Evidence map›Paper›PMID 22854958›Full record

ArticleThe Journal of biological chemistry2012

Znt7-null mice are more susceptible to diet-induced glucose intolerance and insulin resistance.

Liping Huang, Catherine P Kirschke, Yu-An E Lay, Lauren B Levy, Danielle E Lamirande, Patrick H Zhang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Zinc homeostasis and redox alterations in obesity.Frontiers in endocrinology · 2023
    Review
  11. Roles ofInternational journal of molecular sciences · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. The role of labile ZnMolecular and cellular biochemistry · 2021
    Review
  16. Zinc.Advances in food and nutrition research · 2021
    Review
  17. Review
  18. Article
  19. Article
  20. Differential expression of zinc transporters accompanies the differentiation of C2C12 myoblasts.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2018
    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

6 authors at 4 institutions in 1 country.

Liping HuangUnited States Department of Agriculture/Agricultural Research Service/Western Human Nutrition Research Center, Obesity and Metabolism Research Unit, Davis, California 95616, USA. liping.huang@ars.usda.gov
Catherine P Kirschke
Yu-An E Lay
Lauren B Levy
Danielle E Lamirande
Patrick H Zhang
University of California, Davis · USWestern Human Nutrition Research Center · USAgricultural Research Service · USUnited States Department of Agriculture · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Znt7 gene encodes a ubiquitously expressed zinc transporter that is involved in transporting cytoplasmic zinc into the Golgi apparatus and a ZnT7-containing vesicular compartment. Overexpression of ZnT7 in the pancreatic β-cell stimulates insulin synthesis and secretion through regulation of insulin gene transcription. In this study, we demonstrate that ZnT7 is expressed in the mouse skeletal muscle. The activity of the insulin signaling pathway was down-regulated in myocytes isolated from the femoral muscle of Znt7 knock-out (KO) mice. High fat diet consumption (45% kcal) induced weight gain in male Znt7 KO mice but not female Znt7 KO mice. Male Znt7 KO mice fed the high fat diet at 5 weeks of age for 10 weeks exhibited hyperglycemia in the non-fasting state. Oral glucose tolerance tests revealed that male Znt7 KO mice fed the high fat diet had severe glucose intolerance. Insulin tolerance tests showed that male Znt7 KO mice were insulin-resistant. Diet-induced insulin resistance in male Znt7 KO mice was paralleled by a reduction in mRNA expression of Insr, Irs2, and Akt1 in the primary skeletal myotubes isolated from the KO mice. Overexpression of ZnT7 in a rat skeletal muscle cell line (L6) increased Irs2 mRNA expression, Irs2 and Akt phosphorylation, and glucose uptake. We conclude that a combination of decreased insulin secretion and increased insulin resistance accounts for the glucose intolerance observed in Znt7 KO mice.

Indexed as

Insulin ResistanceAnimal FeedAnimalsBody CompositionCation Transport ProteinsDiabetes Mellitus, ExperimentalDietFemaleGene Expression RegulationGlucoseHomeostasisInsulinMaleMiceMice, Inbred C57BLMice, KnockoutCation Transport ProteinsGlucoseInsulinZincZnT7 protein, mouse

Identifiers

PMID22854958
PMCPMC3460483
OpenAlexW1978371202

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.