Evidence map›Paper›PMID 31261663›Full record

ArticleInternational journal of molecular sciences2019

Carbon Monoxide Releasing Molecule-2-Upregulated ROS-Dependent Heme Oxygenase-1 Axis Suppresses Lipopolysaccharide-Induced Airway Inflammation.

Chih-Chung Lin, Li-Der Hsiao, Rou-Ling Cho, Chuen-Mao Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 40 citations in OpenAlex.

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  11. Towards "CO in a pill": Pharmacokinetic studies of carbon monoxide prodrugs in mice.Journal of controlled release : official journal of the Controlled Release Society · 2020
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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 2 institutions in 1 country.

Chih-Chung LinDepartment of Anesthetics, Chang Gung Memorial Hospital at Linkuo, and College of Medicine, Chang Gung University, Kwei-San, Tao-Yuan 33302, Taiwan.
Li-Der HsiaoDepartment of Anesthetics, Chang Gung Memorial Hospital at Linkuo, and College of Medicine, Chang Gung University, Kwei-San, Tao-Yuan 33302, Taiwan.
Rou-Ling ChoDepartment of Physiology and Pharmacology and Health Aging Research Center, College of Medicine, Chang Gung University, 259 Wen-Hwa 1 Road, Kwei-San, Tao-Yuan 33302, Taiwan.ORCID 0000-0002-8970-5562
Chuen-Mao YangDepartment of Anesthetics, Chang Gung Memorial Hospital at Linkuo, and College of Medicine, Chang Gung University, Kwei-San, Tao-Yuan 33302, Taiwan. chuenmao@mail.cgu.edu.tw.
Chang Gung University · TWChang Gung University of Science and Technology · TW

Funding

Chang Gung Medical Foundation CMRPD1F0023Chang Gung Medical Foundation CMRPD1F0552Chang Gung Medical Foundation CMRPD1F0553Chang Gung Medical Foundation CMRPD1I0051-3Chang Gung Medical Foundation CMRPG3F1533Chang Gung Medical Foundation CMRPG3H0062Chang Gung Medical Foundation CMRPG3H0063Chang Gung Medical Foundation CMRPG5F0203Chang Gung Medical Foundation CMRPG5I0041Ministry of Education EMRPD1I0381Ministry of Science and Technology, Taiwan MOST105-2320-B-182-005-MY3Ministry of Science and Technology, Taiwan MOST107-2320-B-182-020-MY2Ministry of Science and Technology, Taiwan MOST107-2320-B-182A-011
6 · The paper itself

Abstract

The up-regulation of heme oxygenase-1 (HO-1) is mediated through nicotinamaide adenine dinucleotide phosphate (NADPH) oxidases (Nox) and reactive oxygen species (ROS) generation, which could provide cytoprotection against inflammation. However, the molecular mechanisms of carbon monoxide-releasing molecule (CORM)-2-induced HO-1 expression in human tracheal smooth muscle cells (HTSMCs) remain unknown. Here, we found that pretreatment with CORM-2 attenuated the lipopolysaccharide (LPS)-induced intercellular adhesion molecule (ICAM-1) expression and leukocyte count through the up-regulation of HO-1 in mice, which was revealed by immunohistochemistrical staining, Western blot, real-time PCR, and cell count. The inhibitory effects of HO-1 by CORM-2 were reversed by transfection with HO-1 siRNA. Next, Western blot, real-time PCR, and promoter activity assay were performed to examine the HO-1 induction in HTSMCs. We found that CORM-2 induced HO-1 expression via the activation of protein kinase C (PKC)α and proline-rich tyrosine kinase (Pyk2), which was mediated through Nox-derived ROS generation using pharmacological inhibitors or small interfering ribonucleic acids (siRNAs). CORM-2-induced HO-1 expression was mediated through Nox-(1, 2, 4) or p47

Indexed as

AnimalsAnti-Inflammatory AgentsCells, CulturedCyclic AMP-Dependent Protein KinasesFocal Adhesion Kinase 2Heme Oxygenase-1HumansIntercellular Adhesion Molecule-1LipopolysaccharidesMaleMAP Kinase Signaling SystemMiceMice, Inbred ICRMyocytes, Smooth MuscleNADPH OxidasesOrganometallic CompoundsAnti-Inflammatory AgentsCyclic AMP-Dependent Protein KinasesFocal Adhesion Kinase 2Heme Oxygenase-1Intercellular Adhesion Molecule-1LipopolysaccharidesNADPH OxidasesOrganometallic CompoundsPtk2b protein, mouseReactive Oxygen Speciestricarbonyldichlororuthenium (II) dimerAP-1CORM-2HO-1NADPH oxidaseROS

Identifiers

PMID31261663
PMCPMC6651427
OpenAlexW2955542628

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.