Effect of prostaglandin E2 injection on the structural properties of the rat patellar tendon.

Scott T Ferry, Hessam M Afshari, Justin A Lee, Laurence E Dahners, Paul S Weinhold
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引用次数: 28

Abstract

Background: Increased tendon production of the inflammatory mediator prostaglandin E2 (PGE2) has been suggested to be a potential etiologic agent in the development of tendinopathy. Repeated injection of PGE2 into tendon has been proposed as a potential animal model for studying treatments for tendinopathy. In contrast, nonsteroidal anti-inflammatory drugs (NSAIDs) which inhibit PGE2 production and are commonly prescribed in treating tendinopathy have been shown to impair the healing of tendon after acute injury in animal models. The contradictory literature suggests the need to better define the functional effects of PGE2 on tendon. Our objective was to characterize the effects of PGE2 injection on the biomechanical and biochemical properties of tendon and the activity of the animals. Our hypothesis was that weekly PGE2 injection to the rat patellar tendon would lead to inferior biomechanical properties.

Methods: Forty rats were divided equally into four groups. Three groups were followed for 4 weeks with the following peritendinous injection procedures: No injection (control), 4 weekly injections of saline (saline), 4 weekly injections of 800 ng PGE2 (PGE2-4 wks). The fourth group received 4 weekly injections of 800 ng PGE2 initially and was followed for a total of 8 weeks. All animals were injected bilaterally. The main outcome measurements included: the structural and material properties of the patellar tendon under tensile loading to failure, tendon collagen content, and weekly animal activity scores.

Results: The ultimate load of PGE2-4 wks tendons at 4 weeks was significantly greater than control or saline group tendons. The stiffness and elastic modulus of the PGE2 injected tendons at 8 weeks was significantly greater than the control or saline tendons. No differences in animal activity, collagen content, or mean fibril diameter were observed between groups.

Conclusions: Four weekly peritendinous injections of PGE2 to the rat patellar tendon were not found to be an effective model of clinical tendinopathy. In contrast, improved structural and material properties of the patellar tendon were found after PGE2 injection. While PGE2 has been thought to have a contributory role in the development of tendinopathy and anti-inflammatory medications remain a common treatment, our results suggest a positive role of PGE2 in tendon remodeling in some circumstances.

Abstract Image

Abstract Image

Abstract Image

前列腺素E2注射对大鼠髌骨肌腱结构特性的影响。
背景:炎症介质前列腺素E2 (PGE2)的肌腱生成增加已被认为是肌腱病变发展的潜在病因。肌腱内重复注射PGE2已被提出作为研究肌腱病变治疗方法的潜在动物模型。相反,非甾体类抗炎药(NSAIDs)抑制PGE2的产生,通常用于治疗肌腱病变,在动物模型中已被证明会损害急性损伤后肌腱的愈合。相互矛盾的文献提示需要更好地定义PGE2对肌腱的功能影响。我们的目的是表征PGE2注射对肌腱生物力学和生化特性以及动物活动的影响。我们的假设是,每周向大鼠髌骨肌腱注射PGE2会导致生物力学性能下降。方法:40只大鼠随机分为4组。三组小鼠连续4周接受腹膜周围注射:不注射(对照组)、每周注射生理盐水(生理盐水)4次、每周注射800 ng PGE2 (PGE2-4周)。第4组小鼠最初每周注射800 ng PGE2,随访8周。所有动物均双侧注射。主要结果测量包括:拉伸载荷下髌骨肌腱的结构和材料特性、肌腱胶原含量和每周动物活动评分。结果:pge2 ~ 4周时,pge2 ~ 4周肌腱的极限负荷明显大于对照组和生理盐水组。PGE2注射肌腱的刚度和弹性模量在8周时明显大于对照或生理盐水肌腱。各组之间的动物活性、胶原含量或平均纤维直径均无差异。结论:每周4次髌腱周注射PGE2并不是临床肌腱病变的有效模型。相比之下,PGE2注射后髌腱的结构和材料性能得到改善。虽然PGE2一直被认为在肌腱病变的发展中起着重要作用,抗炎药物仍然是一种常见的治疗方法,但我们的研究结果表明,在某些情况下,PGE2在肌腱重塑中发挥了积极作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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