QUANTITATIVE-ANALYSIS OF PLATELET-ACTIVATING-FACTOR IN HUMAN PLASMA -APPLICATION TO PATIENTS WITH LIVER-CIRRHOSIS AND DISSEMINATED INTRAVASCULAR COAGULATION

Citation
J. Sugatani et al., QUANTITATIVE-ANALYSIS OF PLATELET-ACTIVATING-FACTOR IN HUMAN PLASMA -APPLICATION TO PATIENTS WITH LIVER-CIRRHOSIS AND DISSEMINATED INTRAVASCULAR COAGULATION, Journal of immunological methods, 166(2), 1993, pp. 251-261
Citations number
31
Categorie Soggetti
Immunology
ISSN journal
00221759
Volume
166
Issue
2
Year of publication
1993
Pages
251 - 261
Database
ISI
SICI code
0022-1759(1993)166:2<251:QOPIHP>2.0.ZU;2-J
Abstract
A simple and reliable analytical procedure was developed for determina tion of platelet-activating factor (PAF) in human plasma using radioim munoassay (RIA). The assay system consisted of lipid extraction with 2 -propanol, lipid separation by Amprep octadecyl minicolumn chromatogra phy and thin-layer chromatography and RIA (charcoal method), and was s uitable for quantitation of 30-1000 pg of PAF. The sensitivity of RIA for PAF was notably higher than that for sn-2-short-chain PAF-like pho sphatidylcholines. This assay system was then applied for measurement of PAF in human plasma. The normal level of plasma PAF was 54 +/- 40 p g/ml (n = 35), whereas plasma PAF levels in patients with liver cirrho sis (LC) and disseminated intravascular coagulation (DIC) were signifi cantly elevated to 238 +/- 314 pg/ml (n = 14) and 591 +/- 328 pg/ml (n = 14), respectively. The values obtained using this assay system were comparable to those obtained by gas chromatography/mass spectrometry analysis and bioassay. These results indicate that our new assay syste m is useful for determining changes in the level of plasma PAF associa ted with diseases such as LC and DIC.