Division of Plastic and Reconstructive Surgery, University of California San Francisco (UCSF).
Division of Plastic and Reconstructive Surgery, University of California San Francisco (UCSF);
J Vis Exp. 2024 May 31(207). doi: 10.3791/66450.
Craniofacial volumetric muscle loss (VML) injuries can occur as a result of severe trauma, surgical excision, inflammation, and congenital or other acquired conditions. Treatment of craniofacial VML involves surgical, functional muscle transfer. However, these procedures are unable to restore normal function, sensation, or expression, and more commonly, these conditions go untreated. Very little research has been conducted on skeletal muscle regeneration in animal models of craniofacial VML. This manuscript describes a rat model for the study of craniofacial VML injury and a protocol for the histological evaluation of biomaterials in the treatment of these injuries. Liquid hydrogel and freeze-dried scaffolds are applied at the time of surgical VML creation, and masseters are excised at terminal time points up to 12 weeks with high retention rates and negligible complications. Hematoxylin and eosin (HE), Masson's Trichrome, and immunohistochemical analysis are used to evaluate parameters of skeletal muscle regeneration as well as biocompatibility and immunomodulation. While we demonstrate the study of a hyaluronic-acid-based hydrogel, this model provides a means for evaluating subsequent iterations of materials in VML injuries.
颅面容积性肌肉损失 (VML) 损伤可由严重创伤、手术切除、炎症以及先天或其他获得性疾病引起。颅面 VML 的治疗包括手术、功能性肌肉转移。然而,这些方法无法恢复正常的功能、感觉或表情,而且这些情况更常见于未治疗的情况。在颅面 VML 动物模型中,针对骨骼肌肉再生的研究很少。本文描述了一种用于研究颅面 VML 损伤的大鼠模型,以及一种用于评估生物材料治疗这些损伤的组织学评估方案。在手术 VML 形成时应用液态水凝胶和冻干支架,并在高达 12 周的时间内切除咬肌,保留率高,并发症可忽略不计。苏木精和伊红 (HE)、马松三色染色和免疫组织化学分析用于评估骨骼肌肉再生以及生物相容性和免疫调节的参数。虽然我们展示了对基于透明质酸的水凝胶的研究,但该模型为评估 VML 损伤中后续材料的迭代提供了一种方法。