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作为对抗脑淀粉样变性中海马过度兴奋和认知缺陷的一种策略,吡仑帕奈对AMPA型谷氨酸受体的非竞争性拮抗作用

Non-competitive AMPA glutamate receptors antagonism by perampanel as a strategy to counteract hippocampal hyper-excitability and cognitive deficits in cerebral amyloidosis.

作者信息

Bellingacci Laura, Tallarico Martina, Mancini Andrea, Megaro Alfredo, De Caro Carmen, Citraro Rita, De Sarro Giovambattista, Tozzi Alessandro, Di Filippo Massimiliano, Sciaccaluga Miriam, Russo Emilio, Leo Antonio, Costa Cinzia

机构信息

Section of Neurology, Department of Medicine and Surgery, University of Perugia, Italy.

System and Applied Pharmacology@University Magna Grecia, Science of Health Department, School of Medicine, Magna Graecia University of Catanzaro, Italy.

出版信息

Neuropharmacology. 2023 Mar 1;225:109373. doi: 10.1016/j.neuropharm.2022.109373. Epub 2022 Dec 9.

Abstract

Pathological accumulation of Aβ oligomers has been linked to neuronal networks hyperexcitability, potentially underpinned by glutamatergic AMPA receptors (AMPARs) dysfunction. We aimed to investigate whether the non-competitive block of AMPARs was able to counteract the alteration of hippocampal epileptic threshold, and of synaptic plasticity linked to Aβ oligomers accumulation, being this glutamate receptor a valuable specific therapeutic target. In this work, we showed that the non-competitive AMPARs antagonist perampanel (PER) which, per se, did not affect physiological synaptic transmission, was able to counteract Aβ-induced hyperexcitability. Moreover, AMPAR antagonism was able to counteract Aβ-induced hippocampal LTP impairment and hippocampal-based cognitive deficits in Aβ oligomers-injected mice, while retaining antiseizure efficacy. Beside this, AMPAR antagonism was also able to reduce the increased expression of proinflammatory cytokines in this mice model, also suggesting the presence of an anti-inflammatory activity. Thus, targeting AMPARs might be a valuable strategy to reduce both hippocampal networks hyperexcitability and synaptic plasticity deficits induced by Aβ oligomers accumulation.

摘要

Aβ寡聚体的病理性积累与神经网络的过度兴奋有关,这可能是由谷氨酸能AMPA受体(AMPARs)功能障碍所导致的。我们旨在研究AMPARs的非竞争性阻断是否能够抵消海马癫痫阈值的改变以及与Aβ寡聚体积累相关的突触可塑性改变,因为这种谷氨酸受体是一个有价值的特异性治疗靶点。在这项研究中,我们发现非竞争性AMPARs拮抗剂吡仑帕奈(PER)本身并不影响生理性突触传递,但能够抵消Aβ诱导的过度兴奋。此外,AMPAR拮抗作用能够抵消Aβ诱导的海马长时程增强(LTP)损伤以及在注射Aβ寡聚体的小鼠中基于海马的认知缺陷,同时保留抗癫痫疗效。除此之外,AMPAR拮抗作用还能够降低该小鼠模型中促炎细胞因子的表达增加,这也表明存在抗炎活性。因此,靶向AMPARs可能是减少Aβ寡聚体积累所诱导的海马网络过度兴奋和突触可塑性缺陷的一种有价值的策略。

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