The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
COX-2-Derived Prostacyclin Confers Atheroprotection on Female Mice
Abstract
Female gender affords relative protection from cardiovascular disease until the menopause. We report that estrogen acts on estrogen receptor subtype alpha to up-regulate the production of atheroprotective prostacyclin, PGI 2 , by activation of cyclooxygenase 2 (COX-2). This mechanism restrained both oxidant stress and platelet activation that contribute to atherogenesis in female mice. Deletion of the PGI 2 receptor removed the atheroprotective effect of estrogen in ovariectomized female mice. This suggests that chronic treatment of patients with selective inhibitors of COX-2 could undermine protection from cardiovascular disease in premenopausal females.
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Self-citationAltered pain perception and inflammatory response in mice lacking prostacyclin receptor
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Self-citationEndothelial–mesenchymal transition in atherosclerosis
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Transcription factor cross-talk: the estrogen receptor and NF-κB
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Metadata
- Authors
- Egan, K. M., Lawson, J. A., Fries, S., Koller, B., Rader, D. J., Smyth, E. M., & FitzGerald, G. A.
- Venue
- Science
- Published
- 2004-12-10
- Volume
- 306
- Issue
- 5703
- Pages
- 1954-1957
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2055691692
- Cited by
- 431
- References
- 15
- FWCI
- 24.05
- Type
- journal article
- Language
- en
- Open access
- closed
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- Egan, K. M., Lawson, J. A., Fries, S., Koller, B., Rader, D. J., Smyth, E. M., & FitzGerald, G. A. (2004). COX-2-Derived Prostacyclin Confers Atheroprotection on Female Mice. Science. https://doi.org/10.1126/science.1103333
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.