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      Heavy metal for a troubled heart

      in-brief
      The Journal of Experimental Medicine
      The Rockefeller University Press

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          Abstract

          Including more copper in your everyday diet could be good for your heart, according to a study on page 657. Jiang et al. now find that dietary supplementation of copper offsets the effects of stress on an overworked heart by preventing its enlargement. Copper-carrying proteins disarm oxygen radicals and power electron transport. Humans with copper deficiency have increased cholesterol levels, clot formation, oxidative tissue damage, and heart disease. Cardiac tissue biopsies of heart attack victims show a great reduction in copper levels. In mice with stress-induced heart disease, the team now shows, increased heart size and decreased heart function can both be restored to normal levels by a small increase in the daily intake of copper, even when the stress stimulus is maintained. But without the copper supplement, stressed mice suffer heart failure after two months. The authors show that mice receiving dietary copper supplements have increased activity of a transcription factor called HIF-1α, leading to increased production of the vascular endothelial growth factor (VEGF) protein, which promotes angiogenesis. Blocking VEGF activity inhibits the ability of copper to reverse heart enlargement and dysfunction. It is not clear, however, how angiogenesis helps decrease muscle mass or how copper gets pushed out of the heart during stress. The human equivalent of the beneficial dose of copper used in this study is ∼3.0 mg/day. The current recommended daily intake for humans, however, is only 0.9 mg/day. Increasing copper intake may be a cheap way to reduce mortality associated with heart disease.

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          Author and article information

          Journal
          J Exp Med
          The Journal of Experimental Medicine
          The Rockefeller University Press
          0022-1007
          1540-9538
          19 March 2007
          : 204
          : 3
          : 455
          Author notes
          Article
          jem.2043iti5
          10.1084/jem.2043iti5
          2137920
          0fe6bf2d-7a35-4ffa-8cd6-50a78c5591a0
          Copyright © 2007, The Rockefeller University Press
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          Medicine
          Medicine

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