Evidence map›Paper›PMID 23092951›Full record

ArticlePhysiological genomics2012

Standardized bioenergetic profiling of adult mouse cardiomyocytes.

Ryan D Readnower, Robert E Brainard, Bradford G Hill, Steven P Jones

Abstract read
In one paragraph

Article in Physiological genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

50 citing papers in PubMed, 77 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Ryan D ReadnowerInstitute of Molecular Cardiology, Diabetes and Obesity Center, University of Louisville, Louisville, Kentucky 40202, USA.
Robert E Brainard
Bradford G Hill
Steven P Jones
University of Louisville · US

Funding

Tumor Necrosis Factor Modulation of CPCsP01HL078825 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BOLLI, ROBERTO · 2005 to 2021
$37.6M
STEM CELLS AND DIABETIC CARDIOMYOPATHY PROJ 2 2009P20RR024489 · NCRR · UNIVERSITY OF LOUISVILLE · PI BHATNAGAR, ARUNI · 2008 to 2011
$10.0M
Metabolic Mechanisms of Cardiac Injury and ProtectionR01HL083320 · NHLBI · UNIVERSITY OF LOUISVILLE · PI JONES, STEVEN P · 2006 to 2010
$1.8M
O-GlcNAc Signaling in Heart FailureR01HL094419 · NHLBI · UNIVERSITY OF LOUISVILLE · PI JONES, STEVEN P · 2009 to 2012
$1.5M
NCRR NIH HHS P20 RR-024489NHLBI NIH HHS P01 HL-078825NHLBI NIH HHS R01 HL-083320NHLBI NIH HHS R01 HL-094419NHLBI NIH HHS R01 HL094419
6 · The paper itself

Abstract

Mitochondria are at the crux of life and death and as such have become ideal targets of intervention in cardiovascular disease. Generally, current methods to measure mitochondrial dysfunction rely on working with the isolated organelle and fail to incorporate mitochondrial function in a cellular context. Extracellular flux methodology has been particularly advantageous in this respect; however, certain primary cell types, such as adult cardiac myocytes, have been difficult to standardize with this technology. Here, we describe methods for using extracellular flux (XF) analysis to measure mitochondrial bioenergetics in isolated, intact, adult mouse cardiomyocytes (ACMs). Following isolation, ACMs were seeded overnight onto laminin-coated (20 μg/ml) microplates, which resulted in high attachment efficiency. After establishing seeding density, we found that a commonly used assay medium (containing a supraphysiological concentration of pyruvate at 1 mmol/l) produced a maximal bioenergetic response. After performing a pyruvate dose-response, we determined that pyruvate titrated to 0.1 mmol/l was optimal for examining alternative substrate oxidation. Methods for measuring fatty acid oxidation were established. These methods lay the framework using XF analysis to profile metabolism of ACMs and will likely augment our ability to understand mitochondrial dysfunction in heart failure and acute myocardial ischemia. This platform could easily be extended to models of diabetes or other metabolic defects.

Indexed as

Energy MetabolismAgingAnimalsCell CountExtracellular SpaceMaleMetabolomicsMiceMice, Inbred C57BLMitochondria, HeartMyocytes, CardiacPalmitatesPyruvatesReference StandardsPalmitatesPyruvates

Identifiers

PMID23092951
PMCPMC3544486
OpenAlexW2144719264

What OpenQuestion holds

Textmetadata
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.