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2017 Fiscal Year Final Research Report

THE MECHANISM OF SALT SENSITIVE HYPERTENSION IN INTERMITTENT HYPOXIA

Research Project

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Project/Area Number 26461262
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Kidney internal medicine
Research InstitutionNihon University

Principal Investigator

KOYAMA Sayoko (オグラサヨコ)  日本大学, 医学部, 助教 (30618202)

Co-Investigator(Renkei-kenkyūsha) SHIMOSAWA Tatsuo  国際医療福祉大学, 医学部, 教授 (90231365)
Research Collaborator Yeerbolati Alimila  
Project Period (FY) 2014-04-01 – 2018-03-31
Keywords間欠的低酸素 / 食塩感受性高血圧 / NCC
Outline of Final Research Achievements

Intermittent hypoxia (IH) increases membrane protein of NCC (The thiazide-sensitive Na+-Cl- cotransporter) in Kidney tubles. It remain by salt loading diet. The other Sodium Chrolide channel in Kidney ENaC(Epithelial sodium channel),NHE3(Na+/H+ exchange),NKCC-2(Na-K-Cl cotransporter) were not changed after IH. Challenge test of Amirolide showed no difference between Control and IH group, but Thiazide test showed remarkably increased IH group. These data suggested NCC is key for salt sensitive hypertension by IH.

Free Research Field

高血圧

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Published: 2019-03-29  

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