Literature DB >> 33654802

Oxygen Consumption Measurements in Caenorhabditis elegans Using the Seahorse XF24.

Suraiya Haroon1, Marc Vermulst2.   

Abstract

Mitochondria generate 90% of the energy required to sustain life. As a result, loss of mitochondrial function compromises almost every facet of human physiology. Accordingly, most mitochondrial diseases tend to present themselves as complex, multi-systemic disorders that can be difficult to diagnose. Depending on the severity of the mitochondrial dysfunction, the pathology can range from mild discomfort to severe epilepsy, blindness and paralysis. To develop therapies to these diseases, it will be important to optimize experimental techniques that can reliably quantify mitochondrial function, particularly in live cells or intact organisms. Here, we describe how a Seahorse XF24 Analyzer can be used to measure both basal and maximal respiration in the nematode Caenorhabditis elegans, and how this data can be interpreted to evaluate mitochondrial function.
Copyright © 2019 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  C. elegans; FCCP; Maximal respiration capacity; Mitochondria; Oxygen consumption; Seahorse XF24

Year:  2019        PMID: 33654802      PMCID: PMC7854111          DOI: 10.21769/BioProtoc.3288

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  5 in total

1.  Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.

Authors:  Yevgenya Kraytsberg; Elena Kudryavtseva; Ann C McKee; Changiz Geula; Neil W Kowall; Konstantin Khrapko
Journal:  Nat Genet       Date:  2006-04-09       Impact factor: 38.330

2.  Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia.

Authors:  J Wanagat; Z Cao; P Pathare; J M Aiken
Journal:  FASEB J       Date:  2001-02       Impact factor: 5.191

Review 3.  Mitochondrial disease in childhood: mtDNA encoded.

Authors:  Russell P Saneto; Margret M Sedensky
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

Review 4.  A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine.

Authors:  Douglas C Wallace
Journal:  Annu Rev Genet       Date:  2005       Impact factor: 16.830

5.  Glutathione S-transferase mediates an ageing response to mitochondrial dysfunction.

Authors:  Beverley M Dancy; Nicole Brockway; Renjini Ramadasan-Nair; Yoing Yang; Margaret M Sedensky; Philip G Morgan
Journal:  Mech Ageing Dev       Date:  2015-12-15       Impact factor: 5.432

  5 in total
  1 in total

1.  PI5P4Ks drive metabolic homeostasis through peroxisome-mitochondria interplay.

Authors:  Archna Ravi; Lavinia Palamiuc; Ryan M Loughran; Joanna Triscott; Gurpreet K Arora; Avi Kumar; Vivian Tieu; Chantal Pauli; Matthias Reist; Rachel J Lew; Shauna L Houlihan; Christof Fellmann; Christian Metallo; Mark A Rubin; Brooke M Emerling
Journal:  Dev Cell       Date:  2021-05-12       Impact factor: 13.417

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.