Evidence map›Paper›PMID 39201689›Full record

ArticleInternational journal of molecular sciences2024

Chronic Neuronal Hyperexcitation Exacerbates Tau Propagation in a Mouse Model of Tauopathy.

Itaru Nishida, Kaoru Yamada, Asami Sakamoto, Tomoko Wakabayashi, Takeshi Iwatsubo

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

5 authors.

Itaru NishidaDepartment of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo 1130033, Japan.
Kaoru YamadaDepartment of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo 1130033, Japan.ORCID 0000-0003-3696-0604
Asami SakamotoDepartment of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo 1130033, Japan.
Tomoko WakabayashiDepartment of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo 1130033, Japan.ORCID 0000-0001-7109-7741
Takeshi IwatsuboNational Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo 1878551, Japan.

Funding

Brain Mapping by Integrated Neurotechnologies for Disease Studies (Brain/MINDS) from Japan Agency for Medical Research and development, AMED JP20dm0207073Grant-in-Aid for Scientific Research (A) 20H00525Grant-in-Aid for Scientific Research (B) 23H02792JST CREST JPMJCR18H3Multidisciplinary Frontier Brain and Neuroscience Discoveries from AMED JP23wm0625001
6 · The paper itself

Abstract

The intracerebral spread of tau is a critical mechanism associated with functional decline in Alzheimer's disease (AD) and other tauopathies. Recently, a hypothesis has emerged suggesting that tau propagation is linked to functional neuronal connections, specifically driven by neuronal hyperactivity. However, experimental validation of this hypothesis remains limited. In this study, we investigated how tau propagation from the entorhinal cortex to the hippocampus, the neuronal circuit most susceptible to tau pathology in AD, is affected by the selective stimulation of neuronal activity along this circuit. Using a mouse model of seed-induced propagation combined with optogenetics, we found that the chronic stimulation of this neuronal connection over a 4-week period resulted in a significant increase in insoluble tau accumulation in both the entorhinal cortex and hippocampus. Importantly, the ratio of tau accumulation in the hippocampus relative to that in the entorhinal cortex, serving as an indicator of transcellular spreading, was significantly higher in mice subjected to chronic stimulation. These results support the notion that abnormal neuronal activity promotes tau propagation, thereby implicating it in the progression of tauopathy.

Indexed as

Disease Models, AnimalEntorhinal CortexHippocampusNeuronsTauopathiestau ProteinsAlzheimer DiseaseAnimalsMaleMiceMice, Inbred C57BLMice, TransgenicOptogeneticstau ProteinsAlzheimer’s diseaseentorhinal cortexhippocampusneuronal activitypropagationtau

Identifiers

PMID39201689
PMCPMC11354494

What OpenQuestion holds

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Registered trials

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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.