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银杏叶提取物EGb 761®可改善5xFAD阿尔茨海默病模型小鼠的认知障碍并减轻TNFα反应。

Ginkgo biloba extract EGb 761® ameliorates cognitive impairment and alleviates TNFα response in 5xFAD Alzheimer's disease model mice.

作者信息

Nguyen Vu Thu Thuy, Slotos Robert Subirana, Guilherme Malena Dos Santos, Nguyen Tinh Thi, Weisenburger Sabrina, Lehner Martin D, Endres Kristina

机构信息

Department of Psychiatry and Psychotherapy, University Medical Center Mainz, Johannes Gutenberg-University Mainz, Mainz, Germany.

Department of Psychiatry and Psychotherapy, University Medical Center Mainz, Johannes Gutenberg-University Mainz, Mainz, Germany.

出版信息

Phytomedicine. 2025 Jan;136:156327. doi: 10.1016/j.phymed.2024.156327. Epub 2024 Dec 15.

Abstract

BACKGROUND

Ginkgo biloba leaf extract EGb 761® has shown clinical efficacy in patients with mild cognitive impairment and dementia. However, the pharmacological action of EGb 761® in Alzheimer's disease (AD) remains unclear and molecular mechanisms targeted in the brain are not completely understood.

HYPOTHESIS/PURPOSE: We aimed to investigate 1) the potential sex-dependent effects of oral administration of EGb 761® in 5xFAD mice, an AD mouse model, and 2) the underlying microglial subtype responsible for the observed anti-inflammatory effects in the brain.

METHODS

Eight-week old 5xFAD and wild type mice received EGb 761®-supplemented diet or control diet for eight weeks. The study investigated changes in cognitive function as well as amyloid plaque load, expression of AD-related genes, and anti-inflammatory effects. Moreover, we used organotypic brain slices for confirmation and assessment of concentration-dependency of the observed EGb 761® effects and performed single cell RNA sequencing on the prefrontal cortex of male mice with focus on microglia.

RESULTS

We demonstrate that EGb 761® treatment improves cognitive function in 5xFAD mice in several behavioral tests. Analysis of the brain tissue from these animals indicated a reduction in amyloid plaque load in the prefrontal cortex (PFC). This brain area was further investigated to assess the molecular changes that occurred following EGb 761® intake. Alterations in the expression of genes related to AD were highly sex-specific with effects on the cholinergic system, the γ-secretase complex, and neuroinflammation. Anti-inflammatory effects of EGb 761® with a particularly pronounced reduction of the TNFα-response could be shown for the PFC but also peripherally in the serum of 5xFAD mice of both sexes. Single-cell RNA sequencing revealed that EGb761® mainly affected disease-associated microglia stage 2 (DAM2), which are thought to have a detrimental role in AD.

CONCLUSIONS

EGb 761® shows efficacy in the treatment of cognitive deficits in the 5xFAD mouse model via multimodal activity, including sex-specific and sex-unrelated mechanisms including the normalization of neuroinflammatory parameters.

摘要

背景

银杏叶提取物EGb 761®已在轻度认知障碍和痴呆患者中显示出临床疗效。然而,EGb 761®在阿尔茨海默病(AD)中的药理作用仍不清楚,其在大脑中的靶向分子机制也未完全明确。

假设/目的:我们旨在研究1)口服EGb 761®对AD小鼠模型5xFAD小鼠潜在的性别依赖性影响,以及2)大脑中负责观察到的抗炎作用的潜在小胶质细胞亚型。

方法

8周龄的5xFAD和野生型小鼠接受补充EGb 761®的饮食或对照饮食8周。该研究调查了认知功能的变化以及淀粉样斑块负荷、AD相关基因的表达和抗炎作用。此外,我们使用脑片培养物来证实和评估观察到的EGb 761®作用的浓度依赖性,并对雄性小鼠的前额叶皮质进行单细胞RNA测序,重点关注小胶质细胞。

结果

我们证明,在多项行为测试中,EGb 761®治疗可改善5xFAD小鼠的认知功能。对这些动物脑组织的分析表明,前额叶皮质(PFC)中的淀粉样斑块负荷减少。对该脑区进行进一步研究,以评估摄入EGb 761®后发生的分子变化。与AD相关的基因表达变化具有高度性别特异性,对胆碱能系统、γ-分泌酶复合物和神经炎症有影响。EGb 761®的抗炎作用在PFC中表现为TNFα反应显著降低,在两性5xFAD小鼠的血清中也有外周抗炎作用。单细胞RNA测序显示,EGb761®主要影响疾病相关小胶质细胞2期(DAM2),这被认为在AD中起有害作用。

结论

EGb 761®通过多模式活性在5xFAD小鼠模型中治疗认知缺陷有效,包括性别特异性和性别无关机制,包括神经炎症参数的正常化。

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