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Hideki Kishikawa

Researcher at Kumamoto University

Publications -  43
Citations -  5091

Hideki Kishikawa is an academic researcher from Kumamoto University. The author has contributed to research in topics: Insulin & Diabetes mellitus. The author has an hindex of 23, co-authored 42 publications receiving 4943 citations.

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Cell-specific regulation of IRS-1 gene expression: role of E box and C/EBP binding site in HepG2 cells and CHO cells.

TL;DR: It is concluded that the two nuclear proteins that bind to the E box regulate IRS-1 gene expression positively in HepG2 cells and the twonuclear proteins thatbind to the C/EBP binding site regulate it negatively in CHO cells.
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Cellular characterization of pituitary adenoma cell line (AtT20 cell) transfected with insulin, glucose transporter type 2 (GLUT2) and glucokinase genes : Insulin secretion in response to physiological concentrations of glucose

TL;DR: The results suggest that both GLUT2 and glucokinase are necessary for the glucose stimulated insulin secretion in at least rodent cell lines, and that other element(s) are needed for a biphasic insulin secretion typically observed in beta cells.
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Effect of α2-adrenoceptor antagonist on platelet activation during insulin-induced hypoglycaemia in Type 2 (non-insulin-dependent) diabetes mellitus

TL;DR: It is suggested that plasma epinephrine plays an important role in platelet activation during hypoglycaemia in Type 2 diabetes mellitus, and that the plateletactivation is prevented by α2-adrenoceptor antagonist.
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Role of α2-Adrenergic Receptor in Platelet Activation During Insulin-Induced Hypoglycemia in Normal Subjects

TL;DR: The results suggest that epinephrine is responsible for some, if not all, of the β-TG release from the platelets during insulin-induced hypoglycemia.
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Bradykinin enhances insulin receptor tyrosine kinase in 32D cells reconstituted with bradykinin and insulin signaling pathways

TL;DR: Results clearly demonstrated that bradykinin enhanced insulin-stimulated tyrosine kinase activity of the insulin receptor and downstream insulin signal cascade through the BK2R mediated signal pathway.