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1997 Fiscal Year Final Research Report Summary

ION HOMEOSTASIS AND METABOLISM IN THE DISEASED HEART-A STUDY USING MULTI-NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY

Research Project

Project/Area Number 07045051
Research Category

Grant-in-Aid for international Scientific Research

Allocation TypeSingle-year Grants
SectionUniversity-to-University Cooperative Research
Research Field Circulatory organs internal medicine
Research InstitutionOSAKA UNIVERSITY

Principal Investigator

KUSUOKA Hideo  OSAKA UNIVERSITY,MEDICAL SCHOOL,ASSOCIATE PROFESSOR, 医学部, 助教授 (00112011)

Co-Investigator(Kenkyū-buntansha) LAWRENCE John  THE JOHNS HOPKINS UNIVERSITY,SCHOOL OF MEDICINE,ASSISTANT PROFESSOR, ホプキンス大学・医学部, 助教授
MARBAN Eduardo  THE JOHNS HOPKINS UNIVERSITY,SCHOOL OF MEDICINE,PROFESSOR, ホプキンス大学・医学部, 教授
MATSUMURA Yasushi  OSAKA UNIVERSITY,MEDICAL HOSPITAL,RESEARCH ASSISTANT, 医学部・附属病院, 助手 (90252642)
Project Period (FY) 1995 – 1997
KeywordsMYOCARDIUM / ION HOMEOSTASIS / ISCHEMIA / REPERFUSION / CALCIUM ION / SODIUM ION / STUNNING / NUCLEAR MAGNETIC RESONANCE
Research Abstract

This project aimed to reveal the relation between the abnormalities in ion homeostasis and contractile failure in the models of diseased hearts. The follwing points were clarified in this research project ;
1. The relation between the abnormalities in intracellular calcium ion homeostasis and contractile failure in the hearts reperfused after acute ischemia. The transient calcium overload during early phase of reperfusion after a brief period of ischemia activates calcium-dependent protease, and protease disappears myofilament-related skeletal proteins, resulting in contractile failure.
2. The mechanism of calcium channel blockers for protection against ischemia/reperfusion injury. Pretreatment of calcium channel blockers prevents calcium overload during ischemia, and protects myocardium against contractile failure induced by ischemia and/or reperfusion. It is clarified that calcium influx from the extracellular space is necessary for the calcium overload during ischemia.
3. The relation between the abnormalities in intracellular sodium ion homeostasis during ischemia and contractile failure after reperfusion. Sodium accumulation during ischemia is mediated by sodium influx via Na/H exchanger, and shows significant negative correlation with contractile recovery after reperfusion. Cardiac protection against ischemia in diabetic hearts is caused by the reduced activity of Na/H exchanger. These results indicate that the abnormalities in ion homeostasis is one of major mechanisms for contractile dysfunction in diseased hearts.

  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] Matsumura Y: "Inhomogeneous disappearance of myofilament-related cytoskeletal proteins in stunned myocardium of guinea pig" Circulation Research. 79. 447-454 (1996)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Imahashi K: "Alteration of intracellular Na during ischemia in diabetic rat hearts" Journal of Molecular and Cellular Cardiology. 30(in press). (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] MATSUMURA Y: "INHOMOGENEOUS DISAPPEARANCE OF MYOFILAMENT-RELATED CYTOSKELETAL PROTEINS IN STUNNED MYOCARDIUM OF GUINEA PIG" CIRCULATION RESEARCH. 79. 447-454 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] IMAHASHI K: "ALTERATION OF INTRACELLULAR Na^+DURING ISCHEMIA IN DIABETIC RAT HEARTS" JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY. 30 (in press). (1998)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1999-03-16  

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