Oxidative stress-induced skeletal muscle injury involves in NF-κB/p53-activated immunosuppression and apoptosis response in copper (II) or/and arsenite-exposed chicken

Chemosphere ◽  
2018 ◽  
Vol 210 ◽  
pp. 76-84 ◽  
Author(s):  
Hongjing Zhao ◽  
Yu Wang ◽  
Yizhi Shao ◽  
Juanjuan Liu ◽  
Sirui Wang ◽  
...  
Author(s):  
Caroline Bomfim Lemos da Cruz ◽  
Luis Fernando Sousa Filho ◽  
Diego Alves Lima ◽  
Joyce Izabel de Gois ◽  
Evaleide Diniz de Oliveira

2015 ◽  
Vol 36 (6) ◽  
pp. 377-393 ◽  
Author(s):  
Magdalena Kozakowska ◽  
Katarzyna Pietraszek-Gremplewicz ◽  
Alicja Jozkowicz ◽  
Jozef Dulak

Redox Report ◽  
2016 ◽  
Vol 22 (6) ◽  
pp. 323-329 ◽  
Author(s):  
Angelina Freitas Siqueira ◽  
Amilton Vieira ◽  
Gracielle Vieira Ramos ◽  
Rita de Cássia Marqueti ◽  
Tania de Fátima Salvini ◽  
...  

2006 ◽  
Vol 38 (Supplement) ◽  
pp. S389
Author(s):  
Richard J. Bloomer ◽  
Michael J. Falvo ◽  
Andrew C. Fry ◽  
Brian K. Schilling ◽  
Webb A. Smith ◽  
...  

RSC Advances ◽  
2021 ◽  
Vol 11 (45) ◽  
pp. 27837-27844
Author(s):  
Luis Fernando Sousa Filho ◽  
Marta Maria Barbosa Santos ◽  
Paula dos Passos Menezes ◽  
Bruno dos Santos Lima ◽  
Adriano Antunes de Souza Araújo ◽  
...  

A gel containing the inclusion complex of quercetin and β-cyclodextrin was developed in order to verify its effects, isolated or using phonophoresis, on oxidative biomarkers after skeletal muscle injury.


2022 ◽  
Vol 12 ◽  
Author(s):  
Ying Xin ◽  
Yifeng Zhang ◽  
Simin Deng ◽  
Xinqun Hu

Vagus nerve stimulation (VNS) has a protective effect on distal organ injury after ischemia/reperfusion (I/R) injury. We aimed to investigate the protective efficacy of VNS on hepatic I/R injury-induced acute skeletal muscle injury and explore its underlying mechanisms. To test this hypothesis, male Sprague-Dawley rats were randomly divided into three groups: sham group (sham operation, n = 6); I/R group (hepatic I/R with sham VNS, n = 6); and VNS group (hepatic I/R with VNS, n = 6). A hepatic I/R injury model was prepared by inducing hepatic ischemia for 1 h (70%) followed by hepatic reperfusion for 6 h. VNS was performed during the entire hepatic I/R process. Tissue and blood samples were collected at the end of the experiment for biochemical assays, molecular biological preparations, and histological examination. Our results showed that throughout the hepatic I/R process, VNS significantly reduced inflammation, oxidative stress, and apoptosis, while significantly increasing the protein levels of silent information regulator 1 (SIRT1) and decreasing the levels of acetylated forkhead box O1 and Ac-p53, in the skeletal muscle. These data suggest that VNS can alleviate hepatic I/R injury-induced acute skeletal muscle injury by suppressing inflammation, oxidative stress, and apoptosis, potentially via the SIRT1 pathway.


2009 ◽  
Vol 28 (1) ◽  
pp. 1-11 ◽  
Author(s):  
Andres J. Quintero ◽  
Vonda J. Wright ◽  
Freddie H. Fu ◽  
Johnny Huard

2020 ◽  
Vol 4 (1) ◽  
Author(s):  
Bruno Paun ◽  
Daniel García Leon ◽  
Alex Claveria Cabello ◽  
Roso Mares Pages ◽  
Elena de la Calle Vargas ◽  
...  

Abstract Background Skeletal muscle injury characterisation during healing supports trauma prognosis. Given the potential interest of computed tomography (CT) in muscle diseases and lack of in vivo CT methodology to image skeletal muscle wound healing, we tracked skeletal muscle injury recovery using in vivo micro-CT in a rat model to obtain a predictive model. Methods Skeletal muscle injury was performed in 23 rats. Twenty animals were sorted into five groups to image lesion recovery at 2, 4, 7, 10, or 14 days after injury using contrast-enhanced micro-CT. Injury volumes were quantified using a semiautomatic image processing, and these values were used to build a prediction model. The remaining 3 rats were imaged at all monitoring time points as validation. Predictions were compared with Bland-Altman analysis. Results Optimal contrast agent dose was found to be 20 mL/kg injected at 400 μL/min. Injury volumes showed a decreasing tendency from day 0 (32.3 ± 12.0mm3, mean ± standard deviation) to day 2, 4, 7, 10, and 14 after injury (19.6 ± 12.6, 11.0 ± 6.7, 8.2 ± 7.7, 5.7 ± 3.9, and 4.5 ± 4.8 mm3, respectively). Groups with single monitoring time point did not yield significant differences with the validation group lesions. Further exponential model training with single follow-up data (R2 = 0.968) to predict injury recovery in the validation cohort gave a predictions root mean squared error of 6.8 ± 5.4 mm3. Further prediction analysis yielded a bias of 2.327. Conclusion Contrast-enhanced CT allowed in vivo tracking of skeletal muscle injury recovery in rat.


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