Evidence map›Paper›PMID 27941940›Full record

ArticleNutrition & diabetes2016

Kefir peptides prevent high-fructose corn syrup-induced non-alcoholic fatty liver disease in a murine model by modulation of inflammation and the JAK2 signaling pathway.

H L Chen, T C Tsai, Y C Tsai, J W Liao, C C Yen, C M Chen

Open access · goldAbstract read
In one paragraph

Article in Nutrition & diabetes, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 62 citations in OpenAlex.

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  16. Protective effect of protein hydrolysates fromIranian journal of basic medical sciences · 2022
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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 3 institutions in 1 country.

H L ChenDepartment of Bioresources, Da-Yeh University, Changhwa, Taiwan.
T C TsaiDepartment of Life Sciences and Agricultural Biotechnology Center, National Chung Hsing University, Taichung, Taiwan.
Y C TsaiDepartment of Life Sciences and Agricultural Biotechnology Center, National Chung Hsing University, Taichung, Taiwan.
J W LiaoGraduate Institute of Veterinary Pathology, National Chung Hsing University, Taichung, Taiwan.
C C YenDepartment of Life Sciences and Agricultural Biotechnology Center, National Chung Hsing University, Taichung, Taiwan.
C M ChenDepartment of Life Sciences and Agricultural Biotechnology Center, National Chung Hsing University, Taichung, Taiwan.
National Chung Hsing University · TWChina Medical University · TWDayeh University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn recent years, people have changed their eating habits, and high-fructose-containing bubble tea has become very popular. High-fructose intake has been suggested to be a key factor that induces non-alcoholic fatty liver disease (NAFLD). Kefir, a fermented milk product composed of microbial symbionts, has demonstrated numerous biological activities, including antibacterial, antioxidant and immunostimulating effects. The present study aims to evaluate the effects of kefir peptides on high-fructose-induced hepatic steatosis and the possible molecular mechanism.

resultsAn animal model of 30% high-fructose-induced NAFLD in C57BL/6J mice was established. The experiment is divided into the following six groups: (1) normal: H

conclusionOur data have demonstrated that kefir peptides can improve the symptoms of NAFLD, including body weight, energy intake, inflammatory reaction and the formation of fatty liver by activating JAK2 signal transduction through the JAK2/STAT3 and JAK2/AMPK pathways in the high-fructose-induced fatty liver animal model. Therefore, kefir peptides may have the potential for clinical application for the prevention or treatment of clinical metabolic syndrome.

Indexed as

KefirAlanine TransaminaseAnimalsBody WeightCytokinesDisease Models, AnimalEnergy IntakeHigh Fructose Corn SyrupInflammationJanus Kinase 2MaleMiceNon-alcoholic Fatty Liver DiseasePhosphorylationSignal TransductionAlanine TransaminaseCytokinesHigh Fructose Corn SyrupJak2 protein, mouseJanus Kinase 2

Identifiers

PMID27941940
PMCPMC5223135
OpenAlexW2564948401

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.