Literature DB >> 3443938

The effects of post-exercise glucose and alanine ingestion on plasma carnitine and ketosis in humans.

J I Carlin1, E B Olson, H A Peters, W G Reddan.   

Abstract

1. Several studies have hypothesized that alanine decreases plasma ketone body levels by increasing availability of oxaloacetate, thus allowing acetyl groups to enter the tricarboxylic acid cycle and releasing co-enzyme A (CoA). 2. Four, fasted adult males exercised at 50% of their maximal oxygen consumption for 1.5 h, then ingested 100 g of either glucose or alanine 2 h into recovery. 3. Post-exercise ketosis had developed at 2 h into recovery, as shown by a significantly elevated concentration of beta-hydroxybutyrate in the plasma. At this time plasma free fatty acids were elevated above resting levels while plasma free carnitine concentrations had fallen below resting values. 4. After either alanine or glucose ingestion beta-hydroxybutyrate concentrations fell to the same extent. After the alanine load free carnitine increased above that seen in the glucose trial. Following either alanine or glucose ingestion free fatty acid levels fell; they remained at resting levels in the alanine trial but decreased below rest in the glucose trial. 5. We assume that plasma carnitine concentrations largely reflect the hepatic carnitine pools; therefore, elevations in the plasma free carnitine are probably the result of an increased utilization of acetyl CoA. The significant elevation in plasma free carnitine concentration found after alanine ingestion is consistent with the hypothesis that alanine increases the oxidation of acetyl CoA by providing oxaloacetate for the tricarboxylic acid cycle.

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Year:  1987        PMID: 3443938      PMCID: PMC1192181          DOI: 10.1113/jphysiol.1987.sp016701

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  16 in total

1.  Microdetermination of (-)carnitine and carnitine acetyltransferase activity.

Authors:  R Parvin; S V Pande
Journal:  Anal Biochem       Date:  1977-05-01       Impact factor: 3.365

2.  Enhancement of mitochondrial carnitine and carnitine acylcarnitine translocase-mediated transport of fatty acids into liver mitochondria under ketogenic conditions.

Authors:  R Parvin; S V Pande
Journal:  J Biol Chem       Date:  1979-06-25       Impact factor: 5.157

3.  Glucose and amino acid metabolism during recovery after exercise.

Authors:  J Wahren; P Felig; R Hendler; G Ahlborg
Journal:  J Appl Physiol       Date:  1973-06       Impact factor: 3.531

4.  Essential roles of insulin and glucagon in regulating glucose fluxes during exercise in dogs.

Authors:  M Vranic; R Kawamori
Journal:  Diabetes       Date:  1979-01       Impact factor: 9.461

5.  Plasma and liver carnitine (free and esterified) levels and their interrelationships in moderately hypercholesterolemic monkeys (Macaca arctoides).

Authors:  F P Bell; A J DeLucia
Journal:  Can J Biochem Cell Biol       Date:  1983-06

6.  Turnover of carnitine by rat tissues.

Authors:  D E Brooks; J E McIntosh
Journal:  Biochem J       Date:  1975-06       Impact factor: 3.857

7.  Carnitine and derivatives in rat tissues.

Authors:  D J Pearson; P K Tubbs
Journal:  Biochem J       Date:  1967-12       Impact factor: 3.857

8.  Relationship between acid-soluble carnitine and coenzyme A pools in vivo.

Authors:  E P Brass; C L Hoppel
Journal:  Biochem J       Date:  1980-09-15       Impact factor: 3.857

9.  The antiketogenic effect of alanine in normal man: evidence for an alanine-ketone body cycle.

Authors:  R Nosadini; K G Alberti; D G Johnston; S Del Prato; C Marescotti; E Duner
Journal:  Metabolism       Date:  1981-06       Impact factor: 8.694

10.  The effects of alanine, glucose and starch ingestion on the ketosis produced by exercise and by starvation.

Authors:  J H Koeslag; T D Noakes; A W Sloan
Journal:  J Physiol       Date:  1982-04       Impact factor: 5.182

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  3 in total

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Authors:  Mark Evans; Karl E Cogan; Brendan Egan
Journal:  J Physiol       Date:  2016-12-07       Impact factor: 5.182

2.  Mitochondrial enzyme GPT2 regulates metabolic mechanisms required for neuron growth and motor function in vivo.

Authors:  Ozan Baytas; Shawn M Davidson; Ralph J DeBerardinis; Eric M Morrow
Journal:  Hum Mol Genet       Date:  2022-02-21       Impact factor: 5.121

Review 3.  Exogenous Ketone Supplements in Athletic Contexts: Past, Present, and Future.

Authors:  Mark Evans; Tyler S McClure; Andrew P Koutnik; Brendan Egan
Journal:  Sports Med       Date:  2022-10-10       Impact factor: 11.928

  3 in total

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