Effects of chronic treatment with gold nanoparticles on inflammatory responses and oxidative stress in Mdx mice.
Animals
Biomarkers
Disease Models, Animal
Dose-Response Relationship, Drug
Gold
/ pharmacology
Inflammation
/ drug therapy
Inflammation Mediators
/ metabolism
Metal Nanoparticles
/ chemistry
Mice
Mice, Inbred mdx
Muscle, Skeletal
/ drug effects
Muscular Dystrophy, Duchenne
/ pathology
Oxidative Stress
/ drug effects
Reactive Nitrogen Species
/ metabolism
Reactive Oxygen Species
/ metabolism
Duchenne muscular dystrophy
Mdx
gold nanoparticles
inflammation
oxidative stress
Journal
Journal of drug targeting
ISSN: 1029-2330
Titre abrégé: J Drug Target
Pays: England
ID NLM: 9312476
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
pubmed:
3
5
2019
medline:
10
6
2021
entrez:
4
5
2019
Statut:
ppublish
Résumé
Duchenne muscular dystrophy (DMD) is an X-linked recessive hereditary myopathy characterised by progressive muscle degeneration in male children. As a consequence of DMD, increased inflammation and oxidative stress occur in muscle tissue along with morphological changes. Several studies have reported anti-inflammatory and antioxidant effects of gold nanoparticles (GNP) in muscle injury models. The objective of this study was to evaluate these effects along with the impacts of the disease on histopathological changes following chronic administration of GNP to Mdx mice. Two-month-old Mdx mice were separated into five groups of eight individuals each, as follows: wild-type (WT), Mdx-modified without treatment, Mdx + 2.5 mg/kg GNP, Mdx + 7.0 mg/kg GNP and Mdx + 21 mg/kg GNP. GNP with a mean diameter of 20 nm were injected subcutaneously at concentrations of 2.5, 7.0 and 21 mg/kg. Treatments continued for 30 d with injections administered at 48-h intervals. Twenty-four hours after the last injection, the animals were killed and the central region of the gastrocnemius muscle was surgically removed. Chronic administration of GNP reduced inflammation in the gastrocnemius muscle of Mdx mice and reduced morphological alterations due to inflammatory responses to muscular dystrophy. In addition, GNP also demonstrated antioxidant potential by reducing the production of reactive oxygen and nitrogen species, reducing oxidative damage and improving antioxidant activity.
Identifiants
pubmed: 31046473
doi: 10.1080/1061186X.2019.1613408
doi:
Substances chimiques
Biomarkers
0
Inflammation Mediators
0
Reactive Nitrogen Species
0
Reactive Oxygen Species
0
Gold
7440-57-5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM