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Swimming exercise alleviates pathological bone features in curdlan-injected SKG mice by inducing irisin expression

病态的 脚踝 炎症 关节炎 强直性脊柱炎 内分泌学 柯德兰 内科学 弗洛斯 脂联素 医学 病理 生物化学 生物 胰岛素抵抗 肥胖 芦丁 抗氧化剂 多糖
作者
Seung Hoon Lee,Bora Nam,Jeehee Youn,Kyu Hoon Lee,Sungsin Jo
出处
期刊:Life Sciences [Elsevier BV]
卷期号:352: 122894-122894 被引量:1
标识
DOI:10.1016/j.lfs.2024.122894
摘要

This study assessed the therapeutic potential of swimming exercise in the curdlan-injected SKG mouse model and investigated the modulatory effects of irisin on inflammation. Curdlan-injected SKG were randomly assigned to either a home-cage group or a swimming group for 6 weeks. Changes in clinical arthritis scores and ankle thickness were measured weekly. Post-swimming program, mice were anesthetized for collection of vastus lateralis muscle and blood, which was followed by histological analysis, micro-CT imaging of the ankle joints, and the measurement of pro-inflammatory cytokines and irisin levels. Additionally, curdlan-injected SKG mice were intravenously injected with recombinant irisin protein and observed. Finally, serum levels of irisin in healthy control and ankylosing spondylitis (AS) patient groups were measured by ELISA. The swimming group of curdlan-injected SKG mice exhibited significant improvements in arthritis and enthesitis compared to the home-cage group. In particular, micro-CT and histological analyses revealed a notable reduction in pathological bone features in the swimming group compared to the home-cage group. Muscle endurance was also enhanced in the swimming group compared to the home-cage group, as determined by the wire-hanging test. Intriguingly, irisin levels not only were statistically increased in the swimming group but, also, TNF-α, IL-1β, and IL-6 levels were decreased. Additionally, injection of irisin protein slightly attenuated both arthritis and enthesitis in curdlan-injected SKG mice. Meanwhile, irisin serum levels were declined in AS patients. Overall, we found that swimming exercise attenuated pathological bone features in an AS animal model, potentially mediated by increased irisin serum levels with associated anti-inflammatory effects.
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