MITOCHONDRIAL FUNCTION IN SEPSIS
- PMID: 26871665
- PMCID: PMC4755359
- DOI: 10.1097/SHK.0000000000000463
MITOCHONDRIAL FUNCTION IN SEPSIS
Abstract
Mitochondria are an essential part of the cellular infrastructure, being the primary site for high-energy adenosine triphosphate production through oxidative phosphorylation. Clearly, in severe systemic inflammatory states, like sepsis, cellular metabolism is usually altered, and end organ dysfunction is not only common, but also predictive of long-term morbidity and mortality. Clearly, interest is mitochondrial function both as a target for intracellular injury and response to extrinsic stress have been a major focus of basic science and clinical research into the pathophysiology of acute illness. However, mitochondria have multiple metabolic and signaling functions that may be central in both the expression of sepsis and its ultimate outcome. In this review, the authors address five primary questions centered on the role of mitochondria in sepsis. This review should be used both as a summary source in placing mitochondrial physiology within the context of acute illness and as a focal point for addressing new research into diagnostic and treatment opportunities these insights provide.
Conflict of interest statement
CD and HG have no disclosures. NA received a research fellowship from the Wellcome Trust. BZ has received research support from NIH (HL120877 and HL074316). PS has received research support from NIH (HL35440 and HL122062). MRP has received research support from Edwards LlifeSciences and NIH (HL07820, NR013912, H L120877 and HL074316). MP has received consulting fees from Masimo. JK has received consulting fees from Abbott, Aethlon, Alere, Alung, AM Pharma, Astute Medical, Atox Bio, Baxter, Cytosorbents, venBio, Gambro, Grifols, Roche, Spectral Diagnostics, Sangart, and Siemens. JK has also received research grants from Alere, Astute Medical, Atox Bio, Bard, Baxter, Cytosorbents, Gambro, Grifols, Kaneka, and Spectral Diagnostics, and has licensed technologies through the University of Pittsburgh to Astute Medical, Cytosorbents and Spectral Diagnostics. AG has received consulting fees from Fresenius Medical Care. PM has received consulting fees from AM Pharma, Abbvie, FAST Diagnostics. He has also received research funding from Abbott, Alere, EKF Diagnostics. CR has received consulting fees from AM Pharma, Astute Medical, Baxter, Gambro, Spectral Diagnostics, GE, FMC and ASAHI.
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- HL07820/HL/NHLBI NIH HHS/United States
- HL122062/HL/NHLBI NIH HHS/United States
- K24 HL067181/HL/NHLBI NIH HHS/United States
- NR013912/NR/NINR NIH HHS/United States
- T32 HL007820/HL/NHLBI NIH HHS/United States
- HL074316/HL/NHLBI NIH HHS/United States
- R01 HL122062/HL/NHLBI NIH HHS/United States
- HL35440/HL/NHLBI NIH HHS/United States
- UM1 HL120877/HL/NHLBI NIH HHS/United States
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- HL120877/HL/NHLBI NIH HHS/United States
- R01 NR013912/NR/NINR NIH HHS/United States
- R01 HL074316/HL/NHLBI NIH HHS/United States
- WT_/Wellcome Trust/United Kingdom
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