# Nobiletin Ameliorates Alzheimer’s Disease Pathology by Reducing Oxidative Stress and Neuroinflammation Through the AMPK/SIRT1/PGC-1α and PI3K/Akt–CREB–BDNF Pathways in 5XFAD Mice

**Authors:** Hana Baek, Miey Park, Hae-Jeung Lee

PMC · DOI: 10.3390/biomedicines14030561 · Biomedicines · 2026-02-28

## TL;DR

Nobiletin, a compound from citrus, helps reduce Alzheimer’s disease symptoms in mice by lowering brain plaques and inflammation through several key biological pathways.

## Contribution

This study reveals nobiletin’s novel dual mechanism in AD via AMPK/SIRT1/PGC-1α and PI3K/Akt–CREB–BDNF pathways.

## Key findings

- Nobiletin reduced amyloid-β40/42 and improved memory in 5XFAD mice.
- It suppressed neuroinflammation by lowering IL-6, IL-1β, and TNF-α levels.
- Nobiletin enhanced antioxidant defenses and synaptic plasticity through key signaling pathways.

## Abstract

Background/Objectives: Alzheimer’s disease (AD) involves amyloid-β (Aβ) deposition, oxidative stress, and neuroinflammation, leading to cognitive decline. Nobiletin, a citrus-derived polymethoxylated flavonoid, exerts antioxidant and anti-inflammatory effects. This study explored its neuroprotective mechanisms in the 5XFAD mouse model. Methods: Male 5XFAD and C57BL/6J mice received oral nobiletin (20 or 40 mg/kg/d) for 4 weeks. Cognitive function was assessed by the Y-maze test. Amyloid-β burden was quantified by Congo red staining and ELISA. Serum cytokine levels and antioxidant enzyme activities were measured by ELISA. Western blotting and RT-PCR were used to assess proteins and genes related to amyloidogenesis, inflammation (TLR4/MyD88/NF-κB), mitochondrial biogenesis (AMPK/SIRT1/PGC-1α), and synaptic plasticity (PI3K/Akt–CREB–BDNF). Results: Nobiletin improved working memory, reduced amyloid-β40/42 deposition, and downregulated APP, BACE1, and PS1 expression, while enhancing ADAM10 expression. It lowered serum IL-6, IL-1β, and TNF-α, increased SOD, CAT, and GPx activities, and suppressed TLR4/MyD88/NF-κB signaling. Furthermore, it activated AMPK/SIRT1/PGC-1α and NRF2 pathways, enhancing antioxidant defenses, and promoted PI3K/Akt–CREB–BDNF signaling, increasing PSD95 and synaptophysin. Conclusions: Nobiletin exerts strong neuroprotective and antioxidant effects by targeting multiple signaling cascades, mitigating amyloid pathology and neuroinflammation, and improving synaptic plasticity. It represents a promising therapeutic agent against AD.

## Linked entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351], BACE1 (beta-secretase 1) [NCBI Gene 23621], PSEN1 (presenilin 1) [NCBI Gene 5663], ADAM10 (ADAM metallopeptidase domain 10) [NCBI Gene 102], TLR4 (toll like receptor 4) [NCBI Gene 7099], MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], SIRT1 (sirtuin 1) [NCBI Gene 23411], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385], BDNF (brain derived neurotrophic factor) [NCBI Gene 627], DLG4 (discs large MAGUK scaffold protein 4) [NCBI Gene 1742]
- **Chemicals:** nobiletin (PubChem CID 72344), IL-6 (PubChem CID 165368475), GPx (PubChem CID 135460989)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Myd88 (myeloid differentiation primary response gene 88) [NCBI Gene 17874], Prdx6-ps2 (peroxiredoxin 6 pseudogene 2) [NCBI Gene 384001] {aka Aop2-rs2, GPx*, Prdx6-rs2}, Bace1 (beta-site APP cleaving enzyme 1) [NCBI Gene 23821] {aka ASP2, Bace}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, Adam10 (a disintegrin and metallopeptidase domain 10) [NCBI Gene 11487] {aka 1700031C13Rik, MADM, kuz, kuzbanian}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Creb1 (cAMP responsive element binding protein 1) [NCBI Gene 12912] {aka 2310001E10Rik, 3526402H21Rik, Creb, Creb-1}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Pik3r1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 18708] {aka PI3K, p50alpha, p55alpha, p85alpha}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, Syp (synaptophysin) [NCBI Gene 20977] {aka A230093K24Rik, Syn, p38}, Sirt1 (sirtuin 1) [NCBI Gene 93759] {aka SIR2L1, Sir2, Sir2a, Sir2alpha}
- **Diseases:** inflammation (MESH:D007249), AD (MESH:D000544), Neuroinflammation (MESH:D000090862), cognitive decline (MESH:D003072), amyloid (MESH:C000718787)
- **Chemicals:** Nobiletin (MESH:C008661), 5XFAD (-), Congo red (MESH:D003224)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023540/full.md

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Source: https://tomesphere.com/paper/PMC13023540