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Yusuke Ito

Researcher at University of Tokyo

Publications -  16
Citations -  7776

Yusuke Ito is an academic researcher from University of Tokyo. The author has contributed to research in topics: Adiponectin & Adiponectin receptor 1. The author has an hindex of 10, co-authored 16 publications receiving 7415 citations. Previous affiliations of Yusuke Ito include Hitotsubashi University.

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Peroxisome proliferator-activated receptor (PPAR)alpha activation increases adiponectin receptors and reduces obesity-related inflammation in adipose tissue: comparison of activation of PPARalpha, PPARgamma, and their combination.

TL;DR: ptive activation of peroxisome proliferator-activated receptor (PPAR)alpha, PPARgamma, and both of them in combination in obese diabetic KKAy mice markedly improved insulin sensitivity and dual activation of PPARalpha and -gamma enhances the action of adip onectin by increasing both adiponectin and AdipoRs, which can result in the amelioration of obesity-induced insulin resistance.
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Generation of Globular Fragment of Adiponectin by Leukocyte Elastase Secreted by Monocytic Cell Line THP-1

TL;DR: Data indicate that the cleavage of adiponectin by leukocyte elastase secreted from activated monocytes and/or neutrophils could be a candidate for the mechanism of the generation of the globular fragment of adip onectin.
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Osmotin Is a Homolog of Mammalian Adiponectin and Controls Apoptosis in Yeast through a Homolog of Mammalian Adiponectin Receptor

TL;DR: It is shown that the protein encoded by ORE20/PHO36 (YOL002c), a seven transmembrane domain receptor-like polypeptide that regulates lipid and phosphate metabolism, is an osmotin binding plasma membrane protein that is required for full sensitivity to osmoton.
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A novel IKKβ inhibitor stimulates adiponectin levels and ameliorates obesity-linked insulin resistance

TL;DR: Observations suggest that "insulin-stimulated Akt activity in adipocytes" may play an important role in the regulation of adiponectin secretion.
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Expression of DGAT2 in white adipose tissue is regulated by central leptin action.

TL;DR: The hypothesis that leptin regulates adipocyte size by altering expression patterns of DGAT via central nervous system to determine the levels of triglyceride synthesis is proposed.