Abstract | OBJECTIVE: STUDY DESIGN: RESULTS: Upregulation of adhesion molecule mRNA or protein was not seen in HUVECs treated with DRSP alone or with 17β-estradiol+DRSP. DRSP alone, 17β-estradiol+DRSP or ethinylestradiol+DRSP did not increase the number of adherent monocytoid cells to HUVECs in the flow chamber system. However, MPA significantly enhanced the monocytoid cell adherence (P<0.05). CONCLUSIONS: DRSP did not increase the expression of adhesion molecules or monocytoid cell adherence to endothelial cells, indicating that DRSP could reduce the risk of atherogenesis caused by MPA. These results suggest that DRSP may be an alternative to MPA in hormone replacement therapy.
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Authors | Fumitake Ito, Taisuke Mori, Osamu Takaoka, Yukiko Tanaka, Akemi Koshiba, Hiroshi Tatsumi, Koichi Iwasa, Jo Kitawaki |
Journal | European journal of obstetrics, gynecology, and reproductive biology
(Eur J Obstet Gynecol Reprod Biol)
Vol. 201
Pg. 113-7
(Jun 2016)
ISSN: 1872-7654 [Electronic] Ireland |
PMID | 27088625
(Publication Type: Journal Article)
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Copyright | Copyright © 2016. Published by Elsevier Ireland Ltd. |
Chemical References |
- Androstenes
- Cell Adhesion Molecules
- E-Selectin
- P-Selectin
- Vascular Cell Adhesion Molecule-1
- Intercellular Adhesion Molecule-1
- Medroxyprogesterone Acetate
- drospirenone
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Topics |
- Androstenes
(pharmacology)
- Cell Adhesion
(drug effects)
- Cell Adhesion Molecules
(metabolism)
- Cells, Cultured
- E-Selectin
(metabolism)
- Female
- Human Umbilical Vein Endothelial Cells
(drug effects, metabolism)
- Humans
- Intercellular Adhesion Molecule-1
(metabolism)
- Medroxyprogesterone Acetate
(pharmacology)
- Monocytes
(drug effects, metabolism)
- P-Selectin
(metabolism)
- Up-Regulation
(drug effects)
- Vascular Cell Adhesion Molecule-1
(metabolism)
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