Copaiba oil suppresses inflammation in asthmatic lungs of BALB/c mice induced with ovalbumin.
Administration, Oral
Animals
Anti-Inflammatory Agents
/ administration & dosage
Asthma
/ blood
Bronchoalveolar Lavage Fluid
/ cytology
Disease Models, Animal
Dose-Response Relationship, Drug
Fabaceae
/ chemistry
Female
Humans
Lung
/ drug effects
Mice
Nitric Oxide
/ metabolism
Oils, Volatile
/ administration & dosage
Ovalbumin
/ immunology
Plant Oils
/ administration & dosage
Th17 Cells
/ drug effects
Th2 Cells
/ drug effects
Toxicity Tests, Acute
Allergic asthma
Copaiba oil
Immunomodulation
Natural products
Journal
International immunopharmacology
ISSN: 1878-1705
Titre abrégé: Int Immunopharmacol
Pays: Netherlands
ID NLM: 100965259
Informations de publication
Date de publication:
Mar 2020
Mar 2020
Historique:
received:
19
10
2019
revised:
05
12
2019
accepted:
30
12
2019
pubmed:
3
2
2020
medline:
24
11
2020
entrez:
3
2
2020
Statut:
ppublish
Résumé
Asthma is a chronic inflammatory disease that represents high hospitalizations and deaths in world. Copaiba oil (CO) is popularly used for relieving asthma symptoms and has already been shown to be effective in many inflammation models. This study aimed to investigate the immunomodulatory relationship of CO in ovalbumin (OVA)-induced allergic asthma. The composition of CO sample analyzed by GC and GC-MS and the toxicity test was performed in mice at doses of 50 or 100 mg/kg (by gavage). After, the experimental model of allergic asthma was induced with OVA and mice were orally treated with CO in two pre-established doses. The inflammatory infiltrate was evaluated in bronchoalveolar lavage fluid (BALF), while cytokines (IL-4, IL-5, IL-17, IFN-γ, TNF-α), IgE antibody and nitric oxide (NO) production was evaluated in BALF and lung homogenate (LH) of mice, together with the histology and histomorphometry of the lung tissue. CO significantly attenuated the number of inflammatory cells in BALF, suppressing NO production and reducing the response mediated by TH2 and TH17 (T helper) cells in both BALF and LH. Histopathological and histomorphometric analysis confirmed that CO significantly reduced the numbers of inflammatory infiltrate in the lung tissue, including in the parenchyma area. Our results indicate that CO has an effective in vivo antiasthmatic effect.
Identifiants
pubmed: 32007706
pii: S1567-5769(19)32398-7
doi: 10.1016/j.intimp.2019.106177
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Oils, Volatile
0
Plant Oils
0
Nitric Oxide
31C4KY9ESH
Ovalbumin
9006-59-1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
106177Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.