Targeting diastolic dysfunction by genetic engineering of calcium handling proteins

被引:19
作者
Coutu, P
Hirsch, JC
Szatkowski, ML
Metzger, JM
机构
[1] Univ Michigan, Dept Physiol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USA
[4] Albert Einstein Coll Med Hosp, Dept Neonatol, Philadelphia, PA USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1050-1738(02)00213-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diastolic heart failure (HF) is associated with significant morbidity and mortality, and is a growing medical problem in this country. Diastolic dysfunction is defined as an abnormality in myocardial relaxation that impairs filling during diastole and contributes to the clinical syndrome of HF Effective clinical strategies to treat diastolic dysfunction are limited. This article focuses on the potential application of parvalbumin-a fast skeletal muscle calcium buffer-for remediation of slow relaxation in the failing heart. (C) 2003, Elsevier Science Inc.
引用
收藏
页码:63 / 67
页数:5
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