Evidence map›Paper›PMID 34921623›Full record

ArticleArchives of microbiology2021

Metabolites from Induratia spp. modulating key enzymes in human hemostasis.

Mauro Guilherme Barros Cardoso, Marcus Vinicius Cardoso Trento, Pedro Henrique Souza Cesar, Silvana Marcussi, Patrícia Gomes Cardoso

Abstract read
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In one paragraph

Article in Archives of microbiology, 2021. 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
0.2field-weighted citation impact, top 36% 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, 1 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

5 authors at 1 institution in 1 country.

Mauro Guilherme Barros CardosoDepartment of Biology, Universidade Federal de Lavras, Lavras, MG, Brazil.
Marcus Vinicius Cardoso TrentoDepartment of Chemistry, Universidade Federal de Lavras, Lavras, MG, Brazil.
Pedro Henrique Souza CesarDepartment of Chemistry, Universidade Federal de Lavras, Lavras, MG, Brazil.
Silvana MarcussiDepartment of Chemistry, Universidade Federal de Lavras, Lavras, MG, Brazil.
Patrícia Gomes CardosoDepartment of Biology, Universidade Federal de Lavras, Lavras, MG, Brazil. patricia@ufla.br.ORCID http://orcid.org/0000-0002-0797-2502
Universidade Federal de Lavras · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induratia spp. fungi have been poorly evaluated for their non-volatile secondary metabolites. In the present work, we evaluated the effects of non-volatile secondary metabolites released into the culture medium by Induratia spp. upon toxic alterations induced by Bothrops spp. venoms. B. atrox venom phospholipase was inhibited by Induratia spp. around 12 and 16%. The extracts of the two strains inhibited 12-25% of the hemolysis induced by B.moojeni venom. Thrombolysis was inhibited by 30-60% by the compounds present in both extracts. The coagulation induced by B. moojeni venom was prolonged by 26-41 s by the action of the extracts of I. coffeana. The fungal extracts did not exert any cytotoxic effect, nor did they induce any alteration in the other evaluated substrates show the potential use of non-volatile metabolites produced by the fungi evaluated as enzyme modulators, especially for proteases with a fundamental role in human hemostasis.

Indexed as

EndopeptidasesHemostasisPeptide HydrolasesAnimalsBothropsCell DeathHumansSnake VenomsXylarialesEndopeptidasesPeptide HydrolasesSnake VenomsBothrops spp.Endophytic fungiMuscodor spp.PhospholipasesProteasesSecondary metabolites

Identifiers

PMID34921623
OpenAlexW4225782351

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.