Evidence map›Paper›PMID 34697722›Full record

ArticleInflammation2022

LASSBio-596: a New Pre-clinical Candidate for Rheumatoid Arthritis?

Max Denisson Maurício Viana, Alyne Almeida de Lima, Geraldo José da Silva Neto, Suellen Maria Albuquerque da Silva, Anderson Brandão Leite, Elane Conceição Dos Santos, Ênio José Bassi, Eliane Aparecida Campesatto, Aline Cavalcanti de Queiroz, Eliezer Jesus Barreiro and 2 more

Abstract read
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In one paragraph

Article in Inflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 3 institutions in 1 country.

Max Denisson Maurício VianaPharmacology and Immunity Laboratory, Institute of Biological and Health Sciences, Federal University of Alagoas, Av. Lourival Melo Mota, SN, Tabuleiro do Martins, Maceio, AL, 57072-900, Brazil. suzana.magna@gmail.com.ORCID http://orcid.org/0000-0002-1650-4460
Alyne Almeida de LimaGonçalo Moniz Institute (Fiocruz, BA), BA, 40296-710, Salvador, Brazil.ORCID https://orcid.org/0000-0002-6174-7402
Geraldo José da Silva NetoLaboratory of Catalysis and Chemical Reactivity, Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceio, AL, 57072-900, Brazil.ORCID https://orcid.org/0000-0002-4872-9269
Suellen Maria Albuquerque da SilvaPharmacology and Immunity Laboratory, Institute of Biological and Health Sciences, Federal University of Alagoas, Maceio, AL, 57072-900, Brazil.ORCID https://orcid.org/0000-0003-1944-9513
Anderson Brandão LeiteInstitute of Biological and Health Sciences, Federal University of Alagoas, Maceio, AL, 57072-900, Brazil.ORCID https://orcid.org/0000-0003-2071-2016
Elane Conceição Dos SantosImmunoregulation Research Group, Laboratory of Research in Virology and Immunology, Institute of Biological and Health Sciences, Federal University of Alagoas, AL, 57072-900, Maceio, Brazil.ORCID https://orcid.org/0000-0002-5959-4654
Ênio José BassiImmunoregulation Research Group, Laboratory of Research in Virology and Immunology, Institute of Biological and Health Sciences, Federal University of Alagoas, AL, 57072-900, Maceio, Brazil.ORCID https://orcid.org/0000-0002-7956-5746
Eliane Aparecida CampesattoPharmacology and Immunity Laboratory, Institute of Biological and Health Sciences, Federal University of Alagoas, Maceio, AL, 57072-900, Brazil.ORCID https://orcid.org/0000-0003-3689-888X
Aline Cavalcanti de QueirozMicrobiology, Immunology and Parasitology Laboratory, Medical and Nursing Sciences Complex, Federal University of Alagoas - Campus Arapiraca, Av. Manoel Severino Barbosa - Bom Sucesso, Arapiraca, AL, 57309-005, Brazil.ORCID https://orcid.org/0000-0002-6362-2726
Eliezer Jesus BarreiroLaboratory for Evaluation and Synthesis of Bioactive Substances, LASSBio®, Institute of Biomedical Sciences, Federal University of Rio de Janeiro, PO Box 68024, Rio de Janeiro, RJ, 21944-910, Brazil.ORCID https://orcid.org/0000-0003-1759-0038
Lidia Moreira LimaLaboratory for Evaluation and Synthesis of Bioactive Substances, LASSBio®, Institute of Biomedical Sciences, Federal University of Rio de Janeiro, PO Box 68024, Rio de Janeiro, RJ, 21944-910, Brazil.ORCID https://orcid.org/0000-0002-8625-6351
Magna Suzana Alexandre-MoreiraPharmacology and Immunity Laboratory, Institute of Biological and Health Sciences, Federal University of Alagoas, Maceio, AL, 57072-900, Brazil.ORCID https://orcid.org/0000-0002-9979-1994
Universidade Federal de Alagoas · BRUniversidade Federal do Rio de Janeiro · BRFundação Oswaldo Cruz · BR

Funding

capes/fapeal 07/2015cnpq 573.564/2008-6faperj E-26/170.020/2008
6 · The paper itself

Abstract

Pain and inflammatory disorders are significant health problems because of prevalence and associated disabilities. In this context, LASSBio-596 is a hybrid compound able to modulate TNF-α and phosphodiesterases 4 and 5, exhibiting an anti-inflammatory effect in the pulmonary inflammatory model. Aiming at a better description of the activities of LASSBio-596, we initially conducted nociception tests (acetic acid-induced abdominal writhing, glutamate, and formalin-induced nociception and hot plate test) and later inflammatory tests (acute, peritonitis; and chronic, arthritis) that directed us to this last one. In the abdominal writhing test, there was a dose-dependent inhibition, whose response occurred at the maximum dose (50 mg/kg, p.o.), used in the subsequent tests. LASSBio-596 also inhibited nociception induced by chemical (glutamate by 31.9%; and formalin, in both phases, 1st phase: 25.7%; 2nd phase: 23.9%) and thermal agents (hotplate, by increased latency for pain at two different times). These effects were independent of the motor function, legitimated in rotarod. As there was a response in the inflammatory component of nociception, we performed the peritonitis test, in which migration was inhibited by LASSBio-596 by 39.9%. As the inflammatory process is present in autoimmune diseases, we also performed the arthritis test. LASSBio-596 reduced paw edema from the 15th day to the 21st day of treatment (no liver changes and with fewer paw injuries). In addition, LASSBio-596 decreased serum levels of TNF-α by 67.1%. These data demonstrated the antinociceptive effect of LASSBio-596 and reinforces its anti-inflammatory property (i.e., RA), amplifying the therapeutic potential of this molecule.

Indexed as

AnalgesicsArthritis, RheumatoidAnti-Inflammatory AgentsEdemaHumansPainPhthalic AcidsPlant ExtractsSulfonamidesAnalgesicsAnti-Inflammatory AgentsLASSBIO596Phthalic AcidsPlant ExtractsSulfonamidesAnti-inflammatoryAnti-nociceptiveLASSBio-596Rheumatoid arthritisThalidomide

Identifiers

PMID34697722
OpenAlexW3210690481

What OpenQuestion holds

Textmetadata
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.