Graduate Course on Pharmacology, Institute of Biomedical Sciences, Universidade de São Paulo, São Paulo, Brazil.
Research Group on Neuropharmacology of Aging, São Paulo, Brazil.
Br J Pharmacol. 2019 Sep;176(17):3193-3205. doi: 10.1111/bph.14744. Epub 2019 Jul 14.
Attention training reverses the neurodegeneration and memory loss promoted by infusion of amyloid-β (Aβ) peptide in rats and increases the density of α7 nicotinic ACh receptors (α7nAChRs) in brain areas related to memory. Hence, we aimed to assess the role of α7nAChRs in the memory recovery promoted by attention training.
C57Bl/6 mice were chronically infused with Aβ, Aβ plus the α7 antagonist methyllycaconitine (MLA), or MLA alone. Control animals were infused with vehicle. Animals were subjected weekly to the active avoidance shuttle box for 4 weeks (attention training). The brain and serum were collected for biochemical and histological analysis.
Aβ caused cognitive impairment, which was reversed by the weekly training, whereas Aβ + MLA also promoted memory loss but with no reversal with weekly training. MLA alone also promoted memory loss but with only partial reversal with the training. Animals infused with Aβ alone showed senile plaques in hippocampus, no change in BDNF levels in cortex, hippocampus, and serum, but increased AChE activity in cortex and hippocampus. Co-treatment with MLA increased AChE activity and senile plaque deposition in hippocampus as well as reducing BDNF in hippocampus and serum, suggesting a lack of α7nAChR function leads to a loss of neuroprotection mechanisms.
The α7nAChR has a determinant role in memory recovery and brain resilience in the presence of neurodegeneration promoted by Aβ peptide. These data support further studies concerning these receptors as pharmacological targets for future therapies.
注意力训练可逆转在大鼠中输注淀粉样蛋白-β(Aβ)肽引起的神经退行性变和记忆丧失,并增加与记忆相关的脑区α7 烟碱型乙酰胆碱受体(α7nAChRs)的密度。因此,我们旨在评估α7nAChRs 在注意力训练促进的记忆恢复中的作用。
C57Bl/6 小鼠被慢性输注 Aβ、Aβ 加α7 拮抗剂甲基-lycaconitine(MLA)或 MLA 单独。对照动物用载体输注。动物每周接受主动回避穿梭箱 4 周(注意力训练)。收集大脑和血清进行生化和组织学分析。
Aβ 引起认知障碍,这种障碍被每周的训练所逆转,而 Aβ+MLA 也促进记忆丧失,但每周的训练不能逆转。单独的 MLA 也促进了记忆丧失,但只有部分逆转了训练。单独输注 Aβ 的动物在海马体中出现老年斑,皮质、海马体和血清中的 BDNF 水平没有变化,但皮质和海马体中的 AChE 活性增加。与 MLA 共同处理增加了 AChE 活性和海马体中的老年斑沉积,并降低了海马体和血清中的 BDNF,表明缺乏α7nAChR 功能会导致神经保护机制丧失。
α7nAChR 在 Aβ 肽促进的神经退行性变存在的情况下,对记忆恢复和大脑弹性具有决定作用。这些数据支持进一步研究这些受体作为未来治疗的药理学靶点。