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Incorporation of 1,2‐ 14 C‐ethanolamine into subfractions of rat liver phosphatidylethanolamines and phosphatidylcholines
Author(s) -
Tinoco J.,
Sheehan G.,
Hopkins S.,
Lyman R. L.
Publication year - 1970
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/bf02532107
Subject(s) - phosphatidylethanolamine , ethanolamine , degree of unsaturation , chemistry , phosphatidylcholine , fraction (chemistry) , specific activity , lipidology , chromatography , biochemistry , phospholipid , endogeny , clinical chemistry , stereochemistry , membrane , enzyme
Abstract The incorporation of 1,2‐ 14 C‐ethanolamine into the liver phosphatidylethanolamines (PE) and phosphatidylcholines (PC) in female rats was studied. These phosphatides were fractionated according to their degrees of unsaturation and the specific activities of monoenoic, dienoic, tetraenoic and hexaenoic fractions were measured at intervals of 1, 20, 60 and 300 min after injection of the labeled precursor. Hexaenoic and dienoic PE incorporated and lost the label rapidly. Although the labeled precursor was incorporated into tetraene PE at a similar rate, this fraction attained a relatively low specific activity that remained essentially constant between 10 and 300 min after injection of the label. Hexaenoic PC had the highest specific activity among the PC fractions at all time periods. Estimations of the rate of loss of radioactivity in the hexaenoic PE fraction and its appearance in hexaenoic PC indicate that the docosahexaenoic acid is conserved, possibly by being reincorporated into PE after becoming a part of the hexaenoic PC species. The high rate of turnover of the hexaenoic PE also suggests that this fraction might have some special role in endogenous choline synthesis.