Evidence map›Paper›PMID 34643986›Full record

ArticleChembiochem : a European journal of chemical biology2022

Head-to-Head Comparison of Selected Extra- and Intracellular CO-Releasing Molecules on Their CO-Releasing and Anti-Inflammatory Properties.

Yingchun Li, Lars Hemmersbach, Bernhard Krause, Nikolay Sitnikov, Anna Schlundt Née Göderz, Diego O Pastene Maldonado, Hans-Günther Schmalz, Benito Yard

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

5 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

8 authors at 2 institutions in 1 country.

Yingchun LiVth medical Department, Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
Lars HemmersbachUniversität zu Köln, Greinstrasse 4, 50939, Köln, Germany.
Bernhard KrauseUniversität zu Köln, Greinstrasse 4, 50939, Köln, Germany.
Nikolay SitnikovUniversität zu Köln, Greinstrasse 4, 50939, Köln, Germany.
Anna Schlundt Née GöderzUniversität zu Köln, Greinstrasse 4, 50939, Köln, Germany.
Diego O Pastene MaldonadoVth medical Department, Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
Hans-Günther SchmalzUniversität zu Köln, Greinstrasse 4, 50939, Köln, Germany.ORCID 0000-0003-0489-1827
Benito YardVth medical Department, Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
University of Cologne · DEHeidelberg University · DE

Funding

Alexander von Humboldt FoundationGerman Research Foundation SCHM 857-20-1
6 · The paper itself

Abstract

Over the past decade, a variety of carbon monoxide releasing molecules (CORMs) have been developed and tested. Some CORMs spontaneously release CO once in solution, while others require a trigger mechanism to release the bound CO from its molecular complex. The modulation of biological systems by CORMs depends largely on the spatiotemporal release of CO, which likely differs among the different types of CORMs. In spontaneously releasing CORMs, CO is released extracellularly and crosses the cell membrane to interact with intracellular targets. Other CORMs can directly release CO intracellularly, which may be a more efficient method to modulate biological systems. In the present study, we compared the efficacy of extracellular and intracellular CO-releasing CORMs that either release CO spontaneously or require an enzymatic trigger. The efficacy of such CORMs to modulate HO-1 and VCAM-1 expression in TNF-α-stimulated human umbilical vein endothelial cells (HUVEC) was evaluated.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalCarbon MonoxideCoordination ComplexesHeme Oxygenase-1HumansHuman Umbilical Vein Endothelial CellsMolecular StructureTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1Anti-Inflammatory Agents, Non-SteroidalCarbon MonoxideCoordination ComplexesHeme Oxygenase-1HMOX1 protein, humanTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1anti-inflammatory agentscarbon monoxideheme oxygenasesiron carbonyl complexesprodrugs

Identifiers

PMID34643986
PMCPMC9298253
OpenAlexW3206359569

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.