Literature DB >> 26523474

Seahorse Xfe 24 Extracellular Flux Analyzer-Based Analysis of Cellular Respiration in Caenorhabditis elegans.

Anthony L Luz1, Latasha L Smith2, John P Rooney1, Joel N Meyer1.   

Abstract

Mitochondria are critical for their role in ATP production as well as multiple nonenergetic functions, and mitochondrial dysfunction is causal in myriad human diseases. Less well appreciated is the fact that mitochondria integrate environmental and intercellular as well as intracellular signals to modulate function. Because mitochondria function in an organismal milieu, there is need for assays capable of rapidly assessing mitochondrial health in vivo. Here, using the Seahorse XF(e) 24 Extracellular Flux Analyzer and the pharmacological inhibitors dicyclohexylcarbodiimide (DCCD, ATP synthase inhibitor), carbonyl cyanide-p-trifluoromethoxyphenylhydrazone (FCCP, mitochondrial uncoupler), and sodium azide (cytochrome c oxidase inhibitor), we describe how to obtain in vivo measurements of the fundamental parameters [basal oxygen consumption rate (OCR), ATP-linked respiration, maximal OCR, spare respiratory capacity, and proton leak] of the mitochondrial respiratory chain in the model organism Caenorhabditis elegans.
Copyright © 2015 John Wiley & Sons, Inc.

Entities:  

Keywords:  Caenorhabditis elegans; Seahorse XFe24; mitochondrial respiration; mitochondrial toxicity

Mesh:

Substances:

Year:  2015        PMID: 26523474      PMCID: PMC4632645          DOI: 10.1002/0471140856.tx2507s66

Source DB:  PubMed          Journal:  Curr Protoc Toxicol        ISSN: 1934-9254


  35 in total

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Review 5.  Mitochondria and cancer.

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Journal:  Toxicol Appl Pharmacol       Date:  2013-05-04       Impact factor: 4.219

7.  Mitochondrial Morphology and Fundamental Parameters of the Mitochondrial Respiratory Chain Are Altered in Caenorhabditis elegans Strains Deficient in Mitochondrial Dynamics and Homeostasis Processes.

Authors:  Anthony L Luz; John P Rooney; Laura L Kubik; Claudia P Gonzalez; Dong Hoon Song; Joel N Meyer
Journal:  PLoS One       Date:  2015-06-24       Impact factor: 3.240

8.  Application of a mathematical model to describe the effects of chlorpyrifos on Caenorhabditis elegans development.

Authors:  Windy A Boyd; Marjolein V Smith; Grace E Kissling; Julie R Rice; Daniel W Snyder; Christopher J Portier; Jonathan H Freedman
Journal:  PLoS One       Date:  2009-09-15       Impact factor: 3.240

9.  Effects of early life exposure to ultraviolet C radiation on mitochondrial DNA content, transcription, ATP production, and oxygen consumption in developing Caenorhabditis elegans.

Authors:  Maxwell C K Leung; John P Rooney; Ian T Ryde; Autumn J Bernal; Amanda S Bess; Tracey L Crocker; Alex Q Ji; Joel N Meyer
Journal:  BMC Pharmacol Toxicol       Date:  2013-02-04       Impact factor: 2.483

10.  Bridging the phenotypic gap: real-time assessment of mitochondrial function and metabolism of the nematode Caenorhabditis elegans.

Authors:  Cristina Lagido; Jonathan Pettitt; Aileen Flett; L Anne Glover
Journal:  BMC Physiol       Date:  2008-04-02
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2.  Effects of reduced mitochondrial DNA content on secondary mitochondrial toxicant exposure in Caenorhabditis elegans.

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Journal:  Mitochondrion       Date:  2016-08-23       Impact factor: 4.160

3.  In Vivo Determination of Mitochondrial Function Using Luciferase-Expressing Caenorhabditis elegans: Contribution of Oxidative Phosphorylation, Glycolysis, and Fatty Acid Oxidation to Toxicant-Induced Dysfunction.

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6.  Deficiencies in mitochondrial dynamics sensitize Caenorhabditis elegans to arsenite and other mitochondrial toxicants by reducing mitochondrial adaptability.

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7.  In Vivo Effects of Silver Nanoparticles on Development, Behavior, and Mitochondrial Function are Altered by Genetic Defects in Mitochondrial Dynamics.

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8.  From the Cover: Arsenite Uncouples Mitochondrial Respiration and Induces a Warburg-like Effect in Caenorhabditis elegans.

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9.  Multiple metabolic changes mediate the response of Caenorhabditis elegans to the complex I inhibitor rotenone.

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