Evidence map›Paper›PMID 31477726›Full record

ArticleNature communications2019

Blunting neuroinflammation with resolvin D1 prevents early pathology in a rat model of Parkinson's disease.

Paraskevi Krashia, Alberto Cordella, Annalisa Nobili, Livia La Barbera, Mauro Federici, Alessandro Leuti, Federica Campanelli, Giuseppina Natale, Gioia Marino, Valeria Calabrese and 16 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
11.8field-weighted citation impact, top 1% 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

108 citing papers in PubMed, 176 citations in OpenAlex.

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  19. Chronic palmitoylethanolamide administrationFrontiers in cellular neuroscience · 2025
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48 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 7 institutions in 3 countries.

Paraskevi Krashia *Department of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.ORCID http://orcid.org/0000-0002-8476-9233
Alberto Cordella *Department of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Annalisa Nobili *Department of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Livia La BarberaDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Mauro FedericiDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.ORCID http://orcid.org/0000-0003-4563-1677
Alessandro LeutiDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Federica CampanelliDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Giuseppina NataleDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Gioia MarinoDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Valeria CalabreseDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.ORCID http://orcid.org/0000-0002-1127-1741
Francescangelo VedeleDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Veronica GhiglieriDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Barbara PicconiDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Giulia Di LazzaroDepartment of Systems Medicine, University of Rome 'Tor Vergata', 00133, Rome, Italy.
Tommaso SchirinziDepartment of Systems Medicine, University of Rome 'Tor Vergata', 00133, Rome, Italy.
Giulia SancesarioDepartment of Clinical and Behavioural Neurology, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Nicolas CasadeiInstitute of Medical Genetics and Applied Genomics, University of Tübingen, 72076, Tübingen, Germany.
Olaf RiessInstitute of Medical Genetics and Applied Genomics, University of Tübingen, 72076, Tübingen, Germany.
Sergio BernardiniDepartment of Experimental Medicine and Surgery, University of Rome 'Tor Vergata', 00133, Rome, Italy.
Antonio PisaniDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.ORCID http://orcid.org/0000-0002-8432-594X
Paolo CalabresiDepartment of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Maria Teresa ViscomiInstitute of Histology and Embryology, Università Cattolica del Sacro Cuore, 00168, Rome, Italy.
Charles Nicholas SerhanCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anaesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital and Harvard Medical School, 02115, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4627-8545
Valerio Chiurchiù *Department of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Marcello D'Amelio *Department of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy.
Nicola Biagio Mercuri *Department of Experimental Neurosciences, IRCCS Santa Lucia Foundation, 00143, Rome, Italy. mercurin@med.uniroma2.it.ORCID http://orcid.org/0000-0001-6700-7491
University of Rome Tor Vergata · ITFondazione Santa Lucia · ITUniversità Campus Bio-Medico · ITUniversity of Perugia · ITUniversity of Tübingen · DEBrigham and Women's Hospital · USUniversità Cattolica del Sacro Cuore · IT

Funding

Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 2011 to 2020
$14.8M
BLOOD CELL LIPOXYGENASE PRODUCTS: FORMATION AND ACTIONR01GM038765 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 1992 to 2020
$4.9M
NIGMS NIH HHS P01 GM095467NIGMS NIH HHS R01 GM038765
6 · The paper itself

Abstract

Neuroinflammation is one of the hallmarks of Parkinson's disease (PD) and may contribute to midbrain dopamine (DA) neuron degeneration. Recent studies link chronic inflammation with failure to resolve early inflammation, a process operated by specialized pro-resolving mediators, including resolvins. However, the effects of stimulating the resolution of inflammation in PD - to modulate disease progression - still remain unexplored. Here we show that rats overexpressing human α-synuclein (Syn) display altered DA neuron properties, reduced striatal DA outflow and motor deficits prior to nigral degeneration. These early alterations are coupled with microglia activation and perturbations of inflammatory and pro-resolving mediators, namely IFN-γ and resolvin D1 (RvD1). Chronic and early RvD1 administration in Syn rats prevents central and peripheral inflammation, as well as neuronal dysfunction and motor deficits. We also show that endogenous RvD1 is decreased in human patients with early-PD. Our results suggest there is an imbalance between neuroinflammatory and pro-resolving processes in PD.

Indexed as

Disease Models, Animalalpha-SynucleinAnimalsDocosahexaenoic AcidsDopaminergic NeuronsHumansInflammationMaleMicrogliaNerve DegenerationParkinson DiseaseRatsRats, Sprague-DawleyRats, TransgenicSubstantia Nigraalpha-SynucleinDocosahexaenoic Acidsresolvin D1SNCA protein, human

Identifiers

PMID31477726
PMCPMC6718379
OpenAlexW2970729530

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.