Literature DB >> 17502492

Validation of renal oxidative metabolism measurement by positron-emission tomography.

Laurent Juillard1, Sandrine Lemoine, Marc F Janier, Paul Y Barthez, Frédéric Bonnefoi, Maurice Laville.   

Abstract

Either in research or in clinical practice, the exploration of renal oxidative metabolism is limited by the lack of noninvasive measurement. Positron-emission tomography using carbon-11 acetate may estimate tissue oxidative metabolism by measuring acetate turnover in the Krebs cycle. Although extensively studied in cardiology, this method has never been validated for renal oxidative metabolism measurement. The aim of this study is the validation of acetate turnover compared with the invasive renal oxygen consumption measurement. Renal oxygen consumption and tubular sodium reabsorption were measured invasively in 10 anesthetized pigs. Simultaneously, acetate turnover was estimated by the clearance of carbon-11 acetate in the renal cortex, after a 166-MBq injection of carbon-11 acetate. Renal oxidative metabolism was measured under various conditions induced by mechanical and pharmacological interventions. Renal oxygen consumption and acetate turnover varied on a wide range from 0.05 to 0.29 mmol min(-1) (>5-fold) and from 0.025 to 0.188 minutes(-1) (>7-fold), respectively. Acetate turnover was very significantly correlated with renal oxygen consumption (P<0.0001; R=0.82) and tubular sodium reabsorption (P=0.001; R=0.67). This study demonstrates that acetate turnover measures renal oxidative metabolism noninvasively and quantitatively, consistent with changes in tubular sodium reabsorption. This method may be applied to assess oxidative metabolism in animal models and in humans.

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Year:  2007        PMID: 17502492     DOI: 10.1161/HYPERTENSIONAHA.107.089607

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  5 in total

1.  [11C]Acetate rest-stress protocol to assess myocardial perfusion and oxygen consumption reserve in a model of congestive heart failure in rats.

Authors:  Etienne Croteau; Suzanne Gascon; M'hamed Bentourkia; Réjean Langlois; Jacques A Rousseau; Roger Lecomte; François Bénard
Journal:  Nucl Med Biol       Date:  2011-11-12       Impact factor: 2.408

2.  Investigation of metabolic changes in STZ-induced diabetic rats with hyperpolarized [1-13C]acetate.

Authors:  Ulrich Koellisch; Christoffer Laustsen; Thomas S Nørlinger; Jakob Appel Østergaard; Allan Flyvbjerg; Concetta V Gringeri; Marion I Menzel; Rolf F Schulte; Axel Haase; Hans Stødkilde-Jørgensen
Journal:  Physiol Rep       Date:  2015-08

Review 3.  Current Use and Complementary Value of Combining in Vivo Imaging Modalities to Understand the Renoprotective Effects of Sodium-Glucose Cotransporter-2 Inhibitors at a Tissue Level.

Authors:  Sjoukje van der Hoek; Jasper Stevens
Journal:  Front Pharmacol       Date:  2022-02-21       Impact factor: 5.810

4.  Current state-of-the-art hyperpolarized 13C-acetate-to-acetylcarnitine imaging is not indicative of the altered balance between glucose and fatty acid utilization associated with diabetes.

Authors:  Ulrich Koellisch; Christoffer Laustsen; Thomas S Nørlinger; Jakob A Østergaard; Allan Flyvbjerg; Concetta V Gringeri; Marion I Menzel; Rolf F Schulte; Axel Haase; Hans Stødkilde-Jørgensen
Journal:  Physiol Rep       Date:  2016-09

5.  Hyperpolarized [1-13C]-acetate Renal Metabolic Clearance Rate Mapping.

Authors:  Emmeli F R Mikkelsen; Christian Østergaard Mariager; Thomas Nørlinger; Haiyun Qi; Rolf F Schulte; Steen Jakobsen; Jørgen Frøkiær; Michael Pedersen; Hans Stødkilde-Jørgensen; Christoffer Laustsen
Journal:  Sci Rep       Date:  2017-11-22       Impact factor: 4.379

  5 in total

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