Evidence map›Paper›PMID 28033347›Full record

ArticlePloS one2016

Inhibitory Effects of Hydroethanolic Leaf Extracts of Kalanchoe brasiliensis and Kalanchoe pinnata (Crassulaceae) against Local Effects Induced by Bothrops jararaca Snake Venom.

Júlia Morais Fernandes, Juliana Félix-Silva, Lorena Medeiros da Cunha, Jacyra Antunes Dos Santos Gomes, Emerson Michell da Silva Siqueira, Luisa Possamai Gimenes, Norberto Peporine Lopes, Luiz Alberto Lira Soares, Matheus de Freitas Fernandes-Pedrosa, Silvana Maria Zucolotto

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 50 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Júlia Morais FernandesGrupo de Pesquisa em Produtos Naturais Bioativos (PNBio), Laboratório de Farmacognosia, Departamento de Farmácia, Universidade Federal do Rio Grande do Norte, (UFRN), Natal, Rio Grande do Norte, Brazil.
Juliana Félix-SilvaLaboratório de Tecnologia & Biotecnologia Farmacêutica (TecBioFar), Programa de Pós-graduação em Ciências Farmacêuticas (PPgCF), Universidade Federal do Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil.
Lorena Medeiros da CunhaGrupo de Pesquisa em Produtos Naturais Bioativos (PNBio), Laboratório de Farmacognosia, Departamento de Farmácia, Universidade Federal do Rio Grande do Norte, (UFRN), Natal, Rio Grande do Norte, Brazil.
Jacyra Antunes Dos Santos GomesLaboratório de Tecnologia & Biotecnologia Farmacêutica (TecBioFar), Programa de Pós-graduação em Ciências Farmacêuticas (PPgCF), Universidade Federal do Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil.
Emerson Michell da Silva SiqueiraGrupo de Pesquisa em Produtos Naturais Bioativos (PNBio), Laboratório de Farmacognosia, Departamento de Farmácia, Universidade Federal do Rio Grande do Norte, (UFRN), Natal, Rio Grande do Norte, Brazil.
Luisa Possamai GimenesNPPNS, Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto-SP, Brasil.
Norberto Peporine LopesNPPNS, Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto-SP, Brasil.
Luiz Alberto Lira SoaresLaboratório de Farmacognosia, Universidade Federal de Pernambuco (UFPE), Recife, Pernambuco, Brazil.
Matheus de Freitas Fernandes-PedrosaLaboratório de Tecnologia & Biotecnologia Farmacêutica (TecBioFar), Programa de Pós-graduação em Ciências Farmacêuticas (PPgCF), Universidade Federal do Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil.
Silvana Maria ZucolottoGrupo de Pesquisa em Produtos Naturais Bioativos (PNBio), Laboratório de Farmacognosia, Departamento de Farmácia, Universidade Federal do Rio Grande do Norte, (UFRN), Natal, Rio Grande do Norte, Brazil.
Universidade Federal do Rio Grande do Norte · BRSUPERA Park of Innovation and Technology of Ribeirão Preto · BRUniversidade Federal de Pernambuco · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The species Kalanchoe brasiliensis and Kalanchoe pinnata, both known popularly as "Saião," are used interchangeably in traditional medicine for their antiophidic properties. Studies evaluating the anti-venom activity of these species are scarce. This study aims to characterize the chemical constituents and evaluate the inhibitory effects of hydroethanolic leaf extracts of K. brasiliensis and K. pinnata against local effects induced by Bothrops jararaca snake venom. Thin Layer Chromatography (TLC) and High Performance Liquid Chromatography coupled with Diode Array Detection and Electrospray Mass Spectrometry (HPLC-DAD-MS/MS) were performed for characterization of chemical markers of the extracts from these species. For antiophidic activity evaluation, B. jararaca venom-induced paw edema and skin hemorrhage in mice were evaluated. In both models, hydroethanolic extracts (125-500 mg/kg) were administered intraperitoneally in different protocols. Inhibition of phospholipase enzymatic activity of B. jararaca was evaluated. The HPLC-DAD-MS/MS chromatographic profile of extracts showed some particularities in the chemical profile of the two species. K. brasileinsis exhibited major peaks that have UV spectra similar to flavonoid glycosides derived from patuletin and eupafolin, while K. pinnata showed UV spectra similar to flavonoids glycosides derived from quercetin and kaempferol. Both extracts significantly reduced the hemorrhagic activity of B. jararaca venom in pre-treatment protocol, reaching about 40% of inhibition, while only K. pinnata was active in post-treatment protocol (about 30% of inhibition). In the antiedematogenic activity, only K. pinnata was active, inhibiting about 66% and 30% in pre and post-treatment protocols, respectively. Both extracts inhibited phospholipase activity; however, K. pinnata was more active. In conclusion, the results indicate the potential antiophidic activity of Kalanchoe species against local effects induced by B. jararaca snake venom, suggesting their potential use as a new source of bioactive molecules against bothropic venom.

Indexed as

BothropsAnimalsCrotalid VenomsEdemaEthanolFemaleHemorrhageKalanchoeMaleMicePlant ExtractsPlant LeavesCrotalid VenomsEthanolPlant Extracts

Identifiers

PMID28033347
PMCPMC5199091
OpenAlexW2569170905

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.