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

Jong Pil Yoon, Sung-Jin Park, Dong-Hyun Kim, Yoon Seong Choi, Hyun Joo Lee, Eugene Jae Jin Park, Chul-Hyun Cho, Seok Won Chung
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Abstract

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.
Ezetimibe/阿托伐他汀治疗高脂血症,抑制棘上肌脂肪浸润,促进大鼠肩袖撕裂模型骨-肌腱界面愈合
背景:肌肉脂肪浸润(FI)、肌腱胶原蛋白含量和胶原蛋白排列等多种因素决定了肩袖(RC)修复后骨-肌腱界面(BTI)的愈合。目的:评价全身给药依替米比-阿托伐他汀(EZE/ATZ)对RC修复大鼠肌肉FI和肌腱胶原密度及排列的影响。研究设计:实验室对照研究。方法:选取雄性Sprague-Dawley大鼠26只,随机分为对照组和EZE/ATZ组,行RC肌腱修复术。术后,EZE/ATZ组大鼠给予EZE (10 mg/kg/d)和ATZ (20 mg/kg/d)联合治疗4周,然后处死。油红O染色评价冈上肌FI。采用实时定量聚合酶链反应测定与肌肉萎缩和FI相关的生物标志物的表达。免疫组织化学染色对fi相关生物标志物进行定性和定量分析。通过生物力学和组织学分析来评估RC修复后BTI的愈合质量。结果:EZE/ATZ组FI明显低于对照组(P <;.001),肌肉萎缩和FI相关基因标记的表达显著下调。组织学分析显示,与对照组相比,EZE/ATZ组I型胶原含量增加,胶原排列一致(P = 0.005),胶原密度显著提高(P = 0.003)。BTI愈合的生物力学分析显示,与对照组相比,EZE/ATZ组的极限强度显著增加(P = 0.006)。结论:系统给药EZE/ATZ通过下调肌萎缩相关基因和FI相关基因抑制冈上肌修复后的FI。此外,EZE/ATZ改善了胶原蛋白的生物合成、密度和BTI的排列,显著提高了抗拉强度。临床意义:本研究结果强烈提倡使用EZE/ATZ来改善RC修复后的肩功能和肌腱愈合。
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