Evidence map›Paper›PMID 39611987›Full record

ArticleHistochemistry and cell biology2024

Cratylia mollis lectin reduces inflammatory burden induced by multidrug-resistant Staphylococcus aureus in diabetic wounds.

Lucas Dos Santos Silva, Simeone Júlio Dos Santos Castelo Branco, Izadora Souza Soeiro Silva, Miria Yasmim Miranda Paiva, Beatriz Gomes Vila Nova, Carlos Emanuel de Matos Chaves Lima, Weslley Felix de Oliveira, Felipe Eduardo Alves de Paiva, Patrícia Maria Guedes Paiva, Andrea de Souza Monteiro and 4 more

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Article in Histochemistry and cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Lucas Dos Santos SilvaLaboratório de Patogenicidade Microbiana, Universidade Ceuma, São Luís, 65075-120, Brazil.
Simeone Júlio Dos Santos Castelo BrancoLaboratório de Bioquímica de Proteínas, Centro de Biociências, Universidade Federal de Pernambuco, Recife, 50740-570, Brazil.
Izadora Souza Soeiro SilvaLaboratório de Patogenicidade Microbiana, Universidade Ceuma, São Luís, 65075-120, Brazil.
Miria Yasmim Miranda PaivaLaboratório de Patogenicidade Microbiana, Universidade Ceuma, São Luís, 65075-120, Brazil.
Beatriz Gomes Vila NovaLaboratório de Patogenicidade Microbiana, Universidade Ceuma, São Luís, 65075-120, Brazil.
Carlos Emanuel de Matos Chaves LimaLaboratório de Odontologia, Universidade Ceuma, São Luís, 65075-120, Brazil.
Weslley Felix de OliveiraLaboratório de Bioquímica de Proteínas, Centro de Biociências, Universidade Federal de Pernambuco, Recife, 50740-570, Brazil.
Felipe Eduardo Alves de PaivaDepartamento de Histologia, Embriologia e Biologia Celular, Universidade Federal de Goiás, Goiânia, 74690-900, Brazil.
Patrícia Maria Guedes PaivaLaboratório de Bioquímica de Proteínas, Centro de Biociências, Universidade Federal de Pernambuco, Recife, 50740-570, Brazil.
Andrea de Souza MonteiroLaboratório de Microbiologia Aplicada, Universidade Ceuma, São Luís, 65075-120, Brazil.
Claudener Souza TeixeiraCentro de Ciências Agrárias e da Biodiversidade, Universidade Federal do Cariri, Crato, Ceará, 63130-025, Brazil.
Cléver Gomes CardosoDepartamento de Histologia, Embriologia e Biologia Celular, Universidade Federal de Goiás, Goiânia, 74690-900, Brazil.
Maria Tereza Dos Santos CorreiaLaboratório de Bioquímica de Proteínas, Centro de Biociências, Universidade Federal de Pernambuco, Recife, 50740-570, Brazil.
Luís Cláudio Nascimento da SilvaLaboratório de Patogenicidade Microbiana, Universidade Ceuma, São Luís, 65075-120, Brazil. luisclaudionsilva@yahoo.com.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In diabetes, tissue repair is impaired, increasing susceptibility to Staphylococcus aureus infections, a pathogen commonly found in wounds. The emergence of S. aureus strains that are highly resistant to antimicrobial agents highlights the urgent need for alternative therapeutic options. One promising candidate is Cramoll (Cratylia mollis seed lectin), known for its immunomodulatory, mitogenic, and healing properties. However, its efficacy in infected diabetic wounds remains unexplored. This study evaluated the effects of topical Cramoll treatment on diabetic wounds infected by S. aureus. Diabetic Swiss mice (induced by streptozotocin) were subjected to an 8-mm wound on the back and subsequently infected with a suspension of multidrug-resistant S. aureus. During the treatment period, the wounds were clinically evaluated for inflammation and the area of injury. After seven days, samples were collected from the wounds to quantify the bacterial load and histopathological and immunological analyses. Wounds infected by S. aureus exhibited more pronounced areas and severity indices, which were significantly reduced by Cramoll treatment (p < 0.05). Histopathological analysis revealed a reduction in inflammatory cells and an increase in revascularization with Cramoll treatment (p < 0.05). Cramoll also promoted greater collagen production compared to controls (p < 0.05). Furthermore, Cramoll treatment significantly reduced the S. aureus load in wounds (p < 0.0001), decreased TNF-α and IL-6 levels in infected wounds, and increased ERK pathway activation (p < 0.05). In conclusion, Cramoll lectin improves the healing of diabetic wounds, and these results contribute to the understanding of Cramoll healing mechanisms, reinforcing its potential as a healing agent in various clinical conditions.

Indexed as

Diabetes Mellitus, ExperimentalAnimalsInflammationMaleMethicillin-Resistant Staphylococcus aureusMicePlant LectinsStaphylococcal InfectionsStaphylococcus aureusWound HealingPlant LectinsBioactive lectinsComplications of diabetesCramollInflammatory responseWound healing

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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.