Department of Otolaryngology - Head and Neck Surgery, University of Missouri School of Medicine, One Hospital Dr. MA314, Columbia, MO, 65212, USA.
Department of Biomedical Sciences, University of Missouri College of Veterinary Medicine, Columbia, MO, USA.
Dysphagia. 2020 Apr;35(2):343-359. doi: 10.1007/s00455-019-10034-9. Epub 2019 Jul 12.
The goal of this study was to compare dysphagia phenotypes in low and high copy number (LCN and HCN) transgenic superoxide dismutase 1 (SOD1) mouse models of ALS to accelerate the discovery of novel and effective treatments for dysphagia and early amyotrophic lateral sclerosis (ALS) diagnosis. Clinicopathological features of dysphagia were characterized in individual transgenic mice and age-matched controls utilizing videofluoroscopy in conjunction with postmortem assays of the tongue and hypoglossal nucleus. Quantitative PCR accurately differentiated HCN-SOD1 and LCN-SOD1 mice and nontransgenic controls. All HCN-SOD1 mice developed stereotypical paralysis in both hindlimbs. In contrast, LCN-SOD1 mice displayed wide variability in fore- and hindlimb involvement. Lick rate, swallow rate, inter-swallow interval, and pharyngeal transit time were significantly altered in both HCN-SOD1 and LCN-SOD1 mice compared to controls. Tongue weight, tongue dorsum surface area, total tongue length, and caudal tongue length were significantly reduced only in the LCN-SOD1 mice compared to age-matched controls. LCN-SOD1 mice with lower body weights had smaller/lighter weight tongues, and those with forelimb paralysis and slower lick rates died at a younger age. LCN-SOD1 mice had a 32% loss of hypoglossal neurons, which differed significantly when compared to age-matched control mice. These novel findings for LCN-SOD1 mice are congruent with reported dysphagia and associated tongue atrophy and hypoglossal nucleus pathology in human ALS patients, thus highlighting the translational potential of this mouse model in ALS research.
本研究的目的是比较低拷贝数(LCN)和高拷贝数(HCN)转超氧化物歧化酶 1(SOD1)ALS 转基因小鼠模型的吞咽困难表型,以加速发现新的、有效的吞咽困难治疗方法和早期肌萎缩侧索硬化症(ALS)诊断方法。通过荧光透视检查与舌和舌下神经核的死后检测相结合,在个体转基因小鼠和年龄匹配的对照中,对吞咽困难的临床病理特征进行了特征描述。实时定量 PCR 可准确区分 HCN-SOD1 和 LCN-SOD1 小鼠和非转基因对照。所有 HCN-SOD1 小鼠的后肢均出现典型瘫痪。相比之下,LCN-SOD1 小鼠的前肢和后肢受累表现出广泛的变异性。与对照组相比,HCN-SOD1 和 LCN-SOD1 小鼠的舔食率、吞咽率、吞咽间隔和咽部通过时间均显著改变。与年龄匹配的对照组相比,LCN-SOD1 小鼠的舌重、舌背表面积、总舌长和舌尾长均显著减小。体重较低的 LCN-SOD1 小鼠的舌体较小/较轻,且前肢瘫痪和舔食率较慢的小鼠死亡年龄较小。LCN-SOD1 小鼠的舌下神经核神经元丢失 32%,与年龄匹配的对照组相比差异显著。LCN-SOD1 小鼠的这些新发现与人类 ALS 患者的吞咽困难及相关的舌萎缩和舌下神经核病理学报告一致,因此突出了该小鼠模型在 ALS 研究中的转化潜力。