Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here to sign up for SAGE Journal Email Alerts today!

Sign In to gain access to subscriptions and/or personal tools.
Journal of the Society for Gynecologic Investigation
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Behrman, H. R.
Right arrow Articles by Gao, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Behrman, H. R.
Right arrow Articles by Kodaman, P. H.
Right arrow Articles by Preston, S. L.
Right arrow Articles by Gao, S.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Oxidative Stress and the Ovary

Harold R. Behrman, PhD

Reproductive Biology Section, Department of Ob/Gyn and Pharmacology, Yale University School of Medicine, New Haven, Connecticut; harold.behrman{at}yale.edu

Pinar H. Kodaman

Sandra L. Preston

Shipig Gao, MD

Reproductive Biology Section, Department of Ob/Gyn and Pharmacology, Yale University School of Medicine, New Haven, Connecticut

Superoxide (O2-), hydrogen preoxide (H2O2), and lipid peroxides are generated in luteal tissue during natural and prostaglandin-induced regression in the rat, and this response is associated with reversible depletion of ascorbic acid. Reactive oxygen species immediately uncouple the luteinizing hormone receptor from adenylate cyclase and inhibit steroideogenesis by interrupting transmitochondrial cholesterol transport. The cellular origin of oxygen radicls in regressing corpora lutea is predominately from resident and infiltrated leukocytes, notably neutrophils. Reactive oxygen species are also produced within the follicle at ovulation and, like the corpus luteum, leukocytes are the major source of the products. Antioxidants block the resumption of meiosis, whereas the generation of reactive oxygen induces oocyte maturation in the follicle. Although oxygen radicals may serve important physiologic roles within the ovary, the cyclic production of these damaging agents over years may lead to an increased cumulative risk of ovarian pathology that would probably be exacerbated under conditions of reduced antioxidant status.

Key Words: Oxygen radicals • antioxidants • corpus luteum • follicle • oocyte.

Journal of the Society for Gynecologic Investigation, Vol. 8, No. 1 suppl, S40-S42 (2001)
DOI: 10.1177/107155760100800113


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?