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2015 Fiscal Year Final Research Report

Identification of regulator of zinc influx in the taste cell for treatment of taste disorder.

Research Project

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Project/Area Number 26870677
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pharmacology in pharmacy
General pharmacology
Research InstitutionAichi Gakuin University

Principal Investigator

Hatano Noriyuki  愛知学院大学, 薬学部, 講師 (50454319)

Project Period (FY) 2014-04-01 – 2016-03-31
Keywords細胞内亜鉛
Outline of Final Research Achievements

We established a system to measure the extracellular zinc influx through zinc transporters in the HEK293 cells overexpressing Zip8 (HEK-Zip8) and Zip14 (HEK-Zip14) using a zinc-sensitive dye FluoZin-3. The extracellular zinc influx in the HEK-Zip8 and HEK-Zip14 were quantitatively measured by quantifying the extracellular zinc content in the medium.
The effects of polaprezinc, a chelate compound of zinc ion, were examined using both HEK293 cells overexpressing TRPA1 (HEK-TRPA1) and human fibroblast-like synoviocytes stimulated by IL-1alpha. The polaprezinc increased intracellular Ca2+ concentration in both HEK-TRPA1 and IL-1alpha-stimulated synoviocytes. Moreover, the effects of a captopril that cause taste disorder were examined. The captopril did not change the response of polaprezinc in the IL-1alpha-stimulated synoviocytes. These results suggest that polaprezinc is effective as a zinc supplementation drug, and the zinc-chelating effect of captopril is very weak.

Free Research Field

薬理

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Published: 2017-05-10  

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