Literature DB >> 24197444

The desaturation and elongation of (14)C-labelled polyunsaturated fatty acids by pike (Esox lucius L.) in vivo.

R J Henderson1, M T Park, J R Sargent.   

Abstract

To examine the ability of pike (Esox lucius L.) to modify exogenous PUFA by desaturation and elongation, (14)C-labelled 18:2(n-6), 18:3(n-3), 20:4(n-6) and 20:5(n-3) were injected intraperitoneally and the distribution of radioactivity in tissue lipid classes and liver PUFA measured. In all tissues examined, radioactivity from all (14)C-PUFA was recovered in many classes of acyl lipids and the level of recovery generally reflected the relative abundance of the lipid classes. Triacylglycerols, CGP and EGP usually contained high levels of all incorporated (14)C-PUFA. PI contained higher levels of radioactivity from (14)C-20:4(n-6) than from other injected substrates. In liver lipid, the Δ6 desaturation products of (14)C-18:2(n-6) and (14)C-18:3(n-3) contained no measurable radioactivity although the elongation products of the Δ6 desaturation products were labelled, as were the direct elongation products of these injected substrates. No radioactivity from (14)C-18:2(n-6) or (14)C-18:3(n-3) was detected in C20 or C22 products of Δ5 and Δ4 desaturation. Almost all radioactivity from injected (14)C-20:4(n-6) was recovered in this PUFA. Of the total radioactivity from (14)C-20:5(n-3) incorporated into liver lipid, 7% was present as 24:5 and 16.4% was recovered in hexaenoic fatty acids. In liver, 24:5(n-3) and 24:6(n-3) each accounted for 1% of the mass of total fatty acids and were located almost exclusively in triacylglycerols. The presence of radioactivity in these C24 PUFA suggests that in pike the synthesis of 22:6(n-3) from 20:5(n-3) may proceed without Δ4 desaturase via the pathway which involves chain shortening of 24:6(n-3). It is concluded that under the circumstances employed in this study pike, do not exhibit Δ5 desaturase activity and are unable to synthesize 20:4(n-6) and 20:5(n-3) from 18:2(n-6) and 18:3(n-3), respectively. This suggests that pike may require 20:4(n-6) and 20:5(n-3) preformed in the diet.

Entities:  

Year:  1995        PMID: 24197444     DOI: 10.1007/BF00004313

Source DB:  PubMed          Journal:  Fish Physiol Biochem        ISSN: 0920-1742            Impact factor:   2.794


  18 in total

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Authors:  A G Hassam; J P Rivers; M A Crawford
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Review 2.  The lipid composition and biochemistry of freshwater fish.

Authors:  R J Henderson; D R Tocher
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3.  Furanoid fatty acids from fish lipids.

Authors:  R L Glass; T P Krick; D M Sand; C H Rahn; H Schlenk
Journal:  Lipids       Date:  1975-11       Impact factor: 1.880

4.  Incorporation and metabolism of (14)C-labelled polyunsaturated fatty acids in juvenile gilthead sea bream Sparus aurata L. in vivo.

Authors:  G Mourente; D R Tocher
Journal:  Fish Physiol Biochem       Date:  1993-04       Impact factor: 2.794

5.  New series of fatty acids in northern pike (Esox lucius).

Authors:  R L Glass; T P Krick; A E Echardt
Journal:  Lipids       Date:  1974-12       Impact factor: 1.880

6.  Incorporation and metabolism of (n-3) and (n-6) polyunsaturated fatty acids in phospholipid classes in cultured turbot (Scophthalmus maximus) cells.

Authors:  D R Tocher; E E Mackinlay
Journal:  Fish Physiol Biochem       Date:  1990-05       Impact factor: 2.794

7.  Fatty acid compositions of the major phosphoglycerides from fish neural tissues; (n-3) and (n-6) polyunsaturated fatty acids in rainbow trout (Salmo gairdneri) and cod (Gadus morhua) brains and retinas.

Authors:  D R Tocher; D G Harvie
Journal:  Fish Physiol Biochem       Date:  1988-10       Impact factor: 2.794

8.  Long and very long chain polyunsaturated fatty acids of the n-6 series in rat seminiferous tubules. Active desaturation of 24:4n-6 to 24:5n-6 and concomitant formation of odd and even chain tetraenoic and pentaenoic fatty acids up to C32.

Authors:  M I Aveldaño; B S Robinson; D W Johnson; A Poulos
Journal:  J Biol Chem       Date:  1993-06-05       Impact factor: 5.157

9.  Metabolism of linoleic acid in the cat.

Authors:  A J Sinclair; J G McLean; E A Monger
Journal:  Lipids       Date:  1979-11       Impact factor: 1.880

10.  The metabolism of 7,10,13,16,19-docosapentaenoic acid to 4,7,10,13,16,19-docosahexaenoic acid in rat liver is independent of a 4-desaturase.

Authors:  A Voss; M Reinhart; S Sankarappa; H Sprecher
Journal:  J Biol Chem       Date:  1991-10-25       Impact factor: 5.157

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2.  Dietary Linseed Oil Reduces Growth While Differentially Impacting LC-PUFA Synthesis and Accretion into Tissues in Eurasian Perch (Perca fluviatilis).

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3.  Minor lipid metabolic perturbations in the liver of Atlantic salmon (Salmo salar L.) caused by suboptimal dietary content of nutrients from fish oil.

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4.  An evolutionary perspective on Elovl5 fatty acid elongase: comparison of Northern pike and duplicated paralogs from Atlantic salmon.

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