Evidence map›Paper›PMID 21079735›Full record

ArticlePloS one2010

Static magnetic field exposure reproduces cellular effects of the Parkinson's disease drug candidate ZM241385.

Zhiyun Wang, Pao-Lin Che, Jian Du, Barbara Ha, Kevin J Yarema

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Review
  3. Cellular and Molecular Effects of Magnetic Fields.International journal of molecular sciences · 2024
    Review
  4. Review
  5. Review
  6. 2-Phenethylamines in Medicinal Chemistry: A Review.Molecules (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. 6-mT 0-120-Hz magnetic fields differentially affect cellular ATP levels.Environmental science and pollution research international · 2018
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Involvement of Na+/K+ pump in fine modulation of bursting activity of the snail Br neuron by 10 mT static magnetic field.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2012
    Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Zhiyun WangDepartment of Biomedical Engineering, The Johns Hopkins University, Baltimore, Maryland, United States of America.
Pao-Lin Che
Jian Du
Barbara Ha
Kevin J Yarema
Johns Hopkins University · US

Funding

Engineering a Carbohydrate-Biomaterial Interface for Control of Wnt Signaling andR01EB005692 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI YAREMA, KEVIN J · 2007 to 2010
$1.4M
NIBIB NIH HHS 5R01EB5692NIBIB NIH HHS R01 EB005692
6 · The paper itself

Abstract

backgroundThis study was inspired by coalescing evidence that magnetic therapy may be a viable treatment option for certain diseases. This premise is based on the ability of moderate strength fields (i.e., 0.1 to 1 Tesla) to alter the biophysical properties of lipid bilayers and in turn modulate cellular signaling pathways. In particular, previous results from our laboratory (Wang et al., BMC Genomics, 10, 356 (2009)) established that moderate strength static magnetic field (SMF) exposure altered cellular endpoints associated with neuronal function and differentiation. Building on this background, the current paper investigated SMF by focusing on the adenosine A(2A) receptor (A(2A)R) in the PC12 rat adrenal pheochromocytoma cell line that displays metabolic features of Parkinson's disease (PD). METHODOLOGY AND PRINCIPAL

findingsSMF reproduced several responses elicited by ZM241385, a selective A(2A)R antagonist, in PC12 cells including altered calcium flux, increased ATP levels, reduced cAMP levels, reduced nitric oxide production, reduced p44/42 MAPK phosphorylation, inhibited proliferation, and reduced iron uptake. SMF also counteracted several PD-relevant endpoints exacerbated by A(2A)R agonist CGS21680 in a manner similar to ZM241385; these include reduction of increased expression of A(2A)R, reversal of altered calcium efflux, dampening of increased adenosine production, reduction of enhanced proliferation and associated p44/42 MAPK phosphorylation, and inhibition of neurite outgrowth. CONCLUSIONS AND SIGNIFICANCE: When measured against multiple endpoints, SMF elicited qualitatively similar responses as ZM241385, a PD drug candidate. Provided that the in vitro results presented in this paper apply in vivo, SMF holds promise as an intriguing non-invasive approach to treat PD and potentially other neurological disorders.

Indexed as

MagneticsAdenosineAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsAdenosine TriphosphateAnalysis of VarianceAnimalsBlotting, WesternCalciumCell ProliferationCyclic AMPIronMagnetic Field TherapyMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neurites2-(4-(2-carboxyethyl)phenethylamino)-5'-N-ethylcarboxamidoadenosineAdenosineAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsAdenosine TriphosphateCalciumCyclic AMPIronMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3PhenethylaminesReceptor, Adenosine A2ATriazinesTriazolesZM 241385

Identifiers

PMID21079735
PMCPMC2975637
OpenAlexW1994714835

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.