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姜酮酸在肌肉中的促再生和抗炎作用评价:治疗杜氏肌营养不良症的潜在疗法。

Evaluation of pro-regenerative and anti-inflammatory effects of isolecanoric acid in the muscle: Potential treatment of Duchenne Muscular Dystrophy.

机构信息

Cardiovascular Development Group, Department of Experimental Biology, Faculty of Experimental Sciences, University of Jaen, Jaen, Spain; Fundación MEDINA, Technology Park of Health Sciences, Granada, Spain.

Fundación MEDINA, Technology Park of Health Sciences, Granada, Spain.

出版信息

Biomed Pharmacother. 2024 Jan;170:116056. doi: 10.1016/j.biopha.2023.116056. Epub 2023 Dec 29.

Abstract

Duchenne muscular dystrophy (DMD) is a devastating degenerative disease of skeletal muscles caused by loss of dystrophin, a key protein that maintains muscle integrity, which leads to progressive muscle degeneration aggravated by chronic inflammation, muscle stem cells' (MuSCs) reduced regenerative capacity and replacement of muscle with fibroadipose tissue. Previous research has shown that pharmacological GSK-3β inhibition favors myogenic differentiation and plays an important role in modulating inflammatory processes. Isolecanoric acid (ILA) is a natural product isolated from a fungal culture displaying GSK-3β inhibitory properties. The present study aimed to investigate the proregenerative and anti-inflammatory properties of this natural compound in the DMD context. Our results showed that ILA markedly promotes myogenic differentiation of myoblasts by increasing β-Catenin signaling and boosting the myogenic potential of mouse and human stem cells. One important finding was that the GSK-3β/β-Catenin pathway is altered in dystrophic mice muscle and ILA enhances the myofiber formation of dystrophic MuSCs. Treatment with this natural compound improves muscle regeneration of dystrophic mice by, in turn, improving functional performance. Moreover, ILA ameliorates the inflammatory response in both muscle explants and the macrophages isolated from dystrophic mice to, thus, mitigate fibrosis after muscle damage. Overall, we show that ILA modulates both inflammation and muscle regeneration to, thus, contribute to improve the dystrophic phenotype.

摘要

杜氏肌营养不良症(DMD)是一种严重的肌肉退行性疾病,由肌营养不良蛋白的缺失引起,肌营养不良蛋白是一种维持肌肉完整性的关键蛋白,其缺失会导致肌肉进行性退化,慢性炎症加剧,肌肉干细胞(MuSCs)的再生能力降低,肌肉被纤维脂肪组织取代。先前的研究表明,药物抑制 GSK-3β 有利于肌生成分化,并在调节炎症过程中发挥重要作用。异亮氨酸(ILA)是一种从真菌培养物中分离出来的天然产物,具有 GSK-3β 抑制特性。本研究旨在探讨这种天然化合物在 DMD 背景下的促再生和抗炎特性。我们的研究结果表明,ILA 通过增加β-连环蛋白信号通路显著促进成肌细胞的肌生成分化,并增强小鼠和人类干细胞的成肌潜能。一个重要的发现是,GSK-3β/β-连环蛋白通路在营养不良小鼠的肌肉中发生改变,ILA 增强了营养不良 MuSCs 的肌纤维形成。这种天然化合物的治疗改善了营养不良小鼠的肌肉再生,从而提高了其功能表现。此外,ILA 改善了肌肉外植体和从营养不良小鼠中分离出的巨噬细胞中的炎症反应,从而减轻了肌肉损伤后的纤维化。总的来说,我们表明 ILA 调节炎症和肌肉再生,从而有助于改善营养不良表型。

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