Evidence map›Paper›PMID 7761392›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

Agouti regulation of intracellular calcium: role in the insulin resistance of viable yellow mice.

M B Zemel, J H Kim, R P Woychik, E J Michaud, S H Kadwell, I R Patel, W O Wilkison

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 143 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Exposure to permethrin promotes high fat diet-induced weight gain and insulin resistance in male C57BL/6J mice.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2018
    Article
  5. Article
  6. Review
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  8. Review
  9. Article
  10. Article
  11. Review
  12. An agouti mutation lacking the basic domain induces yellow pigmentation but not obesity in transgenic mice.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  13. Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  14. Review
  15. Characterization of genes modulated during pheomelanogenesis using differential display.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Combined effects of insulin treatment and adipose tissue-specific agouti expression on the development of obesity.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

M B ZemelDepartment of Nutrition, University of Tennessee, Knoxville 37996-1900, USA.
J H Kim
R P Woychik
E J Michaud
S H Kadwell
I R Patel
W O Wilkison
University of Tennessee at Knoxville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several dominant mutations at the agouti locus in the mouse cause a syndrome of marked obesity, hyperinsulinemia, and insulin resistance. Although it is known that the agouti gene is expressed in an ectopic manner in these mutants, the precise mechanism by which the agouti gene product mediates these effects is unclear. Since intracellular Ca2+ is believed to play a role in mediating insulin action and dysregulation of Ca2+ flux is observed in diabetic animals and humans, we examined the status of intracellular Ca2+ in mice carrying the dominant agouti allele, viable yellow (Avy). We show here that in mice carrying this mutation, the intracellular free calcium concentration ([Ca2+]i) is elevated in skeletal muscle, and the degree of elevation is closely correlated with the degree to which the mutant traits are expressed in individual animals. Moreover, we demonstrate that the agouti gene product is capable of inducing increased [Ca2+]i in cultured and freshly isolated skeletal muscle myocytes from wild-type mice. Based on these findings, we present a model in which we propose that the agouti polypeptide promotes insulin resistance in mutant animals through its ability to increase [Ca2+]i.

Indexed as

Intercellular Signaling Peptides and ProteinsMice, Mutant StrainsAgingAgouti Signaling ProteinAnimalsBody WeightCalciumCells, CulturedDiabetes MellitusFemaleGene ExpressionHumansInsulin ResistanceMaleMiceMice, Inbred C57BLAgouti Signaling ProteinCalciumIntercellular Signaling Peptides and ProteinsProteins

Identifiers

PMID7761392
PMCPMC41781
OpenAlexW2089607284

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.