Pathophysiological Correlation between Cigarette Smoking and Amyotrophic Lateral Sclerosis

被引:1
|
作者
Menounos, Spiro [1 ]
Hansbro, Philip M. [2 ,3 ]
Diwan, Ashish D. [1 ,4 ]
Das, Abhirup [1 ,4 ]
机构
[1] Univ New South Wales, St George & Sutherland Clin Sch, Spine Labs, Kogarah, NSW 2217, Australia
[2] Centenary Inst, Fac Sci, Ctr Inflammat, Sch Life Sci, Sydney, NSW 2050, Australia
[3] Univ Technol Sydney, Sydney, NSW 2050, Australia
[4] St George Hosp, Spine Serv, Kogarah, NSW 2217, Australia
来源
NEUROSCI | 2021年 / 2卷 / 02期
基金
英国医学研究理事会;
关键词
amyotrophic lateral sclerosis (ALS); motor neuron degeneration; cigarette smoking; oxidative stress; neuroinflammation; immunometabolism; epigenetics; blood-spinal cord barrier (BSCB); microbiome; SPINAL CORD BARRIER; OBSTRUCTIVE PULMONARY-DISEASE; MOTOR-NEURON DEGENERATION; CENTRAL-NERVOUS-SYSTEM; OXIDATIVE STRESS; BLOOD-BRAIN; RISK-FACTOR; CEREBROSPINAL-FLUID; GUT MICROBIOTA; MOUSE MODEL;
D O I
10.3390/neurosci2020008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cigarette smoke (CS) has been consistently demonstrated to be an environmental risk factor for amyotrophic lateral sclerosis (ALS), although the molecular pathogenic mechanisms involved are yet to be elucidated. Here, we propose different mechanisms by which CS exposure can cause sporadic ALS pathogenesis. Oxidative stress and neuroinflammation are widely implicated in ALS pathogenesis, with blood-spinal cord barrier disruption also recognised to be involved in the disease process. In addition, immunometabolic, epigenetic and microbiome alterations have been implicated in ALS recently. Identification of the underlying pathophysiological mechanisms that underpin CS-associated ALS will drive future research to be conducted into new targets for treatment.
引用
收藏
页码:120 / 134
页数:15
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