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单磷酸腺苷激活蛋白激酶的激活驱动海马体中的有氧糖酵解,以延缓APP/PS1小鼠电针治疗后的认知衰退。

Activation of Adenosine Monophosphate-Activated Protein Kinase Drives the Aerobic Glycolysis in Hippocampus for Delaying Cognitive Decline Following Electroacupuncture Treatment in APP/PS1 Mice.

作者信息

Li Jianhong, Zhang Bingxue, Jia Weiwei, Yang Minguang, Zhang Yuhao, Zhang Jiayong, Li Le, Jin Tingting, Wang Zhifu, Tao Jing, Chen Lidian, Liang Shengxiang, Liu Weilin

机构信息

TCM Rehabilitation Research Center of SATCM, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

National-Local Joint Engineering Research Center of Rehabilitation Medicine Technology, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

出版信息

Front Cell Neurosci. 2021 Nov 16;15:774569. doi: 10.3389/fncel.2021.774569. eCollection 2021.

Abstract

Aerobic glycolysis (AG), an important pathway of glucose metabolism, is dramatically declined in Alzheimer's disease (AD). AMP-activated protein kinase (AMPK) is a key regulator to maintain the stability of energy metabolism by promoting the process of AG and regulating glucose metabolism. Interestingly, it has been previously reported that electroacupuncture (EA) treatment can improve cognitive function in AD through the enhancement of glucose metabolism. In this study, we generated AMPK-knockdown mice to confirm the EA effect on AMPK activation and further clarify the mechanism of EA in regulating energy metabolism and improving cognitive function in APP/PS1 mice. The behavioral results showed that EA treatment can improve the learning and memory abilities in APP/PS1 mice. At the same time, the glucose metabolism in the hippocampus was increased detected by MRI-chemical exchange saturation transfer (MRI-CEST). The expression of proteins associated with AG in the hippocampus was increased simultaneously, including hexokinase II (HK2), 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3), and pyruvate kinase M2 (PKM2). Moreover, the knockdown of AMPK attenuated AG activated by EA treatment. In conclusion, this study proves that EA can activate AMPK to enhance the process of AG in the early stage of AD.

摘要

有氧糖酵解(AG)是葡萄糖代谢的重要途径,在阿尔茨海默病(AD)中显著下降。AMP激活的蛋白激酶(AMPK)是通过促进AG过程和调节葡萄糖代谢来维持能量代谢稳定性的关键调节因子。有趣的是,此前有报道称电针(EA)治疗可通过增强葡萄糖代谢来改善AD患者的认知功能。在本研究中,我们构建了AMPK基因敲低小鼠,以证实EA对AMPK激活的作用,并进一步阐明EA调节APP/PS1小鼠能量代谢和改善认知功能的机制。行为学结果表明,EA治疗可改善APP/PS1小鼠的学习和记忆能力。同时,通过磁共振成像-化学交换饱和转移(MRI-CEST)检测发现海马区葡萄糖代谢增加。海马区与AG相关的蛋白表达同时增加,包括己糖激酶II(HK2)、6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶3(PFKFB3)和丙酮酸激酶M2(PKM2)。此外,AMPK基因敲低减弱了EA治疗激活的AG。总之,本研究证明EA可激活AMPK以增强AD早期的AG过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8790/8636716/1a0a76cfac01/fncel-15-774569-g001.jpg

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