Literature DB >> 7121717

Ketone-body utilization by homogenates of adult rat brain.

M Lopes-Cardozo, W Klein.   

Abstract

The regulation of ketone-body metabolism and the quantitative importance of ketone bodies as lipid precursors in adult rat brain has been studied in vitro. Utilization of ketone bodies and of pyruvate by homogenates of adult rat brain was measured and the distribution of 14C from [3-14C]ketone bodies among the metabolic products was analysed. The rate of ketone-body utilization was maximal in the presence of added Krebs-cycle intermediates and uncouplers of oxidative phosphorylation. The consumption of acetoacetate was faster than that of D-3-hydroxybutyrate, whereas, pyruvate produced twice as much acetyl-CoA as acetoacetate under optimal conditions. Millimolar concentrations of ATP in the presence of uncoupler lowered the consumption of ketone bodies but not of pyruvate. Indirect evidence is presented suggesting that ATP interferes specifically with the mitochondrial uptake of ketone bodies. Interconversion of ketone bodies and the accumulation of acid-soluble intermediates (mainly citrate and glutamate) accounted for the major part of ketone-body utilization, whereas only a small part was oxidized to CO2. Ketone bodies were not incorporated into lipids or protein. We conclude that adult rat-brain homogenates use ketone bodies exclusively for oxidative purposes.

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Year:  1982        PMID: 7121717     DOI: 10.1007/bf00965522

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  28 in total

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Authors:  D C DeVivo; K Fujimoto; M P Leckie; H C Agrawal
Journal:  J Neurochem       Date:  1976-03       Impact factor: 5.372

2.  Citrate transport and oxidation by isolated rat brain mitochondria.

Authors:  M S Patel
Journal:  Brain Res       Date:  1975-11-21       Impact factor: 3.252

3.  Control of pyruvate and beta-hydroxybutyrate utilization in rat brain mitochondria and its relevance to phenylketonuria and maple syrup urine disease.

Authors:  J M Land; J Mowbray; J B Clark
Journal:  J Neurochem       Date:  1976-04       Impact factor: 5.372

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Authors:  A P Halestrap
Journal:  Biochem J       Date:  1978-06-15       Impact factor: 3.857

5.  The in vivo utilization of acetoacetate, D-(-)-3-hydroxybutyrate, and glucose for lipid synthesis in brain in the 18-day-old rat. Evidence for an acetyl-CoA bypass for sterol synthesis.

Authors:  R J Webber; J Edmond
Journal:  J Biol Chem       Date:  1979-05-25       Impact factor: 5.157

6.  Ketogenesis in isolated rat liver mitochondria. I. Relationships with the citric acid cycle and with the mitochondrial energy state.

Authors:  M Lopes-Cardozo; S G van den Bergh
Journal:  Biochim Biophys Acta       Date:  1972

7.  Control of beta-hydroxybutyrate and acetoacetate oxidation by inorganic phosphate and adenosine-5'-diphosphate in heart mitochondria.

Authors:  Y Hatefi; T Fakouh
Journal:  Arch Biochem Biophys       Date:  1968-04       Impact factor: 4.013

8.  Development and regulation of lipid synthesis from ketone bodies by rat brain.

Authors:  M S Patel; O E Owen
Journal:  J Neurochem       Date:  1977-01       Impact factor: 5.372

9.  The regulation of acetoacetate metabolism in heart [proceedings].

Authors:  J H Ottaway; C L McMinn
Journal:  Biochem Soc Trans       Date:  1979-04       Impact factor: 5.407

10.  Lipogenesis in the brain of suckling rats. Studies on the mechansim of mitochondrial-cytosolic carbon transfer.

Authors:  T B Patel; J B Clark
Journal:  Biochem J       Date:  1980-04-15       Impact factor: 3.857

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  1 in total

1.  Pulmonary surfactant lipid synthesis from ketone bodies, lactate and glucose in newborn rats.

Authors:  P M Sheehan; Y Y Yeh
Journal:  Lipids       Date:  1985-12       Impact factor: 1.880

  1 in total

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