Allen Jacqueline
Department of Surgery University of Auckland Auckland New Zealand.
Laryngoscope Investig Otolaryngol. 2021 Jun 10;6(4):786-793. doi: 10.1002/lio2.602. eCollection 2021 Aug.
To evaluate antifibrotic effects of corticosteroids and halofuginone, a small molecule inhibitor of Smad3, in an ovine model of vocal fold (VF) injury.
Thirty sheep, using a paired study design, underwent controlled right VF injury by biopsy and then were treated with either no treatment, oral dexamethasone, intralesional triamcinolone, or oral halofuginone. Larynges were evaluated for histological evidence of fibrosis, immunohistochemical presence of Smad3, and vibratory parameters. Outcomes were compared across treatment groups.
Following injury, VF collagen density decreased in both halofuginone-treated and dexamethasone-treated sheep but not in triamcinolone treated sheep. A significant difference was noted between halofuginone and triamcinolone treated sheep (27.8% vs 37%, = .017). Elastin was preserved postinjury by halofuginone treatment in contrast with all steroid treated animals where significant loss of elastin was noted ( <.05). Smad3 staining was up-regulated at all injury sites compared to normal left VFs however halofuginone and dexamethasone treatment reduced Smad3 activity significantly whereas triamcinolone treatment did not ( <.05). Ex-vivo stroboscopic evaluation demonstrated mucosal wave in all excised larynges with a normalized glottal gap less than 3, suggesting adequate glottal closure.
VF injury in an ovine model results in a wound response able to be modified by Smad3 inhibitor, halofuginone, with benefit to vibratory function. Halofuginone treated sheep demonstrated reduced collagenization of lamina propria with greater elastin density after injury, than sheep treated with either steroid medication. These data support this pathway as a suitable target for manipulation to prevent or reverse fibrosis in the glottis and restore voice quality.Level of Evidence: NA.
在绵羊声带(VF)损伤模型中评估皮质类固醇和卤夫酮(一种Smad3小分子抑制剂)的抗纤维化作用。
采用配对研究设计,对30只绵羊进行右侧VF活检控制性损伤,然后分别给予不治疗、口服地塞米松、病灶内注射曲安奈德或口服卤夫酮治疗。对喉部进行评估,观察纤维化的组织学证据、Smad3的免疫组化表达及振动参数。比较各治疗组的结果。
损伤后,卤夫酮治疗组和地塞米松治疗组绵羊的VF胶原密度降低,而曲安奈德治疗组绵羊的VF胶原密度未降低。卤夫酮治疗组和曲安奈德治疗组绵羊之间存在显著差异(27.8%对37%,P = 0.017)。与所有类固醇治疗动物相比,卤夫酮治疗可在损伤后保留弹性蛋白,而所有类固醇治疗动物均出现明显的弹性蛋白丢失(P<0.05)。与正常左侧VF相比,所有损伤部位的Smad3染色均上调,但卤夫酮和地塞米松治疗可显著降低Smad3活性,而曲安奈德治疗则无此作用(P<0.05)。体外频闪喉镜评估显示,所有切除的喉部均有黏膜波,声门间隙正常化小于3,提示声门闭合良好。
绵羊模型中的VF损伤会引发伤口反应,Smad3抑制剂卤夫酮可对其进行调节,有利于振动功能。与使用类固醇药物治疗的绵羊相比,卤夫酮治疗的绵羊在损伤后固有层胶原化减少,弹性蛋白密度更高。这些数据支持将该途径作为一个合适的靶点进行调控,以预防或逆转声门纤维化并恢复嗓音质量。证据级别:无。