Evidence map›Paper›PMID 20465991›Full record

ArticleAnalytical biochemistry2010

A high-throughput respirometric assay for mitochondrial biogenesis and toxicity.

Craig C Beeson, Gyda C Beeson, Rick G Schnellmann

Abstract read
In one paragraph

Article in Analytical biochemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

78 citing papers in PubMed, 130 citations in OpenAlex.

  1. The βBritish journal of pharmacology · 2026
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  6. Assays to enhance metabolic phenotyping in the kidney.American journal of physiology. Renal physiology · 2025
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  9. 5-HTFrontiers in cellular neuroscience · 2024
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  17. FDA-approved 5-HTExperimental neurology · 2021
    Article
  18. Off-TargetAntimicrobial agents and chemotherapy · 2021
    Article
  19. Article
  20. Article

18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Craig C BeesonDepartment of Pharmaceutical and Biomedical Sciences, Medical University of South Carolina, Charleston, 29425, USA.
Gyda C Beeson
Rick G Schnellmann
Medical University of South Carolina · US

Funding

Mitochondrial Biogenesis Promotes Recovery From Oxidant InjuryR01GM084147 · NIGMS · UNIVERSITY OF ARIZONA · PI SCHNELLMANN, RICK G · 2008 to 2016
$2.4M
NIGMS NIH HHS GM 084147NIGMS NIH HHS R01 GM084147
6 · The paper itself

Abstract

Mitochondria are a common target of toxicity for drugs and other chemicals and result in decreased aerobic metabolism and cell death. In contrast, mitochondrial biogenesis restores cell vitality, and there is a need for new agents to induce biogenesis. Current cell-based models of mitochondrial biogenesis or toxicity are inadequate because cultured cell lines are highly glycolytic with minimal aerobic metabolism and altered mitochondrial physiology. In addition, there are no high-throughput real-time assays that assess mitochondrial function. We adapted primary cultures of renal proximal tubular cells (RPTCs) that exhibit in vivo levels of aerobic metabolism, are not glycolytic, and retain higher levels of differentiated functions and used the Seahorse Bioscience analyzer to measure mitochondrial function in real time in multiwell plates. Using uncoupled respiration as a marker of electron transport chain (ETC) integrity, the nephrotoxicants cisplatin, HgCl(2), and gentamicin exhibited mitochondrial toxicity prior to decreases in basal respiration and cell death. Conversely, using FCCP (carbonylcyanide p-trifluoromethoxyphenylhydrazone)-uncoupled respiration as a marker of maximal ETC activity, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI), SRT1720, resveratrol, daidzein, and metformin produced mitochondrial biogenesis in RPTCs. The merger of the RPTC model and multiwell respirometry results in a single high-throughput assay to measure mitochondrial biogenesis and toxicity and nephrotoxic potential.

Indexed as

AmphetaminesAnimalsAnti-Infective AgentsAntineoplastic AgentsApoptosisCarbonyl Cyanide m-Chlorophenyl HydrazoneCell RespirationCells, CulturedCisplatinElectron Transport Chain Complex ProteinsGentamicinsHigh-Throughput Screening AssaysKidney Tubules, ProximalMercuric ChlorideMitochondriaOxygen Consumption4-iodo-2,5-dimethoxyphenylisopropylamineAmphetaminesAnti-Infective AgentsAntineoplastic Agentscarbonylcyanide 4-trifluoromethoxyphenylhydrazoneCarbonyl Cyanide m-Chlorophenyl HydrazoneCisplatinElectron Transport Chain Complex ProteinsGentamicinsMercuric Chloride

Identifiers

PMID20465991
PMCPMC2900494
OpenAlexW2025664869

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.