Ezetimibe/Atorvastatin, a Treatment for Hyperlipidemia, Inhibits Supraspinatus Fatty Infiltration and Improves Bone-Tendon Interface Healing in a Rotator Cuff Tear Rat Model

肩袖 阿托伐他汀 医学 肌肉萎缩 肌腱 热情 高脂血症 免疫组织化学 萎缩 泌尿科 外科 内科学 内分泌学 糖尿病
作者
Jong Pil Yoon,S.-H. Park,Dong Hyun Kim,Yun Choi,Hyun‐Joo Lee,Eugene J. Park,Chul‐Hyun Cho,Seok Won Chung
出处
期刊:American Journal of Sports Medicine [SAGE Publishing]
卷期号:53 (1): 80-89 被引量:1
标识
DOI:10.1177/03635465241299408
摘要

Background: Multiple factors, such as muscle fatty infiltration (FI), tendon collagen content, and collagen arrangement, determine bone-tendon interface (BTI) healing after rotator cuff (RC) repair. Purpose: To evaluate the effects of systemic administration of ezetimibe-atorvastatin (EZE/ATZ) combination on muscle FI and tendon collagen density and arrangement in an RC repair rat model. Study design: Controlled laboratory study. Methods: A total of 26 male Sprague-Dawley rats were randomly divided equally into control and EZE/ATZ groups and subjected to RC tendon repair surgery. Postoperatively, the EZE/ATZ group rats received a combination of EZE (10 mg/kg/d) and ATZ (20 mg/kg/d) for 4 weeks, after which they were sacrificed. Oil Red O staining was used to assess FI in the supraspinatus muscle. The expression of biomarkers related to muscle atrophy and FI was measured using quantitative real-time polymerase chain reaction. For the qualitative and quantitative analysis of FI-related biomarkers, immunohistochemical staining was performed. Biomechanical and histological analyses were performed to evaluate the quality of BTI healing after RC repair. Results: The EZE/ATZ group showed significantly lower FI compared with the control group ( P < .001) and significantly downregulated expression of gene markers related to muscle atrophy and FI. On histological analysis, the EZE/ATZ group exhibited increased collagen type I contents, consistent collagen arrangement ( P = .005), and significantly higher collagen density ( P = .003) compared with the control group. Biomechanical analysis of the BTI healing revealed that the EZE/ATZ group had significantly increased ultimate strength ( P = .006) compared with the control group. Conclusion: Systemic EZE/ATZ administration suppressed supraspinatus FI by downregulating muscle atrophy–related and FI-related genes after RC repair. Additionally, EZE/ATZ use improved collagen biosynthesis, density, and arrangement at the BTI and significantly increased tensile strength. Clinical Relevance: The results of the current study strongly advocate the use of EZE/ATZ to improve shoulder function and tendon healing after RC repair.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
3秒前
lixiaolu发布了新的文献求助10
4秒前
hkh发布了新的文献求助10
4秒前
星辰大海应助企鹅采纳,获得10
4秒前
4秒前
5秒前
5秒前
ayn完成签到,获得积分20
6秒前
6秒前
LLM发布了新的文献求助10
6秒前
7秒前
慕青应助肉球球采纳,获得10
7秒前
cheng完成签到,获得积分20
8秒前
8秒前
9秒前
10秒前
cheng发布了新的文献求助10
11秒前
11秒前
11秒前
芭娜55完成签到 ,获得积分10
12秒前
realssr发布了新的文献求助10
13秒前
14秒前
14秒前
15秒前
科研通AI5应助LLM采纳,获得10
15秒前
务实紫发布了新的文献求助10
16秒前
16秒前
17秒前
沉静缘分发布了新的文献求助10
17秒前
科研通AI5应助吴祥坤采纳,获得10
19秒前
深情安青应助温柔的中蓝采纳,获得10
19秒前
李健应助kui采纳,获得10
20秒前
韩冬梅发布了新的文献求助10
20秒前
zm发布了新的文献求助20
20秒前
睡教早祈两年半完成签到,获得积分10
20秒前
20秒前
香蕉觅云应助realssr采纳,获得10
22秒前
22秒前
thomas发布了新的文献求助10
22秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Encyclopedia of Geology (2nd Edition) 2000
CRC Handbook of Chemistry and Physics 104th edition 1000
Izeltabart tapatansine - AdisInsight 600
An International System for Human Cytogenomic Nomenclature (2024) 500
Introduction to Comparative Public Administration Administrative Systems and Reforms in Europe, Third Edition 3rd edition 500
Distinct Aggregation Behaviors and Rheological Responses of Two Terminally Functionalized Polyisoprenes with Different Quadruple Hydrogen Bonding Motifs 450
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3765628
求助须知:如何正确求助?哪些是违规求助? 3310177
关于积分的说明 10153699
捐赠科研通 3025484
什么是DOI,文献DOI怎么找? 1660517
邀请新用户注册赠送积分活动 793415
科研通“疑难数据库(出版商)”最低求助积分说明 755616