Evidence map›Paper›PMID 24688217›Full record

ArticleJournal of clinical biochemistry and nutrition2014

Role of Nrf2 in the alteration of cholesterol and bile acid metabolism-related gene expression by dietary cholesterol in high fat-fed mice.

Toshinori Kamisako, Yuji Tanaka, Yoshizumi Kishino, Takanori Ikeda, Kazuo Yamamoto, Shiori Masuda, Hiroshi Ogawa

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical biochemistry and nutrition, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 45 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

7 authors at 2 institutions in 1 country.

Toshinori KamisakoDepartment of Clinical Laboratory Medicine, Kinki University Faculty of Medicine, Osakasayama, Osaka 589-8511, Japan.
Yuji TanakaDepartment of Clinical Laboratory Medicine, Kinki University Faculty of Medicine, Osakasayama, Osaka 589-8511, Japan.
Yoshizumi KishinoDepartment of Clinical Laboratory Medicine, Kinki University Faculty of Medicine, Osakasayama, Osaka 589-8511, Japan ; Department of Biomedical Informatics, Division of Health Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Takanori IkedaFaculty of Human Sciences, Tezukayama Gakuin University, Sakai, Osaka 590-0113, Japan.
Kazuo YamamotoDivision of Basic Medical Science, Kinki University Faculty of Medicine, Osakasayama, Osaka 589-8511, Japan.
Shiori MasudaDepartment of Clinical Laboratory Medicine, Kinki University Faculty of Medicine, Osakasayama, Osaka 589-8511, Japan.
Hiroshi OgawaFaculty of Human Sciences, Tezukayama Gakuin University, Sakai, Osaka 590-0113, Japan.
Kindai University · JPTezukayama Gakuin University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear factor-E2-related factor 2 (Nrf2) is a regulator of lipid metabolism as well as various cytoprotective enzymes and may be involved in the pathogenesis of non-alcoholic fatty liver disease. Although, bile acids affect lipid metabolism, the role of Nrf2 in bile acid metabolism remains unclear. In this study, it was tested how Nrf2 modulates lipid and bile acid homeostasis in liver in response to changes of cholesterol absorption under high-fat diet using Nrf2-null mice. Eight-week-old male wild-type and Nrf2-null mice (n = 6/group) were divided into three groups fed the following diets: 1) control diet containing 4% soybean oil and 16% lard, 2) control diet plus ezetimibe, 3) control diet plus cholesterol. Blood and livers were removed after 4 weeks feeding. High cholesterol diet increased hepatic expression of liver X receptor α target genes related to fatty acid metabolism (FAS, ACC1, SREBP-1c, SCD-1c and CD36), cholesterol transport (Abcg5/abcg8) and bile acid synthesis (Cyp7a1) in wild type mice. However, these genes were not induced in Nrf2-null mice. These findings suggest that Nrf2 has a relation to liver X receptor α and controls the regulation of gene expressions related to lipid and bile acid metabolism.

Indexed as

bile acid metabolismcholesterol metabolismliver X receptor αnon-alcoholic fatty liver diseasenuclear factor-E2-related factor 2

Identifiers

PMID24688217
PMCPMC3947974
OpenAlexW1982525330

What OpenQuestion holds

Textmetadata
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.