1999
DOI: 10.1006/abio.1999.4322
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A Method for Distinguishing 1-Acyl from 2-Acyl Lysophosphatidylcholines Generated in Biological Systems

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Cited by 14 publications
(10 citation statements)
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“…Recently, using a novel method for distinguishing 1-acyl from 2-acyl LPC, we showed that the LPC found in bovine erythrocyte extracts is predominantly of the type 1-acyl, i.e., the type generated by Plase A 2 (33). Furthermore, we found that no changes in lipid composition occurred in erythrocytes incubated in either heparinized plasma or in TBS-GCM buffer at 37°C for up to 48 h (data not shown).…”
Section: Resultsmentioning
confidence: 78%
“…Recently, using a novel method for distinguishing 1-acyl from 2-acyl LPC, we showed that the LPC found in bovine erythrocyte extracts is predominantly of the type 1-acyl, i.e., the type generated by Plase A 2 (33). Furthermore, we found that no changes in lipid composition occurred in erythrocytes incubated in either heparinized plasma or in TBS-GCM buffer at 37°C for up to 48 h (data not shown).…”
Section: Resultsmentioning
confidence: 78%
“…Most of the papers and our previous methods of positional analysis of PC are based on two different enzymatic reactions (Adlecreutz & Wehtje, 2004;Chojnacka et al, 2009;Florin-Christensen et al, 1999;Gladkowski et al, 2009), which increase their complexity. Some papers also present one-enzymatic reaction methods of determination of FAs composition in PC (Cossignani et al, 1994).…”
Section: Resultsmentioning
confidence: 99%
“…These compounds were chemically hydrolyzed and the released FAs were esterified and analyzed by GC (Adlecreutz & Wehtje, 2004). A two-enzymes system using PLA 2 from bee venom and PLA 1 from T. thermophila was proposed by Florin-Christensen, Narvaez-Vasquez, Florin-Christensen, and Ryan (1999). Although the methods based on enzymatic hydrolysis of PLs are the most common procedures used in positional analysis of PC some other were also proposed.…”
Section: Introductionmentioning
confidence: 99%
“…A 0.2-mL aliquot of the phospholipid fraction obtained by SPE was subjected to phospholipase A 2 catalyzed hydrolysis using the method described by Florin-Christensen et al [20]. Reaction products were separated by TLC on silica gel G plates with chloroform/methanol/acetic acid/ water (65:35:4:2, v/v/v/v).…”
Section: Positional Analysis Of Phospholipidsmentioning
confidence: 99%