Effects of phonophoresis with diclofenac linked gold nanoparticles in model of traumatic muscle injury.


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
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

110681

Informations 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.

Auteurs

Daniela Pacheco Dos Santos Haupenthal (DP)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Diogo Zortea (D)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Rubya Pereira Zaccaron (RP)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Gustavo de Bem Silveira (G)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Maria Eduarda Anastácio Borges Corrêa (MEAB)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Carolini Mendes (C)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Laura de Roch Casagrande (L)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Mariane Bernardo Duarte (MB)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Ricardo Aurino Pinho (RA)

Laboratory of Exercise Biochemistry in Health, Graduate Program in Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná, Curitiba, Paraná, Brazil.

Paulo Emilio Feuser (PE)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Ricardo Andrez Machado-de-Ávila (RA)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil.

Paulo Cesar Lock Silveira (PCL)

Laboratory of Experimental Phisiopatology, Program of postgraduate in Science of Health, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, Santa Catarina State, Brazil. Electronic address: psilveira@unesc.net.

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Classifications MeSH