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临床样冷冻疗法治疗急性膝关节炎可保护股四头肌的神经肌肉接头并减轻小鼠的关节炎症。

Clinical-Like Cryotherapy in Acute Knee Arthritis Protects Neuromuscular Junctions of Quadriceps and Reduces Joint Inflammation in Mice.

机构信息

Department of Physical Therapy, Federal University of São Carlos, São Carlos, SP, Brazil.

Department of Pharmacology, University of São Paulo, Ribeirão Preto, SP, Brazil.

出版信息

Biomed Res Int. 2022 Jan 22;2022:7442289. doi: 10.1155/2022/7442289. eCollection 2022.

Abstract

Rheumatoid arthritis is an autoimmune and inflammatory disease that affects synovial joint tissues and skeletal muscle. Clinical-like cryotherapy benefits signs of joint inflammation in knee osteoarthritis after 60 days of anterior cruciate ligament transection surgery. However, it is unknown whether it also benefits acute knee arthritis (e.g., reduces inflammatory process and protects neuromuscular junction [NMJ] and muscle fibers). We aimed to analyze the effects of clinical-like cryotherapy on NMJ and quadriceps muscle fibers in a model of acute knee arthritis. Twenty-four male C57BL/6 mice (20 to 25 g) were randomly allocated into three groups: control (mice with no intervention), antigen-induced arthritis (AIA; mice sensitized and immunized with intra-articular [i.a.] injection of methylated bovine serum albumin [mBSA]), and AIA+cryotherapy (mice sensitized, immunized with i.a. injection of mBSA, and submitted to a clinical-like cryotherapy protocol). Twenty-one days after sensitization, arthritis was induced in immunized mice via i.a. injection of mBSA (100 g/joint). Two clinical-like cryotherapy sessions (crushed ice pack for 20 min) were applied two hours apart. The first session was applied immediately after i.a. injection of mBSA. The quadriceps was removed two hours after the second clinical-like cryotherapy session for morphological analysis of muscle fibers (cross-sectional area), frequency distribution of muscle fiber area (%), and NMJ (area, perimeter, and maximum diameter). Gene expressions of mRNA involved in NMJ signaling (-nAChR, 1-nAChR, -nAChR, Agrin-MusK-Rapsyn, -dystrobrevin, and utrophin) and atrophy (muscle RING-finger protein-1 and Atrogin-1) pathways were analyzed. Inflammatory signs were assessed in knee joint (swelling, articular surface temperature, and neutrophil migration in synovial fluid). Regarding morphological analysis of muscle fibers, 180 to 270 and >270 m classes were higher in the AIA+cryotherapy than the AIA group. Area, perimeter, and maximum diameter of NMJ also increased in the AIA+cryotherapy compared with the control group. Agrin mRNA expression increased in the AIA+cryotherapy compared with the control and AIA groups. In the atrophy pathway, Atrogin-1 increased compared with the control and AIA groups. The AIA+cryotherapy group reduced knee swelling and neutrophil migration compared with the AIA group. In conclusion, clinical-like cryotherapy increased Agrin expression, contributing to NMJ maintenance and increased Atrogin-1 expression, thus protecting NMJ and muscle fiber. Furthermore, clinical-like cryotherapy reduced inflammatory signs (swelling and neutrophil migration) of acute knee arthritis.

摘要

类风湿关节炎是一种影响滑膜关节组织和骨骼肌的自身免疫性和炎症性疾病。临床类似冷冻疗法有益于前交叉韧带横断术后 60 天膝关节骨关节炎的关节炎症迹象。然而,尚不清楚它是否也有益于急性膝关节炎(例如,减少炎症过程并保护神经肌肉接头[NMJ]和肌肉纤维)。我们旨在分析临床类似冷冻疗法对急性膝关节炎模型中 NMJ 和股四头肌纤维的影响。将 24 只雄性 C57BL/6 小鼠(20-25g)随机分为三组:对照组(无干预组)、抗原诱导性关节炎(AIA;用关节内[IA]注射甲基化牛血清白蛋白[mBSA]致敏和免疫的小鼠)和 AIA+冷冻疗法(用 IA 注射 mBSA 致敏、免疫的小鼠,以及接受临床类似冷冻疗法方案)。致敏后 21 天,通过 IA 注射 mBSA(100μg/关节)诱导免疫小鼠关节炎。两次临床类似冷冻治疗(碎冰袋 20 分钟),间隔两小时进行。第一次治疗在 IA 注射 mBSA 后立即进行。第二次临床类似冷冻治疗后两小时取出股四头肌,用于肌肉纤维的形态分析(横截面积)、肌肉纤维面积(%)的频率分布和 NMJ(面积、周长和最大直径)。分析了参与 NMJ 信号转导的 mRNA(-nAChR、1-nAChR、-nAChR、Agrin-MusK-Rapsyn、-dystrobrevin 和 utrophin)和萎缩(肌肉 RING 指蛋白-1 和 Atrogin-1)途径的基因表达。评估了膝关节的炎症迹象(肿胀、关节表面温度和滑液中的中性粒细胞迁移)。关于肌肉纤维的形态分析,与 AIA 组相比,AIA+冷冻治疗组的 180 至 270m 类和>270m 类更高。与对照组相比,NMJ 的面积、周长和最大直径也增加。与对照组和 AIA 组相比,AIA+冷冻治疗组的 Agrin mRNA 表达增加。在萎缩途径中,与对照组和 AIA 组相比,Atrogin-1 增加。与 AIA 组相比,AIA+冷冻治疗组减少了膝关节肿胀和中性粒细胞迁移。总之,临床类似冷冻疗法增加了 Agrin 的表达,有助于 NMJ 的维持,并增加了 Atrogin-1 的表达,从而保护 NMJ 和肌肉纤维。此外,临床类似冷冻疗法还降低了急性膝关节炎的炎症迹象(肿胀和中性粒细胞迁移)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/8800614/7512e0998549/BMRI2022-7442289.001.jpg

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