Literature DB >> 6810706

Urinary excretion of acetylcarnitine during human diabetic and fasting ketosis.

C L Hoppel, S M Genuth.   

Abstract

The urinary excretion of acetylcarnitine was studied in patients with diabetic ketosis before and during insulin therapy and in normal-weight and obese subjects during fasting. In the diabetic ketotic patients, acetylcarnitine represented 61% of the total acylcarnitine excretion. During the first 24 h of insulin treatment, acetylcarnitine excretion decreased and on the 5th day of treatment was 18% of the acylcarnitines excreted. The urinary excretion of the other acylcarnitines fell slowly. In normal-weight subjects fasted for 3 days, the urinary excretion of acetylcarnitine increased on the 2nd day of fasting, and on the 3rd day acetylcarnitine accounted for 78% of the excreted acylcarnitine. In obese subjects there was a progressive increase in urinary acetylcarnitine excretion, but on day 6 it represented only 55% of the total acylcarnitine excreted. The urinary excretion of acetylcarnitine correlated with blood beta-hydroxybutyrate concentration in the normal-weight subjects during fasting and in the diabetic ketotic patients. Acetylcarnitine accounts for a major fraction of the acylcarnitines excreted in the three ketotic conditions studied. The contribution of acetylcarnitine to the change in acylcarnitines as ketosis appears or disappears is significantly less in the obese subjects than in the normal-weight subjects or in the diabetic patients. This difference may reflect an alteration in the production or disposition of acetyl-CoA and acetylcarnitine in obesity.

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Year:  1982        PMID: 6810706     DOI: 10.1152/ajpendo.1982.243.2.E168

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  6 in total

1.  Inhibition of oxidative metabolism by propionic acid and its reversal by carnitine in isolated rat hepatocytes.

Authors:  E P Brass; P V Fennessey; L V Miller
Journal:  Biochem J       Date:  1986-05-15       Impact factor: 3.857

2.  Cephaloridine-induced nephrotoxicity in the Fischer 344 rat: proton NMR spectroscopic studies of urine and plasma in relation to conventional clinical chemical and histopathological assessments of nephronal damage.

Authors:  M L Anthony; K P Gartland; C R Beddell; J C Lindon; J K Nicholson
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

3.  [Effect of L-carnitine supplemented total parenteral nutrition on postoperative lipid and nitrogen utilization].

Authors:  C Rössle; C Pichard; M Roulet; R Chiolero; Y Schutz; E Temler; C Schindler; F Zurlo; E Jéquier; P Fürst
Journal:  Klin Wochenschr       Date:  1988-12-15

4.  Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

Authors:  C R Roe; C L Hoppel; T E Stacey; R A Chalmers; B M Tracey; D S Millington
Journal:  Arch Dis Child       Date:  1983-11       Impact factor: 3.791

Review 5.  Mitochondria in the elderly: Is acetylcarnitine a rejuvenator?

Authors:  Mariana G Rosca; Hélène Lemieux; Charles L Hoppel
Journal:  Adv Drug Deliv Rev       Date:  2009-08-29       Impact factor: 15.470

6.  Urinary F2-isoprostanes and metabolic markers of fat oxidation.

Authors:  Dora Il'yasova; Lynne E Wagenknecht; Ivan Spasojevic; Steven Watkins; Donald Bowden; Frances Wang; Ralph B D'Agostino
Journal:  Oxid Med Cell Longev       Date:  2015-02-23       Impact factor: 6.543

  6 in total

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