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Role of oxidative stress in female reproduction
Open accessAbstract
In a healthy body, ROS (reactive oxygen species) and antioxidants remain in balance. When the balance is disrupted towards an overabundance of ROS, oxidative stress (OS) occurs. OS influences the entire reproductive lifespan of a woman and even thereafter (i.e. menopause). OS results from an imbalance between prooxidants (free radical species) and the body's scavenging ability (antioxidants). ROS are a double-edged sword - they serve as key signal molecules in physiological processes but also have a role in pathological processes involving the female reproductive tract. ROS affect multiple physiological processes from oocyte maturation to fertilization, embryo development and pregnancy. It has been suggested that OS modulates the age-related decline in fertility. It plays a role during pregnancy and normal parturition and in initiation of preterm labor. Most ovarian cancers appear in the surface epithelium, and repetitive ovulation has been thought to be a causative factor. Ovulation-induced oxidative base damage and damage to DNA of the ovarian epithelium can be prevented by antioxidants. There is growing literature on the effects of OS in female reproduction with involvement in the pathophysiology of preeclampsia, hydatidiform mole, free radical-induced birth defects and other situations such as abortions. Numerous studies have shown that OS plays a role in the pathophysiology of infertility and assisted fertility. There is some evidence of its role in endometriosis, tubal and peritoneal factor infertility and unexplained infertility. This article reviews the role OS plays in normal cycling ovaries, follicular development and cyclical endometrial changes. It also discusses OS-related female infertility and how it influences the outcomes of assisted reproductive techniques. The review comprehensively explores the literature for evidence of the role of oxidative stress in conditions such as abortions, preeclampsia, hydatidiform mole, fetal embryopathies, preterm labour and preeclampsia and gestational diabetes. The review also addresses the growing literature on the role of nitric oxide species in female reproduction. The involvement of nitric oxide species in regulation of endometrial and ovarian function, etiopathogenesis of endometriosis, and maintenance of uterine quiescence, initiation of labour and ripening of cervix at parturition is discussed. Complex interplay between cytokines and oxidative stress in the etiology of female reproductive disorders is discussed. Oxidant status of the cell modulates angiogenesis, which is critical for follicular growth, corpus luteum formation endometrial differentiation and embryonic growth is also highlighted in the review. Strategies to overcome oxidative stress and enhance fertility, both natural and assisted are delineated. Early interventions being investigated for prevention of preeclampsia are enumerated. Trials investigating combination intervention strategy of vitamin E and vitamin C supplementation in preventing preeclampsia are highlighted. Antioxidants are powerful and there are few trials investigating antioxidant supplementation in female reproduction. However, before clinicians recommend antioxidants, randomized controlled trials with sufficient power are necessary to prove the efficacy of antioxidant supplementation in disorders of female reproduction. Serial measurement of oxidative stress biomarkers in longitudinal studies may help delineate the etiology of some of the diosorders in female reproduction such as preeclampsia.
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“The placenta itself produces ROS since it is rich in mitochondria, is hemomonochorial and allows electrons to pass that are converted into O2•-radicals (Casanueva and Viteri, 2003;Fuji, et al., 2005;Agarwal et al., 2005).”
From Iron, Oxidative Stress and Health (2012) · cites this paper as Agarwal et al., 2005
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“Also, higher levels of 8-hydroxy-2-deoxyguanosine, an indicator of DNA damage caused by oxidative stress, have been observed in granulosa cells of patients with endometriosis and were associated with lower fertilization rates and poor embryo quality (Agarwal et al., 2005).”
From Iron, Oxidative Stress and Health (2012) · cites this paper as Agarwal et al., 2005
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“It is known that in places affected by endometriosis, oxidative stress further intensifies the immune response, as a result of which there may be an exacerbation of the development of endometriosis [151,152,153].”
From Endometriosis: Epidemiology, Classification, Pathogenesis, Treatment and Genetics (Review of Literature) (2021) · cites this paper as [151]
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Citations
Cites
Free radicals, antioxidants, and human disease: where are we now?
Halliwell, B. B., Gutteridge, J. M. C., & Cross, C. E. (1992) · PubMed · Cited by 2,156
Oxidative Stress and Vascular Disease
Madamanchi, N. R., Vendrov, A., & Runge, M. S. (2005) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000150649.39934.13 · Cited by 1,618
Role of reactive oxygen species in the pathophysiology of human reproduction.
