Literature DB >> 2233704

Characterization and analysis of the subclasses and molecular species of choline phosphoglycerides from porcine heart by successive chemical hydrolyses and reverse phase high-performance liquid chromatography.

N A Shaikh1.   

Abstract

Choline phosphoglycerides (CPG) represent the major fraction of heart phospholipids. Since depletion of membrane phospholipids and accumulation of lyso-compounds, particularly lysophosphatidylcholines, have been implicated in arrhythmogenesis, it was of great interest to study the composition of this major phospholipid fraction of the heart at a molecular level in an established animal model. The data presented here describe the first report on the detailed chemical examination of CPG and resolution, characterization and quantitative analysis of the molecular species of this phospholipid fraction from porcine heart by high performance liquid chromatography (HPLC). This fraction constitutes 37.5 +/- 0.7% (n = 21) of the total phospholipids and upon successive mild acid and alkaline hydrolyses revealed the presence of essentially three subclasses: diacyl-, alkenylacyl-, and alkylacyl glycerophosphorylcholines, in a relative abundance of 57.7 +/- 2.2% (n = 8), 37.3 +/- 1.3% (n = 8) and 4.6 +/- 0.2% (n = 8), respectively. The fourth subclass, dialkyl CPG was found only in minute amounts (0.43 +/- 0.05%, n = 8) and the presence of dialkenyl and alkenylalkyl analogues could not be detected. Alternatively, by converting the CPG fraction to benzoate derivatives after phospholipase C digestion, it was possible to isolate and quantitate subclass composition by TLC/spectroscopy or both subclass compositions and molecular species analysis by HPLC directly by a UV detector online with the column. By these techniques, subclass composition was found to be very similar to that obtained by the chemical hydrolysis technique. By HPLC, up to 25 species can be identified and quantitated in each subclass, their identity being confirmed by gas-liquid chromatography, after their isolation from the column. The analyses showed that up to 74% of the diacyl moiety consisted of 16:0-18:2 (34%), 16:0-18:1 (27%), and 18:0-18:2 (13%) species, while the major species of the alkenylacyl moiety were 16:0-18:2 (44%) 16:0-18:1 (13%), 16:0-20:4 (12%) and 18:1-18:2 (9%) making up more than 75% of the total mass of this subclass. The major molecular species of the alkylacyl moiety was 16:0-18:2, constituting up to 47% of this fraction, while others constituted about 10% (16:0-18:1), 9% (18:1-18:2), 8% (16:0-20:4) and 6% (18:0-18:2), making up 80% of the total mass. The ether chain composition of akylacyl CPG whether determined after isolation of this fraction by the chemical hydrolysis technique or by HPLC was indistinguishable.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2233704     DOI: 10.1007/bf00228452

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  35 in total

1.  METABOLISM OF PLASMALOGEN: II. THE DETERMINATION OF ALKENYL ETHERS IN THE PRESENCE OF FREE ALDEHYDES.

Authors:  H R WARNER; W E LANDS
Journal:  J Lipid Res       Date:  1963-04       Impact factor: 5.922

Review 2.  Metabolism of molecular species of diacylglycerophospholipids.

Authors:  B J Holub; A Kuksis
Journal:  Adv Lipid Res       Date:  1978

3.  Separation of molecular species of sphingomyelin and ceramide by argentation and reversed-phase HPLC.

Authors:  M Smith; P Monchamp; F B Jungalwala
Journal:  J Lipid Res       Date:  1981-05       Impact factor: 5.922

4.  Lysophosphatidylcholine causes cardiac arrhythmia.

Authors:  R Y Man; P C Choy
Journal:  J Mol Cell Cardiol       Date:  1982-03       Impact factor: 5.000

5.  Separation of alkenylacyl, alkylacyl, and diacyl analogues and their molecular species by high performance liquid chromatography.

Authors:  Y Nakagawa; L A Horrocks
Journal:  J Lipid Res       Date:  1983-09       Impact factor: 5.922

Review 6.  Membrane lipid composition and cellular function.

Authors:  A A Spector; M A Yorek
Journal:  J Lipid Res       Date:  1985-09       Impact factor: 5.922

7.  Differentiation of primary or metastatic lung carcinoma by phospholipid analysis. A new approach for lung carcinoma differentiation.

Authors:  K Itoh; H Natori; A Suzuki; T Akino
Journal:  Cancer       Date:  1986-04-01       Impact factor: 6.860

8.  Separation of phospholipid molecular species by high performance liquid chromatography: potentials for use in metabolic studies.

Authors:  S J Robins; G M Patton
Journal:  J Lipid Res       Date:  1986-02       Impact factor: 5.922

9.  Correlation of alterations in cation exchange and sarcolemmal ultrastructure produced by neuraminidase and phospholipases in cardiac cell tissue culture.

Authors:  G A Langer; J S Frank; K D Philipson
Journal:  Circ Res       Date:  1981-12       Impact factor: 17.367

10.  1-O-alkyl-2-acyl-sn-glycero-3-phosphocholine: a novel source of arachidonic acid in neutrophils stimulated by the calcium ionophore A23187.

Authors:  C L Swendsen; J M Ellis; F H Chilton; J T O'Flaherty; R L Wykle
Journal:  Biochem Biophys Res Commun       Date:  1983-05-31       Impact factor: 3.575

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