Astiz Lab

Laboratory of Circadian Physiology | Achucarro Basque Center for Neuroscience

GLUT12—A promising new target for the treatment of insulin resistance in obesity and type 2 diabetes


Journal article


M. Astiz, H. Oster
Acta Physiologica, 2019

Semantic Scholar DOI PubMed
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APA   Click to copy
Astiz, M., & Oster, H. (2019). GLUT12—A promising new target for the treatment of insulin resistance in obesity and type 2 diabetes. Acta Physiologica.


Chicago/Turabian   Click to copy
Astiz, M., and H. Oster. “GLUT12—A Promising New Target for the Treatment of Insulin Resistance in Obesity and Type 2 Diabetes.” Acta Physiologica (2019).


MLA   Click to copy
Astiz, M., and H. Oster. “GLUT12—A Promising New Target for the Treatment of Insulin Resistance in Obesity and Type 2 Diabetes.” Acta Physiologica, 2019.


BibTeX   Click to copy

@article{m2019a,
  title = {GLUT12—A promising new target for the treatment of insulin resistance in obesity and type 2 diabetes},
  year = {2019},
  journal = {Acta Physiologica},
  author = {Astiz, M. and Oster, H.}
}

Abstract

In this issue of Acta Physiologica, Gil-Iturbe et al. show how activity of the facilitative glucose transporter 12 (GLUT12, SLC2A12) in adipose tissues is regulated by metabolic signals such as insulin, leptin, adiponectin, tumour necrosis factor alpha (TNFα), and hypoxia. Using both in-vitro and in-vivo approaches the authors compare the hormonal modulation of GLUT12 expression and activity to that of GLUT4, the main insulin sensitive transporter responsible for glucose uptake. This article is protected by copyright. All rights reserved.





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