Evidence map›Paper›PMID 30070033›Full record

ArticleJournal of diabetes investigation2019

Hepatocyte growth factor alleviates hepatic insulin resistance and lipid accumulation in high-fat diet-fed mice.

Yali Jing, Qingmin Sun, Xiaolu Xiong, Ran Meng, Sunyinyan Tang, Shu Cao, Yan Bi, Dalong Zhu

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  20. Effects of Acute Cold Stress on LiverInternational journal of molecular sciences · 2018
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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

8 authors at 2 institutions in 1 country.

Yali JingDepartment of Endocrinology, Drum Tower Clinical Medical College of Nanjing Medical University, Nanjing, China.
Qingmin SunDepartment of Pharmacy, The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Xiaolu XiongDepartment of Endocrinology, Drum Tower Hospital, Affiliated to Nanjing University Medical School, Nanjing, China.
Ran MengDepartment of Endocrinology, Drum Tower Hospital, Affiliated to Nanjing University Medical School, Nanjing, China.
Sunyinyan TangDepartment of Endocrinology, Drum Tower Hospital, Affiliated to Nanjing University Medical School, Nanjing, China.
Shu CaoDepartment of Endocrinology, Drum Tower Hospital, Affiliated to Nanjing University Medical School, Nanjing, China.
Yan BiDepartment of Endocrinology, Drum Tower Clinical Medical College of Nanjing Medical University, Nanjing, China.ORCID http://orcid.org/0000-0003-3914-7854
Dalong ZhuDepartment of Endocrinology, Drum Tower Clinical Medical College of Nanjing Medical University, Nanjing, China.ORCID http://orcid.org/0000-0002-5492-3017
Nanjing Drum Tower Hospital · CNNanjing University of Chinese Medicine · CN

Funding

Jiangsu Provincial Key Medical Discipline ZDXKB2016012Jiangsu Provincial Medical Talent ZDRCA2016062Jiangsu Provincial Medical Youth Talent QNRC2016018Jiangsu Provincial Medical Youth Talent QNRC2016019Jiangsu Provincial Medical Youth Talent QNRC2016020Key Project of Nanjing Clinical Medical Science, the Key Research and Development Program of Jiangsu Province of China BE2015604Key Project of Nanjing Clinical Medical Science, the Key Research and Development Program of Jiangsu Province of China BE2016606Nanjing Science and Technology Development Project 201605019Nanjing Science and Technology Development Project YKK16105Nanjing Science and Technology Development Project ZKX16036National Key Research and Development Program of China 2016YFC1304804National Key Research and Development Program of China 2017YFC1309605National Natural Science Foundation of China 81200587National Natural Science Foundation of China 81370947National Natural Science Foundation of China 81400832National Natural Science Foundation of China 81500612National Natural Science Foundation of China 81570736National Natural Science Foundation of China 81570737National Natural Science Foundation of China 81600632National Natural Science Foundation of China 81600637National Natural Science Foundation of China 81703294National Natural Science Foundation of China 81770819Natural Science Foundation of Jiangsu Province of China BK20170125Six Talent Peaks Project of Jiangsu Province of China SWYY-091Six Talent Peaks Project of Jiangsu Province of China WSN-165
6 · The paper itself

Abstract

AIMS/

introductionType 2 diabetes mellitus is frequently accompanied by fatty liver disease. Lipid accumulation within the liver is considered as one of the risk factors for insulin resistance. Hepatocyte growth factor (HGF) is used to treat liver dysfunction; however, the effect and mechanism of HGF on hepatic lipid metabolism are still not fully understood. MATERIALS AND

methodsMale C57BL/6 mice were induced with a high-fat diet for 12 weeks, followed by a 4-week treatment of HGF or vehicle saline. The levels of fasting blood glucose, fasting insulin and homeostatic model assessment of insulin resistance were calculated for insulin sensitivity. Biochemical plasma parameters were also measured to assess the effect of HGF on lipid accumulation. Additionally, genes in the lipid metabolism pathway were evaluated in palmitic acid-treated HepG2 cells and high-fat diet mice.

resultsHGF treatment significantly decreased the levels of fasting blood glucose, hepatic triglyceride and cholesterol contents. Additionally, HGF-regulated expression levels of sterol regulatory element-binding protein-1c/fatty acid synthase, peroxidase proliferator-activated receptor-α, and upstream nuclear receptors, such as farnesoid X receptor and small heterodimer partner. Furthermore, c-Met inhibitor could partially reverse the effects of HGF.

conclusionsHGF treatment can ameliorate hepatic insulin resistance and steatosis through regulation of lipid metabolism. These effects might occur through farnesoid X receptor-small heterodimer partner axis-dependent transcriptional activity.

Indexed as

Diet, High-FatInsulin ResistanceAnimalsBlood GlucoseBody WeightHepatocyte Growth FactorHep G2 CellsHumansLipid MetabolismLiverMaleMiceMice, Inbred C57BLBlood GlucoseHepatocyte Growth FactorHepatocyte growth factorInsulin resistanceLipid metabolism

Identifiers

PMID30070033
PMCPMC6400203
OpenAlexW2887100081

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.