Evidence map›Paper›PMID 28980850›Full record

ArticleAutophagy2018

Rilmenidine promotes MTOR-independent autophagy in the mutant SOD1 mouse model of amyotrophic lateral sclerosis without slowing disease progression.

Nirma D Perera, Rebecca K Sheean, Chew L Lau, Yea Seul Shin, Philip M Beart, Malcolm K Horne, Bradley J Turner

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
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  9. Article
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  11. Molecular hallmarks of ageing in amyotrophic lateral sclerosis.Cellular and molecular life sciences : CMLS · 2024
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Fountain of youth-Targeting autophagy in aging.Frontiers in aging neuroscience · 2023
    Review
  17. Article
  18. Frontiers in molecular neuroscience · 2023
    Review
  19. Review
  20. Review
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

7 authors at 2 institutions in 1 country.

Nirma D Pereraa The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Rebecca K Sheeana The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Chew L Laua The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Yea Seul Shina The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Philip M Bearta The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Malcolm K Hornea The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Bradley J Turnera The Florey Institute of Neuroscience and Mental Health, University of Melbourne , Parkville , Victoria , Australia.
Florey Institute of Neuroscience and Mental Health · AUUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macroautophagy/autophagy is the main intracellular catabolic pathway in neurons that eliminates misfolded proteins, aggregates and damaged organelles associated with ageing and neurodegeneration. Autophagy is regulated by both MTOR-dependent and -independent pathways. There is increasing evidence that autophagy is compromised in neurodegenerative disorders, which may contribute to cytoplasmic sequestration of aggregation-prone and toxic proteins in neurons. Genetic or pharmacological modulation of autophagy to promote clearance of misfolded proteins may be a promising therapeutic avenue for these disorders. Here, we demonstrate robust autophagy induction in motor neuronal cells expressing SOD1 or TARDBP/TDP-43 mutants linked to amyotrophic lateral sclerosis (ALS). Treatment of these cells with rilmenidine, an anti-hypertensive agent and imidazoline-1 receptor agonist that induces autophagy, promoted autophagic clearance of mutant SOD1 and efficient mitophagy. Rilmenidine administration to mutant SOD1

Indexed as

Amyotrophic Lateral SclerosisAnimalsAutophagyDisease Models, AnimalDNA-Binding ProteinsHumansMice, TransgenicMotor NeuronsRilmenidineSuperoxide Dismutase-1TOR Serine-Threonine KinasesDNA-Binding ProteinsMTOR protein, humanmTOR protein, mouseRilmenidineSOD1 protein, humanSod1 protein, mouseSuperoxide Dismutase-1TOR Serine-Threonine KinasesALSautophagymotor neuronrilmenidineSOD1TARDBP

Identifiers

PMID28980850
PMCPMC5915012
OpenAlexW2761647282

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.