Hyperpolarized magnetic resonance shows that the anti-ischemic drug meldonium leads to increased flux through pyruvate dehydrogenase in vivo resulting in improved post-ischemic function in the diabetic heart.


Journal

NMR in biomedicine
ISSN: 1099-1492
Titre abrégé: NMR Biomed
Pays: England
ID NLM: 8915233

Informations de publication

Date de publication:
04 2021
Historique:
received: 02 09 2020
revised: 20 11 2020
accepted: 20 12 2020
pubmed: 19 1 2021
medline: 15 12 2021
entrez: 18 1 2021
Statut: ppublish

Résumé

The diabetic heart has a decreased ability to metabolize glucose. The anti-ischemic drug meldonium may provide a route to counteract this by reducing l-carnitine levels, resulting in improved cardiac glucose utilization. Therefore, the aim of this study was to use the novel technique of hyperpolarized magnetic resonance to investigate the in vivo effects of treatment with meldonium on cardiac metabolism and function in control and diabetic rats. Thirty-six male Wistar rats were injected either with vehicle, or with streptozotocin (55 mg/kg) to induce a model of type 1 diabetes. Daily treatment with either saline or meldonium (100 mg/kg/day) was undertaken for three weeks. in vivo cardiac function and metabolism were assessed with CINE MRI and hyperpolarized magnetic resonance respectively. Isolated perfused hearts were challenged with low-flow ischemia/reperfusion to assess the impact of meldonium on post-ischemic recovery. Meldonium had no significant effect on blood glucose concentrations or on baseline cardiac function. However, hyperpolarized magnetic resonance revealed that meldonium treatment elevated pyruvate dehydrogenase flux by 3.1-fold and 1.2-fold in diabetic and control animals, respectively, suggesting an increase in cardiac glucose oxidation. Hyperpolarized magnetic resonance further demonstrated that meldonium reduced the normalized acetylcarnitine signal by 2.1-fold in both diabetic and control animals. The increase in pyruvate dehydrogenase flux in vivo was accompanied by an improvement in post-ischemic function ex vivo, as meldonium elevated the rate pressure product by 1.3-fold and 1.5-fold in the control and diabetic animals, respectively. In conclusion, meldonium improves in vivo pyruvate dehydrogenase flux in the diabetic heart, contributing to improved cardiac recovery after ischemia.

Identifiants

pubmed: 33458907
doi: 10.1002/nbm.4471
pmc: PMC8609426
doi:

Substances chimiques

Methylhydrazines 0
Pyruvate Dehydrogenase Complex 0
Streptozocin 5W494URQ81
3-(2,2,2-trimethylhydrazine)propionate 73H7UDN6EC
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e4471

Subventions

Organisme : Medical Research Council
ID : G0601490
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/14/17/30634
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/17/58/33072
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/10/002/28078
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/19/18/34252
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/16/7/31843
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/13/1/30181
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd.

