ArticleMolecular neurobiology2026
Gallein-Loaded Albumin Nanoparticles Prevent Amyloid-β-Induced Amyloidogenic APP Processing, Synaptic Loss, and Dendritic Pathology.
Article in Molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
Abstract
Alzheimer's disease (AD) is a multifactorial and highly debilitating disorder with a long clinical course. The development of new therapeutic strategies capable of mitigating or delaying disease progression remains a major challenge. We previously identified the amyloid precursor protein (APP) as a receptor for aggregated amyloid-β (Aβ) species that signals through a Go/Gβγ-dependent pathway, thereby promoting amyloidogenesis and neurotoxicity. In this context, gallein (GAL), a selective inhibitor of Gβγ signaling, has demonstrated robust neuroprotective effects in preclinical AD models. However, GAL exhibits poor stability and limited aqueous solubility, which may restrict brain bioavailability. To overcome these limitations, a nanotechnology-based formulation strategy was implemented. Here, we report the design and generation of human serum albumin-based nanoparticles (HSA NPs) loaded with GAL (NP-GAL) using a green desolvation method followed by thermal stabilization. Using murine neuroblastoma cells, primary rat cortical neurons, and human iPSC-derived neurons, we demonstrate that NP-GAL effectively prevents Aβ-induced amyloidogenic APP processing, dendritic dystrophy, and presynaptic loss. In addition, both empty NPs and NP-GAL exhibit association with Aβ aggregates, suggesting an additional benefit, as these nanoparticles mitigate amyloid-associated toxicity. Notably, the nanoparticles themselves exert beneficial effects on dendritic morphology and provide protection against neurotoxic insults beyond amyloid pathology, including those induced by rotenone, a widely used experimental model of Parkinson's disease. Together, these in vitro findings suggest that HSA-based nanoparticles hold potential as a platform to stabilize GAL and exert intrinsic neuroprotective effects. These results provide a proof-of-concept for exploring nanoparticle-mediated Gβγ inhibition to counteract Aβ-induced neuronal dysfunction and synaptic pathology.
Indexed as
Identifiers
42563066What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.