Evidence map›Paper›PMID 32076070›Full record

ArticleScientific reports2020

Cysteine redox state regulates human β2-adrenergic receptor binding and function.

Kalyn M Rambacher, Nader H Moniri

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 12 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

2 authors at 1 institution in 1 country.

Kalyn M RambacherDepartment of Pharmaceutical Sciences, College of Pharmacy, Mercer University Health Sciences Center, Mercer University, Atlanta, GA30341, United States.
Nader H MoniriDepartment of Pharmaceutical Sciences, College of Pharmacy, Mercer University Health Sciences Center, Mercer University, Atlanta, GA30341, United States. moniri_nh@mercer.edu.
Mercer University Health Sciences Center · US

Funding

The role of ROS on beta-2-adrenergic receptor function in human airwayR15HL138603 · NHLBI · MERCER UNIVERSITY MACON · PI MONIRI, NADER H · 2017 to 2022
$887k
NHLBI NIH HHS R15 HL138603
6 · The paper itself

Abstract

Bronchoconstrictive airway disorders such as asthma are characterized by inflammation and increases in reactive oxygen species (ROS), which produce a highly oxidative environment. β2-adrenergic receptor (β2AR) agonists are a mainstay of clinical therapy for asthma and provide bronchorelaxation upon inhalation. We have previously shown that β2AR agonism generates intracellular ROS, an effect that is required for receptor function, and which post-translationally oxidizes β2AR cysteine thiols to Cys-S-sulfenic acids (Cys-S-OH). Furthermore, highly oxidative environments can irreversibly oxidize Cys-S-OH to Cys-S-sulfinic (Cys-SO

Indexed as

Adrenergic beta-2 Receptor AgonistsBinding SitesCyclic AMPCyclohexanonesCysteineDihydroalprenololEpithelial CellsHEK293 CellsHumansHydrogen PeroxideLungOxidation-ReductionProtein BindingReactive Oxygen SpeciesReceptors, Adrenergic, beta-2Signal TransductionAdrenergic beta-2 Receptor AgonistsCyclic AMPCyclohexanonesCysteineDihydroalprenololdimedoneHydrogen PeroxideReactive Oxygen SpeciesReceptors, Adrenergic, beta-2Sulfenic AcidsTritium

Identifiers

PMID32076070
PMCPMC7031529
OpenAlexW3008909067

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.