肌萎缩侧索硬化
促炎细胞因子
肿瘤坏死因子α
医学
免疫印迹
炎症
免疫学
病理
内科学
生物
生物化学
基因
疾病
作者
Jing Jiang,Eun Jin Yang,Myung Gi Baek,Seon Hwy Kim,Sang Min Lee,Sun‐Mi Choi
出处
期刊:Neurodegenerative Diseases
[S. Karger AG]
日期:2011-01-01
卷期号:8 (6): 504-514
被引量:29
摘要
<i>Background:</i> Because amyotrophic lateral sclerosis (ALS) is a progressive inflammatory disease, treatment of the pulmonary system plays a key role in ALS patients’ care. Previous studies have mainly examined the pathological mechanism of ALS in the central nervous system; however, there has been relatively little research regarding the pulmonary system in ALS animal models. In inflammatory diseases, including asthma and arthritis, electroacupuncture (EA) is commonly used for its anti-inflammatory effects. The goal of this study was to determine whether EA treatment affects inflammation in the pulmonary system in an ALS animal model. <i>Methods:</i> EA treatment at ST36 (Zusanli) acupoint was performed with 14-week-old hSOD1<sup>G93A</sup> transgenic mice. Immunohistochemical analysis was performed using anti-ionized calcium binding adaptor molecule 1 (Iba-1) and anti-tumor necrosis factor alpha (TNF-α) antibodies. To investigate the expression level of inflammatory proteins, Western blot analyses were performed using anti-Iba-1, anti-TNF-α, anti-nuclear factor kappa B (NF-ĸB), and anti-interleukin 6 (IL-6) antibodies. The activation of Ser435-phospho-specific RAC-alpha serine/threonine-protein kinase 1 (pAKT) and the increase of phosphorylated extracellular-signal-regulated kinases (pERK) protein in lung tissues of EA-treated and untreated hSOD1<sup>G93A</sup> mice were also evaluated by Western blot. <i>Results:</i> EA treatment decreased the expression of the proinflammatory proteins such as TNF-α and IL-6, pNF-ĸB, and Iba-1 and increased the level of activated pAKT and pERK compared to control hSOD1<sup>G93A</sup> mice. <i>Conclusions:</i> Our findings suggest that EA could be an effective anti-inflammatory treatment for the respiratory impairment that occurs in ALS animal models.
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