Evidence map›Paper›PMID 22761303›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2012

Aldehyde dehydrogenase type 2 activation by adenosine and histamine inhibits ischemic norepinephrine release in cardiac sympathetic neurons: mediation by protein kinase Cε.

Pablo A Robador, Nahid Seyedi, Noel Yan-Ki Chan, Kenichiro Koda, Roberto Levi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  4. Review
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.

Pablo A RobadorDepartment of Pharmacology, Weill Cornell Medical College, New York, NY 10065, USA.
Nahid Seyedi
Noel Yan-Ki Chan
Kenichiro Koda
Roberto Levi
Cornell University · US

Funding

Histamine Receptor/Norepinephrine in Cardiac DysfunctionR01HL034215 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEVI, ROBERTO · 1985 to 2013
$6.6M
Cell-Cell Interactions in Thrombosis -Request for Extension of Merit AwardR37HL047073 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MARCUS, AARON JACOB · 2004 to 2011
$3.7M
NHLBI NIH HHS HL034215NHLBI NIH HHS R01 HL034215NHLBI NIH HHS R37 HL047073
6 · The paper itself

Abstract

During myocardial ischemia/reperfusion, lipid peroxidation leads to the formation of toxic aldehydes that contribute to ischemic dysfunction. Mitochondrial aldehyde dehydrogenase type 2 (ALDH2) alleviates ischemic heart damage and reperfusion arrhythmias via aldehyde detoxification. Because excessive norepinephrine release in the heart is a pivotal arrhythmogenic mechanism, we hypothesized that neuronal ALDH2 activation might diminish ischemic norepinephrine release. Incubation of cardiac sympathetic nerve endings with acetaldehyde, at concentrations achieved in myocardial ischemia, caused a concentration-dependent increase in norepinephrine release. A major increase in norepinephrine release also occurred when sympathetic nerve endings were incubated in hypoxic conditions. ALDH2 activation substantially reduced acetaldehyde- and hypoxia-induced norepinephrine release, an action prevented by inhibition of ALDH2 or protein kinase Cε (PKCε). Selective activation of G(i/o)-coupled adenosine A(1), A(3), or histamine H(3) receptors markedly inhibited both acetaldehyde- and hypoxia-induced norepinephrine release. These effects were also abolished by PKCε and/or ALDH2 inhibition. Moreover, A(1)-, A(3)-, or H(3)-receptor activation increased ALDH2 activity in a sympathetic neuron model (differentiated PC12 cells stably transfected with H(3) receptors). This action was prevented by the inhibition of PKCε and ALDH2. Our findings suggest the existence in sympathetic neurons of a protective pathway initiated by A(1)-, A(3)-, and H(3)-receptor activation by adenosine and histamine released in close proximity of these terminals. This pathway comprises the sequential activation of PKCε and ALDH2, culminating in aldehyde detoxification and inhibition of hypoxic norepinephrine release. Thus, pharmacological activation of PKCε and ALDH2 in cardiac sympathetic nerves may have significant protective effects by alleviating norepinephrine-induced life-threatening arrhythmias that characterize myocardial ischemia/reperfusion.

Indexed as

Aldehyde DehydrogenaseAldehyde Dehydrogenase, MitochondrialAnimalsEnzyme ActivationGuinea PigsHypoxiaMitochondrial ProteinsMyocardial IschemiaMyocytes, CardiacNorepinephrinePC12 CellsProtein Kinase C-epsilonRatsReceptors, HistamineReceptors, Purinergic P1Sympathetic Fibers, PostganglionicAldehyde DehydrogenaseAldehyde Dehydrogenase, MitochondrialAldh2 protein, ratMitochondrial ProteinsNorepinephrineProtein Kinase C-epsilonReceptors, HistamineReceptors, Purinergic P1

Identifiers

PMID22761303
PMCPMC3464041
OpenAlexW2156228251

What OpenQuestion holds

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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.