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Physiological and pharmacological study for ATP sensitive K channel in human heart

Research Project

Project/Area Number 10670767
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionNippon Medical School

Principal Investigator

KATSUBE Yasuhiro  Nippon Medical School, Pediatrics, Assistant, 医学部, 助手 (20246523)

Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1999: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1998: ¥2,500,000 (Direct Cost: ¥2,500,000)
Keywordshuman cardiac cell / ATP sensitive K channel / patch clamp / PDE inhibitor / levosimendan / イオンチャネル / カルシウム感受性増強薬
Research Abstract

We had explored the ionic channels of human cardiac cells using whole-cell voltage clamp method. To activate the ionic channels, we used a novel Ca sensitizer, levosimendan, which has the action of opening the ATP sensitive K channel and of phosphodiesterase III inhibition. We studied about the ATP sensitive K channel mainly in 1998, and about the stimulation of L-type Ca channel through phosphodiesterase III inhibition in 1999. We found the following results.
1. Levosimendan is reported to have an action of opening the ATP sensitive K channel in rat ventricular cells and mesenteric artery cells. According to our experiments, levosimendan also has the action of opening the ATP sensitive K channel in human atrial cells.
2. ATP sensitive K channel was not activated in clinically relevant concentration (【approximately equal】nM), gut was activated in more high concentration such as 10 mM. These showed that levosimendan act as a cardioprotective agent by opening ATP sensitive K channels in the pathophysiological conditions such as regional ischemia.
3. Levosimendan stimulated the nifedipine sensitive Ca current (L-type Ca channel) by inhibiting the phosphodiesterase III with ECィイD250ィエD2 value of 56 nM, and maximal effect was 134% of control at 1μM.
These resuls were presented at the following meetings.
1. 15ィイD1thィエD1 Society of Japanese Electrocardiography (1998, 10/1-2, Kagoshima)
2. 35ィイD1thィエD1 Carduikiguca Paediatrica Japonica (1999, 7/7-9, Fukuoka)
3. 21ィイD1stィエD1 European Society of Cardiology (1999, 8/28-9/1, Barcelona, Spain)

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report

URL: 

Published: 1998-04-01   Modified: 2016-04-21  

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