenylcholine was hydrolysed by phospolipase A2 activities in cardiac microsomal, mitochondrial and cytosolic fractions. Phospholipase A2 activities in these fractions had an alkaline pH optimum and were enhanced by Ca2+. The enzymes also displayed high specificity for plasmenylcholine with linoleoyl or oleoyl at the C-2 position. Lysoplasmalogenase activity for lysoplasmenycholine was also detected and characterized in the microsomal and mitochondrial fractions. Since the cardiac plasmalogenase is only active towards plasmenylethanolamine but not plasmenylcholine, the catabolism of these two plasmalogens must be different from each other. We postulate that the major pathway for the catabolism of plasmenycholine involves the hydrolysis of the C-2 fatty acid by phospholipase A2, and hydrolysis of the vinyl ether group of the resultant lysoplasmenylcholine by lysoplasmalogenase.

Full text

PDF
475

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ANSELL G. B., SPANNER S. THE MAGNESIUM-ION-DEPENDENT CLEAVAGE OF THE VINYL ETHER LINKAGE OF BRAIN ETHANOLAMINE PLASMALOGEN. Biochem J. 1965 Jan;94:252–258. doi: 10.1042/bj0940252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arthur G., Choy P. C. Acyl specificity of hamster heart CDP-choline 1,2-diacylglycerol phosphocholine transferase in phosphatidylcholine biosynthesis. Biochim Biophys Acta. 1984 Sep 12;795(2):221–229. doi: 10.1016/0005-2760(84)90069-9. [DOI] [PubMed] [Google Scholar]
  3. Arthur G., Choy P. C. Acylation of 1-alkenyl-glycerophosphocholine and 1-acyl-glycerophosphocholine in guinea pig heart. Biochem J. 1986 Jun 1;236(2):481–487. doi: 10.1042/bj2360481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Arthur G., Covic L., Wientzek M., Choy P. C. Plasmalogenase in hamster heart. Biochim Biophys Acta. 1985 Feb 8;833(2):189–195. doi: 10.1016/0005-2760(85)90189-4. [DOI] [PubMed] [Google Scholar]
  5. BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
  6. Bers D. M. Isolation and characterization of cardiac sarcolemma. Biochim Biophys Acta. 1979 Jul 19;555(1):131–146. doi: 10.1016/0005-2736(79)90078-6. [DOI] [PubMed] [Google Scholar]
  7. D'Amato R. A., Horrocks L. A., Richardson K. E. Kinetic properties of plasmalogenase from bovine brain. J Neurochem. 1975 Jun;24(6):1251–1255. doi: 10.1111/j.1471-4159.1975.tb03906.x. [DOI] [PubMed] [Google Scholar]
  8. 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. 1984 Apr 18;793(2):221–231. doi: 10.1016/0005-2760(84)90324-2. [DOI] [PubMed] [Google Scholar]
  9. Dorman R. V., Toews A. D., Horrocks L. A. Plasmalogenase activities in neuronal perikarya, astroglia, and oligodendroglia isolated from bovine brain. J Lipid Res. 1977 Jan;18(1):115–117. [PubMed] [Google Scholar]
  10. FOLCH J., LEES M., SLOANE STANLEY G. H. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957 May;226(1):497–509. [PubMed] [Google Scholar]
  11. GOTTFRIED E. L., RAPPORT M. M. The biochemistry of plasmalogens. I. Isolation and characterization of phosphatidal choline, a pure native plasmalogen. J Biol Chem. 1962 Feb;237:329–333. [PubMed] [Google Scholar]
  12. Gross R. W. High plasmalogen and arachidonic acid content of canine myocardial sarcolemma: a fast atom bombardment mass spectroscopic and gas chromatography-mass spectroscopic characterization. Biochemistry. 1984 Jan 3;23(1):158–165. doi: 10.1021/bi00296a026. [DOI] [PubMed] [Google Scholar]
  13. Gunawan J., Debuch H. Lysoplasmalogenase--a microsomal enzyme from rat brain. J Neurochem. 1982 Sep;39(3):693–699. doi: 10.1111/j.1471-4159.1982.tb07948.x. [DOI] [PubMed] [Google Scholar]
  14. Horrocks L. A., Fu S. C. Pathway for hydrolysis of plasmalogens in brain. Adv Exp Med Biol. 1978;101:397–406. doi: 10.1007/978-1-4615-9071-2_37. [DOI] [PubMed] [Google Scholar]
  15. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  16. PENNINGTON R. J. Biochemistry of dystrophic muscle. Mitochondrial succinate-tetrazolium reductase and adenosine triphosphatase. Biochem J. 1961 Sep;80:649–654. doi: 10.1042/bj0800649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Tam S. W., Man R. Y., Choy P. C. The hydrolysis of phosphatidylcholine by phospholipase A2 in hamster heart. Can J Biochem Cell Biol. 1984 Dec;62(12):1269–1274. doi: 10.1139/o84-161. [DOI] [PubMed] [Google Scholar]
  18. WARNER H. R., LANDS W. E. The metabolism of plasmalogen: enzymatic hydrolysis of the vinyl ether. J Biol Chem. 1961 Sep;236:2404–2409. [PubMed] [Google Scholar]
  19. Woelk H., Goracci G., Porcellati G. The action of brain phospholipases A2 on purified, specifically labelled 1,2-diacyl-, 2-acyl-1-alk-1'-enyl- and 2-acyl-1-alkyl-sn-glycero-3-phosphorylcholine. Hoppe Seylers Z Physiol Chem. 1974 Jan;355(1):75–81. doi: 10.1515/bchm2.1974.355.1.75. [DOI] [PubMed] [Google Scholar]
  20. Woelk H. The action of phospholipase A2 in isolated fat cells on specifically labelled 2-acyl-1-alk-1'-enyl- and 2-acyl-1-alkyl-sn-glycero-3-phosphorylcholine. Biochem Biophys Res Commun. 1974 Aug 19;59(4):1278–1285. doi: 10.1016/0006-291x(74)90452-5. [DOI] [PubMed] [Google Scholar]
  21. Wolf R. A., Gross R. W. Identification of neutral active phospholipase C which hydrolyzes choline glycerophospholipids and plasmalogen selective phospholipase A2 in canine myocardium. J Biol Chem. 1985 Jun 25;260(12):7295–7303. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES