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抑制 PDE2 和 PDE4 协同作用可改善记忆巩固过程。

Inhibition of PDE2 and PDE4 synergistically improves memory consolidation processes.

机构信息

School for Mental Health and Neuroscience, Department of Psychiatry and Neuropsychology, Maastricht University, Universiteitssingel 50, 6229, ER Maastricht, the Netherlands.

In Vitro Pharmacology, Dart Neuroscience, LLC, 12278 Scripps Summit Drive, San Diego, CA, 92131, USA.

出版信息

Neuropharmacology. 2021 Feb 15;184:108414. doi: 10.1016/j.neuropharm.2020.108414. Epub 2020 Nov 26.

Abstract

Phosphodiesterases (PDE) are the only enzymes that degrade cAMP and cGMP which are second messengers crucial to memory consolidation. Different PDE inhibitors have been developed and tested for their memory-enhancing potential, but the occurrence of side effects has hampered clinical progression. As separate inhibition of the PDE2 and PDE4 enzyme family has been shown to enhance memory, we investigated whether concurrent treatment with a PDE2 and PDE4 inhibitor can have synergistic effects on memory consolidation processes. We found that combined administration of PF-999 (PDE2 inhibitor) and roflumilast (PDE4 inhibitor) increases the phosphorylation of the AMPA receptor subunit GluR1 and induces CRE-mediated gene expression. Moreover, when combined sub-effective and effective doses of PF-999 and roflumilast were administered after learning, time-dependent forgetting was abolished in an object location memory task. Pharmacokinetic assessment indicated that combined treatment does not alter exposure of the individual compounds. Taken together, these findings suggest that combined PDE2 and PDE4 inhibition has synergistic effects on memory consolidation processes at sub-effective doses, which could therefore provide a therapeutic strategy with an improved safety profile.

摘要

磷酸二酯酶(PDE)是唯一能够降解 cAMP 和 cGMP 的酶,而 cAMP 和 cGMP 是记忆巩固的关键第二信使。已经开发出了不同的 PDE 抑制剂,并对其增强记忆的潜力进行了测试,但副作用的发生阻碍了其临床进展。由于单独抑制 PDE2 和 PDE4 酶家族已被证明可以增强记忆,我们研究了同时使用 PDE2 和 PDE4 抑制剂是否对记忆巩固过程具有协同作用。我们发现,PF-999(PDE2 抑制剂)和罗氟司特(PDE4 抑制剂)联合给药会增加 AMPA 受体亚基 GluR1 的磷酸化,并诱导 CRE 介导的基因表达。此外,当在学习后给予 PF-999 和罗氟司特的亚有效和有效剂量联合给药时,在物体位置记忆任务中,时程依赖性遗忘被消除。药代动力学评估表明,联合治疗不会改变单个化合物的暴露。综上所述,这些发现表明,联合使用 PDE2 和 PDE4 抑制剂在亚有效剂量下对记忆巩固过程具有协同作用,因此可以提供一种具有改善安全性特征的治疗策略。

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