Evidence map›Paper›PMID 25400906›Full record

ReviewCell & bioscience2014

Recent advances in hydrogen peroxide imaging for biological applications.

Hengchang Guo, Hossein Aleyasin, Bryan C Dickinson, Renée E Haskew-Layton, Rajiv R Ratan

Open access · goldAbstract readReview
In one paragraph

Review in Cell & bioscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 111 citations in OpenAlex.

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  13. Evaluation of borinic acids as new, fast hydrogen peroxide-responsive triggers.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

5 authors at 4 institutions in 1 country.

Hengchang GuoFischell Department of Bioengineering, University of Maryland, College Park, MD 20742 USA ; Burke Medical Research Institute, Weill Medical College of Cornell University, White Plains, NY 10605 USA.
Hossein AleyasinBurke Medical Research Institute, Weill Medical College of Cornell University, White Plains, NY 10605 USA ; Fishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029 USA.
Bryan C DickinsonDepartment of Chemistry, The University of Chicago, Chicago, IL 60637 USA.
Renée E Haskew-LaytonBurke Medical Research Institute, Weill Medical College of Cornell University, White Plains, NY 10605 USA ; School of Health and Natural Sciences, Mercy College, Dobbs Ferry, NY 10522 USA.
Rajiv R RatanBurke Medical Research Institute, Weill Medical College of Cornell University, White Plains, NY 10605 USA.
Cornell University · USBurke Medical Research Institute · USUniversity of Chicago · USUniversity of Maryland, College Park · US

Funding

TRANSCRIPTIONAL RESPONSES TO MITOCHONDRIAL DYSFUNCTIONP01AG014930 · NIA · WINIFRED MASTERSON BURKE MED RES INST · PI GIBSON, GARY E · 1999 to 2020
$30.7M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
NCATS NIH HHS UL1 TR000430NIA NIH HHS P01 AG014930
6 · The paper itself

Abstract

Mounting evidence supports the role of hydrogen peroxide (H2O2) in physiological signaling as well as pathological conditions. However, the subtleties of peroxide-mediated signaling are not well understood, in part because the generation, degradation, and diffusion of H2O2 are highly volatile within different cellular compartments. Therefore, the direct measurement of H2O2 in living specimens is critically important. Fluorescent probes that can detect small changes in H2O2 levels within relevant cellular compartments are important tools to study the spatial dynamics of H2O2. To achieve temporal resolution, the probes must also be photostable enough to allow multiple readings over time without loss of signal. Traditional fluorescent redox sensitive probes that have been commonly used for the detection of H2O2 tend to react with a wide variety of reactive oxygen species (ROS) and often suffer from photostablilty issues. Recently, new classes of H2O2 probes have been designed to detect H2O2 with high selectivity. Advances in H2O2 measurement have enabled biomedical scientists to study H2O2 biology at a level of precision previously unachievable. In addition, new imaging techniques such as two-photon microscopy (TPM) have been employed for H2O2 detection, which permit real-time measurements of H2O2 in vivo. This review focuses on recent advances in H2O2 probe development and optical imaging technologies that have been developed for biomedical applications.

Indexed as

ChemiluminescenceFluorescence lifetime imaging microscopy (FLIM)Fluorescent probeHydrogen peroxide (H2O2)Molecular imagingNanoparticlesRatiometric imagingReactive oxygen species (ROS)Two-photon microscopy

Identifiers

PMID25400906
PMCPMC4232666
OpenAlexW2158082165

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.