Evidence map›Paper›PMID 26569269›Full record

ArticleMarine drugs2015

Polyphenol-Rich Fraction of Ecklonia cava Improves Nonalcoholic Fatty Liver Disease in High Fat Diet-Fed Mice.

Eun-Young Park, Hojung Choi, Ji-Young Yoon, In-Young Lee, Youngwan Seo, Hong-Seop Moon, Jong-Hee Hwang, Hee-Sook Jun

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.7field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Brown AlgaeMarine drugs · 2024
    Article
  3. Article
  4. Nutrients · 2023
    Article
  5. Article
  6. Article
  7. Protective Effect ofMolecules (Basel, Switzerland) · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Phlorotannins fromMarine drugs · 2019
    Article
  12. Nutrients · 2019
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. 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

8 authors at 3 institutions in 1 country.

Eun-Young ParkCollege of Pharmacy, Mokpo National University, Muan-gun, Jeonnam 58554, Korea. parkey@mokpo.ac.kr.
Hojung ChoiCollege of Pharmacy, Gachon Institute of Pharmaceutical Science, Gachon University, Yeonsu-gu, Incheon 21999, Korea. hchoi@gachon.ac.kr.
Ji-Young YoonCollege of Pharmacy, Gachon Institute of Pharmaceutical Science, Gachon University, Yeonsu-gu, Incheon 21999, Korea. yoonj6@naver.com.
In-Young LeeKorea Mouse Metabolic Phenotyping Center (KMMPC), Lee Gil Ya Cancer and Diabetes Institute, Gachon University, Yeonsu-gu, Incheon 21999, Korea. 76pey@naver.com.
Youngwan SeoOcean Science & Technology School, Korea Maritime and Ocean University, Yeongdo-gu, Busan 49112, Korea. ywseo@kmou.ac.kr.
Hong-Seop MoonCollege of Pharmacy, Mokpo National University, Muan-gun, Jeonnam 58554, Korea. hbsmoon@mokpo.ac.kr.
Jong-Hee HwangKorea Mouse Metabolic Phenotyping Center (KMMPC), Lee Gil Ya Cancer and Diabetes Institute, Gachon University, Yeonsu-gu, Incheon 21999, Korea. jonghhwang@gachon.ac.kr.
Hee-Sook JunCollege of Pharmacy, Gachon Institute of Pharmaceutical Science, Gachon University, Yeonsu-gu, Incheon 21999, Korea. hsjun@gachon.ac.kr.
Gachon University · KRMokpo National University · KRKorea Maritime and Ocean University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ecklonia cava (E. cava; CA) is an edible brown alga with beneficial effects in diabetes via regulation of various metabolic processes such as lipogenesis, lipolysis, inflammation, and the antioxidant defense system in liver and adipose tissue. We investigated the effect of the polyphenol-rich fraction of E. cava produced from Gijang (G-CA) on nonalcoholic fatty liver disease (NAFLD) in high-fat diet (HFD)-fed mice. C57BL6 mice were fed a HFD for six weeks and then the HFD group was administered 300 mg/kg of G-CA extracts by oral intubation for 10 weeks. Body weight, fat mass, and serum biochemical parameters were reduced by G-CA extract treatment. MRI/MRS analysis showed that liver fat and liver volume in HFD-induced obese mice were reduced by G-CA extract treatment. Further, we analyzed hepatic gene expression related to inflammation and lipid metabolism. The mRNA expression levels of inflammatory cytokines and hepatic lipogenesis-related genes were decreased in G-CA-treated HFD mice. The mRNA expression levels of cholesterol 7 alpha-hydroxylase 1 (CYP7A1), the key enzyme in bile acid synthesis, were dramatically increased by G-CA treatment in HFD mice. We suggest that G-CA treatment ameliorated hepatic steatosis by inhibiting inflammation and improving lipid metabolism.

Indexed as

AnimalsCholesterol 7-alpha-HydroxylaseCytokinesDiet, High-FatDisease Models, AnimalGene Expression RegulationInflammationLipid MetabolismLipogenesisLiverMaleMiceMice, Inbred C57BLNon-alcoholic Fatty Liver DiseaseObesityPhaeophyceaeCholesterol 7-alpha-HydroxylaseCyp7a1 protein, mouseCytokinesPolyphenolsRNA, MessengerEcklonia cavafatty liverhepatic steatosisMRIMRSNAFLD

Identifiers

PMID26569269
PMCPMC4663557
OpenAlexW2106900623

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.