Literature DB >> 8573096

Reduction pathway of cis-5 unsaturated fatty acids in intact rat-liver and rat-heart mitochondria: assessment with stable-isotype-labelled substrates.

K Y Tserng1, S J Jin, L S Chen.   

Abstract

Besides the conventional isomerase-mediated pathway, unsaturated fatty acids with old-numbered double bonds are also metabolized by reduction pathways with NADPH as cofactor. The relative contributions of these pathways were measured in intact rat-liver and rat-heart mitochondria with a novel stable isotope tracer technique. A mixture of equal amounts of unlabelled cis-5-enoyl-CoA and 13C4-labelled acyl-CoA of equal chain lengths was incubated with mitochondria. The isotope distribution of 3-hydroxy fatty acids produced from the first cycle of beta-oxidation was analysed with selected ion monitoring by gas chromatograph-mass spectrometer. 3-Hydroxy fatty acids produced from the reduction pathway of unsaturated fatty acids were unlabelled (m + 0) whereas those produced from saturated fatty acids were labelled (m + 4). The m + 0 content serves to indicate the extent of reduction pathway. Rotenone treatment was used to switch the pathway completely to reduction. The extent of m + 0 enrichment in untreated mitochondria normalized to the m + 0 enrichment of rotenone-treated mitochondria was the percentage of reduction pathway. With this technique, cis-4-decenoate was found to be metabolized completely by the reduction pathway in both liver and heart mitochondria. cis-5-Dodecenoate was metabolized essentially by the reduction pathway in liver mitochondria, but only to 75% in heart mitochondria. When the chain length was extended to cis-5-tetradecenoate, the reduction pathway in liver mitochondria decreased to 86% and that in heart mitochondria to 65%. The effects of carnitine, clofibrate and other conditions on the reduction pathway were also studied. Enrichments of the label on saturated fatty acids and 3-hydroxy fatty acids indicated that the major pathway of reduction was not by the direct reduction of the cis-5 double bond. Instead, it is most probably by a pathway that does not involve forming a reduced saturated fatty acid first.

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Year:  1996        PMID: 8573096      PMCID: PMC1216947          DOI: 10.1042/bj3130581

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  24 in total

1.  Studies on the metabolism of unsaturated fatty acids. XI. Alterations in the activities of enoyl-CoA hydratase, 3-hydroxyacyl-CoA epimerase and 2,4-dienyl-CoA reductase in rat liver mitochondria and peroxisomes by clofibrate.

Authors:  M Mizugaki; T Nishimaki; H Yamamoto; M Sagi; H Yamanaka
Journal:  J Biochem       Date:  1982-12       Impact factor: 3.387

2.  Metabolic origin of urinary 3-hydroxy dicarboxylic acids.

Authors:  K Y Tserng; S J Jin
Journal:  Biochemistry       Date:  1991-03-05       Impact factor: 3.162

Review 3.  Physiological roles of nicotinamide nucleotide transhydrogenase.

Authors:  J B Hoek; J Rydström
Journal:  Biochem J       Date:  1988-08-15       Impact factor: 3.857

4.  Metabolic origins of urinary unsaturated dicarboxylic acids.

Authors:  S J Jin; K Y Tserng
Journal:  Biochemistry       Date:  1990-09-18       Impact factor: 3.162

5.  Calculation of substrate turnover rate in stable isotope tracer studies.

Authors:  K Y Tserng; S C Kalhan
Journal:  Am J Physiol       Date:  1983-09

6.  A role for 2,4-enoyl-CoA reductase in mitochondrial beta-oxidation of polyunsaturated fatty acids. Effects of treatment with clofibrate on oxidation of polyunsaturated acylcarnitines by isolated rat liver mitochondria.

Authors:  H Osmundsen; J Cervenka; J Bremer
Journal:  Biochem J       Date:  1982-12-15       Impact factor: 3.857

7.  Degradation of unsaturated fatty acids in peroxisomes. Existence of a 2,4-dienoyl-CoA reductase pathway.

Authors:  V Dommes; C Baumgart; W H Kunau
Journal:  J Biol Chem       Date:  1981-08-25       Impact factor: 5.157

8.  [Metabolism of unsaturated fatty acids. V. On the beta-oxidation of mono- and polyene-fatty acids. Mechanism of enzymatic reactions of delta-2-cis-enoyl-CoA compounds].

Authors:  W Stoffel; H Caesar
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1965

9.  Relationships between the NAD(P) redox state, fatty acid oxidation, and inner membrane permeability in rat liver mitochondria.

Authors:  D Lê-Quôc; K Lê-Quôc
Journal:  Arch Biochem Biophys       Date:  1989-09       Impact factor: 4.013

10.  Studies on the metabolism of unsaturated fatty acids. XV. Purification and properties of 2,4-dienoyl-CoA reductase from rat liver peroxisomes.

Authors:  C Kimura; A Kondo; N Koeda; H Yamanaka; M Mizugaki
Journal:  J Biochem       Date:  1984-11       Impact factor: 3.387

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  3 in total

1.  The questionable role of a microsomal delta8 acyl-coA-dependent desaturase in the biosynthesis of polyunsaturated fatty acids.

Authors:  Q Chen; F Q Yin; H Sprecher
Journal:  Lipids       Date:  2000-08       Impact factor: 1.880

Review 2.  Mammalian mitochondrial beta-oxidation.

Authors:  S Eaton; K Bartlett; M Pourfarzam
Journal:  Biochem J       Date:  1996-12-01       Impact factor: 3.857

3.  The effect of fasting, long-chain triglyceride load and carnitine load on plasma long-chain acylcarnitine levels in mitochondrial very long-chain acyl-CoA dehydrogenase deficiency.

Authors:  C G Costa; L Dorland; I T de Almeida; C Jakobs; M Duran; B T Poll-The
Journal:  J Inherit Metab Dis       Date:  1998-06       Impact factor: 4.982

  3 in total

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