Evidence map›Paper›PMID 31478124›Full record

ArticleNeurotoxicity research2020

Differential Effects of LPS and 6-OHDA on Microglia's Morphology in Rats: Implications for Inflammatory Model of Parkinson's Disease.

Irving Parra, Isabel Martínez, Gabriel Ramírez-García, Yousef Tizabi, Liliana Mendieta

Abstract read
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In one paragraph

Article in Neurotoxicity research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 28 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

5 authors at 3 institutions in 2 countries.

Irving ParraLaboratorio de Neuroquímica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, 14 Sur y Av. San Claudio CU, Col. San Manuel, 72570, Puebla, Mexico.
Isabel MartínezLaboratorio de Neuroquímica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, 14 Sur y Av. San Claudio CU, Col. San Manuel, 72570, Puebla, Mexico.
Gabriel Ramírez-GarcíaUnidad Periférica de Neurociencias, Facultad de Medicina, Universidad Nacional Autónoma de México, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suárez", Ciudad de Mexico, Mexico.
Yousef TizabiDepartment of Pharmacology, Howard University College of Medicine, Washington, DC, USA.
Liliana MendietaLaboratorio de Neuroquímica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, 14 Sur y Av. San Claudio CU, Col. San Manuel, 72570, Puebla, Mexico. liliana.martinezmen@correo.buap.mx.ORCID http://orcid.org/0000-0001-6049-2770
Benemérita Universidad Autónoma de Puebla · MXHoward University · USInstituto Nacional de Neurología y Neurocirugía · MX

Funding

VIEP-BUAP 2019
6 · The paper itself

Abstract

Parkinson's disease (PD) is an idiopathic and progressive neurodegenerative disease characterized by the loss of ~ 80% of dopaminergic neurons in substantia nigra pars compacta (SNpc). Because activation of the innate cellular immune response, mediated by microglia, has been linked to the neurodegeneration in PD, in the present study, we evaluated the effects of lipopolysaccharide (LPS) and 6-hydroxydopamine (6-OHDA) on microglia's morphology, reflective of their activity, as well as tyrosine hydroxylase (TH)-positive neurons in SNpc and motor behavior. Adult male Wistar rats were stereotactically injected with LPS or 6-OHDA into the left dorsolateral striatum. Control groups received appropriate vehicle. The morphological changes of microglial cells and neurotoxic effects were examined at 1, 7, and 14 post-injection days. Both LPS and 6-OHDA caused activation and morphological changes in microglial cells as well as loss of dopaminergic neurons in SNpc. These effects were maximal at 14 days post-injection where motor impairments were also evident. However, our findings indicate that 6-OHDA causes a low degree of microglia activation compared to LPS. Hence, it may be concluded that LPS model of PD might be a better representation of inflammatory involvement in this devastating disease.

Indexed as

AnimalsCorpus StriatumDisease Models, AnimalDopaminergic NeuronsLipopolysaccharidesMaleMicrogliaMicroinjectionsMotor ActivityOxidopamineParkinson Disease, SecondaryPars CompactaRatsTime FactorsTyrosine 3-MonooxygenaseLipopolysaccharidesOxidopamineTyrosine 3-Monooxygenase6-HydroxydopamineInflammationLipopolysaccharideMicrogliaParkinson’s diseaseSubstantia nigra

Identifiers

PMID31478124
OpenAlexW2972193916

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.