Tonnesen 2021 Mol Cell Biochem

From Bioblast
Publications in the MiPMap
Tonnesen PT, Hjortbak MV, Lassen TR, Seefeldt JM, BΓΈtker HE, Jespersen NR (2021) Myocardial salvage by succinate dehydrogenase inhibition in ischemia-reperfusion injury depends on diabetes stage in rats. Mol Cell Biochem 476:2675-84.

Β» PMID: 33666828 Open Access

Tonnesen Pernille Tilma, Hjortbak Marie Vognstoft, Lassen Thomas Ravn, Seefeldt Jacob Marthinsen, Boetker Hans Erik, Jespersen Nichlas Riise (2021) Mol Cell Biochem

Abstract: Inhibition of succinate dehydrogenase (SDH) by Dimethyl Malonate (DiMal) reduces cardiac ischemia-reperfusion (IR) injury. We investigated the cardioprotective effect of DiMal in a rat model during advancing type 2 diabetes. Zucker Diabetic Fatty rats and lean controls were investigated corresponding to prediabetes, onset and mature diabetes. Hearts were mounted in an isolated perfused model, and subjected to IR for investigation of infarct size (IS) and mitochondrial respiratory control ratio (RCR). DiMal was administered for 10 min before ischemia. Compared with age-matched non-diabetic rats, prediabetic rats had larger IS (49 Β± 4% vs. 36 Β± 2%, p = 0.007), rats with onset diabetes smaller IS (51 Β± 3% vs. 62 Β± 3%, p = 0.05) and rats with mature diabetes had larger IS (79 Β± 3% vs. 69 Β± 2%, p = 0.06). At the prediabetic stage DiMal did not alter IS. At onset of diabetes DiMal 0.6 mM increased IS in diabetic but not in non-diabetic control rats (72 Β± 4% vs. 51 Β± 3%, p = 0.003). At mature diabetes DiMal 0.1 and 0.6 mM reduced IS (68 Β± 3% vs. 79 Β± 3% and 64 Β± 5% vs. 79 Β± 3%, p = 0.1 and p = 0.01), respectively. DiMal 0.1 mM alone reduced IS in age-matched non-diabetic animals (55 Β± 3% vs. 69 Β± 2% p = 0.01). RCR was reduced at mature diabetes but not modulated by DiMal. Modulation of SDH activity results in variable infarct size reduction depending on presence and the stage of diabetes. Modulation of SDH activity may be an unpredictable cardioprotective approach. β€’ Keywords: Cardioprotection, Cardiovascular metabolism, Diabetes mellitus, Ischemia–reperfusion injury, Mitochondrial function β€’ Bioblast editor: Plangger M β€’ O2k-Network Lab: DK Aarhus Boetker HE

Labels: MiParea: Respiration, Pharmacology;toxicology  Pathology: Diabetes  Stress:Ischemia-reperfusion  Organism: Rat  Tissue;cell: Heart  Preparation: Permeabilized tissue 

Coupling state: LEAK, OXPHOS  Pathway: F, N  HRR: Oxygraph-2k 


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