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草药配方提取物通过调节创伤后应激障碍小鼠模型中的Reelin/Dab-1通路改善焦虑和认知障碍。

Herbal Formula Extract Ameliorates Anxiety and Cognitive Impairment via Regulation of the Reelin/Dab-1 Pathway in a Murine Model of Post-Traumatic Stress Disorder.

作者信息

Park Hee Ra, Cai Mudan, Yang Eun Jin

机构信息

Department of KM Science Research, Korea Institute of Oriental Medicine (KIOM), Daejeon 34054, Republic of Korea.

出版信息

Pharmaceutics. 2024 Aug 30;16(9):1150. doi: 10.3390/pharmaceutics16091150.

DOI:10.3390/pharmaceutics16091150
PMID:39339187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11434737/
Abstract

We investigated the effects of epigenetic modifications on post-traumatic stress disorder (PTSD) using a novel combination of herbal medicines from , , , and . The herbal formula extract (HFE) (250 mg/kg) was administered orally once daily for 14 days to determine its effects on PTSD in mice by combining prolonged stress and foot shock. The open field and Y-maze tests determined the effect of HFE on PTSD-induced anxiety and cognition. Hippocampal neuronal plastic changes and molecular mechanism were verified. Treatment with HFE decreased anxiety-like behavior and enhanced cognition. Moreover, it reduced the number of PTSD-related hilar ectopic granule cells in the dentate gyrus (DG). PTSD mice showed reduced neuronal plasticity of doublecortin cells in the DG, which was restored by HFE treatment. HFE reversed PTSD-induced inhibition of the Reelin/Dab1 pathway, a critical signaling cascade involved in brain development, and regulated methylation. Furthermore, DNA methylation, methyl-CpG binding protein 2, and DNA methyltransferase 1, which were elevated in the hippocampus of PTSD mice, were restored following HFE treatment. HFE increased the expression of synaptic plasticity-related factors in the hippocampus of PTSD mice. Our findings suggest that HFE can facilitate PTSD treatment by alleviating behavioral abnormalities through the restoration of hippocampal dysfunction via regulation of the Reelin/Dab-1 pathway and DNA methylation in the hippocampus.

摘要

我们使用来自[具体来源1]、[具体来源2]、[具体来源3]和[具体来源4]的草药新组合,研究了表观遗传修饰对创伤后应激障碍(PTSD)的影响。将草药配方提取物(HFE)(250毫克/千克)每天口服一次,持续14天,通过结合长期应激和足部电击来确定其对小鼠PTSD的影响。旷场试验和Y迷宫试验确定了HFE对PTSD诱导的焦虑和认知的影响。验证了海马神经元可塑性变化和分子机制。HFE治疗可减少焦虑样行为并增强认知。此外,它减少了齿状回(DG)中与PTSD相关的 hilar异位颗粒细胞数量。PTSD小鼠DG中双皮质素细胞的神经元可塑性降低,而HFE治疗可使其恢复。HFE逆转了PTSD诱导的Reelin/Dab1信号通路抑制,该信号级联在大脑发育中起关键作用,并调节[具体甲基化相关内容]。此外,PTSD小鼠海马中升高的DNA甲基化、甲基-CpG结合蛋白2和DNA甲基转移酶1在HFE治疗后恢复。HFE增加了PTSD小鼠海马中突触可塑性相关因子的表达。我们的研究结果表明,HFE可以通过调节海马中的Reelin/Dab-1信号通路和DNA甲基化来恢复海马功能障碍,从而缓解行为异常,促进PTSD的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/8ff910f839b8/pharmaceutics-16-01150-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/814d55497898/pharmaceutics-16-01150-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/9467b7722dcd/pharmaceutics-16-01150-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/3af63d34e53a/pharmaceutics-16-01150-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/c65822a18326/pharmaceutics-16-01150-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/8ff910f839b8/pharmaceutics-16-01150-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/814d55497898/pharmaceutics-16-01150-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/9467b7722dcd/pharmaceutics-16-01150-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/3af63d34e53a/pharmaceutics-16-01150-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/c65822a18326/pharmaceutics-16-01150-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/11434737/8ff910f839b8/pharmaceutics-16-01150-g006a.jpg

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