Methylene blue stimulates substrate-level phosphorylation catalysed by succinyl–CoA ligase in the citric acid cycle

T. Komlódi, L. Tretter

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Methylene blue (MB), a potential neuroprotective agent, is efficient in various neurodegenerative disease models. Beneficial effects of MB have been attributed to improvements in mitochondrial functions. Substrate-level phosphorylation (SLP) results in the production of ATP independent from the ATP synthase (ATP-ase). In energetically compromised mitochondria, ATP produced by SLP can prevent the reversal of the adenine nucleotide translocase and thus the hydrolysis of glycolytic ATP. The aim of the present study was to investigate the effect of MB on mitochondrial SLP catalysed by succinyl-CoA ligase. Measurements were carried out on isolated guinea pig cortical mitochondria respiring on α-ketoglutarate, glutamate, malate or succinate. The mitochondrial functions and parameters like ATP synthesis, oxygen consumption, membrane potential, and NAD(P)H level were followed online, in parallel with the redox state of MB. SLP-mediated ATP synthesis was measured in the presence of inhibitors for ATP-ase and adenylate kinase. In the presence of the ATP-ase inhibitor oligomycin MB stimulated respiration with all of the respiratory substrates. However, the rate of ATP synthesis increased only with substrates α-ketoglutarate and glutamate (forming succinyl–CoA). MB efficiently stimulated SLP and restored the membrane potential in mitochondria also with the combined inhibition of Complex I and ATP synthase. ATP formed by SLP alleviated the energetic insufficiency generated by the lack of oxidative phosphorylation. Thus, the MB-mediated stimulation of SLP might be important in maintaining the energetic competence of mitochondria and in preventing the mitochondrial hydrolysis of glycolytic ATP. The mitochondrial effects of MB are explained by the ability to accept electrons from reducing equivalents and transfer them to cytochrome c bypassing the respiratory Complexes I and III.

Original languageEnglish
Pages (from-to)287-298
Number of pages12
JournalNeuropharmacology
Volume123
DOIs
Publication statusPublished - Sep 1 2017

Fingerprint

Citric Acid Cycle
Methylene Blue
Ligases
Adenosine Triphosphate
Phosphorylation
Mitochondria
Membrane Potentials
Glutamic Acid
Hydrolysis
ATP Translocases Mitochondrial ADP
Electron Transport Complex I
Oligomycins
Adenylate Kinase
Glycogen Synthase
Aptitude
Oxidative Phosphorylation
Succinic Acid
Neuroprotective Agents
Cytochromes c
Oxygen Consumption

Keywords

  • Citric acid cycle
  • Methylene blue
  • Mitochondria
  • Neurodegeneration
  • Neuroprotection
  • Substrate-level phosphorylation

ASJC Scopus subject areas

  • Pharmacology
  • Cellular and Molecular Neuroscience

Cite this

Methylene blue stimulates substrate-level phosphorylation catalysed by succinyl–CoA ligase in the citric acid cycle. / Komlódi, T.; Tretter, L.

In: Neuropharmacology, Vol. 123, 01.09.2017, p. 287-298.

Research output: Contribution to journalArticle

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