Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage (original) (raw)
- Letter
- Published: 13 April 2000
- Diane Edelstein1,
- Xue Liang Du1,
- Sho-ichi Yamagishi1,
- Takeshi Matsumura1,
- Yasufumi Kaneda2,
- Mark A. Yorek3,
- David Beebe4,
- Peter J. Oates4,
- Hans-Peter Hammes5,
- Ida Giardino1 &
- …
- Michael Brownlee1
Nature volume 404, pages 787–790 (2000)Cite this article
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Abstract
Diabetic hyperglycaemia causes a variety of pathological changes in small vessels, arteries and peripheral nerves1. Vascular endothelial cells are an important target of hyperglycaemic damage, but the mechanisms underlying this damage are not fully understood. Three seemingly independent biochemical pathways are involved in the pathogenesis: glucose-induced activation of protein kinase C isoforms2; increased formation of glucose-derived advanced glycation end-products3; and increased glucose flux through the aldose reductase pathway4. The relevance of each of these pathways is supported by animal studies in which pathway-specific inhibitors prevent various hyperglycaemia-induced abnormalities3,5,6,7. Hyperglycaemia increases the production of reactive oxygen species inside cultured bovine aortic endothelial cells8. Here we show that this increase in reactive oxygen species is prevented by an inhibitor of electron transport chain complex II, by an uncoupler of oxidative phosphorylation, by uncoupling protein-1 and by manganese superoxide dismutase. Normalizing levels of mitochondrial reactive oxygen species with each of these agents prevents glucose-induced activation of protein kinase C, formation of advanced glycation end-products, sorbitol accumulation and NFκB activation.
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Acknowledgements
We thank K. Preissner for his critical reading of the manuscript and M. Quon for his gift of plasmid pCIS-eGFP. This research was supported by grants from the National Institutes of Health (USA).
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- Takeshi Nishikawa
Present address: Department of Medicine, Kumamoto University School of Medicine, Kumamoto, Japan
Authors and Affiliations
- Albert Einstein College of Medicine, Diabetes Research Centre, 1,300 Morris Park Ave, Bronx, 10461, New York, USA
Takeshi Nishikawa, Diane Edelstein, Xue Liang Du, Sho-ichi Yamagishi, Takeshi Matsumura, Ida Giardino & Michael Brownlee - Division of Gene Therapy Science Osaka University Medical School, Suita, 5650871, Osaka, Japan
Yasufumi Kaneda - Department of Internal Medicine University of Iowa, Iowa City, 52246, Iowa, USA
Mark A. Yorek - Department of Metabolic Diseases Central Research Division, Pfizer Inc., Groton, 06340, Connecticut, USA
David Beebe & Peter J. Oates - Justus-Liebig University III Medical Department, Giessen, D-35385, Germany
Hans-Peter Hammes
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Correspondence toMichael Brownlee.
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Nishikawa, T., Edelstein, D., Du, X. et al. Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage.Nature 404, 787–790 (2000). https://doi.org/10.1038/35008121
- Received: 24 November 1999
- Accepted: 26 January 2000
- Issue Date: 13 April 2000
- DOI: https://doi.org/10.1038/35008121
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