Evidence map›Paper›PMID 26009763›Full record

ReviewPhilosophical transactions of the Royal Society of London. Series B, Biological sciences2015

Levodopa-induced plasticity: a double-edged sword in Parkinson's disease?

Paolo Calabresi, Veronica Ghiglieri, Petra Mazzocchetti, Ilenia Corbelli, Barbara Picconi

Open access · bronzeAbstract readReview
In one paragraph

Review in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. mRNA mProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced Dyskinesia.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Pathological cell assembly dynamics in a striatal MSN network model.Frontiers in computational neuroscience · 2024
    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 3 institutions in 1 country.

Paolo CalabresiClinica Neurologica, Dipartimento di Medicina, Università degli Studi di Perugia, Ospedale Santa Maria della Misericordia, S. Andrea delle Fratte, Via Gambuli, Perugia 06156, Italy Fondazione Santa Lucia, IRCCS, via del Fosso di Fiorano 64, Rome 00143, Italy paolo.calabresi@unipg.it.
Veronica GhiglieriDipartimento di Filosofia, Scienze Sociali, Umane e della Formazione, Università degli Studi di Perugia, Piazza Ermini 1, Perugia 06123, Italy Fondazione Santa Lucia, IRCCS, via del Fosso di Fiorano 64, Rome 00143, Italy.
Petra MazzocchettiClinica Neurologica, Dipartimento di Medicina, Università degli Studi di Perugia, Ospedale Santa Maria della Misericordia, S. Andrea delle Fratte, Via Gambuli, Perugia 06156, Italy Fondazione Santa Lucia, IRCCS, via del Fosso di Fiorano 64, Rome 00143, Italy.
Ilenia CorbelliClinica Neurologica, Dipartimento di Medicina, Università degli Studi di Perugia, Ospedale Santa Maria della Misericordia, S. Andrea delle Fratte, Via Gambuli, Perugia 06156, Italy.
Barbara PicconiFondazione Santa Lucia, IRCCS, via del Fosso di Fiorano 64, Rome 00143, Italy.
Fondazione Santa Lucia · ITOspedale Santa Maria · ITUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The long-term replacement therapy with the dopamine (DA) precursor 3,4-dihydroxy-l-phenylalanine (L-DOPA) is a milestone in the treatment of Parkinson's disease (PD). Although this drug precursor can be metabolized into the active neurotransmitter DA throughout the brain, its therapeutic benefit is due to restoring extracellular DA levels within the dorsal striatum, which lacks endogenous DA as a consequence of the neurodegenerative process induced by the disease. In the early phases of PD, L-DOPA treatment is able to restore both long-term depression (LTD) and long-term potentiation (LTP), two major forms of corticostriatal synaptic plasticity that are altered by dopaminergic denervation. However, unlike physiological DA transmission, this therapeutic approach in the advanced phase of the disease leads to abnormal peaks of DA, non-synaptically released, which are supposed to trigger behavioural sensitization, namely L-DOPA-induced dyskinesia. This condition is characterized by a loss of synaptic depotentiation, an inability to reverse previously induced LTP. In the advanced stages of PD, L-DOPA can also induce non-motor fluctuations with cognitive dysfunction and neuropsychiatric symptoms such as compulsive behaviours and impulse control disorders. Although the mechanisms underlying the role of L-DOPA in both motor and behavioural symptoms are still incompletely understood, recent data from electrophysiological and imaging studies have increased our understanding of the function of the brain areas involved and of the mechanisms implicated in both therapeutic and adverse actions of L-DOPA in PD patients.

Indexed as

Cerebral CortexCorpus StriatumDopamineDose-Response Relationship, DrugHippocampusHumansLevodopaNeuronal PlasticityParkinson DiseaseDopamineLevodopaanimal modelsLevodopa treatmentParkinson's diseasesynaptic plasticity

Identifiers

PMID26009763
PMCPMC4455753
OpenAlexW2177709963

What OpenQuestion holds

Textmetadata
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.