Evidence map›Paper›PMID 32365648›Full record

ArticleInternational journal of molecular sciences2020

Designing Single-Molecule Magnets as Drugs with Dual Anti-Inflammatory and Anti-Diabetic Effects.

Arturo Navas, Fatin Jannus, Belén Fernández, Javier Cepeda, Marta Medina O'Donnell, Luis Díaz-Ruiz, Cristina Sánchez-González, Juan Llopis, José M Seco, E Rufino-Palomares and 9 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

8 citing papers in PubMed, 14 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

19 authors at 6 institutions in 1 country.

Arturo NavasDepartment of Inorganic Chemistry, C/ Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.
Fatin JannusDepartment of Biochemistry and Molecular Biology I, Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.ORCID 0000-0001-7419-8492
Belén FernándezInstitute of Parasitology and Biomedicine "López-Neyra", CSIC, Av. Conocimiento s/n, 18600 Granada, Spain.ORCID 0000-0001-9987-1495
Javier CepedaDepartment of Applied Chemistry, University of The Basque Country (UPV/EHU), 20018 San Sebastián, Spain.ORCID 0000-0002-0147-1360
Marta Medina O'DonnellDepartment of Organic Chemistry, C/ Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-2662-0238
Luis Díaz-RuizDepartment of Biochemistry and Molecular Biology I, Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.
Cristina Sánchez-GonzálezDepartment of Physiology, University Campus of Cartuja, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-1044-4858
Juan LlopisDepartment of Physiology, University Campus of Cartuja, University of Granada, 18071 Granada, Spain.
José M SecoDepartment of Applied Chemistry, University of The Basque Country (UPV/EHU), 20018 San Sebastián, Spain.
E Rufino-PalomaresDepartment of Biochemistry and Molecular Biology I, Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-9650-825X
José Antonio LupiáñezDepartment of Biochemistry and Molecular Biology I, Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.ORCID 0000-0001-9095-7145
Santiago Gómez-RuizDepartment of Biology and Geology, Physics and Inorganic Chemistry, Rey Juan Carlos University, Calle Tulipán s/n, 28933 Móstoles (Madrid), Spain.ORCID 0000-0001-9538-8359
José Luis QuilesDepartment of Physiology. Institute of Nutrition and Food Technology "Jose Mataix", Biomedical Research Center, Avda. Conocimiento s/n, 18100 Armilla, Spain.ORCID 0000-0002-9048-9086
Maurizio BattinoDepartment of Clinical Specialist and Odontostomatological Sciences (DISCO) -Sez. Biochemistry, Faculty of Medicine, Polytechnic University of Marche, 60131 Ancona, Italy.ORCID 0000-0002-7250-1782
Duane Choquesillo-LazarteLaboratorio de Estudios Cristalográficos, IACT (CSIC-UGR), Avda. de las Palmeras 4, 18100 Armilla, Spain.ORCID 0000-0002-7077-8972
Ana Belén Ruiz-MuelleDepartment of Chemistry and Physics, Research Centre CIAIMBITAL, University of Almería, Ctra. Sacramento s/n, 04120 Almería, Spain.
Ignacio FernándezDepartment of Chemistry and Physics, Research Centre CIAIMBITAL, University of Almería, Ctra. Sacramento s/n, 04120 Almería, Spain.ORCID 0000-0001-8355-580X
Fernando Reyes-ZuritaDepartment of Biochemistry and Molecular Biology I, Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.ORCID 0000-0003-3438-0753
Antonio Rodríguez-DiéguezDepartment of Inorganic Chemistry, C/ Severo Ochoa s/n, University of Granada, 18071 Granada, Spain.ORCID 0000-0003-3198-5378
Universidad de Granada · ESUniversity of Almería · ESUniversity of the Basque Country · ESConsejo Superior de Investigaciones Científicas · ESInstituto de Parasitología y Biomedicina "López - Neyra" · ESUniversidad Rey Juan Carlos · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have designed and synthesized two novel cobalt coordination compounds using bumetanide (bum) and indomethacin (ind) therapeutic agents. The anti-inflammatory effects of cobalt metal complexes with ind and bum were assayed in lipopolysaccharide stimulated RAW 264.7 macrophages by inhibition of nitric oxide production. Firstly, we determined the cytotoxicity and the anti-inflammatory potential of the cobalt compounds and ind and bum ligands in RAW 264.7 cells. Indomethacin-based metal complex was able to inhibit the NO production up to 35% in a concentration-dependent manner without showing cytotoxicity, showing around 6-37 times more effective than indomethacin. Cell cycle analysis showed that the inhibition of NO production was accompanied by a reversion of the differentiation processes in LPS-stimulated RAW 264.7 cells, due to a decreased of cell percentage in G0/G1 phase, with the corresponding increase in the number of cells in S phase. These two materials have mononuclear structures and show slow relaxation of magnetization. Moreover, both compounds show anti-diabetic activity with low in vitro cell toxicities. The formation of metal complexes with bioactive ligands is a new and promising strategy to find new compounds with high and enhanced biochemical properties and promises to be a field of great interest.

Indexed as

Drug DesignAlgorithmsAnimalsAnti-Inflammatory AgentsCell Cycle CheckpointsCell SurvivalDose-Response Relationship, DrugHypoglycemic AgentsMagnetsMiceModels, ChemicalModels, MolecularMolecular ConformationNitric OxideRAW 264.7 CellsSolubilityAnti-Inflammatory AgentsHypoglycemic AgentsNitric Oxidebumetadinecobaltcoordination compounddiabetesindomethacininflammatorysingle-ion magnet

Identifiers

PMID32365648
PMCPMC7246571
OpenAlexW3023430694

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.