Garbugino Luciana, Golini Elisabetta, Giuliani Alessandro, Mandillo Silvia
Istituto di Biologia Cellulare e Neurobiologia, Consiglio Nazionale delle Ricerche, Rome, Italy.
Environment and Health Department, Istituto Superiore di Sanità, Rome, Italy.
Front Behav Neurosci. 2018 Nov 13;12:275. doi: 10.3389/fnbeh.2018.00275. eCollection 2018.
Amyotrophic Lateral Sclerosis (ALS) is a disease in which physical activity plays a controversial role. Epidemiological studies indicate an association between intense exercise and risk of developing ALS. To study the impact of physical activity on ALS, mouse models rely mostly on forced exercise. In this study we hypothesized that voluntary wheel running could represent a better model of the influence of exercise in the pathogenesis of ALS. We used an automated home-cage running-wheel system that enables individual monitoring of performance. To verify the effect of voluntary running on disease progression, prognosis and survival as well as motor functions, we challenged SOD1G93A low-copy male and female mice on one (1 RW, at age 24 weeks) or multiple (3 RW) running sessions at age 13, 18, and 24 weeks. In parallel we measured performance on Rotarod and Grip strength tests at different ages. Several parameters were analyzed through Principal Component Analysis in order to detect what indices correlate and may be useful for deeper understanding of the relation between exercise and disease development. We found mutant male mice more negatively affected than females by prolonged and repeated exercise. SOD1G93A low-copy male mice showed shorter survival, increased body weight loss and poorer disease prognosis when exposed to multiple running sessions. These findings could encourage the investigation of the pathogenetic mechanisms underlying the supposedly increased risk to develop ALS in humans engaged in specific and intense exercise activities.
肌萎缩侧索硬化症(ALS)是一种身体活动在其中起着争议性作用的疾病。流行病学研究表明高强度运动与患ALS的风险之间存在关联。为了研究身体活动对ALS的影响,小鼠模型大多依赖强制运动。在本研究中,我们假设自愿轮转跑步可能是运动对ALS发病机制影响的更好模型。我们使用了一种自动的笼内跑步轮系统,该系统能够对性能进行个体监测。为了验证自愿跑步对疾病进展、预后和生存以及运动功能的影响,我们在13周、18周和24周龄时,对SOD1G93A低拷贝雄性和雌性小鼠进行一次(1次跑步,24周龄时)或多次(3次跑步)跑步实验。同时,我们在不同年龄测量了它们在转棒试验和握力测试中的表现。通过主成分分析对几个参数进行了分析,以检测哪些指标相关,并且可能有助于更深入地理解运动与疾病发展之间的关系。我们发现,长时间和重复的运动对突变雄性小鼠的负面影响比对雌性小鼠更大。当暴露于多次跑步实验时,SOD1G93A低拷贝雄性小鼠的生存期缩短,体重减轻增加,疾病预后更差。这些发现可能会促使人们对从事特定高强度运动的人群中患ALS风险可能增加的潜在发病机制进行研究。