Evidence map›Paper›PMID 31540057›Full record

ArticleInternational journal of molecular sciences2019

Niacin Ameliorates Neuro-Inflammation in Parkinson's Disease via GPR109A.

Banabihari Giri, Kasey Belanger, Marissa Seamon, Eric Bradley, Sharad Purohit, Raymond Chong, John C Morgan, Babak Baban, Chandramohan Wakade

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 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
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  7. The Role of NADPharmaceuticals (Basel, Switzerland) · 2024
    Review
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  13. ProbioticMicroorganisms · 2023
    Article
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  15. Malaysian brown macroalgaIranian journal of basic medical sciences · 2023
    Article
  16. Article
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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

9 authors at 3 institutions in 1 country.

Banabihari GiriCharlie Norwood VA Medical Center, Augusta, GA 30904, USA. bgiri@augusta.edu.
Kasey BelangerDepartment of Physiology, Augusta University, Augusta, GA 30912, USA. kbelanger@augusta.edu.ORCID 0000-0003-0209-8905
Marissa SeamonCharlie Norwood VA Medical Center, Augusta, GA 30904, USA. mseamon@augusta.edu.
Eric BradleyEdward Via College of Osteopathic Medicine, Greenville, SC 29303, USA. Ebradley@carolinas.vcom.edu.
Sharad PurohitCharlie Norwood VA Medical Center, Augusta, GA 30904, USA. spurohit@augusta.edu.ORCID 0000-0003-0385-3829
Raymond ChongCharlie Norwood VA Medical Center, Augusta, GA 30904, USA. rchong@augusta.edu.
John C MorganCharlie Norwood VA Medical Center, Augusta, GA 30904, USA. jmorgan@augusta.edu.
Babak BabanDepartment of Oral Biology and Diagnostic Sciences, Augusta University, Augusta, GA 30912, USA. bbaban@augusta.edu.ORCID 0000-0002-3144-2288
Chandramohan WakadeCharlie Norwood VA Medical Center, Augusta, GA 30904, USA. cwakade@augusta.edu.
Augusta University · USCharlie Norwood VA Medical Center · USEdward Via College of Osteopathic Medicine · US

Funding

GPR109A and Parkinson's Disease: Role of Niacin in Outcome MeasuresI01RX001613 · VA · CHARLIE NORWOOD VA MEDICAL CENTER · PI WAKADE, CHANDRAMOHAN · 2016 to 2020
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RRD VA I01 RX001613U.S. Department of Veterans Affairs RX001613
6 · The paper itself

Abstract

In this study, we used macrophage RAW264.7 cells to elucidate the molecular mechanism underlying the anti-inflammatory actions of niacin. Anti-inflammatory actions of niacin and a possible role of its receptor GPR109A have been studied previously. However, the precise molecular mechanism of niacin's action in reducing inflammation through GPR109A is unknown. Here we observed that niacin reduced the translocation of phosphorylated nuclear kappa B (p-NF-κB) induced by lipopolysaccharide (LPS) in the nucleus of RAW264.7 cells. The reduction in the nuclear translocation in turn decreased the expression of pro-inflammatory cytokines IL-1β, IL-6 in RAW264.7 cells. We observed a decrease in the nuclear translocation of p-NF-κB and the expression of inflammatory cytokines after knockdown of GPR109A in RAW264.7 cells. Our results suggest that these molecular actions of niacin are mediated via its receptor GPR109A (also known as HCAR2) by controlling the translocation of p-NF-κB to the nucleus. Overall, our findings suggest that niacin treatment may have potential in reducing inflammation by targeting GPR109A.

Indexed as

AnimalsAnti-Inflammatory AgentsHumansInflammationInterleukin-1betaInterleukin-6LipopolysaccharidesMacrophagesMiceMice, Inbred BALB CNF-kappa BNiacinParkinson DiseaseRAW 264.7 CellsReceptors, G-Protein-CoupledAnti-Inflammatory AgentsHCAR2 protein, humanHcar2 protein, mouseIL1B protein, humanInterleukin-1betaInterleukin-6LipopolysaccharidesNF-kappa BNiacinReceptors, G-Protein-CoupledcytokineGPR109Alipopolysaccharidemacrophageneurodegenerative diseaseneuroinflammationniacinParkinson’s diseasevitamin B3

Identifiers

PMID31540057
PMCPMC6770365
OpenAlexW2972991237

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.