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臭氧疗法对大鼠肩周炎的治疗效果:一项实验研究。

Efficacy of ozone therapy in the treatment of frozen shoulder in rats: An experimental study.

作者信息

Kaya Simsek Ekin, Turkbey Simsek Duygu, Ayan Deniz Mert, Araz Coskun, Haberal Bahtiyar

机构信息

Başkent Üniversitesi Tıp Fakültesi Ortopedi ve Travmatoloji Anabilim Dalı, 06490, Bahçelievler, Ankara, Türkiye.

出版信息

Jt Dis Relat Surg. 2025 Jan 20;36(2):272-282. doi: 10.52312/jdrs.2025.2055.

DOI:10.52312/jdrs.2025.2055
PMID:40235405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12086470/
Abstract

OBJECTIVES

This study aims to explore the therapeutic effects of medical ozone therapy on the frozen shoulder (FS) model and compares it with traditional corticosteroid treatments in rats.

MATERIALS AND METHODS

A total of 30 Sprague-Dawley rats aged 18 to 20 months weighing between 400 to 450 g were included in the study. The rats were randomly divided into three equal groups: a control group (C, n=10, FS model only), a corticosteroid treatment group (CST, n=10, FS model + intraarticular 0.5 mg/kg betamethasone), and an ozone treatment group (OT, n=10, FS model + intraarticular 1 mg/kg ozone). Frozen shoulder was induced via surgical immobilization, and treatments were administered intraarticularly. Outcomes were measured through histopathological and functional assessments.

RESULTS

The CST and OT significantly reduced inflammation (p<0.001), capillary proliferation (p<0.001), fibroblastic proliferation (p=0.002), collagen type 3 staining (p=0.022), and mean capsular thickness (p<0.001), while improving the range of motion in all directions compared to the control group. Ozone therapy showed a comparable reduction in fibrosis and improvement in joint mobility to CST (p=0.001).

CONCLUSION

Ozone therapy effectively reduces fibrosis and improves mobility in an FS rat model, presenting a promising alternative to corticosteroids. However, further studies are still needed to elucidate the molecular mechanisms and optimize treatment protocols, underscoring the potential for future discoveries in this area.

摘要

目的

本研究旨在探讨医用臭氧疗法对大鼠肩周炎(FS)模型的治疗效果,并与传统皮质类固醇治疗进行比较。

材料与方法

本研究共纳入30只18至20个月大、体重400至450克的Sprague-Dawley大鼠。将大鼠随机分为三组,每组10只:对照组(C组,仅建立FS模型)、皮质类固醇治疗组(CST组,建立FS模型+关节内注射0.5毫克/千克倍他米松)和臭氧治疗组(OT组,建立FS模型+关节内注射1毫克/千克臭氧)。通过手术固定诱导肩周炎,并进行关节内给药。通过组织病理学和功能评估来测量结果。

结果

与对照组相比,CST组和OT组显著减轻了炎症(p<0.001)、毛细血管增生(p<0.001)、成纤维细胞增生(p=0.002)、Ⅲ型胶原染色(p=0.022)以及平均关节囊厚度(p<0.001),同时改善了各个方向的活动范围。臭氧疗法在纤维化减轻和关节活动度改善方面与CST组相当(p=0.001)。

结论

臭氧疗法能有效减轻FS大鼠模型的纤维化并改善活动度,是皮质类固醇的一种有前景的替代方法。然而,仍需进一步研究以阐明分子机制并优化治疗方案,这突出了该领域未来发现的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/78dfddae450b/JDRS-2025-36-2-272-282-F8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/704fec810bc7/JDRS-2025-36-2-272-282-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/6d65c2334bf0/JDRS-2025-36-2-272-282-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/ec87246d0628/JDRS-2025-36-2-272-282-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/8f8eb8a1308e/JDRS-2025-36-2-272-282-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/3f92ed862455/JDRS-2025-36-2-272-282-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/648964dcf13f/JDRS-2025-36-2-272-282-F6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/9026535d2b8d/JDRS-2025-36-2-272-282-F7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/78dfddae450b/JDRS-2025-36-2-272-282-F8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/704fec810bc7/JDRS-2025-36-2-272-282-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/6d65c2334bf0/JDRS-2025-36-2-272-282-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/ec87246d0628/JDRS-2025-36-2-272-282-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/8f8eb8a1308e/JDRS-2025-36-2-272-282-F4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/3f92ed862455/JDRS-2025-36-2-272-282-F5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/648964dcf13f/JDRS-2025-36-2-272-282-F6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/9026535d2b8d/JDRS-2025-36-2-272-282-F7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d05/12086470/78dfddae450b/JDRS-2025-36-2-272-282-F8.jpg

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