Evidence map›Paper›PMID 25681575›Full record

ArticleExperimental neurology2015

Tricyclic antidepressant treatment evokes regional changes in neurotrophic factors over time within the intact and degenerating nigrostriatal system.

Katrina L Paumier, Caryl E Sortwell, Lalitha Madhavan, Brian Terpstra, Brian F Daley, Timothy J Collier

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 29 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Katrina L PaumierDepartment of Translational Science and Molecular Medicine, Michigan State University, Grand Rapids, MI, USA. Electronic address: Katrina.paumier@hc.msu.edu.
Caryl E SortwellDepartment of Translational Science and Molecular Medicine, Michigan State University, Grand Rapids, MI, USA.
Lalitha MadhavanDepartment of Neurology, University of Arizona, Tucson, AZ, USA.
Brian TerpstraThe Parkinson's Disease Rehabilitation Institute, Cincinnati, OH, USA.
Brian F DaleyDepartment of Translational Science and Molecular Medicine, Michigan State University, Grand Rapids, MI, USA.
Timothy J CollierDepartment of Translational Science and Molecular Medicine, Michigan State University, Grand Rapids, MI, USA.
Michigan State University · USOrthopaedic Associates of Michigan · USUniversity of Arizona · US

Funding

STN Deep Brain Stimulation and NeuroprotectionP50NS058830 · NINDS · UNIVERSITY OF CINCINNATI · PI COLLIER, TIMOTHY J. · 2009 to 2015
$5.9M
NINDS NIH HHS P50 NS058830
6 · The paper itself

Abstract

In addition to alleviating depression, trophic responses produced by antidepressants may regulate neural plasticity in the diseased brain, which not only provides symptomatic benefit but also potentially slows the rate of disease progression in Parkinson's disease (PD). Recent in vitro and in vivo data provide evidence that neurotrophic factors such as brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF) may be key mediators of the therapeutic response to antidepressants. As such, we conducted a cross-sectional time-course study to determine whether antidepressant-mediated changes in neurotrophic factors occur in relevant brain regions in response to amitriptyline (AMI) treatment before and after intrastriatal 6-hydroxydopamine (6OHDA). Adult male Wistar rats were divided into seven cohorts and given daily injections (i.p.) of AMI (5mg/kg) or saline throughout the duration of the study. In parallel, various cohorts of intact or parkinsonian animals were sacrificed at specific time points to determine the impact of AMI treatment on trophic factor levels in the intact and degenerating nigrostriatal system. The left and right hemispheres of the substantia nigra, striatum, frontal cortex, piriform cortex, hippocampus, and anterior cingulate cortex were dissected, and BDNF and GDNF levels were measured with ELISA. Results show that chronic AMI treatment elicits effects in multiple brain regions and differentially regulates levels of BDNF and GDNF depending on the region. Additionally, AMI halts the progressive degeneration of dopamine (DA) neurons elicited by an intrastriatal 6-OHDA lesion. Taken together, these results suggest that AMI treatment elicits significant trophic changes important to DA neuron survival within both the intact and degenerating nigrostriatal system.

Indexed as

AmitriptylineAnimalsAntidepressive Agents, TricyclicBrain ChemistryBrain-Derived Neurotrophic FactorDopaminergic NeuronsGlial Cell Line-Derived Neurotrophic FactorMaleNerve DegenerationNerve Growth FactorsOxidopamineRatsRats, WistarSubstantia NigraSympathectomy, ChemicalSympatholyticsAmitriptylineAntidepressive Agents, TricyclicBrain-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic FactorNerve Growth FactorsOxidopamineSympatholyticsAmitriptylineAntidepressantsNeuroprotectionParkinson's diseaseTrophic factors

Identifiers

PMID25681575
PMCPMC4382385
OpenAlexW2075745941

What OpenQuestion holds

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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.