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罗氟司特,一种磷酸二酯酶-4 抑制剂,可改善 C57BL/6J 小鼠的睡眠剥夺诱导的认知功能障碍。

Roflumilast, a Phosphodiesterase-4 Inhibitor, Ameliorates Sleep Deprivation-Induced Cognitive Dysfunction in C57BL/6J Mice.

机构信息

Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysuru 570015, Karnataka, India.

Centre for Experimental Pharmacology and Toxicology, JSS Academy of Higher Education & Research, Mysuru 570015, Karnataka, India.

出版信息

ACS Chem Neurosci. 2022 Jul 6;13(13):1938-1947. doi: 10.1021/acschemneuro.2c00127. Epub 2022 Jun 23.

Abstract

Sleep deprivation (SD) interferes with long-term memory and cognitive functions by overactivation of phosphodiesterase (PDEs) enzymes. PDE4, a nonredundant regulator of the cyclic nucleotides (cAMP), is densely expressed in the hippocampus and is involved in learning and memory processes. In the present study, we investigated the effects of Roflumilast (ROF), a PDE4B inhibitor, on sleep deprivation-induced cognitive dysfunction in a mouse model. Memory assessment was performed using a novel object recognition task, and the hippocampal cAMP level was estimated by the ELISA method. The alterations in the expressions of PDE4B, amyloid-β (Aβ), CREB, BDNF, and synaptic proteins (Synapsin I, SAP 97, PSD 95) were assessed to gain insights into the possible mechanisms of action of ROF using the Western blot technique. Results show that ROF reversed SD-induced cognitive decline in mice. ROF downregulated PDE4B and Aβ expressions in the brain. Additionally, ROF improved the cAMP level and the protein expressions of synapsin I, SAP 97, and PSD 95 in the hippocampal region of SD mice. Taken together, these results suggest that ROF can suppress the deleterious effects of SD-induced cognitive dysfunction via the PDE4B-mediated cAMP/CREB/BDNF signaling cascade.

摘要

睡眠剥夺(SD)通过磷酸二酯酶(PDEs)酶的过度激活干扰长期记忆和认知功能。PDE4 是环核苷酸(cAMP)的非冗余调节剂,在海马体中高度表达,参与学习和记忆过程。在本研究中,我们研究了 PDE4B 抑制剂罗氟司特(ROF)对小鼠模型中睡眠剥夺引起的认知功能障碍的影响。使用新物体识别任务进行记忆评估,并通过 ELISA 方法估计海马体 cAMP 水平。使用 Western blot 技术评估 PDE4B、淀粉样蛋白-β(Aβ)、CREB、BDNF 和突触蛋白(Synapsin I、SAP 97、PSD 95)的表达变化,以深入了解 ROF 的可能作用机制。结果表明,ROF 逆转了 SD 诱导的小鼠认知下降。ROF 下调了大脑中的 PDE4B 和 Aβ 表达。此外,ROF 改善了 SD 小鼠海马区 cAMP 水平和突触素 I、SAP 97 和 PSD 95 的蛋白表达。综上所述,这些结果表明,ROF 可以通过 PDE4B 介导的 cAMP/CREB/BDNF 信号级联抑制 SD 诱导的认知功能障碍的有害影响。

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