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制何首乌通过抑制 HDAC4/JNK 通路保护糖尿病脑病中海马神经元凋亡。

Radix polygoni multiflori protects against hippocampal neuronal apoptosis in diabetic encephalopathy by inhibiting the HDAC4/JNK pathway.

机构信息

Guizhou Prenatal Diagnosis Center, Affiliated Hospital of Guizhou Medical University, Guiyang 550004, Guizhou, PR China; School of Public Health, Key Laboratory of Environmental Pollution Monitoring and Disease Control, Guizhou Medical University, Guiyang 550004, Guizhou, PR China; School of Medical Laboratory, Guizhou Medical University, Guiyang 550004, Guizhou, PR China.

Reproductive Medical Center, Affiliated Hospital of Guizhou Medical University, Guiyang 550004, Guizhou, PR China.

出版信息

Biomed Pharmacother. 2022 Sep;153:113427. doi: 10.1016/j.biopha.2022.113427. Epub 2022 Jul 21.

Abstract

With an poorly characterized pathogenesis, Diabetic encephalopathy (DE), one of the main chronic complications of diabetes, would require further studies. Recent studies have proven that DE developing in conjunction with neuronal apoptosis, which is tightly regulated by a variety of processes and involved with histone acetylation and molecular signaling or so on. Though the histone deacetylase 4 (HDAC4), HDAC5, HDAC7, and HDAC9 form class IIa of the HDAC superfamily have been found participating in multiple neurodegenerative diseases, while JNK signaling pathway activation was hypothesized as a key cause leading to cell apoptosis, the correlation between HDAC4 and JNK signaling pathway remains unknown. Studies have found that Radix Polygoni Multiflori (RPM) contains a variety of ingredients, such as TSG and Emodin, could exert antioxidant effects, scavenge free radicals, inhibit cell apoptosis and provide neuroprotection, but the underlying mechanism has not fully elucidated yet. In the present study, we further explored the mechanism by which RPM improves the cognitive function of diabetic rats. Simultaneously, TSG and Emodin were used to stimulate HT-22 hippocampal neurons treated with high glucose. After RPM extracts or TSG, Emodin treatments, the cognitive functions of DE rats improved while the hippocampal neurons arranged tighter and increased. Meanwhile, the expression level of HAT, HDAC, HDAC4 and JNK signaling pathway and apoptosis related genes were decreased. Our finds indicates that RPM and Emodin would inhibit HDAC4 expression, curb the activation of the JNK pathway, reduce hippocampal neuron apoptosis and ultimately meliorate the cognitive function from diabetes. Additionally, the markedly inhibitory effects of the RPM and Emodin on HAT and HDAC was identified for the first time in this study, which provides a basis for future drug targeting histones acetylation development and application.

摘要

由于糖尿病性脑病(DE)的发病机制尚不清楚,它是糖尿病的主要慢性并发症之一,需要进一步研究。最近的研究已经证明,与神经元凋亡有关的 DE 的发展,这是由多种过程严格调节的,并涉及组蛋白乙酰化和分子信号等。尽管组蛋白脱乙酰酶 4(HDAC4)、HDAC5、HDAC7 和 HDAC9 形成 HDAC 超家族的 IIa 类已被发现参与多种神经退行性疾病,而 JNK 信号通路的激活被假设为导致细胞凋亡的关键原因,但 HDAC4 和 JNK 信号通路之间的相关性尚不清楚。研究发现,何首乌(RPM)含有多种成分,如 TSG 和大黄素,可发挥抗氧化作用,清除自由基,抑制细胞凋亡并提供神经保护作用,但潜在的机制尚未完全阐明。在本研究中,我们进一步探讨了 RPM 改善糖尿病大鼠认知功能的机制。同时,使用 TSG 和大黄素刺激高糖处理的 HT-22 海马神经元。在 RPM 提取物或 TSG、大黄素处理后,DE 大鼠的认知功能得到改善,而海马神经元排列更紧密,数量增加。同时,HAT、HDAC、HDAC4 和 JNK 信号通路以及凋亡相关基因的表达水平降低。我们的研究结果表明,RPM 和大黄素可抑制 HDAC4 的表达,抑制 JNK 通路的激活,减少海马神经元凋亡,最终改善糖尿病引起的认知功能障碍。此外,本研究首次确定了 RPM 和大黄素对 HAT 和 HDAC 的明显抑制作用,为未来针对组蛋白乙酰化的药物靶点开发和应用提供了依据。

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