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Cited by 166

The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.

Mitochondrial Respiratory Complex I Regulates Neutrophil Activation and Severity of Lung Injury

Open access
Zmijewski, Jaroslaw W., Lorne, Emmanuel, Zhao, Xia, Tsuruta, Yuko, Sha, Yonggang, Liu, Gang, Siegal, Gene P., Abraham, Edward·2008·American Journal of Respiratory and Critical Care Medicine

Abstract

RATIONALE: Mitochondria have important roles in intracellular energy generation, modulation of apoptosis, and redox-dependent intracellular signaling. Although reactive oxygen species (ROS) participate in the regulation of intracellular signaling pathways, including activation of nuclear factor (NF)-kappaB, there is only limited information concerning the role of mitochondrially derived ROS in modulating cellular activation and tissue injury associated with acute inflammatory processes. OBJECTIVES: To examine involvement of the mitochondrial electron transport chain complex I on LPS-mediated NF-kappaB activation in neutrophils and neutrophil-dependent acute lung injury. METHODS: Neutrophils incubated with rotenone or metformin were treated with bacterial lipopolysaccharide (LPS) to determine the effects of mitochondrial complex I inhibition on intracellular concentrations of reactive oxygen species, NF-kappaB activation, and proinflammatory cytokine expression. Acute lung injury was produced by intratracheal injection of LPS into control, metformin, or rotenone-treated mice. MEASUREMENTS AND MAIN RESULTS: Inhibition of complex I with either rotenone or the antihyperglycemic agent metformin was associated with increased intracellular levels of both superoxide and hydrogen peroxide, as well as inhibition of LPS-induced I kappaB-alpha degradation, NF-kappaB nuclear accumulation, and proinflammatory cytokine production. Treatment of LPS-exposed mice with rotenone or metformin resulted in inhibition of complex I in the lungs, as well as diminished severity of lung injury. CONCLUSIONS: These results demonstrate that mitochondrial complex I plays an important role in modulating Toll-like receptor 4-mediated neutrophil activation and suggest that metformin, as well as other agents that inhibit mitochondrial complex I, may be useful in the prevention or treatment of acute inflammatory processes in which activated neutrophils play a major role, such as acute lung injury.

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Metadata

Authors
Zmijewski, J. W., Lorne, E., Zhao, X., Tsuruta, Y., Sha, Y., Liu, G., Siegal, G. P., & Abraham, E.
Venue
American Journal of Respiratory and Critical Care Medicine
Published
2008-07-15
Volume
178
Issue
2
Pages
168-179
ISSN
  • 1073-449X (ISSN-L)
  • 1535-4970
OpenAlex
W1991832824
Cited by
166
References
14
FWCI
3.15
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Mitochondrial Respiratory Complex I Regulates Neutrophil Activation and Severity of Lung Injury. https://app.cochat.ai/papers/10.1164/rccm.200710-1602oc
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Zmijewski, J. W., Lorne, E., Zhao, X., Tsuruta, Y., Sha, Y., Liu, G., Siegal, G. P., & Abraham, E. (2008). Mitochondrial Respiratory Complex I Regulates Neutrophil Activation and Severity of Lung Injury. American Journal of Respiratory and Critical Care Medicine. https://doi.org/10.1164/rccm.200710-1602oc

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