Evidence map›Paper›PMID 30375462›Full record

ArticleScientific reports2018

Standardized phytotherapic extracts rescue anomalous locomotion and electrophysiological responses of TDP-43 Drosophila melanogaster model of ALS.

Riccardo Maccioni, Maria Dolores Setzu, Giuseppe Talani, Paolo Solari, Ameya Kasture, Sonja Sucic, Simona Porru, Patrizia Muroni, Enrico Sanna, Sanjay Kasture and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Ashwagandha Extract as a Promising Source of Immunology Support forAnimals : an open access journal from MDPI · 2026
    Article
  2. Article
  3. Invertebrate genetic models of amyotrophic lateral sclerosis.Frontiers in molecular neuroscience · 2024
    Review
  4. Article
  5. Article
  6. Nutrients · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

12 authors at 3 institutions in 2 countries.

Riccardo MaccioniUniversity of Cagliari, Department of Biomedical Sciences, Monserrato, 09042, Italy.
Maria Dolores SetzuUniversity of Cagliari, Department of Biomedical Sciences, Monserrato, 09042, Italy.
Giuseppe TalaniNational Research Council (CNR), Institute of Neuroscience, Monserrato, 09042, Italy.
Paolo SolariUniversity of Cagliari, Department of Biomedical Sciences, Monserrato, 09042, Italy.ORCID http://orcid.org/0000-0001-8785-1438
Ameya KastureMedical University of Vienna, Institute of Pharmacology, Center of Physiology and Pharmacology, Vienna, A-1090, Austria.
Sonja SucicMedical University of Vienna, Institute of Pharmacology, Center of Physiology and Pharmacology, Vienna, A-1090, Austria.ORCID http://orcid.org/0000-0001-5136-8022
Simona PorruUniversity of Cagliari, Department of Life and Environmental Sciences, Cagliari, 09126, Italy.
Patrizia MuroniUniversity of Cagliari, Department of Biomedical Sciences, Monserrato, 09042, Italy.
Enrico SannaUniversity of Cagliari, Department of Life and Environmental Sciences, Cagliari, 09126, Italy.
Sanjay KasturePinnacle Biomedical Research Institute, Bhopal, 462003, India.
Elio AcquasUniversity of Cagliari, Department of Life and Environmental Sciences, Cagliari, 09126, Italy.
Anna LisciaUniversity of Cagliari, Department of Biomedical Sciences, Monserrato, 09042, Italy. liscia@unica.it.ORCID http://orcid.org/0000-0002-1629-2090
University of Cagliari · ITMedical University of Vienna · ATNational Research Council · IT

Funding

Austrian Science Fund FWF P 31255
6 · The paper itself

Abstract

Findings from studies using animal models expressing amyotrophic lateral sclerosis (ALS) mutations in RNA-binding proteins, such as Transactive Response DNA-binding protein-43 (TDP-43), indicate that this protein, which is involved in multiple functions, including transcriptional regulation and pre-mRNA splicing, represents a key candidate in ALS development. This study focuses on characterizing, in a Drosophila genetic model of ALS (TDP-43), the effects of Mucuna pruriens (Mpe) and Withania somnifera (Wse). Electrophysiological and behavioural data in TDP-43 mutant flies revealed anomalous locomotion (i.e. impaired climbing with unexpected hyperactivity) and sleep dysregulation. These features, in agreement with previous findings with a different ALS model, were at least partially, rescued by treatment with Mpe and Wse. In addition, electrophysiological recordings from dorsal longitudinal muscle fibers and behavioral observations of TDP-43 flies exposed to the volatile anaesthetics, diethyl ether or chloroform, showed paradoxical responses, which were normalized upon Mpe or Wse treatment. Hence, given the involvement of some potassium channels in the effects of anaesthetics, our results also hint toward a possible dysregulation of some potassium channels in the ALS-TDP-43 Drosophila model, that might shed new light on future therapeutic strategies pertaining to ALS.

Indexed as

Amyotrophic Lateral SclerosisAnimalsDisease Models, AnimalDrosophila melanogasterElectrophysiological PhenomenaGenetic Association StudiesGenetic Predisposition to DiseaseHumansLocomotionMotor NeuronsMutationPhytochemicalsPlant ExtractsTDP-43 ProteinopathiesPhytochemicalsPlant Extracts

Identifiers

PMID30375462
PMCPMC6207707
OpenAlexW2898217469

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.