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光生物调节干预改善肝硬化 Wistar 大鼠骨骼肌的氧化、炎症和形态学参数。

Photobiomodulation intervention improves oxidative, inflammatory, and morphological parameters of skeletal muscle in cirrhotic Wistar rats.

机构信息

Laboratory of Genetic Toxicology, Lutheran University of Brazil, Avenida Farroupilha, 8001, Canoas, RS, CEP 92425900, Brazil.

Lutheran University of Brazil (ULBRA), Avenida Farroupilha, 8001, São José, Canoas, RS, CEP 92425900, Brazil.

出版信息

Lasers Med Sci. 2022 Apr;37(3):1973-1982. doi: 10.1007/s10103-021-03458-z. Epub 2021 Nov 4.

Abstract

Photobiomodulation (PBM) might be an intervention method to mitigate sarcopenia in cirrhotic patients. Given the lack of research on this issue, the goal of this study was to evaluate possible beneficial effects of PBM on the structural and functional properties of skeletal muscle from cirrhotic rats. Cirrhosis was induced by secondary bile duct ligation (BDL). Wistar rats were randomized into four groups: sham-operated control (Sham), Sham + PBM, BDL, and BDL + PBM. After cirrhosis induction, a dose of PBM (1 J; 100mW; 10 s; 880 nm; 6 × per week) was applied to each quadriceps, from the 15th to the 45th day after surgery. The locomotor ability was performed using an open-field task. The muscle structure was analyzed using histological methods. Cell damage was also evaluated assessing oxidative stress and DNA damage markers, and IL-1β pro-inflammatory interleukin by immunohistochemical analysis. An increase in the number of crossings was observed in the BDL + PBM group in relation to BDL. The BDL group showed muscle atrophy and increased IL-1β in relation to Sham, while in the BDL + PBM group, the fiber muscle was restructured and there was a decrease of IL-1 β. TBARS increased in the liver and muscle tissues in the BDL group and decreased it in the BDL + PBM group. SOD increased while CAT decreased in the BDL + PBM group in relation to the BDL group. No genotoxic or mutagenic effect was observed for PBM treatment. PBM improved the locomotion and the morphology of the muscle fibers, decreasing oxidative stress and inflammation, without causing DNA damage in cirrhotic rats.

摘要

光生物调节(PBM)可能是一种减轻肝硬化患者肌少症的干预方法。鉴于此问题研究较少,本研究旨在评估 PBM 对肝硬化大鼠骨骼肌结构和功能特性的可能有益影响。采用次级胆管结扎(BDL)诱导肝硬化。Wistar 大鼠随机分为四组:假手术对照(Sham)、Sham+PBM、BDL 和 BDL+PBM。在肝硬化诱导后,从手术后第 15 天到第 45 天,对每个四头肌应用 1 剂量的 PBM(1 J;100 mW;10 s;880 nm;每周 6 次)。使用旷场任务进行运动能力测试。采用组织学方法分析肌肉结构。通过免疫组织化学分析评估氧化应激和 DNA 损伤标志物以及促炎细胞因子白细胞介素 1β(IL-1β)来评估细胞损伤。与 BDL 组相比,BDL+PBM 组的穿越次数增加。BDL 组与 Sham 组相比,肌肉萎缩和 IL-1β 增加,而 BDL+PBM 组的纤维肌肉结构重构,IL-1β 减少。BDL 组肝和肌肉组织中 TBARS 增加,BDL+PBM 组减少。BDL+PBM 组的 SOD 增加,CAT 减少。PBM 治疗未观察到遗传毒性或致突变作用。PBM 改善了运动能力和肌肉纤维的形态,减轻了氧化应激和炎症,而不会在肝硬化大鼠中引起 DNA 损伤。

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