The protective effect of Nigella sativa extract on lung inflammation and oxidative stress induced by lipopolysaccharide in rats.
Animals
Anti-Inflammatory Agents
/ pharmacology
Antioxidants
/ pharmacology
Bronchoalveolar Lavage Fluid
/ chemistry
Cytokines
/ immunology
Dinoprostone
/ immunology
Leukocyte Count
Lipopolysaccharides
Lung
/ drug effects
Male
Nigella sativa
Oxidative Stress
/ drug effects
Plant Extracts
/ pharmacology
Pneumonia
/ drug therapy
Rats, Wistar
Inflammation
LPS
Lung injury
Nigella sativa
Oxidative stress
Journal
Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310
Informations de publication
Date de publication:
10 May 2020
10 May 2020
Historique:
received:
10
10
2019
revised:
01
02
2020
accepted:
04
02
2020
pubmed:
9
2
2020
medline:
5
1
2021
entrez:
9
2
2020
Statut:
ppublish
Résumé
Oxidative stress during inflammation can increase inflammation and damage tissue. Nigella sativa L. (NS) showed many pharmacological properties including antioxidant and anti-inflammatory activities. In this study, the preventive effect of NS on lung inflammation and oxidative stress induced by lipopolysaccharide (LPS) in the rats was investigated. Male rats were assigned to: Control, LPS (1 mg/kg, i.p.), LPS + NS (100, 200, 400 mg/kg, i.p.), (10 per group). Saline (1 ml/kg) was intra-peritoneal (i.p.) injected instead of LPS in the rats of the control group. LPS dissolved in saline and injected i.p. daily for 14 days. Treatment with NS extracts started two days before LPS administration and treatment continued during LPS administration. White blood cells (WBC), total and differential as well as oxidative stress index in bronchoalveolar fluid (BALF) and serum, TGF-β1, IFN-γ, PGE LPS administration increased total WBC, eosinophils, neutrophils, basophils, and monocytes counts as well as oxidative stress markers in the BALF and serum as well as TGF-β1, IFN-γ, PGE These results suggested the protective effects of NS extract on lung inflammation and oxidative stress as well as its effect on lung pathology induced by LPS dose-dependently.
Identifiants
pubmed: 32035219
pii: S0378-8741(19)34062-0
doi: 10.1016/j.jep.2020.112653
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Antioxidants
0
Cytokines
0
Lipopolysaccharides
0
Plant Extracts
0
Dinoprostone
K7Q1JQR04M
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112653Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that there are no conflicts of interest.