Rehabilitation Medicine School of Henan University of Chinese Medicine, The First Affiliated Hospital of Henan University of Chinese Medicine, People's Hospital of Henan University of Chinese Medicine, Department of Rehabilitation Medicine of Zhengzhou People's Hospital (South Hospital), Zhengzhou, Henan, China.
Rehabilitation Medicine School of Henan University of Chinese Medicine, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Brain Res. 2024 Dec 1;1844:149139. doi: 10.1016/j.brainres.2024.149139. Epub 2024 Aug 5.
In recent years, the mechanism of acupuncture in the treatment of post-stroke cognitive impairment (PSCI) has not been fully elucidated. The balance between mitochondrial fission and fusion is important for PSCI. Our previous research demonstrated that electroacupuncture can improve learning and memory in middle cerebral artery ischemia reperfusion (MCAO/R) rats. However, the specific mechanism by which electroacupuncture improves learning and memory in MCAO/R rats by regulating mitochondrial fission and fusion needs to be further investigated. The MCAO/R rats was developed using the line-bolt method. The rats were randomly divided into sham-operated (Sham), model (MCAO/R), electroacupuncture (MCAO/R + EA) and sham-electroacupuncture (MCAO/R + sham EA) groups. Investigating the effects of EA on the expression of Sirtuin1 (SIRT1), peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α), Optic atrophy 1R + (OPA1) and Dynamin-related protein 1 (DRP1) in hippocampal neurons and on the morphology and function of hippocampal neurons and mitochondria. EA was able to reduce neurologic deficit scores and cerebral infarct volume and improve new object discrimination in MCAO/R rats, but there were no significant changes in these indices in the sham-electroacupuncture group. Moreover, EA increased the expression of SIRT1, PGC-1α, and OPA1 in hippocampal tissues, inhibited the expression of DRP1, attenuated neuronal and mitochondrial damage, and reduced mitochondrial fragmentation. The mechanism by which EA improves learning memory deficits in MCAO/R rats may be related to the inhibition of SIRT1/PGC-1α expression, the enhancement of mitochondrial fusion and the obstruction of its fission, and the reduction of hippocampal neuronal damage.
近年来,针刺治疗中风后认知障碍(PSCI)的机制尚未完全阐明。线粒体分裂和融合的平衡对 PSCI 很重要。我们之前的研究表明,电针对大脑中动脉缺血再灌注(MCAO/R)大鼠的学习和记忆有改善作用。然而,电针对 MCAO/R 大鼠学习和记忆的改善作用,通过调节线粒体分裂和融合的具体机制,需要进一步研究。MCAO/R 大鼠采用线锤法建立。将大鼠随机分为假手术(Sham)、模型(MCAO/R)、电针(MCAO/R+EA)和假电针(MCAO/R+sham EA)组。探讨 EA 对海马神经元中 Sirtuin1(SIRT1)、过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC-1α)、视神经萎缩 1R+(OPA1)和动力相关蛋白 1(DRP1)的表达,以及海马神经元和线粒体的形态和功能的影响。EA 能降低 MCAO/R 大鼠的神经功能缺损评分、脑梗死体积,改善新物体识别,但 sham EA 组这些指标无明显变化。此外,EA 增加了海马组织中 SIRT1、PGC-1α 和 OPA1 的表达,抑制了 DRP1 的表达,减轻了神经元和线粒体的损伤,减少了线粒体的碎片化。EA 改善 MCAO/R 大鼠学习记忆障碍的机制可能与抑制 SIRT1/PGC-1α 的表达、增强线粒体融合和阻断其分裂、减少海马神经元损伤有关。