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Addition of Nitric Oxide Through Nitric Oxide-paracetamol Enhances Healing Rat Achilles Tendon

机译:通过一氧化氮-扑热息痛添加一氧化氮可增强大鼠跟腱腱的愈合

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摘要

Nitric oxide is an important messenger molecule in many physiological processes. The addition of NO via NO-flurbiprofen enhances the material properties of healing tendon, however, flurbiprofen has a detrimental effect on healing. We asked if NO delivered by a cyclooxygenase 3 inhibitor (paracetamol/acetaminophen) would enhance healing in a rat Achilles tendon healing model. Rats were injected subcutaneously daily with NO-paracetamol, paracetamol or vehicle from two days before surgery to the day of tissue harvesting. Paracetamol had no effect on tendon healing compared with vehicle alone. NO-paracetamol did not change the failure load, but did decrease the water content, enhance the collagen content, reduce the cross-sectional area and improve the ultimate stress of healing tendon compared with paracetamol and vehicle. The collagen organization of the healing tendon in the NO-paracetamol group, as determined by polarized light microscopy, was enhanced. Our data suggests NO-paracetamol increases the total collagen content and enhances organization while decreasing the cross-sectional area of healing rat Achilles tendon and is consistent with human clinical trials where NO has improved the symptoms and signs of tendinopathy.
机译:一氧化氮是许多生理过程中的重要信使分子。通过NO-氟比洛芬添加NO可以增强愈合肌腱的物质特性,但是氟比洛芬对愈合有不利影响。我们询问环氧化酶3抑制剂(扑热息痛/对乙酰氨基酚)传递的NO是否会增强大鼠跟腱愈合模型中的愈合。从手术前两天到组织收集的当天,每天向大鼠皮下注射NO-对乙酰氨基酚,扑热息痛或溶媒。与单独使用赋形剂相比,扑热息痛对肌腱的愈合没有影响。与扑热息痛和赋形剂相比,NO-扑热息痛没有改变破坏负荷,但确实降低了水分含量,增加了胶原蛋白含量,减小了横截面积,并改善了愈合肌腱的最终应力。通过偏光显微镜观察,NO-扑热息痛组的愈合肌腱胶原组织得到增强。我们的数据表明,NO-扑热息痛增加了总胶原蛋白含量并增强了组织,同时减小了愈合的大鼠跟腱的横截面积,并且与人体临床试验一致,在该试验中,NO改善了肌腱病的症状和体征。

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