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西地那非,一种磷酸二酯酶-5 抑制剂,可刺激小鼠萎缩性骨不连模型中的血管生成和骨再生。

Sildenafil, a phosphodiesterase-5 inhibitor, stimulates angiogenesis and bone regeneration in an atrophic non-union model in mice.

机构信息

Department of Trauma and Reconstructive Surgery, Eberhard Karls University Tuebingen, BG Trauma Center Tuebingen, 72076, Tuebingen, Germany.

Institute for Clinical and Experimental Surgery, Saarland University, 66421, Homburg, Saar, Germany.

出版信息

J Transl Med. 2023 Sep 8;21(1):607. doi: 10.1186/s12967-023-04441-8.

Abstract

Non-union formation represents a major complication in trauma and orthopedic surgery. The phosphodiesterase-5 (PDE-5) inhibitor sildenafil has been shown to exert pro-angiogenic and pro-osteogenic effects in vitro and in vivo. Therefore, the aim of the present study was to analyze the impact of sildenafil in an atrophic non-union model in mice. After creation of a 1.8 mm segmental defect, mice femora were stabilized by pin-clip fixation. Bone regeneration was analyzed by means of X-ray, biomechanics, photoacoustic and micro-computed tomography (µCT) imaging as well as histological, immunohistochemical and Western blot analyses at 2, 5 and 10 weeks after surgery. The animals were treated daily with either 5 mg/kg body weight sildenafil (n = 35) or saline (control; n = 35) per os. Bone formation was markedly improved in defects of sildenafil-treated mice when compared to controls. This was associated with a higher bending stiffness as well as an increased number of CD31-positive microvessels and a higher oxygen saturation within the callus tissue. Moreover, the bone defects of sildenafil-treated animals contained more tartrate-resistant acid phosphatase (TRAP)-positive osteoclasts and CD68-positive macrophages and exhibited a higher expression of the pro-angiogenic and pro-osteogenic markers cysteine rich protein (CYR)61 and vascular endothelial growth factor (VEGF) when compared to controls. These findings demonstrate that sildenafil acts as a potent stimulator of angiogenesis and bone regeneration in atrophic non-unions.

摘要

非愈合形成是创伤和骨科手术中的主要并发症。磷酸二酯酶-5(PDE-5)抑制剂西地那非已被证明在体外和体内具有促血管生成和促成骨作用。因此,本研究旨在分析西地那非在小鼠萎缩性骨不连模型中的影响。在创建 1.8mm 节段性缺损后,通过钉夹固定稳定小鼠股骨。通过 X 射线、生物力学、光声和微计算机断层扫描(µCT)成像以及手术后 2、5 和 10 周的组织学、免疫组织化学和 Western blot 分析来分析骨再生。动物每天通过口服 5mg/kg 体重的西地那非(n=35)或生理盐水(对照组;n=35)进行治疗。与对照组相比,西地那非治疗小鼠的骨缺损中的骨形成明显改善。这与更高的弯曲刚度以及在骨痂组织中更高数量的 CD31 阳性微血管和更高的氧饱和度相关。此外,与对照组相比,西地那非治疗动物的骨缺损含有更多的抗酒石酸酸性磷酸酶(TRAP)阳性破骨细胞和 CD68 阳性巨噬细胞,并表现出更高的促血管生成和促成骨标志物半胱氨酸丰富蛋白(CYR)61 和血管内皮生长因子(VEGF)的表达。这些发现表明西地那非作为萎缩性骨不连中血管生成和骨再生的有效刺激物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eda6/10486066/cf85f0197289/12967_2023_4441_Fig1_HTML.jpg

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