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在阿尔茨海默病的 5XFAD 小鼠模型中,慢性使用布洛芬治疗后没有改善。

No improvement after chronic ibuprofen treatment in the 5XFAD mouse model of Alzheimer's disease.

机构信息

Division of Molecular Psychiatry and Alzheimer Ph.D. Graduate School, Department of Psychiatry, University Medicine Goettingen, Goettingen, Germany.

出版信息

Neurobiol Aging. 2012 Apr;33(4):833.e39-50. doi: 10.1016/j.neurobiolaging.2011.08.006. Epub 2011 Sep 22.

Abstract

Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID) that has been reported to reduce the risk of developing Alzheimer's disease (AD). Its preventive effects in AD are likely pleiotropic as ibuprofen displays both anti-inflammatory activity by inhibition of cyclooxygenases and anti-amyloidogenic activity by modulation of γ-secretase. In order to study the anti-inflammatory properties of ibuprofen independent of its anti-amyloidogenic activity, we performed a long-term treatment study with ibuprofen in 5XFAD mice expressing a presenilin-1 mutation that renders this AD model resistant to γ-secretase modulation. As expected, ibuprofen treatment for 3 months resulted in a reduction of the inflammatory reaction in the 5XFAD mouse model. Importantly, an unchanged amyloid beta (Aβ) plaque load, an increase in soluble Aβ42 levels, and an aggravation of some behavioral parameters were noted, raising the question whether suppression of inflammation by nonsteroidal anti-inflammatory drug is beneficial in AD.

摘要

布洛芬是一种非甾体抗炎药 (NSAID),据报道它可以降低患阿尔茨海默病 (AD) 的风险。其在 AD 中的预防作用可能是多效的,因为布洛芬通过抑制环氧化酶显示出抗炎活性,并且通过调节 γ-分泌酶显示出抗淀粉样蛋白形成活性。为了研究布洛芬的抗炎特性而不考虑其抗淀粉样蛋白形成活性,我们在表达早老素-1 突变的 5XFAD 小鼠中进行了长期的布洛芬治疗研究,该突变使这种 AD 模型对 γ-分泌酶调节具有抗性。正如预期的那样,布洛芬治疗 3 个月导致 5XFAD 小鼠模型中的炎症反应减少。重要的是,注意到淀粉样β (Aβ) 斑块载量不变、可溶性 Aβ42 水平增加以及某些行为参数恶化,这提出了一个问题,即通过非甾体抗炎药抑制炎症是否对 AD 有益。

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