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低剂量的磷酸二酯酶 4 和 5 抑制剂可改善阿尔茨海默病小鼠模型的记忆。

Sub-efficacious doses of phosphodiesterase 4 and 5 inhibitors improve memory in a mouse model of Alzheimer's disease.

机构信息

Dept. Biomedical and Biotechnological Sciences, Section of Physiology, University of Catania, Catania, Italy.

Dept. of Pathology and Cell Biology, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.

出版信息

Neuropharmacology. 2018 Aug;138:151-159. doi: 10.1016/j.neuropharm.2018.06.002. Epub 2018 Jun 6.

Abstract

Cyclic nucleotides cAMP and cGMP cooperate to ensure memory acquisition and consolidation. Increasing their levels by phosphodiesterase inhibitors (PDE-Is) enhanced cognitive functions and rescued memory loss in different models of aging and Alzheimer's disease (AD). However, side effects due to the high doses used limited their application in humans. Based on previous studies suggesting that combinations of sub-efficacious doses of cAMP- and cGMP-specific PDE-Is improved synaptic plasticity and memory in physiological conditions, here we aimed to study whether this treatment was effective to counteract the AD phenotype in APPswe mice. We found that a 3-week chronic treatment with a combination of sub-efficacious doses of the cAMP-specific PDE4-I roflumilast (0.01 mg/kg) and the cGMP-specific PDE5-I vardenafil (0.1 mg/kg) improved recognition, spatial and contextual fear memory. Importantly, the cognitive enhancement persisted for 2 months beyond administration. This long-lasting action, and the possibility to minimize side effects due to the low doses used, might open feasible therapeutic strategies against AD.

摘要

环核苷酸 cAMP 和 cGMP 合作确保记忆的获得和巩固。通过磷酸二酯酶抑制剂 (PDE-Is) 增加它们的水平可以增强认知功能,并在不同的衰老和阿尔茨海默病 (AD) 模型中挽救记忆丧失。然而,由于使用的高剂量产生的副作用限制了它们在人类中的应用。基于先前的研究表明,cAMP- 和 cGMP-特异性 PDE-Is 的亚有效剂量组合可改善生理条件下的突触可塑性和记忆,我们旨在研究这种治疗方法是否能有效对抗 APPswe 小鼠的 AD 表型。我们发现,用 cAMP 特异性 PDE4-I 罗氟司特(0.01mg/kg)和 cGMP 特异性 PDE5-I 伐地那非(0.1mg/kg)的亚有效剂量组合进行 3 周的慢性治疗可改善识别、空间和情景恐惧记忆。重要的是,认知增强在给药后持续了 2 个月以上。这种长效作用以及由于使用低剂量而最小化副作用的可能性,可能为针对 AD 的可行治疗策略开辟了道路。

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