Epigallocatechin-3-Gallate (EGCG)-Loaded Hyaluronic Acid Hydrogel Seems to Be Effective in a Rat Model of Collagenase-Induced Achilles Tendinopathy.

IF 5.2 3区 医学 Q1 ENGINEERING, BIOMEDICAL Journal of Functional Biomaterials Pub Date : 2025-02-10 DOI:10.3390/jfb16020055
Hwa Jun Kang, Sivakumar Allur Subramanian, Si Young Song, Jihyun Hwang, Collin Lee, Sung Jae Kim
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Abstract

Tendon injuries account for 45% of musculoskeletal injuries. However, research on the occurrence and pathogenesis of tendinopathy is insufficient, and there is still much debate regarding treatment methods. It is important to understand the molecular mechanisms of oxidative stress and inflammatory responses because oxidative stress in tendon tissue is induced by various factors, including inflammatory cytokines, drug exposure, and metabolic abnormalities. In this study, 28 rats were divided into four groups (7 rats assigned to each group): control group (CON), collagenase injection group (CL), collagenase injection and hyaluronic acid injection group (CL + HA), and collagenase injection and EGCG-loaded hyaluronic acid injection group (CL + HA + EGCG). Seven weeks after the start of the study, all rats underwent histochemical analysis, immunofluorescence staining, and Western blot. The results showed increased inflammatory cells, disarray of collagen matrix, and degradation of the collagen matrix in the CL group. However, in the EGCG-treated group, there was a significant increase in type I collagen expression and a significant decrease in type III collagen expression, compared to the CL group. Additionally, there was an increase in the expression of antioxidant markers SOD (Superoxide Dismutase) and CAT (Catalase), tenogenic markers COLL-1 (collagen type I), and SCX (Scleraxis), and a downregulated expression of apoptosis markers cas-3 and cas-7. Our findings suggest that EGCG-loaded hyaluronic acid hydrogel exhibits potential in preventing tendon damage and promoting the regeneration process in a rat model of Achilles tendinopathy. The insights gained from our histological and molecular investigations highlight the future potential for testing novel tendinopathy treatments in human subjects.

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表没食子儿茶素-3-棓酸盐(EGCG)负载透明质酸水凝胶似乎对胶原酶诱发的跟腱病大鼠模型有效。
肌腱损伤占肌肉骨骼损伤的45%。然而,对腱鞘病的发生、发病机制的研究还很不足,治疗方法也存在很大争议。了解氧化应激和炎症反应的分子机制是很重要的,因为肌腱组织中的氧化应激是由多种因素引起的,包括炎症细胞因子、药物暴露和代谢异常。本研究将28只大鼠分为4组(每组7只):对照组(CON)、胶原酶注射组(CL)、胶原酶注射加透明质酸注射组(CL + HA)、胶原酶注射加透明质酸注射组(CL + HA + EGCG)。研究开始7周后,所有大鼠进行组织化学分析、免疫荧光染色和Western blot。结果显示CL组炎症细胞增多,胶原基质紊乱,胶原基质降解。然而,在egcg处理组中,与CL组相比,I型胶原蛋白表达显著增加,III型胶原蛋白表达显著降低。此外,抗氧化标志物SOD(超氧化物歧化酶)和CAT(过氧化氢酶)、肌腱生成标志物col -1 (I型胶原)和SCX(硬化剂)的表达增加,凋亡标志物cas3和cas7的表达下调。我们的研究结果表明,在大鼠跟腱病模型中,含有egcg的透明质酸水凝胶具有预防跟腱损伤和促进跟腱再生的潜力。从我们的组织学和分子研究中获得的见解强调了在人类受试者中测试新型肌腱病变治疗的未来潜力。
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来源期刊
Journal of Functional Biomaterials
Journal of Functional Biomaterials Engineering-Biomedical Engineering
CiteScore
4.60
自引率
4.20%
发文量
226
审稿时长
11 weeks
期刊介绍: Journal of Functional Biomaterials (JFB, ISSN 2079-4983) is an international and interdisciplinary scientific journal that publishes regular research papers (articles), reviews and short communications about applications of materials for biomedical use. JFB covers subjects from chemistry, pharmacy, biology, physics over to engineering. The journal focuses on the preparation, performance and use of functional biomaterials in biomedical devices and their behaviour in physiological environments. Our aim is to encourage scientists to publish their results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Several topical special issues will be published. Scope: adhesion, adsorption, biocompatibility, biohybrid materials, bio-inert materials, biomaterials, biomedical devices, biomimetic materials, bone repair, cardiovascular devices, ceramics, composite materials, dental implants, dental materials, drug delivery systems, functional biopolymers, glasses, hyper branched polymers, molecularly imprinted polymers (MIPs), nanomedicine, nanoparticles, nanotechnology, natural materials, self-assembly smart materials, stimuli responsive materials, surface modification, tissue devices, tissue engineering, tissue-derived materials, urological devices.
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