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

dc.contributor.authorNguyen, Vu Thu Thuy
dc.contributor.authorSubirana Slotos, Robert
dc.contributor.authorDos Santos Guilherme, Malena
dc.contributor.authorNguyen, Tinh Thi
dc.contributor.authorWeisenburger, Sabrina
dc.contributor.authorLehner, Martin D.
dc.contributor.authorEndres, Kristina
dc.date.accessioned2026-07-16T14:10:12Z
dc.date.issued2025
dc.description.abstractBackground 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.doihttps://doi.org/10.25358/openscience-15202
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/15223
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 Medizinde
dc.subject.ddc610 Medical sciencesen
dc.titleGinkgo biloba extract EGb 761® ameliorates cognitive impairment and alleviates TNFα response in 5xFAD Alzheimer‘s disease model miceen
dc.typeZeitschriftenaufsatz
jgu.apc.netprice2312,63
jgu.apc.price2474,51
jgu.apc.taxrate7
jgu.apc.transformationcontractElsevier
jgu.dfg.year2025
jgu.identifier.uuid8b147bed-bb90-44db-90a4-95717c4da761
jgu.journal.titlePhytomedicine
jgu.journal.volume136
jgu.nationalcurrency.eur2312,63
jgu.organisation.departmentFB 04 Medizin
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative156327
jgu.publisher.doi10.1016/j.phymed.2024.156327
jgu.publisher.eissn1618-095X
jgu.publisher.nameElsevier
jgu.publisher.placeMünchen
jgu.publisher.year2025
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610
jgu.subject.dfgLebenswissenschaften
jgu.type.contenttypeScientific article
jgu.type.dinitypeArticleen_GB
jgu.type.resourceText
jgu.type.versionPublished version

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