Evidence map›Paper›PMID 25550814›Full record

ArticleInternational journal of clinical and experimental pathology2014

α-Naphthoflavone modulates inflammatory response in adipocytes-macrophages interaction through NFκB signaling.

Yanmei Sun, Minghua Xie, Tingting Huang, Xu Zhang, Sicong Lei, Qun Shi, Suqing Wang, Cuifang Fan, Jie Zhang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 1 institution in 1 country.

Yanmei SunDepartment of Obstetrics and Gynecology, Renmin Hospital, Wuhan University China.
Minghua XieDepartment of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.
Tingting HuangDepartment of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.
Xu ZhangDepartment of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.
Sicong LeiDepartment of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.
Qun ShiDepartment of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.
Suqing WangDepartment of Nutrition and Food Hygiene, School of Public Health, Wuhan University China.
Cuifang FanDepartment of Obstetrics and Gynecology, Renmin Hospital, Wuhan University China.
Jie ZhangDepartment of Urology, Renmin Hospital, Wuhan University China ; Hubei Key Laboratory of Kidney Disease Pathogenesis and Intervention Huangshi, China.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveOur previous study demonstrated that α-naphthoflavone (α-NF) inhibits mouse 3T3-L1 pre-adipocytes differentiation via PPARγ, a key transcription factor in adipogenesis. Due to the critical role of inflammation in adipogenesis, we speculated that the suppression role of α-NF in adipogenesis might involve in modulation of cytokines secretion raised by adipocyte differentiation cocktail. Therefore, the present study aims to investigate the role of α-NF in modulating of inflammatory response during adipocytes differentiation and adipocyte-macrophage interaction.

methodsConditioned medium from different doses of α-NF treated 10-day differentiated 3T3-L1 adipocytes were collected to culture RAW264.7 macrophages. Conditioned medium from activated macrophages and α-NF pre-treated macrophage were used to investigate the effects of α-NF in adipocytes differentiation. Cultured cells and medium were harvested for RT-PCR, Western blot and ELISA.

resultsα-NF dose-dependently decreased TNF-α and IL-6 and increased IL-10 expression induced by IDM (Insulin, dexamethasone, isobutylmethylxanthine) in 3T3-L1 pre-adipocytes. Conditioned medium from α-NF treated 3T3-L1 differentiated cells inhibited inflammatory response in mouse macrophage cell line RAW264.7 in contrast to IDM control medium. NFĸB activation elicited by IDM was suppressed by α-NF in a dose-response manner. Consequently, decreased TNF-α and increased IL-10 secretion, downstream targets of NFĸB signaling pathway, were observed with α-NF in macrophages. Finally, Conditioned medium from α-NF pre-treated, LPS-activated macrophages ameliorated the suppression of 3T3-L1 adipogenesis by LPS activated macrophages.

conclusionOur results suggest that α-NF regulates inflammation response in both adipocytes and macrophages and adipocyte-macrophage interaction which contributes to pre-adipocyte differentiation.

Indexed as

3T3-L1 CellsAdipocytesAnimalsBenzoflavonesDose-Response Relationship, DrugInterleukin-10Interleukin-6MacrophagesMiceNF-kappa BSignal TransductionTumor Necrosis Factor-alphaalpha-naphthoflavoneBenzoflavonesInterleukin-10Interleukin-6NF-kappa BTumor Necrosis Factor-alphaAdipocyte-macrohage interactioncondition mediuminflammationα-NF

Identifiers

PMID25550814
PMCPMC4270567
OpenAlexW2200390719

What OpenQuestion holds

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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.