Sites of reactive oxygen species generation by mitochondria oxidizing different substrates

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Sites of reactive oxygen species generation by mitochondria oxidizing different substrates. / Quinlan, Casey L; Perevoshchikova, IrinaV; Hey-Mogensen, Martin; Orr , Adam l; Brand, Martin D.

In: Redox Biology, Vol. 1, No. 1, 2013, p. 304-312.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Quinlan, CL, Perevoshchikova, I, Hey-Mogensen, M, Orr , AL & Brand, MD 2013, 'Sites of reactive oxygen species generation by mitochondria oxidizing different substrates', Redox Biology, vol. 1, no. 1, pp. 304-312. https://doi.org/10.1016/j.redox.2013.04.005

APA

Quinlan, C. L., Perevoshchikova, I., Hey-Mogensen, M., Orr , A. L., & Brand, M. D. (2013). Sites of reactive oxygen species generation by mitochondria oxidizing different substrates. Redox Biology, 1(1), 304-312. https://doi.org/10.1016/j.redox.2013.04.005

Vancouver

Quinlan CL, Perevoshchikova I, Hey-Mogensen M, Orr AL, Brand MD. Sites of reactive oxygen species generation by mitochondria oxidizing different substrates. Redox Biology. 2013;1(1):304-312. https://doi.org/10.1016/j.redox.2013.04.005

Author

Quinlan, Casey L ; Perevoshchikova, IrinaV ; Hey-Mogensen, Martin ; Orr , Adam l ; Brand, Martin D. / Sites of reactive oxygen species generation by mitochondria oxidizing different substrates. In: Redox Biology. 2013 ; Vol. 1, No. 1. pp. 304-312.

Bibtex

@article{13874fc579ee4d3897d6121116c5bcb0,
title = "Sites of reactive oxygen species generation by mitochondria oxidizing different substrates",
abstract = "Mitochondrial radical production is important in redox signaling, aging and disease, but the relative contributions of different production sites are poorly understood. We analyzed the rates of superoxide/H2O2 production from different defined sites in rat skeletal muscle mitochondria oxidizing a variety of conventional substrates in the absence of added inhibitors: succinate; glycerol 3-phosphate; palmitoylcarnitine plus carnitine; or glutamate plus malate. In all cases, the sum of the estimated rates accounted fully for the measured overall rates. There were two striking results. First, the overall rates differed by an order of magnitude between substrates. Second, the relative contribution of each site was very different with different substrates. During succinate oxidation, most of the superoxide production was from the site of quinone reduction in complex I (site IQ), with small contributions from the flavin site in complex I (site IF) and the quinol oxidation site in complex III (site IIIQo). However, with glutamate plus malate as substrate, site IQ made little or no contribution, and production was shared between site IF, site IIIQo and 2-oxoglutarate dehydrogenase. With palmitoylcarnitine as substrate, the flavin site in complex II (site IIF) was a major contributor (together with sites IF and IIIQo), and with glycerol 3-phosphate as substrate, five different sites all contributed, including glycerol 3-phosphate dehydrogenase. Thus, the relative and absolute contributions of specific sites to the production of reactive oxygen species in isolated mitochondria depend very strongly on the substrates being oxidized, and the same is likely true in cells and in vivo.",
author = "Quinlan, {Casey L} and IrinaV Perevoshchikova and Martin Hey-Mogensen and Orr, {Adam l} and Brand, {Martin D}",
year = "2013",
doi = "10.1016/j.redox.2013.04.005",
language = "English",
volume = "1",
pages = "304--312",
journal = "Redox Biology",
issn = "2213-2317",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Sites of reactive oxygen species generation by mitochondria oxidizing different substrates

AU - Quinlan, Casey L

AU - Perevoshchikova, IrinaV

AU - Hey-Mogensen, Martin

AU - Orr , Adam l

AU - Brand, Martin D

PY - 2013

Y1 - 2013

N2 - Mitochondrial radical production is important in redox signaling, aging and disease, but the relative contributions of different production sites are poorly understood. We analyzed the rates of superoxide/H2O2 production from different defined sites in rat skeletal muscle mitochondria oxidizing a variety of conventional substrates in the absence of added inhibitors: succinate; glycerol 3-phosphate; palmitoylcarnitine plus carnitine; or glutamate plus malate. In all cases, the sum of the estimated rates accounted fully for the measured overall rates. There were two striking results. First, the overall rates differed by an order of magnitude between substrates. Second, the relative contribution of each site was very different with different substrates. During succinate oxidation, most of the superoxide production was from the site of quinone reduction in complex I (site IQ), with small contributions from the flavin site in complex I (site IF) and the quinol oxidation site in complex III (site IIIQo). However, with glutamate plus malate as substrate, site IQ made little or no contribution, and production was shared between site IF, site IIIQo and 2-oxoglutarate dehydrogenase. With palmitoylcarnitine as substrate, the flavin site in complex II (site IIF) was a major contributor (together with sites IF and IIIQo), and with glycerol 3-phosphate as substrate, five different sites all contributed, including glycerol 3-phosphate dehydrogenase. Thus, the relative and absolute contributions of specific sites to the production of reactive oxygen species in isolated mitochondria depend very strongly on the substrates being oxidized, and the same is likely true in cells and in vivo.

AB - Mitochondrial radical production is important in redox signaling, aging and disease, but the relative contributions of different production sites are poorly understood. We analyzed the rates of superoxide/H2O2 production from different defined sites in rat skeletal muscle mitochondria oxidizing a variety of conventional substrates in the absence of added inhibitors: succinate; glycerol 3-phosphate; palmitoylcarnitine plus carnitine; or glutamate plus malate. In all cases, the sum of the estimated rates accounted fully for the measured overall rates. There were two striking results. First, the overall rates differed by an order of magnitude between substrates. Second, the relative contribution of each site was very different with different substrates. During succinate oxidation, most of the superoxide production was from the site of quinone reduction in complex I (site IQ), with small contributions from the flavin site in complex I (site IF) and the quinol oxidation site in complex III (site IIIQo). However, with glutamate plus malate as substrate, site IQ made little or no contribution, and production was shared between site IF, site IIIQo and 2-oxoglutarate dehydrogenase. With palmitoylcarnitine as substrate, the flavin site in complex II (site IIF) was a major contributor (together with sites IF and IIIQo), and with glycerol 3-phosphate as substrate, five different sites all contributed, including glycerol 3-phosphate dehydrogenase. Thus, the relative and absolute contributions of specific sites to the production of reactive oxygen species in isolated mitochondria depend very strongly on the substrates being oxidized, and the same is likely true in cells and in vivo.

U2 - 10.1016/j.redox.2013.04.005

DO - 10.1016/j.redox.2013.04.005

M3 - Journal article

C2 - 24024165

VL - 1

SP - 304

EP - 312

JO - Redox Biology

JF - Redox Biology

SN - 2213-2317

IS - 1

ER -

ID: 48877842