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地塞米松治疗通过改变愈合过程的分辨率和对肌腱细胞的直接作用来影响肌腱愈合。

Dexamethasone treatment influences tendon healing through altered resolution and a direct effect on tendon cells.

机构信息

Department of Biomedical and Clinical Sciences, Faculty of Medicine and Health Science, Linköping University, 581 83, Linköping, Sweden.

Division of Immunology, Department of Pathology, University of Cambridge, Cambridge, UK.

出版信息

Sci Rep. 2024 Jul 3;14(1):15304. doi: 10.1038/s41598-024-66038-5.

Abstract

Inflammation, corticosteroids, and loading all affect tendon healing, with an interaction between them. However, underlying mechanisms behind the effect of corticosteroids and the interaction with loading remain unclear. The aim of this study was to investigate the role of dexamethasone during tendon healing, including specific effects on tendon cells. Rats (n = 36) were randomized to heavy loading or mild loading, the Achilles tendon was transected, and animals were treated with dexamethasone or saline. Gene and protein analyses of the healing tendon were performed for extracellular matrix-, inflammation-, and tendon cell markers. We further tested specific effects of dexamethasone on tendon cells in vitro. Dexamethasone increased mRNA levels of S100A4 and decreased levels of ACTA2/α-SMA, irrespective of load level. Heavy loading + dexamethasone reduced mRNA levels of FN1 and TenC (p < 0.05), while resolution-related genes were unaltered (p > 0.05). In contrast, mild loading + dexamethasone increased mRNA levels of resolution-related genes ANXA1, MRC1, PDPN, and PTGES (p < 0.03). Altered protein levels were confirmed in tendons with mild loading. Dexamethasone treatment in vitro prevented tendon construct formation, increased mRNA levels of S100A4 and decreased levels of SCX and collagens. Dexamethasone during tendon healing appears to act through immunomodulation by promoting resolution, but also through an effect on tendon cells.

摘要

炎症、皮质类固醇和负荷都会影响肌腱愈合,并相互作用。然而,皮质类固醇的作用和与负荷相互作用的潜在机制仍不清楚。本研究旨在探讨地塞米松在肌腱愈合过程中的作用,包括对肌腱细胞的特定影响。将大鼠(n=36)随机分为重负荷或轻负荷组,切断跟腱,并给予地塞米松或生理盐水治疗。对愈合肌腱的细胞外基质、炎症和肌腱细胞标志物进行基因和蛋白分析。我们进一步在体外测试地塞米松对肌腱细胞的特定影响。无论负荷水平如何,地塞米松均增加 S100A4 的 mRNA 水平并降低 ACTA2/α-SMA 的水平。重负荷+地塞米松降低 FN1 和 TenC 的 mRNA 水平(p<0.05),而与组织修复相关的基因则不变(p>0.05)。相比之下,轻负荷+地塞米松增加了与组织修复相关的基因 ANXA1、MRC1、PDPN 和 PTGES 的 mRNA 水平(p<0.03)。轻度负荷的肌腱中证实了改变的蛋白水平。体外地塞米松处理可防止肌腱构建体的形成,增加 S100A4 的 mRNA 水平,并降低 SCX 和胶原蛋白的水平。地塞米松在肌腱愈合过程中的作用似乎是通过促进组织修复的免疫调节作用,同时也通过对肌腱细胞的作用来实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5236/11222440/77dfe1aee6bb/41598_2024_66038_Fig1_HTML.jpg

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