Monocyclic dienoic fatty acids formed from γ-linolenic acid in heated evening primrose oil

1999 ◽  
Vol 97 (2) ◽  
pp. 105-118 ◽  
Author(s):  
Gary Dobson ◽  
Jean Louis Sebedio
1994 ◽  
Vol 71 (6) ◽  
pp. 569-573 ◽  
Author(s):  
M. S. K. Syed Rahmatullah ◽  
V. K. S. Shukla ◽  
K. D. Mukherjee

1985 ◽  
Vol 53 (3) ◽  
pp. 441-448 ◽  
Author(s):  
S. C Cunnane ◽  
M. S. Manku ◽  
D. F. Horrobin

1. Genetically obese mice (ob/ob) and their lean litter-mates were given diets iso-energetically supplemented with sucrose, hydrogenated coconut oil, safflower oil or evening primrose (Oenothera biennis) oil.2. Weight gain over 15 weeks was significantly greater in the evening primrose oil-supplemented obese mice than in the other groups.3. In all the groups of obese mice, liver total phospholipids contained proportionally less linoleic acid and more dihomo-γ-linolenic acid and arachidonic acid than did the lean controls.4. As a percentage of total fatty acids, n-3 essential fatty acids (EFA) in liver and adipose tissue lipids were significantly lower in the obese mice than in the lean controls.5. Supplementation with EFA-rich oils (safflower and evening primrose oil) increased the proportional composition of n-6 EFA and decreased the n-3 EFA more in the liver total phospholipids of the lean than the obese mice.


2014 ◽  
Vol 91 (7) ◽  
pp. 1147-1153 ◽  
Author(s):  
Ramiro Baeza-Jiménez ◽  
Da Som No ◽  
Christina Otero ◽  
Hugo S. García ◽  
Jeom Sig Lee ◽  
...  

2008 ◽  
Vol 99 (2) ◽  
pp. 360-369 ◽  
Author(s):  
Julia Geppert ◽  
Hans Demmelmair ◽  
Gerard Hornstra ◽  
Berthold Koletzko

Fish oil supplementation during pregnancy not only improves maternal and neonatal DHA status, but often reduces γ-linolenic acid (GLA), dihomo-GLA (DGLA), and arachidonic acid (ARA) levels also, which may compromise foetal and infant development. The present study investigated the effects of a fish oil/evening primrose oil (FSO/EPO) blend (456 mg DHA/d and 353 mg GLA/d) compared to a placebo (mixture of habitual dietary fatty acids) on the plasma fatty acid (FA) composition in two groups of twenty non-pregnant women using a randomised, double-blind, placebo-controlled parallel design. FA were quantified in plasma total lipids, phospholipids, cholesterol esters, and TAG at weeks 0, 4, 6 and 8. After 8 weeks of intervention, percentage changes from baseline values of plasma total lipid FA were significantly different between FSO/EPO and placebo for GLA (+49·9 % v. +2·1 %, means), DGLA (+13·8 % v. +0·7 %) and DHA (+59·6 % v. +5·5 %), while there was no significant difference for ARA ( − 2·2 % v. − 5·9 %). FA changes were largely comparable between plasma lipid fractions. In both groups three subjects reported mild adverse effects. As compared with placebo, FSO/EPO supplementation did not result in any physiologically relevant changes of safety parameters (blood cell count, liver enzymes). In women of childbearing age the tested FSO/EPO blend was well tolerated and appears safe. It increases plasma GLA, DGLA, and DHA levels without impairing ARA status. These data provide a basis for testing this FSO/EPO blend in pregnant women for its effects on maternal and neonatal FA status and infant development.


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