Evidence map›Paper›PMID 30006580›Full record

ArticleInternational journal of obesity (2005)2018

Zinc alpha2 glycoprotein protects against obesity-induced hepatic steatosis.

Xin-Hua Xiao, Ya-Di Wang, Xiao-Yan Qi, Yuan-Yuan Wang, Jiao-Yang Li, Han Li, Pei-Ying Zhang, Hai-Lin Liao, Mei-Hua Li, Zhe-Zhen Liao and 4 more

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Zinc.Advances in food and nutrition research · 2021
    Review
  11. Adipokines in the Skin and in Dermatological Diseases.International journal of molecular sciences · 2020
    Review
  12. Article
  13. [An in vitro study of zinc-alpha-2-glycoprotein inhibits activation and proliferation of hepatic stellate cells].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Polyphenol-richPeerJ · 2019
    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

14 authors at 3 institutions in 2 countries.

Xin-Hua XiaoDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Ya-Di WangDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Xiao-Yan QiDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Yuan-Yuan WangDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Jiao-Yang LiDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Han LiDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Pei-Ying ZhangDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Hai-Lin LiaoDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Mei-Hua LiDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Zhe-Zhen LiaoDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Jing YangDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Can-Xin XuDepartment of Pathology & Immunology, Washington University in, St. Louis, MO, 63110, USA.
Ge-Bo WenDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China.
Jiang-Hua LiuDepartment of Metabolism and Endocrinology, The First Affiliated Hospital of University of South China, Hengyang, 421001, China. jianghua990@hotmail.com.
First Affiliated Hospital of University of South China · CNUniversity of South China · CNWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimNonalcoholic fatty liver disease (NAFLD) is characterized by hepatic steatosis, impaired insulin sensitivity, and chronic low-grade inflammation. Our previous studies indicated that zinc alpha2 glycoprotein (ZAG) alleviates palmitate (PA)-induced intracellular lipid accumulation in hepatocytes. This study is to further characterize the roles of ZAG on the development of hepatic steatosis, insulin resistance (IR), and inflammation.

methodsZAG protein levels in the livers of NAFLD patients, high-fat diet (HFD)-induced or genetically (ob/ob) induced obese mice, and in PA-treated hepatocytes were determined by western blotting. C57BL/6J mice injected with an adenovirus expressing ZAG were fed HFD for indicated time to induce hepatic steatosis, IR, and inflammation, and then biomedical, histological, and metabolic analyses were conducted to identify pathologic alterations in these mice. The molecular mechanisms underlying ZAG-regulated hepatic steatosis were further explored and verified in mice and hepatocytes.

resultsZAG expression was decreased in NAFLD patient liver biopsy samples, obese mice livers, and PA-treated hepatocytes. Simultaneously, ZAG overexpression alleviated intracellular lipid accumulation via upregulating adiponectin and lipolytic genes (FXR, PPARα, etc.) while downregulating lipogenic genes (SREBP-1c, LXR, etc.) in obese mice as well as in cultured hepatocytes. ZAG improved insulin sensitivity and glucose tolerance via activation of IRS/AKT signaling. Moreover, ZAG significantly inhibited NF-ĸB/JNK signaling and thus resulting in suppression of obesity-associated inflammatory response in hepatocytes.

conclusionsOur results revealed that ZAG could protect against NAFLD by ameliorating hepatic steatosis, IR, and inflammation.

Indexed as

AnimalsHumansLiverMaleMiceMice, Inbred C57BLMice, ObeseNon-alcoholic Fatty Liver DiseaseObesitySeminal Plasma ProteinsSignal TransductionUp-RegulationZn-Alpha-2-GlycoproteinSeminal Plasma ProteinsZn-Alpha-2-Glycoprotein

Identifiers

PMID30006580
OpenAlexW2883230127

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.