Effects of phonophoresis with diclofenac linked gold nanoparticles in model of traumatic muscle injury.
Animals
Catalase
/ metabolism
Diclofenac
/ pharmacology
Disease Models, Animal
Glutathione
/ metabolism
Gold
/ chemistry
Hyperalgesia
/ complications
Metal Nanoparticles
/ chemistry
Muscle, Skeletal
/ drug effects
Phonophoresis
Rats, Wistar
Spectroscopy, Fourier Transform Infrared
Superoxide Dismutase
/ metabolism
Wounds and Injuries
/ complications
Gold nanoparticles
Inflammation and oxidative stress
Muscle injury
Phonophoresis
Sodium diclofenac
Journal
Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
05
09
2019
revised:
16
01
2020
accepted:
19
01
2020
entrez:
25
3
2020
pubmed:
25
3
2020
medline:
5
1
2021
Statut:
ppublish
Résumé
The use of nanotechnology for administering drugs is a recent development that presents promising results. Therapeutic Pulsed Ultrasound (TPU) is one such therapeutic option and is widely used for treating soft tissue lesions. Thus, the objective of this study was to investigate the therapeutic effect of phonophoresis using diclofenac (DC) linked to gold nanoparticles (GNPs) in the skeletal muscle of rats used as a model of traumatic muscular injury. Wistar rats were divided into eight groups (N = 10): Sham, Muscle injury (MI), MI + TPU, MI + DC, MI + GNPs, MI + TPU + DC, MI + TPU + GNPs, and MI + TPU + DC-GNPs. The traumatic injury was performed in the gastrocnemius with a single direct traumatic impact via an injuring press. The animals received daily treatment for 5 consecutive days with TPU and gel with DC and/or GNPs. Two hours after the last treatment session, animals were euthanized and the gastrocnemius muscle surgically removed for histological and biochemical analysis. The groups exposed to some therapies (MI + TPU + DC, MI + TPU + GNPs and MI + TPU + DC-GNPs) showed reduced levels of pro-inflammatory cytokines, whereas an increase in anti-inflammatory cytokine levels was observed in the group exposed to all therapies combined (MI + TPU + DC-GNPs). Reactive species production and protein damage resulting from oxidative damage was lower for the group exposed to all tested therapies had lower production. Lower protein damage was also observed in the TPU + GNPs group. The group that underwent all tested therapies combined showed a significant increase in antioxidants compared to the MI group. During histological analysis, the MI group showed large amounts of cell infiltration and centralized nuclei, whereas the MI + TPU + DC-GNPs group showed structural improvements. Pain levels in the MI + TPU + DC-GNPs group were lower than those of the MI group. We believe that the association of TPU with DC linked to GNPs decreases the inflammation caused by traumatic muscle injury and accelerates tissue repair.
Identifiants
pubmed: 32204109
pii: S0928-4931(19)33311-9
doi: 10.1016/j.msec.2020.110681
pii:
doi:
Substances chimiques
Diclofenac
144O8QL0L1
Gold
7440-57-5
Catalase
EC 1.11.1.6
Superoxide Dismutase
EC 1.15.1.1
Glutathione
GAN16C9B8O
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
110681Informations 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.