Evidence map›Paper›PMID 27209494›Full record

ArticleEnvironmental health and preventive medicine2016

Importance of detoxifying enzymes in differentiating fibrotic development between SHRSP5/Dmcr and SHRSP rats.

Hisao Naito, Xiaofang Jia, Husna Yetti, Yukie Yanagiba, Hazuki Tamada, Kazuya Kitamori, Yumi Hayashi, Dong Wang, Masashi Kato, Akira Ishii and 1 more

Open access · goldAbstract read
In one paragraph

Article in Environmental health and preventive medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 15 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

11 authors at 3 institutions in 1 country.

Hisao NaitoDepartment of Public Health, Fujita Health University School of Medicine, Dengakugakubo 1-98, Kutsukake-cho, Toyoake, 470-1192, Japan. naitoh@med.nagoya-u.ac.jp.
Xiaofang JiaDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Husna YettiDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yukie YanagibaDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hazuki TamadaDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kazuya KitamoriDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yumi HayashiDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Dong WangDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masashi KatoDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Akira IshiiDepartment of Legal Medicine and Bioethics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Tamie NakajimaDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nagoya University · JPChubu University · JPFujita Health University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesHigh-fat and -cholesterol diet (HFC) induced fibrotic steatohepatitis in stroke-prone spontaneously hypertensive rat (SHRSP) 5/Dmcr, the fifth substrain from SHRSP, by dysregulating bile acid (BA) kinetics. This study aimed to clarify the histopathological and BA kinetic differences in HFC-induced fibrosis between SHRSP5/Dmcr and SHRSP.

methodsTen-week-old male SHRSP5/Dmcr and SHRSP were randomly allocated to groups and fed with either control diet or HFC for 2 and 8 weeks. The liver histopathology, biochemical features, and molecular signaling involved in BA kinetics were measured.

resultsHFC caused more severe hepatocyte ballooning, macrovesicular steatosis and fibrosis in SHRSP5/Dmcr than in SHRSP. It was noted that fibrosis was disproportionately formed in retroperitoneal side of both strains. As for BA kinetics, HFC greatly increased the level of Cyp7a1 and Cyp7b1 to the same degree in both strains at 8 weeks, while multidrug resistance-associated protein 3 was greater in SHRSP5/Dmcr than SHRSP. The diet decreased the level of bile salt export pump by the same degree in both strains, while constitutive androstane receptor, pregnane X receptor, and UDP-glucuronosyltransferase activity more prominent in SHRSP5/Dmcr than SHRSP at 8 weeks. In the fibrosis-related genes, only expression of collagen, type I, alpha 1 mRNA was greater in SHRSP5/Dmcr than SHRSP.

conclusionsThe greater progression of fibrosis in SHRSP5/Dmcr induced by HFC may be due to greater suppression of UDP-glucuronosyltransferase activity detoxifying toxicants, such as hydrophobic BAs.

Indexed as

AnimalsCholesterol, DietaryDiet, High-FatDisease ProgressionFatty LiverFibrosisInactivation, MetabolicLiverMaleRandom AllocationRatsRats, Inbred SHRCholesterol, DietaryBile acidConstitutive androstane receptorPregnane X receptorResistance-associated protein 3UDP-glucuronosyltransferase activity

Identifiers

PMID27209494
PMCPMC5305991
OpenAlexW2406755174

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Registered trials

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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.