Ginkgo biloba extract EGb 761® ameliorates cognitive impairment and alleviates TNFα response in 5xFAD Alzheimer‘s disease model mice
| dc.contributor.author | Nguyen, Vu Thu Thuy | |
| dc.contributor.author | Subirana Slotos, Robert | |
| dc.contributor.author | Dos Santos Guilherme, Malena | |
| dc.contributor.author | Nguyen, Tinh Thi | |
| dc.contributor.author | Weisenburger, Sabrina | |
| dc.contributor.author | Lehner, Martin D. | |
| dc.contributor.author | Endres, Kristina | |
| dc.date.accessioned | 2026-07-16T14:10:12Z | |
| dc.date.issued | 2025 | |
| dc.description.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. | en |
| dc.identifier.doi | https://doi.org/10.25358/openscience-15202 | |
| dc.identifier.uri | https://openscience.ub.uni-mainz.de/handle/20.500.12030/15223 | |
| dc.language.iso | eng | |
| dc.rights | CC-BY-4.0 | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject.ddc | 610 Medizin | de |
| dc.subject.ddc | 610 Medical sciences | en |
| dc.title | Ginkgo biloba extract EGb 761® ameliorates cognitive impairment and alleviates TNFα response in 5xFAD Alzheimer‘s disease model mice | en |
| dc.type | Zeitschriftenaufsatz | |
| jgu.apc.netprice | 2312,63 | |
| jgu.apc.price | 2474,51 | |
| jgu.apc.taxrate | 7 | |
| jgu.apc.transformationcontract | Elsevier | |
| jgu.dfg.year | 2025 | |
| jgu.identifier.uuid | 8b147bed-bb90-44db-90a4-95717c4da761 | |
| jgu.journal.title | Phytomedicine | |
| jgu.journal.volume | 136 | |
| jgu.nationalcurrency.eur | 2312,63 | |
| jgu.organisation.department | FB 04 Medizin | |
| jgu.organisation.name | Johannes Gutenberg-Universität Mainz | |
| jgu.organisation.number | 2700 | |
| jgu.organisation.place | Mainz | |
| jgu.organisation.ror | https://ror.org/023b0x485 | |
| jgu.pages.alternative | 156327 | |
| jgu.publisher.doi | 10.1016/j.phymed.2024.156327 | |
| jgu.publisher.eissn | 1618-095X | |
| jgu.publisher.name | Elsevier | |
| jgu.publisher.place | München | |
| jgu.publisher.year | 2025 | |
| jgu.rights.accessrights | openAccess | |
| jgu.subject.ddccode | 610 | |
| jgu.subject.dfg | Lebenswissenschaften | |
| jgu.type.contenttype | Scientific article | |
| jgu.type.dinitype | Article | en_GB |
| jgu.type.resource | Text | |
| jgu.type.version | Published version |