Evidence map›Paper›PMID 31311094›Full record

ArticleInternational journal of molecular sciences2019

NLRP3 Inflammasome Modulation by Melatonin Supplementation in Chronic Pristane-Induced Lupus Nephritis.

Francesca Bonomini, Mariane Dos Santos, Francisco Veríssimo Veronese, Rita Rezzani

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  5. Obesity-Related Glomerulosclerosis-How Adiposity Damages the Kidneys.International journal of molecular sciences · 2025
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  13. Research Progress of Pyroptosis in Renal Diseases.Current medicinal chemistry · 2024
    Review
  14. Review
  15. Review
  16. Article
  17. Does Pyroptosis Play a Role in Inflammasome-Related Disorders?International journal of molecular sciences · 2022
    Review
  18. Article
  19. Review
  20. 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

4 authors at 2 institutions in 2 countries.

Francesca BonominiAnatomy and Physiopathology Division, Department of Clinical and Experimental Sciences, University o of Brescia, Viale Europa, 25123 Brescia, Italy.ORCID 0000-0001-7210-0308
Mariane Dos SantosLaboratory of Molecular Biology Applied to Nephrology, Experimental Research Center, Hospital de Clínicas de Porto Alegre, 90035-903 Porto Alegre, Brazil.
Francisco Veríssimo VeroneseLaboratory of Molecular Biology Applied to Nephrology, Experimental Research Center, Hospital de Clínicas de Porto Alegre, 90035-903 Porto Alegre, Brazil.
Rita RezzaniAnatomy and Physiopathology Division, Department of Clinical and Experimental Sciences, University o of Brescia, Viale Europa, 25123 Brescia, Italy. rita.rezzani@unibs.it.ORCID 0000-0002-7515-5846
Hospital de Clínicas de Porto Alegre · BRUniversity of Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lupus nephritis (LN) is a kidney inflammatory disease caused by systemic lupus erythematosus (SLE). NLRP3 inflammasome activation is implicated in LN pathogenesis, suggesting its potential targets for LN treatment. Melatonin, an endogenous indoleamine, is considered an important multitasking molecule that has been reported to have anti-inflammatory effects by inhibiting nuclear factor-kappa B (NF-κB)-mediated inflammatory responses in vivo. This molecule has also protective effects against the activation of the inflammasomes and, in particular, the NLRP3 inflammasome. Thus, this work evaluated the effect of melatonin on morphological alteration and NLRP3 inflammasome activation in LN pristane mouse models. To evaluate the melatonin effects in these mice, we studied the renal cytoarchitecture by means of morphological analyses and immunohistochemical expression of specific markers related to oxidative stress, inflammation and inflammasome activation. Our results showed that melatonin attenuates pristane-induced LN through restoring of morphology and attenuation of oxidative stress and inflammation through a pathway that inhibited activation of NLRP3 inflammasome signaling. Our data clearly demonstrate that melatonin has protective activity on lupus nephritis in these mice that is highly associated with its effect on enhancing the Nrf2 antioxidant signaling pathway and decreasing renal NLRP3 inflammasome activation.

Indexed as

AnimalsAnti-Inflammatory AgentsAntioxidantsFemaleInflammasomesLupus NephritisMelatoninMiceMice, Inbred BALB CNLR Family, Pyrin Domain-Containing 3 ProteinTerpenesAnti-Inflammatory AgentsAntioxidantsInflammasomesMelatoninNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousepristaneTerpenesinflammationLupus nephritismelatoninoxidative stress

Identifiers

PMID31311094
PMCPMC6678949
OpenAlexW2959479777

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.