Neuroprotective effects of traditional Chinese medicine Naofucong on diabetic cognitive impairment: Mechanisms involving insulin-degrading enzyme-mediated degradation of Amyloid-β and inhibition of ERK/JNK/p38 MAPK signaling pathway.

IF 2.7 4区 医学 Q3 NEUROSCIENCES Brain Research Pub Date : 2025-02-15 Epub Date: 2024-11-29 DOI:10.1016/j.brainres.2024.149365
Yue Tian, Guangchan Jing, Ruiying Yin, Mei Ma, Weiwei Cao, Mengren Zhang
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Abstract

The increasing prevalence of diabetes and its related cognitive impairments is a significant public health concern. With limited clinical treatment options and an incomplete understanding of the underlying mechanisms, traditional Chinese medicine (TCM) Naofucong is proposed as a potential neuroprotective agent against diabetic cognitive impairment (DCI). This study aims to investigate the therapeutic mechanisms of Naofucong in DCI. We hypothesize that Naofucong may improve cognitive function in diabetic rats by modulating the extracellular regulated protein kinases (ERK)/c-Jun N-terminal kinase (JNK)/p38 mitogen-activated protein kinases (MAPK) signaling pathway, enhancing insulin-degrading enzyme (IDE) expression, reducing amyloid-beta (Aβ) deposition, decreasing phosphorylated Tau (p-Tau) levels, and alleviating oxidative stress. Diabetes was induced in specific-pathogen-free male Sprague-Dawley rats using streptozotocin, and the rats were treated with oral Naofucong for 12 weeks. We assessed cognitive function and measured neuronal damage, oxidative stress injury, and the expression levels of IDE, Aβ, amyloid precursor protein (APP), p-Tau, and components of the ERK/JNK/p38 MAPK pathway. Diabetic rats showed significant declines in cognitive function, neuronal damage, oxidative stress, low IDE expression, Aβ accumulation, high APP expression, abnormal Tau phosphorylation, and overactivation of the ERK/JNK/p38 MAPK pathway. Naofucong treatment significantly reversed these symptoms. Our findings suggest that Naofucong improves cognitive impairment in diabetic rats by inhibiting the ERK/JNK/p38 MAPK pathway, upregulating IDE, reducing Aβ deposition, suppressing APP and p-Tau expression, and alleviating neuronal damage and oxidative stress. This research provides a reference for the clinical prevention and treatment of DCI using TCM Naofucong.

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中药脑复通对糖尿病认知功能障碍的神经保护作用:涉及胰岛素降解酶介导的淀粉样蛋白-β降解和ERK/JNK/p38 MAPK信号通路抑制的机制
糖尿病及其相关认知障碍的日益流行是一个重大的公共卫生问题。由于临床治疗方案有限,对其机制的了解不完全,中药脑复聪被认为是一种潜在的糖尿病认知功能障碍(DCI)的神经保护剂。本研究旨在探讨脑复聪治疗DCI的作用机制。我们推测脑复通可能通过调节细胞外调节蛋白激酶(ERK)/c-Jun n-末端激酶(JNK)/p38丝裂原活化蛋白激酶(MAPK)信号通路,增强胰岛素降解酶(IDE)表达,减少β淀粉样蛋白(Aβ)沉积,降低磷酸化Tau蛋白(p-Tau)水平,减轻氧化应激,从而改善糖尿病大鼠的认知功能。采用链脲佐菌素诱导无特异性病原体雄性sd大鼠患糖尿病,口服脑复聪12 周。我们评估了认知功能,测量了神经元损伤、氧化应激损伤,以及IDE、Aβ、淀粉样蛋白前体蛋白(APP)、p-Tau和ERK/JNK/p38 MAPK通路组分的表达水平。糖尿病大鼠表现出认知功能、神经元损伤、氧化应激、IDE低表达、Aβ积累、APP高表达、Tau磷酸化异常、ERK/JNK/p38 MAPK通路过度激活等显著下降。脑复聪治疗可明显逆转上述症状。我们的研究结果表明,脑复通通过抑制ERK/JNK/p38 MAPK通路,上调IDE,减少Aβ沉积,抑制APP和p-Tau表达,减轻神经元损伤和氧化应激,改善糖尿病大鼠认知功能障碍。本研究为临床应用中药脑复聪防治DCI提供参考。
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来源期刊
Brain Research
Brain Research 医学-神经科学
CiteScore
5.90
自引率
3.40%
发文量
268
审稿时长
47 days
期刊介绍: An international multidisciplinary journal devoted to fundamental research in the brain sciences. Brain Research publishes papers reporting interdisciplinary investigations of nervous system structure and function that are of general interest to the international community of neuroscientists. As is evident from the journals name, its scope is broad, ranging from cellular and molecular studies through systems neuroscience, cognition and disease. Invited reviews are also published; suggestions for and inquiries about potential reviews are welcomed. With the appearance of the final issue of the 2011 subscription, Vol. 67/1-2 (24 June 2011), Brain Research Reviews has ceased publication as a distinct journal separate from Brain Research. Review articles accepted for Brain Research are now published in that journal.
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