Evidence map›Paper›PMID 34165214›Full record

ArticleCell proliferation2021

Nodakenin represses obesity and its complications via the inhibition of the VLDLR signalling pathway in vivo and in vitro.

Bo-Ram Jin, Minho Lee, Hyo-Jin An

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Herbal Combination ofFood science & nutrition · 2025
    Article
  4. Article
  5. Anti-Obesity and Anti-Diabetic Effects ofInternational journal of molecular sciences · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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

3 authors at 2 institutions in 1 country.

Bo-Ram JinDepartment of Pharmacology, College of Korean Medicine, Sangji University, Wonju, Korea.
Minho LeeDepartment of Life Science, Dongguk University-Seoul, Goyang-si, Korea.
Hyo-Jin AnDepartment of Pharmacology, College of Korean Medicine, Sangji University, Wonju, Korea.ORCID https://orcid.org/0000-0002-2937-874X
Sangji University · KRDongguk University · KR

Funding

Korean Government NRF-2017M3A9B6061511Korean Government NRF-2017R1C1B2008617
6 · The paper itself

Abstract

objectivesNodakenin (NK) is a coumarin glucoside that is found in the roots of Angelicae gigas. A limited number of studies have been conducted on the pharmacological activities of NK. Although NK is an important natural resource having anti-inflammatory and antioxidant effects, no investigation has been conducted to examine the effects of NK on obesity and obesity-induced inflammation. MATERIALS AND

methodsThe present study investigated the therapeutic effects of NK treatment on obesity and its complications, and its mechanism of action using differentiated 3T3-L1 adipocytes and high-fat diet (HFD)-induced obese mice. Oil red O staining, western blot assay, qRT-PCR assay, siRNA transfection, enzyme-linked immunosorbent assay, H&E staining, immunohistochemistry, molecular docking and immunofluorescence staining were utilized.

resultsTreatment with NK demonstrated anti-adipogenesis effects via the regulation of adipogenic transcription factors and genes associated with triglyceride synthesis in differentiated 3T3-L1 adipocytes. Compared with the control group, the group administered NK showed a suppression in weight gain, dyslipidaemia and the development of fatty liver in HFD-induced obese mice. In addition, NK administration inhibited adipogenic differentiation and obesity-induced inflammation and oxidative stress via the suppression of the VLDLR and MEK/ERK1/2 pathways. This is the first study that has documented the interaction between NK and VLDLR structure.

conclusionThese results demonstrate the potential of NK as a natural product-based therapeutic candidate for the treatment of obesity and its complications by targeting adipogenesis and adipose tissue inflammation-associated markers.

Indexed as

3T3-L1 CellsAdipogenesisAnimalsCell DifferentiationCholesterolCoumarinsDiet, High-FatGlucosidesMaleMiceMice, Inbred C57BLMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3ObesityReceptors, LDLRNA InterferenceCholesterolCoumarinsGlucosidesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3nodakeninReceptors, LDLRNA, Small InterferingVLDL receptoradipogenesisMetainflammationNodakeninobesityoxidative stressVLDLR

Identifiers

PMID34165214
PMCPMC8349651
OpenAlexW3176405814

What OpenQuestion holds

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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.