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Hiroyuki Odaka

Researcher at Takeda Pharmaceutical Company

Publications -  97
Citations -  2527

Hiroyuki Odaka is an academic researcher from Takeda Pharmaceutical Company. The author has contributed to research in topics: Insulin & Diabetes mellitus. The author has an hindex of 29, co-authored 97 publications receiving 2449 citations. Previous affiliations of Hiroyuki Odaka include Osaka University & Hirosaki University.

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Activation of Human Peroxisome Proliferator-Activated Receptor (PPAR) Subtypes by Pioglitazone

TL;DR: Results showed that pioglitazone significantly increased the apoA-I secretion from the human hepatoma cell line HepG2 and binding assay indicated that the transactivation of hPPARgamma1 or hPParalpha by piog Litazone is due to direct binding of piog litazone to each subtype.
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Increased glucose metabolism and insulin sensitivity in transgenic skinny mice overexpressing leptin.

TL;DR: Evidence is provided that leptin is an adipocyte-derived antidiabetic hormone in vivo and its pathophysiologic and therapeutic implications in diabetes are suggested and suggested.
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Overexpression of GPR40 in Pancreatic β-Cells Augments Glucose-Stimulated Insulin Secretion and Improves Glucose Tolerance in Normal and Diabetic Mice

TL;DR: The results suggest that G PR40 may have a role in regulating glucose-stimulated insulin secretion and plasma glucose levels in vivo and that pharmacological activation of GPR40 may provide a novel insulin secretagogue beneficial for the treatment of type 2 diabetes.
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Novel 5-Substituted 2,4-Thiazolidinedione and 2,4-Oxazolidinedione Derivatives as Insulin Sensitizers with Antidiabetic Activities

TL;DR: The antidiabetic effects of this compound are considered to be due to its potent agonistic activity for peroxisome proliferator-activated receptor gamma (EC(50) = 8.87 nM).
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Effect of an intestinal disaccharidase inhibitor (AO-128) on obesity and diabetes.

TL;DR: A new disaccharidase inhibitor, AO-128, showed 190-3900-fold more potent inhibition of purified rat small intestine sucrase-isomaltase (S-1) complex and 23-33-fold greater inhibition of semipurified porcine small intestine disacchcharidases than acarbose, and is useful as an adjunct to the dietary management of obesity and diabetes.