Department of Neuroscience, IRCCS, Istituto di Ricerhe Farmacologiche Mario Negri, Milano, Italy.
Department of Biochemistry and Molecular Biology, University of Parma, Parma, Italy.
Neurobiol Aging. 2018 Oct;70:128-139. doi: 10.1016/j.neurobiolaging.2018.06.002. Epub 2018 Jun 12.
β-Amyloid oligomers (AβOs) and neuroinflammation are 2 main culprits to counteract in Alzheimer's disease (AD). Doxycycline (DOXY) is a second generation antibiotic of the tetracycline class that are promising drugs tested in many clinical trials for a number of different pathologies. DOXY is endowed with antiamyloidogenic properties and better crosses the blood-brain barrier, but its efficacy has never been tested in AD mice. We herein show that 15- to 16-month-old APP/PS1dE9 (APP/PS1) AD mice receiving DOXY under different treatment regimens recovered their memory without plaque reduction. An acute DOXY treatment was, also, sufficient to improve APP/PS1 mouse memory, suggesting an action against soluble AβOs. This was confirmed in an AβO-induced mouse model, where the AβO-mediated memory impairment was abolished by a DOXY pretreatment. Although AβOs induce memory impairment through glial activation, assessing the anti-inflammatory action of DOXY, we found that in both the AβO-treated and APP/PS1 mice, the memory recovery was associated with a lower neuroinflammation. Our data promote DOXY as a hopeful repositioned drug counteracting crucial neuropathological AD targets.
β-淀粉样寡聚体 (AβOs) 和神经炎症是阿尔茨海默病 (AD) 中需要对抗的两个主要罪魁祸首。强力霉素 (DOXY) 是四环素类的第二代抗生素,在许多临床试验中被测试用于多种不同的病理病症,是一种很有前途的药物。DOXY 具有抗淀粉样蛋白特性,并且可以更好地穿过血脑屏障,但它在 AD 小鼠中的疗效从未得到过测试。我们在此表明,接受不同治疗方案的 15 至 16 个月大的 APP/PS1dE9 (APP/PS1) AD 小鼠在没有斑块减少的情况下恢复了记忆。急性 DOXY 治疗也足以改善 APP/PS1 小鼠的记忆,表明其可以对抗可溶性 AβOs。在 AβO 诱导的小鼠模型中得到了证实,其中 DOXY 预处理可消除 AβO 介导的记忆障碍。虽然 AβOs 通过神经胶质细胞激活导致记忆损伤,但评估 DOXY 的抗炎作用时,我们发现,在 AβO 处理和 APP/PS1 小鼠中,记忆的恢复与较低的神经炎症有关。我们的数据表明 DOXY 是一种有希望的重新定位药物,可以对抗 AD 的关键神经病理学靶点。