Evidence map›Paper›PMID 24406899›Full record

ArticlePeptides2014

Dynamic changes in dopamine neuron function after DNSP-11 treatment: effects in vivo and increased ERK 1/2 phosphorylation in vitro.

Joshua L Fuqua, Ofelia M Littrell, Martin Lundblad, Jadwiga Turchan-Cholewo, Lina G Abdelmoti, Emilia Galperin, Luke H Bradley, Wayne A Cass, Don M Gash, Greg A Gerhardt

Abstract read
In one paragraph

Article in Peptides, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Research progress on intranasal treatment for Parkinson's disease.Neuroprotection (Chichester, England) · 2024
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. 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

10 authors at 2 institutions in 2 countries.

Joshua L FuquaDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA.
Ofelia M LittrellDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA.
Martin LundbladExperimental Medical Science, Neurobiology, Lund University, BMCA11, 221, 84 Lund, Sweden.
Jadwiga Turchan-CholewoDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA.
Lina G AbdelmotiDepartment of Molecular & Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY, USA; Center of Structural Biology, University of Kentucky College of Medicine, Lexington, KY, USA.
Emilia GalperinDepartment of Molecular & Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY, USA; Center of Structural Biology, University of Kentucky College of Medicine, Lexington, KY, USA.
Luke H BradleyDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA; Department of Molecular & Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY, USA; Center of Structural Biology, University of Kentucky College of Medicine, Lexington, KY, USA.
Wayne A CassDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA.
Don M GashDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA.
Greg A GerhardtDepartment of Anatomy and Neurobiology, Parkinson's Disease Translational Center of Excellence, University of Kentucky Medical Center, MN 206 Medical Sciences Building, 800 Rose St., Lexington, KY 40536, USA. Electronic address: greg.gerhardt@uky.edu.
University of Kentucky · USLund University · SE

Funding

WKU Lead Faculty AwardP20GM103436 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ERIC C ROUCHKA · 2012 to 2026
$60.1M
ZEBRAFISH VISUAL FUNCTION RECOVERY FOLLOWING OPTIC NERVE DAMAGEP20RR016481 · NCRR · UNIVERSITY OF LOUISVILLE · PI BARTON, HAZEL A · 2001 to 2011
$34.8M
UNDERSTANDING THE MOLECULAR BASIS OF EPIGENETIC TRANSCRIPTIONAL SILENCINGP20RR020171 · NCRR · UNIVERSITY OF KENTUCKY · PI LOUIS HERSH, LOUIS HERSH LOUIS HERSH · 2004 to 2011
$16.5M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
Restoration of Dopaminergic Function in Parkinson's DiseaseP50NS039787 · NINDS · UNIVERSITY OF KENTUCKY · PI GASH, DON MARSHALL · 1999 to 2009
$10.9M
NEUROCHEMICAL STUDIES OF THE AGING BASAL GANGLIAP01AG013494 · NIA · UNIVERSITY OF KENTUCKY · PI GASH, DON MARSHALL · 1997 to 2007
$5.5M
THE MOLECULAR AND CELLULAR BASIS OF BRAIN AGINGT32AG000242 · NIA · UNIVERSITY OF KENTUCKY · PI GERHARDT, GREG A. · 1994 to 2013
$3.4M
Neurobiology of CNS Injury and RepairT32NS077889 · NINDS · UNIVERSITY OF KENTUCKY · PI Warren Joseph Alilain, JOHN C GENSEL · 2012 to 2026
$2.4M
Neurochem Chip: Methodology to Study Untethered RatsR01DA017186 · NIDA · UNIVERSITY OF KENTUCKY · PI GERHARDT, GREG A. · 2003 to 2007
$2.0M
Therapeutic Strategies for Neurodegeneration Training GrantT32DA022738 · NIDA · UNIVERSITY OF KENTUCKY · PI HALL, EDWARD D. · 2006 to 2010
$1.2M
Regulation of MAPK Activity by EGFR EndocytosisR00CA126161 · NCI · UNIVERSITY OF KENTUCKY · PI GALPERIN, EMILIA · 2010 to 2012
$731k
Calcitriol and Methamphetamine NeurotoxicityR21DA022314 · NIDA · UNIVERSITY OF KENTUCKY · PI CASS, WAYNE A · 2007 to 2008
$363k
NCATS NIH HHS UL1 TR000117NCATS NIH HHS UL1TR000117NCI NIH HHS R00 CA126161NCRR NIH HHS 5P20RR016481-12NCRR NIH HHS P20 RR020171NCRR NIH HHS P20RR20171NIA NIH HHS 5T32 AG000242NIA NIH HHS 5T32 AG000242-14NIA NIH HHS AG13494NIA NIH HHS P01 AG013494NIA NIH HHS T32 AG000242NIA NIH HHS T32-AG00242NIDA NIH HHS 1T32 DA022738NIDA NIH HHS DA22314NIDA NIH HHS R01 DA017186NIDA NIH HHS R21 DA022314NIDA NIH HHS T32 DA022738NIGMS NIH HHS 8 P20 GM103436-12NINDS NIH HHS NS075694NINDS NIH HHS NS39787NINDS NIH HHS NS60924NINDS NIH HHS P50 NS039787NINDS NIH HHS P50-NS039787NINDS NIH HHS R03 NS075694NINDS NIH HHS R21 NS060924NINDS NIH HHS T32 NS077889PHS HHS P01-13494
6 · The paper itself

Abstract

Glial cell-line derived neurotrophic factor (GDNF) has demonstrated robust effects on dopamine (DA) neuron function and survival. A post-translational processing model of the human GDNF proprotein theorizes the formation of smaller, amidated peptide(s) from the proregion that exhibit neurobiological function, including an 11-amino-acid peptide named dopamine neuron stimulating peptide-11 (DNSP-11). A single treatment of DNSP-11 was delivered to the substantia nigra in the rat to investigate effects on DA-neuron function. Four weeks after treatment, potassium (K+) and D-amphetamine evoked DA release were studied in the striatum using microdialysis. There were no significant changes in DA-release after DNSP-11 treatment determined by microdialysis. Dopamine release was further examined in discrete regions of the striatum using high-speed chronoamperometry at 1-, 2-, and 4-weeks after DNSP-11 treatment. Two weeks after DNSP-11 treatment, potassium-evoked DA release was increased in specific subregions of the striatum. However, spontaneous locomotor activity was unchanged by DNSP-11 treatment. In addition, we show that a single treatment of DNSP-11 in the MN9D dopaminergic neuronal cell line results in phosphorylation of ERK1/2, which suggests a novel cellular mechanism responsible for increases in DA function.

Indexed as

AnimalsCell LineDopamineGlial Cell Line-Derived Neurotrophic FactorHumansIn Vitro TechniquesMaleMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Motor ActivityNeuronsOligopeptidesPeptide FragmentsPhosphorylationRats, Inbred F344Substantia NigraDopamineGlial Cell Line-Derived Neurotrophic FactorMAPK1 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3OligopeptidesPeptide Fragmentsprolyl-prolyl-glutamyl-alanyl-prolyl-alanyl-glutamyl-aspartyl-arginyl-seryl-leucinamideDopamineGlial cell line-derived neurotrophic factorParkinson's diseasePeptideStriatum

Identifiers

PMID24406899
PMCPMC3989369
OpenAlexW1998096796

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.