Reinkemeier Felix, Wallner Christoph, Drysch Marius, Schmidt Sonja Verena, Puscz Flemming, Steubing Yonca, Bakri Ali, Theiss Carsten, Lehnhardt Marcus, Behr Bjoörn, Wagner Johannes Maximilian
Department of Plastic Surgery and Hand Surgery, BG-University Hospital Bergmannsheil, Bochum, Germany.
Department of Cytology, Institute for Anatomy, Ruhr-University Bochum, Bochum, Germany.
PLoS One. 2025 Sep 16;20(9):e0332067. doi: 10.1371/journal.pone.0332067. eCollection 2025.
Posttraumatic lymphedema is a common complication after open and closed fractures with soft tissue trauma. Even though there is quite certain consensus about the basic mechanisms of lymphedema formation, the pathophysiology on a cellular and molecular base is largely unknown. Furthermore, there is currently no data on the interaction of lymphedema and bone regeneration. Subsequently, the aim of this study was to establish an animal model specific to posttraumatic lymphedema, which can be used to conduct future investigations into the pathophysiology and bone regeneration in lymphedema.
The test animals (rats)In wild-type Fisher 344 rats were divided into three groups: group one had an isolated bone defect, group two had an isolated soft tissue defect, and group three had a combination of bone and soft tissue trauma.
Using volumetric and circumferential measurements, a significant increase in circumference and volume in the sense of lymphedema could be detected, particularly 3-4 weeks after trauma in the groups with soft tissue trauma, whereas the creation of a bony defect did not appear to have a significant influence on the swelling. Microscopic images of the lymphatic drainage pathways verified the lymphatic drainage disorder weeks after soft tissue trauma.
Consequently, the established model can be used to investigate the exact pathophysiology of post-traumatic lymphedema. Furthermore, it seems to be suitable as a model for investigating bone regeneration in manifest lymphedema.
创伤后淋巴水肿是开放性和闭合性骨折合并软组织损伤后的常见并发症。尽管关于淋巴水肿形成的基本机制已达成相当一致的共识,但细胞和分子层面的病理生理学在很大程度上仍不清楚。此外,目前尚无关于淋巴水肿与骨再生相互作用的数据。因此,本研究的目的是建立一种创伤后淋巴水肿特异性动物模型,可用于未来对淋巴水肿病理生理学和骨再生的研究。
将野生型费希尔344大鼠作为实验动物,分为三组:第一组有孤立性骨缺损,第二组有孤立性软组织缺损,第三组有骨和软组织联合创伤。
通过体积和周径测量,可检测到淋巴水肿意义上的周径和体积显著增加,特别是在软组织创伤组创伤后3 - 4周,而骨缺损的形成似乎对肿胀没有显著影响。软组织创伤数周后,淋巴引流途径的微观图像证实了淋巴引流障碍。
因此,所建立的模型可用于研究创伤后淋巴水肿的确切病理生理学。此外,它似乎适合作为研究明显淋巴水肿中骨再生的模型。