Evidence map›Paper›PMID 25278902›Full record

ReviewFrontiers in physiology2014

Mitochondrial targets for volatile anesthetics against cardiac ischemia-reperfusion injury.

Bhawana Agarwal, David F Stowe, Ranjan K Dash, Zeljko J Bosnjak, Amadou K S Camara

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.2field-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

28 citing papers in PubMed, 41 citations in OpenAlex.

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  15. Metformin attenuates ER stress-induced mitochondrial dysfunction.Translational research : the journal of laboratory and clinical medicine · 2017
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  20. The cardioprotective compound cloxyquin uncouples mitochondria and induces autophagy.American journal of physiology. Heart and circulatory physiology · 2016
    Article
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 1 institution in 1 country.

Bhawana AgarwalDepartment of Anesthesiology, Medical College of Wisconsin Milwaukee, WI, USA.
David F StoweDepartment of Anesthesiology, Medical College of Wisconsin Milwaukee, WI, USA ; Department of Physiology, Medical College of Wisconsin Milwaukee, WI, USA ; Cardiovascular Research Center, Medical College of Wisconsin Milwaukee, WI, USA ; Zablocki VA Medical Center Milwaukee, WI, USA ; Department of Biomedical Engineering, Marquette University Milwaukee, WI, USA.
Ranjan K DashDepartment of Physiology, Medical College of Wisconsin Milwaukee, WI, USA ; Department of Biomedical Engineering, Marquette University Milwaukee, WI, USA ; Biotechnology and Bioengineering Center, Medical College of Wisconsin Milwaukee, WI, USA.
Zeljko J BosnjakDepartment of Anesthesiology, Medical College of Wisconsin Milwaukee, WI, USA ; Department of Physiology, Medical College of Wisconsin Milwaukee, WI, USA ; Cardiovascular Research Center, Medical College of Wisconsin Milwaukee, WI, USA.
Amadou K S CamaraDepartment of Anesthesiology, Medical College of Wisconsin Milwaukee, WI, USA ; Cardiovascular Research Center, Medical College of Wisconsin Milwaukee, WI, USA.
Medical College of Wisconsin · US

Funding

Stem Cell CoreP01GM066730 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI DASH, RANJAN K · 2003 to 2019
$23.6M
Cations and ROS in Modulating Mitochondrial Function in Normal and Ischemic HeartR01HL095122 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI CAMARA, AMADOU K., DASH, RANJAN K · 2010 to 2013
$2.1M
Mitochondrial Ca-sensitive K channel-induced superoxide and cardiac protectionR01HL089514 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI STOWE, DAVID F · 2009 to 2012
$1.4M
NHLBI NIH HHS R01 HL089514NHLBI NIH HHS R01 HL095122NIGMS NIH HHS P01 GM066730
6 · The paper itself

Abstract

Mitochondria are critical modulators of cell function and are increasingly recognized as proximal sensors and effectors that ultimately determine the balance between cell survival and cell death. Volatile anesthetics (VA) are long known for their cardioprotective effects, as demonstrated by improved mitochondrial and cellular functions, and by reduced necrotic and apoptotic cell death during cardiac ischemia and reperfusion (IR) injury. The molecular mechanisms by which VA impart cardioprotection are still poorly understood. Because of the emerging role of mitochondria as therapeutic targets in diseases, including ischemic heart disease, it is important to know if VA-induced cytoprotective mechanisms are mediated at the mitochondrial level. In recent years, considerable evidence points to direct effects of VA on mitochondrial channel/transporter protein functions and electron transport chain (ETC) complexes as potential targets in mediating cardioprotection. This review furnishes an integrated overview of targets that VA impart on mitochondrial channels/transporters and ETC proteins that could provide a basis for cation regulation and homeostasis, mitochondrial bioenergetics, and reactive oxygen species (ROS) emission in redox signaling for cardiac cell protection during IR injury.

Indexed as

cardiac IR injurycardioprotectionelectron transport chainisofluranemitochondrial bioenergeticsvolatile anesthetics

Identifiers

PMID25278902
PMCPMC4165278
OpenAlexW2151005532

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.