Pro-inflammatory response induced by the venom of Parachartergus fraternus wasp.


Journal

Toxicon : official journal of the International Society on Toxinology
ISSN: 1879-3150
Titre abrégé: Toxicon
Pays: England
ID NLM: 1307333

Informations de publication

Date de publication:
30 Jan 2021
Historique:
received: 09 08 2020
revised: 30 10 2020
accepted: 30 11 2020
pubmed: 9 12 2020
medline: 27 1 2021
entrez: 8 12 2020
Statut: ppublish

Résumé

The sting of different wasp species triggers local and systemic reactions in victims that can lead to death. Parachartergus fraternus is responsible for frequent accidents in Latin America; however, few studies have been conducted on this insect and its venom. In this study, the inflammatory process induced by the venom of the P. fraternus wasp (Pfv; 100, 200, and 400 μg/kg) was characterized. Mice were used to assess paw edema, vascular permeability, mast cell degranulation, leukocyte influx, nitric oxide (NO) production, expression of inflammatory genes, and histopathological changes. Pfv triggered edema formation with a peak dose of 200 μg/kg at 10 min. There was an increase in permeability in all periods and doses evaluated, with no differences between them. The 200 μg/kg dose induced mast cell degranulation in all periods, with a peak at 15 min. This same dose induced leukocyte influx with a predominance of mononuclear cells and triggered a peak in NO production in the 12th hour. The increase in COX-2, iNOS, and IFN-γ mRNA expression occurred after 1 and 6 h, and there was an increase in IL-10 expression after 48 h. In addition, Pfv triggered edema and induced an influx of macrophages and mast cells into the injection site. Therefore, Pfv induces an inflammatory process from the first 5 min of inoculation that can persist for up to 48 h.

Identifiants

pubmed: 33290790
pii: S0041-0101(20)30620-6
doi: 10.1016/j.toxicon.2020.11.176
pii:
doi:

Substances chimiques

Venoms 0
Wasp Venoms 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11-19

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Jéssica Araujo Isaias Muller (JAI)

Laboratory of Pharmacology and Inflammation, FACFAN/Federal University of Mato Grosso do Sul, Brazil; PhD student of the Multicenter Program of Post-Graduation in Biochemistry and Molecular Biology, INBIO/Federal University of Mato Grosso do Sul, Brazil.

Iluska Senna Bonfá Moslaves (ISB)

Laboratory of Pharmacology and Inflammation, FACFAN/Federal University of Mato Grosso do Sul, Brazil.

Edwin José Torres Oliveira (EJT)

Center for Study and Stem Cells, Cell Therapy and Toxicological Genetics, Federal University of Mato Grosso do Sul, Brazil.

Luciane Candeloro Portugal (LC)

Laboratory of Histology, INBIO/Federal University of Mato Grosso do Sul, Brazil.

Rodrigo Juliano Oliveira (RJ)

Center for Study and Stem Cells, Cell Therapy and Toxicological Genetics, Federal University of Mato Grosso do Sul, Brazil.

Márcia Renata Mortari (MR)

Laboratory of Neuropharmacology, ICB/University of Brasilia, Brazil.

Mônica Cristina Toffoli-Kadri (MC)

Laboratory of Pharmacology and Inflammation, FACFAN/Federal University of Mato Grosso do Sul, Brazil. Electronic address: monica.kadri@ufms.br.

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Classifications MeSH