Evidence map›Paper›PMID 41629683›Full record

ArticleNpj imaging2026

Accelerated and localized synucleinopathy in a hybrid mouse model: implications for positron emission tomography studies.

Chunfang A Xia, Hsiu-Ming Tsai, Sandra Diaz Garcia, Shuanglong Liu, Alessandra Matzeu, Mani Salarian, Wouter Bruinzeel, Anna K Szardenings

Abstract read
In one paragraph

Article in Npj imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Development and characterization of a novel TDP-43 positron emission tomography tracer: [Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Chunfang A XiaDiscovery Technologies and Molecular Pharmacology, Johnson & Johnson, San Diego, CA, USA. cxia1@its.jnj.com.
Hsiu-Ming TsaiDiscovery Technologies and Molecular Pharmacology, Johnson & Johnson, San Diego, CA, USA.
Sandra Diaz GarciaPreclinical Sciences and Translational Safety, Johnson & Johnson, San Diego, CA, USA.
Shuanglong LiuGlobal Discovery Chemistry, Johnson & Johnson, San Diego, CA, USA.
Alessandra MatzeuPreclinical Sciences and Translational Safety, Johnson & Johnson, San Diego, CA, USA.
Mani SalarianDiscovery Technologies and Molecular Pharmacology, Johnson & Johnson, San Diego, CA, USA.
Wouter BruinzeelNeuroscience Discovery, Johnson & Johnson, Beerse, Belgium.
Anna K SzardeningsDiscovery Technologies and Molecular Pharmacology, Johnson & Johnson, San Diego, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is characterized by alpha-synuclein (α-syn) aggregation, dopaminergic (DA) neuron loss, and neuroinflammation. Synucleinopathy, the α-syn-related pathology, is the central to the pathogenetic processes observed in the brains of patients with PD, dementia with Lewy bodies (DLB), and multiple system atrophy (MSA). We are seeking an animal model with synucleinopathy that can comprehensively replicate these pathologies and adhere to suitable timeframes for preclinical research for positron emission tomography (PET) imaging studies. Adeno-associated virus (AAV) carrying the mutated human α-syn gene and S87N α-syn preformed fibrils (PFF) were co-injected into the left substantia nigra (SN) of mouse brains. Immunohistochemistry (IHC) and PET/CT imaging were performed at different time points to detect the key pathologies in the brain. This model resulted in accelerated α-syn pathology, detectable as early as two weeks post-injection, alongside DA neuron loss, microglial activation, reduced synaptic density, and impaired mitochondrial function within five weeks. Pathology remained spatially localized. In summary, this AAV/PFF hybrid model offers a rapid, region-specific platform for studying synucleinopathies such as PD, as well as for evaluating PET ligands for disease diagnosis and monitoring.

Identifiers

PMID41629683
PMCPMC12864980

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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 OpenQuestion graph.