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沙利度胺通过抑制阿尔茨海默病小鼠模型中的β-分泌酶改善淀粉样蛋白样病理。

Long-term treatment of thalidomide ameliorates amyloid-like pathology through inhibition of β-secretase in a mouse model of Alzheimer's disease.

机构信息

Center for Advanced Therapeutic Strategies of Brain Disorders, Roskamp Institute, Sarasota, FL, USA.

出版信息

PLoS One. 2013;8(2):e55091. doi: 10.1371/journal.pone.0055091. Epub 2013 Feb 6.

Abstract

Thalidomide is a tumor necrosis factor alpha (TNFα) inhibitor which has been found to have abilities against tumor growth, angiogenesis and inflammation. Recently, it has been applied in clinic for the treatment of multiple myeloma as well as some inflammatory diseases. However, whether thalidomide has any therapeutic effects on neurodegenerative disorders, i.e. Alzheimer's disease (AD) is not clear. AD is characterized by excessive amount of amyloid β peptides (Aβ), which results in a significant release of inflammatory factors, including TNFα in the brain. Studies have shown that inhibition of TNFα reduces amyloid-associated pathology, prevents neuron loss and improves cognition. Our recent report showed that genetic inhibition of TNFα/TNF receptor signal transduction down-regulates β amyloid cleavage enzyme 1 (BACE1) activity, reduces Aβ generation and improves learning and memory deficits. However, the mechanism of thalidomide involving in the mitigation of AD neuropathological features remains unclear. Here, we chronically administrated thalidomide on human APPswedish mutation transgenic (APP23) mice from 9 months old (an onset of Aβ deposits and early stage of AD-like changes) to 12 months old. We found that, in addition of dramatic decrease in the activation of both astrocytes and microglia, thalidomide significantly reduces Aβ load and plaque formation. Furthermore, we found a significant decrease in BACE1 level and activity with long-term thalidomide application. Interestingly, these findings cannot be observed in the brains of 12-month-old APP23 mice with short-term treatment of thalidomide (3 days). These results suggest that chronic thalidomide administration is an alternative approach for AD prevention and therapeutics.

摘要

沙利度胺是一种肿瘤坏死因子-α(TNFα)抑制剂,已被发现具有抑制肿瘤生长、血管生成和炎症的作用。最近,它已被应用于多发性骨髓瘤以及一些炎症性疾病的临床治疗。然而,沙利度胺是否对神经退行性疾病,如阿尔茨海默病(AD)有治疗作用尚不清楚。AD 的特征是淀粉样β肽(Aβ)的含量过多,导致大脑中炎症因子,包括 TNFα的大量释放。研究表明,TNFα 的抑制可减少淀粉样相关病理,防止神经元丢失,并改善认知功能。我们最近的报告显示,TNFα/TNF 受体信号转导的基因抑制可下调β淀粉样肽前体裂解酶 1(BACE1)的活性,减少 Aβ的生成,并改善学习和记忆障碍。然而,沙利度胺在减轻 AD 神经病理学特征中的作用机制尚不清楚。在这里,我们从 9 个月大(Aβ沉积和 AD 样变化的早期阶段)开始对人 APPswedish 突变转基因(APP23)小鼠长期给予沙利度胺,一直持续到 12 个月大。我们发现,除了星形胶质细胞和小胶质细胞的激活明显减少外,沙利度胺还显著减少了 Aβ负荷和斑块形成。此外,我们发现长期应用沙利度胺可显著降低 BACE1 水平和活性。有趣的是,在给予 APP23 小鼠 12 个月大时短期(3 天)应用沙利度胺,无法观察到这些发现。这些结果表明,长期沙利度胺给药是 AD 预防和治疗的一种替代方法。

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