Références

Front Nutr. 2016 Apr 19;3:10
pubmed: 27148535
J Clin Invest. 1960 May;39:717-23
pubmed: 13796251
Circ Res. 2016 Nov 11;119(11):1177-1182
pubmed: 27635086
J Cardiovasc Pharmacol. 2006 Mar;47(3):493-9
pubmed: 16633095
Heart Fail Rev. 2014 Jan;19(1):35-48
pubmed: 23443849
NMR Biomed. 2019 Jun;32(6):e4091
pubmed: 30968985
Magn Reson Med. 2018 Nov;80(5):1882-1890
pubmed: 29607535
J Chromatogr Sci. 2011;49(6):463-8
pubmed: 21682996
Circ Res. 1995 Oct;77(4):726-34
pubmed: 7554119
Cardiovasc Drugs Ther. 2009 Aug;23(4):281-8
pubmed: 19536647
Klin Med (Mosk). 2007;85(7):39-42
pubmed: 17882808
Mol Cell Biochem. 2004 Mar;258(1-2):171-82
pubmed: 15030182
NMR Biomed. 2018 Jun;31(6):e3912
pubmed: 29637642
Eur J Pharmacol. 2011 May 11;658(2-3):277-83
pubmed: 21371472
Commun Biol. 2020 May 20;3(1):247
pubmed: 32433536
NMR Biomed. 2021 Apr;34(4):e4471
pubmed: 33458907
Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):12051-6
pubmed: 18689683
Sci Rep. 2016 May 06;6:25573
pubmed: 27150735
J Ethnopharmacol. 2008 May 8;117(2):215-20
pubmed: 18359177
Magn Reson Med. 2016 Apr;75(4):1515-24
pubmed: 25991606
Diabetes Obes Metab. 2019 Apr;21(4):949-960
pubmed: 30536560
Biochem Pharmacol. 1988 Jan 15;37(2):195-202
pubmed: 3342076
Lancet. 1963 Apr 13;1(7285):785-9
pubmed: 13990765
Proc Natl Acad Sci U S A. 1977 Jun;74(6):2485-9
pubmed: 142253
Magn Reson Med. 2014 May;71(5):1663-9
pubmed: 23798473
Arterioscler Thromb Vasc Biol. 2014 Jun;34(6):1126-35
pubmed: 24675660
Diabetologia. 2018 Jan;61(1):21-28
pubmed: 28776083
J Magn Reson. 2011 Dec;213(2):533-41
pubmed: 22152368
Diabetes Res Clin Pract. 2019 Nov;157:107843
pubmed: 31518657
Circ Res. 1996 Nov;79(5):940-8
pubmed: 8888686
JAMA. 1979 May 11;241(19):2035-8
pubmed: 430798
Life Sci. 1980 Dec 1;27(22):2121-4
pubmed: 7207010
Circ Res. 2013 Aug 30;113(6):709-24
pubmed: 23989714
Circulation. 2003 Jun 24;107(24):3040-6
pubmed: 12810608
NMR Biomed. 2020 Mar;33(3):e4243
pubmed: 31904900
Diabetes. 2015 Aug;64(8):2735-43
pubmed: 25795215
Diabetes Metab J. 2018 Aug;42(4):270-281
pubmed: 30136450
Circ Heart Fail. 2013 Sep 1;6(5):1058-66
pubmed: 23940308
Cell Biochem Funct. 2011 Jan-Feb;29(1):55-63
pubmed: 21264891
J Cardiovasc Magn Reson. 2013 Feb 18;15:19
pubmed: 23414451
J Magn Reson. 1997 Nov;129(1):35-43
pubmed: 9405214
Proc Natl Acad Sci U S A. 2003 Sep 2;100(18):10158-63
pubmed: 12930897
Diabetologia. 2006 Apr;49(4):660-6
pubmed: 16432708
J Med Food. 2008 Sep;11(3):518-24
pubmed: 18800901
NMR Biomed. 2012 Feb;25(2):305-11
pubmed: 21774012
Exp Diabetes Res. 2008;2008:305403
pubmed: 18769499
Sci Rep. 2019 Apr 2;9(1):5532
pubmed: 30940842
Prog Nucl Magn Reson Spectrosc. 2018 Jun - Aug;106-107:66-87
pubmed: 31047602
Am J Physiol Endocrinol Metab. 2009 Sep;297(3):E578-91
pubmed: 19531645
NMR Biomed. 2011 Feb;24(2):201-208
pubmed: 20799252
Circ Res. 2020 Mar 13;126(6):725-736
pubmed: 32078413

Auteurs

Dragana Savic (D)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Vicky Ball (V)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.

Lorenz Holzner (L)

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.

David Hauton (D)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Metabolomics Research Group, Department of Chemistry, University of Oxford, Oxford, UK.

Kerstin N Timm (KN)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.

M Kate Curtis (MK)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.

Lisa C Heather (LC)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.

Damian J Tyler (DJ)

Cardiac Metabolism Research Group (CMRG), Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Oxford Centre for Clinical Magnetic Resonance Research (OCMR), Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH