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电针对快速老化小鼠 prone 8(SAMP8)中食欲素 A 介导的 cAMP/PKA/CREB 信号通路的调节增强神经可塑性。

Electroacupuncture Enhances Neuroplasticity by Regulating the Orexin A-Mediated cAMP/PKA/CREB Signaling Pathway in Senescence-Accelerated Mouse Prone 8 (SAMP8) Mice.

机构信息

Key Laboratory of Chinese Internal Medicine of the Ministry of Education, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Beijing 100700, China.

College of Basic Medical and Sciences, Heilongjiang University of Chinese Medicine, Harbin, 150040 Heilongjiang, China.

出版信息

Oxid Med Cell Longev. 2022 Feb 4;2022:8694462. doi: 10.1155/2022/8694462. eCollection 2022.

Abstract

Learning and memory disorders and decreased neuroplasticity are the main clinical manifestations of age-induced cognitive dysfunction. Orexin A (OxA) has been reported to show abnormally elevated expression in the cerebrospinal fluid (CSF) of patients with Alzheimer's disease (AD) and to be associated with cognitive impairment. Here, we further assessed whether the excitatory neurotransmitter OxA is involved in neuroplasticity and cognitive function in senescence-accelerated mouse prone 8 (SAMP8) mice. In this study, we investigated the mechanism of OxA by using behavioral tests, CSF microdialysis, immunofluorescence, toluidine blue staining, gene silencing, transmission electron microscopy, and Western blotting. The results showed that 10 Hz electroacupuncture (EA) effectively alleviated learning and memory impairment in 7-month-old SAMP8 mice, reduced OxA levels in the CSF, increased the level of the neurotransmitter glutamate, alleviated pathological damage to hippocampal tissue, improved the synaptic structure, enhanced synaptic transmission, and regulated the expression of cAMP/PKA/CREB signaling pathway-related proteins. These results suggest that EA enhances neuroplasticity in SAMP8 mice by regulating the OxA-mediated cAMP/PKA/CREB signaling pathway, thus improving cognitive function. These findings suggest that EA may be beneficial for the prevention and treatment of age-induced cognitive impairment.

摘要

学习和记忆障碍以及神经可塑性降低是年龄相关性认知功能障碍的主要临床表现。有报道称,食欲素 A(OxA)在阿尔茨海默病(AD)患者的脑脊液(CSF)中表达异常升高,并与认知障碍有关。在这里,我们进一步评估了兴奋性神经递质 OxA 是否参与衰老加速模型 8 号小鼠(SAMP8)的神经可塑性和认知功能。在这项研究中,我们通过行为测试、CSF 微透析、免疫荧光、甲苯胺蓝染色、基因沉默、透射电子显微镜和 Western blot 研究了 OxA 的作用机制。结果表明,10 Hz 电针(EA)有效缓解了 7 月龄 SAMP8 小鼠的学习和记忆障碍,降低了 CSF 中的 OxA 水平,增加了神经递质谷氨酸的水平,减轻了海马组织的病理损伤,改善了突触结构,增强了突触传递,并调节了 cAMP/PKA/CREB 信号通路相关蛋白的表达。这些结果表明,EA 通过调节 OxA 介导的 cAMP/PKA/CREB 信号通路增强 SAMP8 小鼠的神经可塑性,从而改善认知功能。这些发现表明,EA 可能有益于预防和治疗年龄相关性认知障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0986/8837456/4e14cb88483e/OMCL2022-8694462.001.jpg

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