Suppr超能文献

多发性硬化症中的疲劳:机制与管理。

Fatigue in multiple sclerosis: mechanisms and management.

机构信息

Department of Neurology, Westmead Hospital and Western Clinical School, University of Sydney, Sydney, NSW, Australia.

出版信息

Clin Neurophysiol. 2010 Jun;121(6):809-17. doi: 10.1016/j.clinph.2009.12.013. Epub 2010 Jan 25.

Abstract

Multiple sclerosis [MS] is a chronic immune-mediated disorder of the central nervous system [CNS]. Fatigue may be a debilitating symptom in MS patients, adversely impacting on their quality of life. Clinically, fatigue may manifest as exhaustion, lack of energy, increased somnolence, or worsening of MS symptoms. Activity and heat typically serve to exacerbate symptoms of fatigue. There is now strong evidence to suggest that fatigue results from reduced voluntary activation of muscles by means of central mechanisms. Given that axonal demyelination is a pathological hallmark of MS, activity-dependent conduction block [ADCB] has been proposed as a mechanism underlying fatigue in MS. This ADCB results from axonal membrane hyperpolarization, mediated by the Na(+)/K(+) electrogenic pump, with conduction failure precipitated in demyelinated axons with a reduced safety factor of impulse transmission. In addition, Na(+)/K(+) pump dysfunction, as reported in MS, may induce a depolarizing conduction block associated with inactivation of Na(+) channels. These processes may induce secondary effects including axonal degeneration triggered by raised levels of intracellular Ca(2+) through reverse operation of the Na(+)-Ca(2+) exchanger. Restoration of normal conduction in demyelinated axons with selective channel blockers improves fatigue and may yet prove useful as a neuroprotective strategy, in preventing secondary axonal degeneration and consequent functional impairment.

摘要

多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性免疫介导疾病。疲劳可能是 MS 患者的一种使人衰弱的症状,对他们的生活质量产生负面影响。临床上,疲劳可能表现为疲惫、缺乏能量、嗜睡增加或 MS 症状恶化。活动和热量通常会加剧疲劳症状。现在有强有力的证据表明,疲劳是由于中枢机制导致肌肉的自愿激活减少所致。鉴于轴突脱髓鞘是 MS 的病理标志,活动依赖性传导阻滞(ADCB)已被提出作为 MS 疲劳的机制。这种 ADCB 是由轴突膜超极化引起的,由 Na(+) / K(+) 电致泵介导,在冲动传输安全系数降低的脱髓鞘轴突中引发传导失败。此外,如 MS 中报道的那样,Na(+) / K(+) 泵功能障碍可能会引起与 Na(+) 通道失活相关的去极化传导阻滞。这些过程可能会引起继发性效应,包括通过 Na(+) -Ca(2+) 交换器的反向作用,细胞内 Ca(2+) 水平升高引发的轴突退化。使用选择性通道阻滞剂恢复脱髓鞘轴突的正常传导可改善疲劳,并且可能作为一种神经保护策略很有用,可防止继发性轴突退化和随后的功能障碍。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验