Evidence map›Paper›PMID 36293338›Full record

ArticleInternational journal of molecular sciences2022

The Citrus Flavonoid Nobiletin Downregulates Angiopoietin-like Protein 3 (ANGPTL3) Expression and Exhibits Lipid-Modulating Effects in Hepatic Cells and Adult Zebrafish Models.

Ching-Yen Lin, Pei-Yi Chen, Hao-Jen Hsu, Wan-Yun Gao, Ming-Jiuan Wu, Jui-Hung Yen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 13 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

6 authors at 2 institutions in 1 country.

Ching-Yen LinDepartment of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 970374, Taiwan.ORCID 0000-0002-8543-5059
Pei-Yi ChenDepartment of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 970374, Taiwan.ORCID 0000-0003-4270-7031
Hao-Jen HsuDepartment of Life Science, Tzu Chi University, Hualien 970374, Taiwan.ORCID 0000-0001-6096-7481
Wan-Yun GaoInstitute of Medical Sciences, Tzu Chi University, Hualien 970374, Taiwan.
Ming-Jiuan WuDepartment of Biotechnology, Chia-Nan University of Pharmacy and Science, Tainan 717301, Taiwan.ORCID 0000-0003-3327-828X
Jui-Hung YenDepartment of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 970374, Taiwan.ORCID 0000-0003-2551-350X
Tzu Chi University · TWChia Nan University of Pharmacy and Science · TW

Funding

National Science and Technology Council, Taiwan. MOST 108-2320-B-320-002-MY3National Science and Technology Council, Taiwan. MOST 110-2320-B-041-002-MY3National Science and Technology Council, Taiwan. MOST 110-2320-B-303-003-MY2
6 · The paper itself

Abstract

Nobiletin, a dietary citrus flavonoid, exerts biological activities against hyperlipidemia, obesity, and atherosclerotic cardiovascular diseases (ASCVDs). The aim of this study was to explore the lipid-lowering effects of nobiletin and the underlying molecular mechanisms in vitro in hepatic cells and in vivo in zebrafish models. Transcriptome and gene ontology (GO) analyses of differentially expressed genes (DEGs) by gene set enrichment analysis (GSEA) showed that a set of twenty-eight core enrichment DEGs associated with "GO BP regulation of lipid metabolic process" (GO: 0019216) were significantly downregulated in nobiletin-treated cells. Among these genes, angiopoietin-like 3 (ANGPTL3), an inhibitor of lipoprotein lipase (LPL) activity that regulates TG-rich lipoprotein (TGRL) metabolism in circulation, was the protein most markedly downregulated by nobiletin. Nobiletin (20 and 40 μM) significantly reduced the levels of ANGPTL3 mRNA and intracellular and secreted ANGPTL3 proteins in hepatic cell lines. Furthermore, alleviation of secreted ANGPTL3 production by nobiletin was found to reinstate LPL catalytic activity. Nobiletin significantly inhibited ANGPTL3 promoter activity and attenuated the transcription factor liver X receptor-α (LXRα)-mediated ANGPTL3 transcription. Molecular docking analysis predicted that nobiletin could bind to the ligand-binding domain of LXRα, thereby counteracting LXRα activation. In animal studies, orally administered nobiletin significantly alleviated the levels of plasma triglycerides (TGs) and cholesterol in zebrafish fed a high-fat diet. Moreover, nobiletin significantly reduced the amounts of hepatic ANGPTL3 protein in zebrafish. Our findings suggest that nobiletin may regulate the LXRα-ANGPTL3-LPL axis and exhibit lipid-modulating effects in vitro and in vivo. Thus, nobiletin is a potential ANGPTL3 inhibitor for the regulation of lipid metabolism to ameliorate dyslipidemia and ASCVDs.

Indexed as

Angiopoietin-Like Protein 3CitrusAngiopoietin-like ProteinsAngiopoietinsAnimalsFlavonesFlavonoidsHepatocytesLigandsLipoprotein LipaseLipoproteinsLiver X ReceptorsMolecular Docking SimulationRNA, MessengerTranscription FactorsTriglyceridesAngiopoietin-Like Protein 3Angiopoietin-like ProteinsAngiopoietinsFlavonesFlavonoidsLigandsLipoprotein LipaseLipoproteinsLiver X ReceptorsnobiletinRNA, MessengerTranscription FactorsTriglyceridesANGPTL3lipoprotein lipaseLXRαnobiletinTG-rich lipoprotein

Identifiers

PMID36293338
PMCPMC9604320
OpenAlexW4306765265

What OpenQuestion holds

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LicenceCC BY
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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.