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Department of Surgery and Physiology and Biophysics, Mayo Clinic and Foundation, Rochester, Minnesota 55905
Platelets participate in normal and
pathological thrombotic processes. Hormone replacement in
postmenopausal women is associated with increase risk for thrombosis.
However, little is known regarding how platelets are affected by
hormonal status. Nitric oxide (NO) modulates platelet functions and is
modulated by hormones. Therefore, the present study was designed to
determine how loss of ovarian hormones changes expression of estrogen
receptors and regulatory proteins for NO synthase (NOS) in platelets.
Estrogen receptors (ER
and ER
), NOS, heat shock proteins 70 and
90 (HSP70 and HSP90), caveolin-1, -2, and -3, calmodulin, NOS activity,
and cGMP were analyzed in a lysate of platelets from gonadally intact
and ovariectomized female pigs. Expression of ER
and ER
receptors, endothelial NOS (eNOS), HSP70, and HSP90 increased with
ovariectomy. NOS activity and cGMP also increased; calmodulin was
unchanged. Caveolins were not detected. These results suggest that
ovarian hormones influence expression of estrogen receptors and eNOS in
platelets. Changes in estrogen receptors and NOS could affect platelet
aggregation in response to hormone replacement.
17
-estradiol; hormones; nitric oxide synthase; endothelial
nitric oxide synthase; megakaryocytes; inducible nitric oxide synthase; heat shock protein
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