Translational Neuropharmacology, Department of Comparative Medicine, Yale University School of Medicine, 310 Cedar St, New Haven, CT, 06520, USA.
Alzheimers Res Ther. 2018 Oct 10;10(1):105. doi: 10.1186/s13195-018-0433-4.
Translational research in Alzheimer's disease (AD) pathology provides evidence that accumulation of amyloid-β and hyperphosphorylated tau, neuropathological hallmarks of AD, is associated with complex disturbances in synaptic and neuronal function leading to oscillatory abnormalities in the neuronal networks that support memory and cognition. Accordingly, our recent study on transgenic TgF344-AD rats modeling AD showed an age-dependent reduction of stimulation-induced oscillations in the hippocampus, and disrupted long-range connectivity together with enhanced neuronal excitability in the cortex, reflected in greatly increased expression of high-voltage spindles, an epileptic absence seizure-like activity. To better understand the translational value of observed oscillatory abnormalities in these rats, we examine here the effects of donepezil, an acetylcholine esterase inhibitor clinically approved for AD treatment.
Brainstem nucleus pontis oralis stimulation-induced hippocampal oscillations were recorded under urethane anesthesia in adult (6-month-old) and aged (12-month-old) TgF344-AD and wild-type rats. Spontaneous cortical activity was monitored in a cohort of freely behaving aged rats implanted with frontal and occipital cortical electroencephalography (EEG) electrodes.
Subcutaneous administration of donepezil significantly augmented stimulation-induced hippocampal theta oscillation in aged wild-type rats and both adult and aged TgF344-AD rats, which have been previously shown to have diminished response to nucleus pontis oralis stimulation. Moreover, in adult TgF344-AD rats, donepezil also significantly increased theta phase-gamma amplitude coupling in the hippocampus during stimulation. However, neither of these effects were significantly changed in adult wild-type rats. Under freely behaving conditions, donepezil treatment had the opposite effect on cortical oscillatory connectivity in TgF344-AD and wild-type rats, and it reduced the occurrence of high-voltage spindle activity in TgF344-AD rats.
Together, these results imply that pharmacologically enhancing cholinergic tone with donepezil could partially reverse oscillatory abnormalities in TgF344-AD rats, which is in line with its clinical effectiveness in AD patients. Therefore, our study suggests good translational opportunities for these neurophysiological signals recorded in TgF344-AD rats, and their application could be considered in drug discovery efforts for developing therapies with disease-modifying potential.
阿尔茨海默病(AD)病理学的转化研究提供了证据,表明淀粉样β和过度磷酸化 tau 的积累,AD 的神经病理学标志物,与突触和神经元功能的复杂紊乱有关,导致支持记忆和认知的神经元网络中的振荡异常。因此,我们最近对模拟 AD 的转基因 TgF344-AD 大鼠的研究表明,随着年龄的增长,海马体中刺激诱导的振荡会出现依赖性减少,并且皮质中的长程连接被破坏,同时神经元兴奋性增强,表现为高电压纺锤波的表达大大增加,这是一种癫痫失神样发作活动。为了更好地理解这些大鼠中观察到的振荡异常的转化价值,我们在这里检查了多奈哌齐的作用,多奈哌齐是一种已被批准用于 AD 治疗的乙酰胆碱酯酶抑制剂。
在成年(6 个月大)和老年(12 个月大)TgF344-AD 和野生型大鼠的尿嘧啶麻醉下记录脑桥核口刺激诱导的海马体振荡。在一组植入额皮质和枕皮质脑电图(EEG)电极的自由活动老年大鼠中监测自发皮质活动。
皮下给予多奈哌齐可显著增强老年野生型大鼠以及成年和老年 TgF344-AD 大鼠对脑桥核口刺激的海马体θ振荡反应,此前研究表明,这些大鼠对脑桥核口刺激的反应减弱。此外,在成年 TgF344-AD 大鼠中,多奈哌齐还显著增加了刺激过程中海马体的θ相-γ幅度耦合。然而,在成年野生型大鼠中,这些影响均未发生显著变化。在自由活动条件下,多奈哌齐治疗对 TgF344-AD 和野生型大鼠的皮质振荡连接产生了相反的影响,并减少了 TgF344-AD 大鼠高电压纺锤波活动的发生。
总的来说,这些结果表明,用多奈哌齐增强胆碱能张力可以部分逆转 TgF344-AD 大鼠的振荡异常,这与它在 AD 患者中的临床疗效一致。因此,我们的研究表明,这些在 TgF344-AD 大鼠中记录的神经生理信号具有良好的转化机会,并且可以考虑将其应用于开发具有疾病修饰潜力的治疗方法的药物发现工作中。