Evidence map›Paper›PMID 20161443›Full record

ReviewFuture medicinal chemistry2009

mGluR4-positive allosteric modulation as potential treatment for Parkinson's disease.

Corey R Hopkins, Craig W Lindsley, Colleen M Niswender

Open access · greenAbstract readReview
In one paragraph

Review in Future medicinal chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 67 citations in OpenAlex.

  1. Update on mGlu4 modulator patents: 2017 to present.Expert opinion on therapeutic patents · 2025
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  10. Review
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  12. Discovery of VU2957 (Valiglurax): An mGluACS medicinal chemistry letters · 2019
    Article
  13. Article
  14. Review
  15. N-Pyrrylarylsulfones with High Therapeutic Potential.Molecules (Basel, Switzerland) · 2017
    Review
  16. Article
  17. Article
  18. Article
  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

3 authors at 1 institution in 1 country.

Corey R HopkinsDepartment of Pharmacology, Vanderbilt Program in Drug Discovery, Vanderbilt University Medical Center, Nashville, TN 37232-36000, USA. corey.r.hopkins@vanderbilt.edu
Craig W Lindsley
Colleen M Niswender
Vanderbilt University Medical Center · US

Funding

Metabotropic Glutamate Receptors in Basal GangliaR01NS048334 · NINDS · VANDERBILT UNIVERSITY · PI NISWENDER, COLLEEN M · 2005 to 2009
$1.7M
NINDS NIH HHS R01 NS048334
6 · The paper itself

Abstract

Although Parkinson's disease was first diagnosed nearly 200 years ago, its effective treatment still remains elusive for most of those diagnosed. The gold standard of treatment for most patients is 3,4-dihydroxy-L-phenylalanine. This drug works for most individuals early in the disease; however, resistant symptoms start to emerge after several years of treatment. There has been increased interest in finding novel therapies to help Parkinson's disease patients. Such strategies may have the benefit of not only treating the symptomatic issues of the disorder, but might also offer promise in protecting dopaminergic neurons from further degeneration. One such target that is now receiving much attention from the scientific community is the metabotropic glutamate receptor mGluR4. In this article, we briefly review Parkinson's disease and then recent work in the mGluR area, with a focus on the efforts being made toward finding and optimizing novel mGluR4 positive allosteric modulators (PAMs). Preclinically in rodent models, mGluR4 activation has offered much promise as a novel treatment of Parkinson's disease. Additionally, the specific use of PAMs, rather than direct-acting agonists at the orthosteric glutamate site, continues to be validated as a viable treatment option for this target. It is anticipated that continued progress in this area will further our understanding of the potential of mGluR4 modulation as a novel symptomatic and potentially disease-modifying treatment for Parkinson's disease.

Indexed as

Allosteric RegulationBenzopyransGlutamatesHumansParkinson DiseaseReceptors, Metabotropic GlutamateBenzopyransGlutamatesmetabotropic glutamate receptor 4N-phenyl-7-(hydroxyimino)cyclopropa(b)chromen-1a-carboxamideReceptors, Metabotropic Glutamate

Identifiers

PMID20161443
PMCPMC2790174
OpenAlexW2082439372

What OpenQuestion holds

Textmetadata
LicenceTDM
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.