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Mechanism By Which Progesterone Protects Against Heart Disease Identified
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WESTPORT, Sep 02 (Reuters) - Harvard scientists report in the current issue
of Nature Medicine that progesterone protects against cardiovascular
disease through direct inhibition of DNA synthesis in smooth muscle cells,
which blocks the proliferation of arterial smooth muscle cells, a major
factor in formation of atherosclerotic plaque.

The research team that reports this finding is the same that first reported
three years ago that elevated homocysteine levels are linked to heart disease.

Principal author Dr. Edgar Haber says that he and his colleagues analyzed
the action of progesterone receptors in smooth muscle cells and found that
the hormone directly blocks DNA synthesis in a dose-dependent manner. They
also discovered that pretreatment of rat aorta with the progesterone
antagonist RU486 blocks progesterone's inhibitory action.

The Boston team analyzed both human and rat aortic smooth muscle cells in
vivo and in vitro. They observed that levels of cyclin A and E mRNA decline
in the presence of progesterone, which suggests that the hormone interrupts
the cell cycle at the G1/S transition; that progesterone inhibits
[3H]thymidine incorporation into the cell, which is an indication of a stop
in DNA synthesis; and that progesterone causes a decrease in the growth
rate of smooth muscle cell proliferation.

Dr. Haber notes in his conclusion that the relative risk of coronary artery
disease in postmenopausal women who take both estrogens and progestins as
hormone replacement therapy is 0.39.

The relative risk in age-matched women who take estrogens alone is 0.60.

The relative risk in women who are not on hormone replacement therapy is 1.0.

Nature Medicine 1997;3:000-000.
Copyright 1997 Reuters Limited.
<http://www.reutershealth.com/news/docs/199709/19970902scd.html>
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