Evidence map›Paper›PMID 29929501›Full record

ArticleBMC complementary and alternative medicine2018

Naringin ameliorates the high glucose-induced rat mesangial cell inflammatory reaction by modulating the NLRP3 Inflammasome.

Fenqin Chen, Guozhu Wei, Jiao Xu, Xiaoyu Ma, Qiuyue Wang

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

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  19. Targeting Pyroptosis: New Insights into the Treatment of Diabetic Microvascular Complications.Evidence-based complementary and alternative medicine : eCAM · 2022
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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 2 institutions in 1 country.

Fenqin ChenDepartments of Geriatric, the First Affiliated Hospital, China Medical University, Shenyang, 110001, China.
Guozhu WeiDepartment of Radiology, Orthopedic Hospital of Shenyang, Shenyang, 110001, China.
Jiao XuDepartments of Geriatric, the First Affiliated Hospital, China Medical University, Shenyang, 110001, China.
Xiaoyu MaDepartments of Geriatric, the First Affiliated Hospital, China Medical University, Shenyang, 110001, China.
Qiuyue WangDepartments of Endocrinology, the First Affiliated Hospital, China Medical University, Shenyang, 110001, China. wqycmu123@163.com.
China Medical University · CNFirst Hospital of China Medical University · CN

Funding

Department of Education of Liaoning Province L2015564Shenyang Municipal Science and Technology project F17-231-1-56
6 · The paper itself

Abstract

backgroundThe Nucleotide binding and oligomerization domain-like receptorfamily pyrin domain-containing 3 (NLRP3)-inflammasome plays an important role in various diseases, including a variety of kidney diseases. Naringin exhibits anti-inflammatory and anti-oxidation effects among others, but its specific mechanisms are not clear. We investigated the expression of the NLRP3-inflammasome under high-glucose conditions, assessed the effects of naringin on that process, and further elucidated the role of naringin in the pathogenesis of diabetic kidney disease(DKD).

methodsTo assess the therapeutic potential of naringin and the mechanisms involved, we cultured rat glomerular mesangial cells and grouped them according to different glucose concentrations, different action times, different concentrations of MCC950, and different concentrations of naringin.The cell proliferation was measured by MTT assay. The expression of Interleukin-1β(IL-1β) and Interleukin18 (IL-18) in the cell supernatant were detected by ELISA. The expression and activity of NLPR3, apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC) and Caspase-1 were detected by Western Blot.

resultsThe expressions of NLRP3, ASC, caspase-1, IL-1β, and IL-18 in rat glomerular mesangial cells were significantly higher in the high glucose (HG) group than in the control normal glucose (NG) group and exhibited time-dependence activity. The expression levels of NLRP3, caspase-1, IL-1β, and IL-18 in different treatment groups were significantly lower compared with the HG group after 48 h of MCC950 pre-treatment (p < 0.05). Pre-treatment with naringin produced the same results. Naringin also inhibited the proliferation of cells.

conclusionsThe NLRP3-inflammasome potentially plays a role in the process of activation and inflammation of glomerular mesangial cells as induced by high-glucose conditions. Naringin inhibited the proliferation of cells that were induced by high glucose. Further, it reduced the expression of inflammatory factors that are mediated by NLRP3 through the NLRP3-caspase-1-IL-1β/IL-18 signaling pathway, which makes naringin a potentially novel treatment for DKD disease.

Indexed as

AnimalsDiabetic NephropathiesFlavanonesGlucoseInflammasomesInterleukin-1betaMesangial CellsNLR Family, Pyrin Domain-Containing 3 ProteinProtective AgentsRatsFlavanonesGlucoseInflammasomesInterleukin-1betanaringinNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratProtective AgentsDiabetes mellitusDiabetic kidney diseaseNaringinNLRP3-caspase-1-IL-1β/IL-18 signaling pathwayNLRP3 inflammasome

Identifiers

PMID29929501
PMCPMC6014005
OpenAlexW2809055337

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.