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Futoshi Izumi

Researcher at University of Occupational and Environmental Health Japan

Publications -  116
Citations -  2679

Futoshi Izumi is an academic researcher from University of Occupational and Environmental Health Japan. The author has contributed to research in topics: Adrenal medulla & Catecholamine. The author has an hindex of 28, co-authored 116 publications receiving 2655 citations.

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Influx of 22Na through acetylcholine receptor-associated Na channels: relationship between 22Na influx, 45Ca influx and secretion of catecholamines in cultured bovine adrenal medulla cells.

TL;DR: Results indicate that cultured bovine adrenal medulla cells have at least three distinct ion channels: nicotinic acetylcholine receptor-associated Na channels which are not inhibited by tetrodotoxin, voltage-dependent Na channelsWhich are kept activated by veratridine and inhibited by Tetrodtoxin and (3) voltage- dependent Ca channels.
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Staurosporine: an effective inhibitor for Ca2+/calmodulin-dependent protein kinase II.

TL;DR: It is suggested that staurosporine inhibits CaM kinase II by interacting with the catalytic domain, distinct from the ATP‐binding site or substrate‐ binding site, of the enzyme and that Staurospora is an effective inhibitor for CaM Kinase II in the cell system.
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Evidence that multiple P2X purinoceptors are functionally expressed in rat supraoptic neurones.

TL;DR: The results suggest that multiple P2x receptors, including P2X3, are functionally expressed in SON neurones, and that activation of these receptors induces cationic currents and Ca2+ entry.
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ATP activates DNA synthesis by acting on P2X receptors in human osteoblast-like MG-63 cells.

TL;DR: It is concluded that ATP increases DNA synthesis and enhances the proliferative effects of growth factors through P2X receptors by activating a mitogen-activated protein kinase pathway.
Journal Article

Coupling of the expressed cannabinoid CB1 and CB2 receptors to phospholipase C and G protein-coupled inwardly rectifying K+ channels.

TL;DR: Signaling of the cannabinoid CB1 and CB2 receptors through phospholipase C and G protein-coupled inwardly rectifying K+ channels (GIRK) was studied after their expression in COS7 cells and Xenopus oocytes to suggest two new signaling pathways for the cannabinoid receptors.