Experimental Lung Transplant Unit of the Department of Experimental Surgery, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas, Mexico City, Mexico.
Division of Pulmonary, Critical and Sleep Medicine, Department of Internal Medicine, Davis Heart and Lun Research Institute, Ohio State University, Columbus, Ohio, USA.
J Invest Surg. 2022 Jul;35(7):1551-1561. doi: 10.1080/08941939.2022.2081388. Epub 2022 Jun 1.
Tracheal stenosis (TS) is a complication of prolonged intubation, tracheotomy, and tracheal surgery that compromises the vascular supply. Animal models are essential for studying its pathophysiology and the effect of interventions.
To establish a TS model in rats secondary to tracheal autotransplantation with a graft submerged in bleomycin (Atx-Bleo). Additionally, to evaluate the clinical and histological changes, as well as the expression of newly formed collagen (NFC), isoforms of transforming growth factor beta (TGFβ), fibronectin (FN), elastin (ELN), integrin β1 (ITGβ1), and matrix metalloproteinase 1 (MMP1) in TS.
Twenty Wistar rats were divided into three groups: group I (n = 20) control; group II (n = 10) end-to-end anastomosis of the trachea (tracheoplasty); and group III (n = 10) Atx-Bleo. The animals were evaluated clinically, tomographically, macroscopically, morphometrically, and microscopically. NFC deposition, and the expression of profibrotic and antifibrotic proteins were evaluated in tracheal scars.
All animals survived the surgical procedure and the study period. Compared with the other study groups, the Atx-Bleo group developed TS and fibrosis, exhibited higher expression of NFC, TGFβ1, TGFβ2, FN, ELN, and ITGβ1, and mild expression of TGFβ3 and MMP1 (p < 0.005; analysis of variance, Dunnett and Tukey tests).
Atx-Bleo in TS model rats produces tomographic and histological changes, and induces the upregulation of profibrotic proteins (TGFβ1, TGFβ2, collagen, FN, ELN, ITGβ1) and downregulation of antifibrotic proteins (TGFβ3, MMP1). Therefore, this model may be used to test new pharmacological treatments for reversing or preventing TS, and conduct basic studies regarding its pathophysiology.
气管狭窄(TS)是长期插管、气管切开和气管手术导致血管供应受损的并发症。动物模型对于研究其病理生理学和干预措施的效果至关重要。
通过气管自体移植,使移植物浸泡在博来霉素(Atx-Bleo)中,建立大鼠 TS 模型。此外,评估临床和组织学变化,以及新形成的胶原蛋白(NFC)、转化生长因子β(TGFβ)同工型、纤维连接蛋白(FN)、弹性蛋白(ELN)、整合素β1(ITGβ1)和基质金属蛋白酶 1(MMP1)在 TS 中的表达。
将 20 只 Wistar 大鼠分为三组:I 组(n=20)对照组;II 组(n=10)气管端端吻合术(气管成形术);III 组(n=10)Atx-Bleo。对动物进行临床、影像学、大体、形态学和显微镜评估。评估气管瘢痕中 NFC 沉积和促纤维化和抗纤维化蛋白的表达。
所有动物均存活至手术和研究期结束。与其他研究组相比,Atx-Bleo 组发展为 TS 和纤维化,表现出更高的 NFC、TGFβ1、TGFβ2、FN、ELN 和 ITGβ1 表达,以及轻度表达的 TGFβ3 和 MMP1(p<0.005;方差分析、Dunnett 和 Tukey 检验)。
Atx-Bleo 在 TS 模型大鼠中引起影像学和组织学变化,并诱导促纤维化蛋白(TGFβ1、TGFβ2、胶原蛋白、FN、ELN、ITGβ1)上调和抗纤维化蛋白(TGFβ3、MMP1)下调。因此,该模型可用于测试逆转或预防 TS 的新药物治疗,并进行关于其病理生理学的基础研究。