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基质金属蛋白酶抑制作为治疗慢性心力衰竭的潜在策略。

MMP inhibition as a potential therapeutic strategy for CHF.

作者信息

Lindsey M, Lee R T

机构信息

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Drug News Perspect. 2000 Aug;13(6):350-4.

Abstract

Congestive heart failure (CHF) is a leading cause of death in developed countries and its prevalence is increasing throughout the world. Progressive left ventricular dilation and contractile dysfunction cause most cases of CHF. Recent therapies have targeted the neurohumoral system, with few therapies directed toward the actual dilation process; however, emerging data indicate that certain members of the family of metalloenzymes, the matrix metalloproteinases, are not only associated with ventricular dilation, but may actually mediate the dilation process. Because these enzymes are extracellular and are pharmacologic targets, matrix metalloproteinase inhibition is a novel potential therapy for delaying or preventing heart failure.

摘要

充血性心力衰竭(CHF)是发达国家主要的死亡原因,且其患病率在全球范围内呈上升趋势。进行性左心室扩张和收缩功能障碍导致了大多数CHF病例。近期的治疗方法主要针对神经体液系统,针对实际扩张过程的治疗方法很少;然而,新出现的数据表明,金属酶家族中的某些成员,即基质金属蛋白酶,不仅与心室扩张有关,而且可能实际上介导了扩张过程。由于这些酶存在于细胞外且是药物作用靶点,抑制基质金属蛋白酶是一种用于延缓或预防心力衰竭的新型潜在治疗方法。

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