Komlodi 2017 Neuropharmacology
|Komlódi T, Tretter L (2017) Methylene blue stimulates substrate-level phosphorylation catalysed by succinyl-CoA ligase in the citric acid cycle. Neuropharmacology 123:287-98.|
Komlodi Timea, Tretter Laszlo (2017) Neuropharmacology
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.
Copyright © 2017 Elsevier Ltd. All rights reserved. • Keywords: Carbonylcyanide-p-triflouromethoxy-phenylhydrazone (PubChem CID: 3330), Carboxyatractilozide (PubChem CID: 101834999), Citric acid cycle; Malate (PubChem CID: 222656), Methylene blue, Methylene blue (PubChem CID: 6099), Mitochondria, Neurodegeneration, Neuroprotection, Oligomycin (PubChem CID: 78358496), P(1), P(5)-di(adenosine-5′) pentaphosphate (PubChem CID: 6419779), Substrate-level phosphorylation, Succinate (PubChem CID: 1110), α-ketoglutarate (PubChem CID: 51) • Bioblast editor: Kandolf G, Komlodi T • O2k-Network Lab: HU Budapest Tretter L
- Gnaiger E et al ― MitoEAGLE Task Group (2020) Mitochondrial physiology. Bioenerg Commun 2020.1. doi:10.26124/bec:2020-0001.v1.
Labels: MiParea: Respiration, Pharmacology;toxicology Pathology: Neurodegenerative
Organism: Guinea pig Tissue;cell: Nervous system Preparation: Isolated mitochondria
Regulation: ATP production Coupling state: LEAK, OXPHOS, ET Pathway: N, S HRR: Oxygraph-2k
2017-05, BEC 2020.1