Evidence map›Paper›PMID 30905766›Full record

ArticleNeurobiology of disease2019

Neuropathological changes and cognitive deficits in rats transgenic for human mutant tau recapitulate human tauopathy.

Janice C Malcolm, Lionel Breuillaud, Sonia Do Carmo, Hélène Hall, Lindsay A Welikovitch, Jennifer A Macdonald, Michel Goedert, A Claudio Cuello

Open access · hybridAbstract read
In one paragraph

Article in Neurobiology of disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. PET Imaging of a Transgenic Tau Rat Model SHR24 with [Molecular imaging and biology · 2025
    Article
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  10. Review
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  12. Magnetic Resonance Imaging in Tauopathy Animal Models.Frontiers in aging neuroscience · 2021
    Review
  13. 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 at 3 institutions in 2 countries.

Janice C MalcolmDepartment of Anatomy and Cell Biology, McGill University, Montréal, QC H3A 0C7, Canada.
Lionel BreuillaudDepartment of Pharmacology and Therapeutics, McGill University, Montréal, QC H3G 1Y6, Canada.
Sonia Do CarmoDepartment of Pharmacology and Therapeutics, McGill University, Montréal, QC H3G 1Y6, Canada.
Hélène HallDepartment of Pharmacology and Therapeutics, McGill University, Montréal, QC H3G 1Y6, Canada.
Lindsay A WelikovitchDepartment of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 2B4, Canada.
Jennifer A MacdonaldMedical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
Michel GoedertMedical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
A Claudio CuelloDepartment of Anatomy and Cell Biology, McGill University, Montréal, QC H3A 0C7, Canada; Department of Pharmacology and Therapeutics, McGill University, Montréal, QC H3G 1Y6, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 2B4, Canada. Electronic address: claudio.cuello@mcgill.ca.
McGill University · CAMedical Research Council · GBMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_U105184291
6 · The paper itself

Abstract

The assembly of tau protein into abnormal filaments and brain cell degeneration are characteristic of a number of human neurodegenerative diseases, including Alzheimer's disease and frontotemporal dementia and parkinsonism linked to chromosome 17. Several murine models have been generated to better understand the mechanisms contributing to tau assembly and neurodegeneration. Taking advantage of the more elaborate central nervous system and higher cognitive abilities of the rat, we generated a model expressing the longest human tau isoform (2N4R) with the P301S mutation. This transgenic rat line, R962-hTau, exhibits the main features of human tauopathies, such as: age-dependent increase in inclusions comprised of aggregated-tau, neuronal loss, global neurodegeneration as reflected by brain atrophy and ventricular dilation, alterations in astrocytic and microglial morphology, and myelin loss. In addition, substantial deficits across multiple memory and learning paradigms, including novel object recognition, fear conditioning and Morris water maze tasks, were observed at the time of advanced tauopathy. These results support the concept that progressive tauopathy correlates with brain atrophy and cognitive impairment.

Indexed as

AnimalsBrainCognitive DysfunctionDisease Models, AnimalInclusion BodiesRatsRats, TransgenicTauopathiestau Proteinstau ProteinsAlzheimer's diseaseFTDP-17TGliosisInflammationNeurodegenerationNeuronal lossRat modelTauopathy

Identifiers

PMID30905766
PMCPMC6597947
OpenAlexW2922829546

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.