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The effect of a fish oil diet on the fatty acid composition of individual phospholipids and eicosanoid production by rat platelets
Author(s) -
CareagaHouck Mónica,
Sprecher Howard
Publication year - 1989
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/bf02535125
Subject(s) - glycerophospholipids , fish oil , polyunsaturated fatty acid , eicosapentaenoic acid , arachidonic acid , phospholipid , composition (language) , chemistry , food science , docosahexaenoic acid , biochemistry , calcium , ethanolamine , platelet , fatty acid , eicosanoid , lipoxygenase , choline , biology , fish <actinopterygii> , enzyme , linguistics , philosophy , organic chemistry , membrane , fishery , immunology
When rats were fed a diet containing chow or fish oil for six weeks, the platelet phospholipid content and percent distribution were similar. In the fish oil fed animals there was a 54, 40, 41, and 24% reduction, respectively, in the levels of 20∶4(n−6) in the choline‐, ethanolamine‐, inositol‐and serine‐containing glycerophospholipids. Dietary fish oil increased the total (n−3) polyunsaturated fatty acid content in all lipids. This effect was most pronounced in the ethanolamine glycerophospholipids which now contained 26, 11, and 4 nmols of 20∶5(n−3), 22∶5(n−3), and 22∶6(n−3) in 10 9 cells. Ionophore A23187 stimulation of platelets from the chow fed rats resulted in the synthesis of 7, 64, and 3.5 nmols of 12‐hydroxy‐5,8,10‐heptadecatrienoic acid, 12‐hydroxy‐5,8,10,14‐eicosatetraenoic acid and 12‐hydroxy‐5,8,10,14,17‐eicosapentaenoic acid, respectively, from 1×10 9 cells. The values from animals fed fish oil were 4, 18, and 27 nmol/10 9 platelets. It was not possible to detect any lipoxygenase products from 22∶5(n−3) or 22∶6(n−3), even though both acids are readily metabolized by lipoxygenase when added directly to platelets. These findings suggest that 22‐carbon (n−3) fatty acids are not liberated when phospholipases are activated by calcium mobilization.