Evidence map›Paper›PMID 27568038›Full record

ArticleEndocrine2016

20-HETE attenuates the response of glucose-stimulated insulin secretion through the AKT/GSK-3β/Glut2 pathway.

Bijun Zhang, Guangrui Lai, Jingjing Wu, Ru Sun, Runhong Xu, Xianghong Yang, Yafei Qi, Yanyan Zhao

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Gpr75 Deletion in Adipocytes Protects From Diet-Induced Obesity: Changes in Glucose Homeostasis and Inflammatory Responses.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Article
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  4. Article
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  6. GPR21 Inhibition Increases Glucose-Uptake in HepG2 Cells.International journal of molecular sciences · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. High-fat diet-induced obesity and insulin resistance in CYP4a14American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Article
  13. 20-HETE: Hypertension and Beyond.Hypertension (Dallas, Tex. : 1979) · 2018
    Review
  14. Fatty Acid-Stimulated Insulin Secretion vs. Lipotoxicity.Molecules (Basel, Switzerland) · 2018
    Review
  15. 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

8 authors.

Bijun ZhangDepartment of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Guangrui LaiDepartment of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Jingjing WuDepartment of Medical Genetics, China Medical University, Shenyang, Liaoning, China.
Ru SunDepartment of Medical Genetics, China Medical University, Shenyang, Liaoning, China.
Runhong XuDepartment of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Xianghong YangDepartment of Pathology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Yafei QiDepartment of Pathology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Yanyan ZhaoDepartment of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China. yyzhao@sj-hospital.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously generated cytochrome P450 4F2 (CYP4F2) transgenic mice that have high levels of 20-hydroxyeicosatetraenoic acid (20-HETE) production; these mice exhibit both hypertension and hyperglycemia without insulin resistance. Currently, it is unclear whether and how 20-HETE affects insulin secretion, thus resulting in hyperglycemia. In this study, we found that 20-HETE attenuated glucose-stimulated insulin secretion (GSIS) in CYP4F2 transgenic mice as well as in rat insulinoma INS-1E cells treated with 0.5 μM 20-HETE. HET0016, a selective inhibitor of 20-HETE synthesis, reversed the reduction in GSIS leading to a decrease in blood glucose in the transgenic mice. Furthermore, the expression of glucose transporter 2 (Glut2), Ser

Indexed as

AnimalsBlood GlucoseCell Line, TumorCytochrome P450 Family 4GlucoseGlucose Transporter Type 2Glycogen Synthase Kinase 3 betaHydroxyeicosatetraenoic AcidsInsulinInsulin-Secreting CellsInsulin SecretionMiceMice, TransgenicPhosphorylationProto-Oncogene Proteins c-aktRats20-hydroxy-5,8,11,14-eicosatetraenoic acidBlood GlucoseCyp4f1 protein, ratCytochrome P450 Family 4GlucoseGlucose Transporter Type 2Glycogen Synthase Kinase 3 betaHydroxyeicosatetraenoic AcidsInsulinProto-Oncogene Proteins c-akt20-hydroxyeicosatetraenoic acidGlucose-stimulated insulin secretionGlucose transporter 2Glycogen synthase kinase-3β

Identifiers

What Socratic 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 Socratic graph.