Agarwal, A., Saleh, R., & Bedaiwy, M. (2003) · Fertility and Sterility · doi:10.1016/s0015-0282(02)04948-8 · Cited by 1,578
Self-citationEffects of antioxidant enzymes in the molecular control of reactive oxygen species toxicology
Matés, J. M. (2000) · Toxicology · doi:10.1016/s0300-483x(00)00306-1 · Cited by 1,540
Guerin, P. J. (2001) · Human Reproduction Update · doi:10.1093/humupd/7.2.175 · Cited by 1,419
Oxidative DNA damage and disease: induction, repair and significance
Evans, M. D., Dizdaroglu, M., & Cooke, M. S. (2004) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2003.11.001 · Cited by 1,372
Acute Renal Failure and Sepsis
Schrier, R. W., & Wang, W. (2004) · New England Journal of Medicine · doi:10.1056/nejmra032401 · Cited by 1,263
Onset of Maternal Arterial Blood Flow and Placental Oxidative Stress
Jauniaux, E., Watson, A. L., Hempstock, J., Bao, Y.-P., Skepper, J. N., & Burton, G. J. (2000) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)64849-3 · Cited by 1,057
Trophoblastic invasion of human decidua from 8 to 18 weeks of pregnancy
Pijnenborg, R., Dixon, G., Robertson, W. B., & Brosens, I. A. (1980) · Placenta · doi:10.1016/s0143-4004(80)80012-9 · Cited by 848
Oxidative stress in the placenta
Myatt, L., & Cui, X.-L. (2004) · Histochemistry and Cell Biology · doi:10.1007/s00418-004-0677-x · Cited by 803
Research works printed but not linked: 1
- Knott L, Hartridge T, Brown NL, Mansell JP, Sandy JR: Homocysteine oxidation and apoptosis: a potential cause of cleft palate. In Vitro Cell Dev Biol Anim. 2003, 39: 98-105. 10.1290/1543-706X(2003)039<0098:HOAAAP>2.0.CO;2. · DOI
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The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989
ESHRE guideline: management of women with endometriosis
Dunselman, G. A. J., Vermeulen, N., Becker, C., Calhaz-Jorge, C., D'Hooghe, T., De Bie, B., Heikinheimo, O., Horne, A. W., Kiesel, L., Nap, A., et al. (2014) · Human Reproduction · doi:10.1093/humrep/det457 · Cited by 2,211
Smolarz, B., Szyłło, K., & Romanowicz, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910554 · Cited by 560
Oxidative Stress and Endometriosis: A Systematic Review of the Literature
Scutiero, G., Iannone, P., Bernardi, G., Bonaccorsi, G., Spadaro, S., Volta, C. A., Greco, P., & Nappi, L. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/7265238 · Cited by 436
Critical review on the presence of phthalates in food and evidence of their biological impact
Giuliani, A., Zuccarini, M., Cichelli, A., Khan, H., & Reale, M. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17165655 · Cited by 420
Oxidative stress in the pelvic cavity and its role in the pathogenesis of endometriosis
Donnez, J., Binda, M. M., Donnez, O., & Dolmans, M.-M. (2016) · Fertility and Sterility · doi:10.1016/j.fertnstert.2016.07.1075 · Cited by 251
Hanna, C. W., Bloom, M. S., Robinson, W. P., Kim, D., Parsons, P. J., vom Saal, F. S., Taylor, J. A., Steuerwald, A. J., & Fujimoto, V. Y. (2012) · Human Reproduction · doi:10.1093/humrep/des038 · Cited by 163
Placental membrane aging and HMGB1 signaling associated with human parturition
Menon, R., Behnia, F., Polettini, J., Saade, G. R., Campisi, J., & Velarde, M. (2016) · Aging · doi:10.18632/aging.100891 · Cited by 143
The incidence and origin of segmental aneuploidy in human oocytes and preimplantation embryos
Babariya, D., Fragouli, E., Alfarawati, S., Spath, K., & Wells, D. (2017) · Human Reproduction · doi:10.1093/humrep/dex324 · Cited by 142
The role of the oxidative-stress in the endometriosis-related infertility
Augoulea, A., Mastorakos, G., Lambrinoudaki, I., Christodoulakos, G., & Creatsas, G. (2009) · Gynecological Endocrinology · doi:10.1080/09513590802485012 · Cited by 129
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Cacciottola, L., Donnez, J., & Dolmans, M.-M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137138 · Cited by 118
Qi, Q.-R., Zhao, X.-Y., Zuo, R.-J., Wang, T.-S., Gu, X.-W., Liu, J.-L., & Yang, Z.-M. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1033593 · Cited by 58
Kwon, C.-Y., Cho, I.-H., & Park, K. S. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01192 · Cited by 52
Role of Oxidative Stress and Antioxidant Therapies in Endometriosis
Baboo, K. D., Chen, Z.-Y., & Zhang, X.-M. (2019) · Reproductive and Developmental Medicine · doi:10.4103/2096-2924.268154 · Cited by 20
“OS results from an imbalance between prooxidants (free radical species) and antioxidants.[6] Free radical species including reactive oxygen species (ROS) and reactive nitrogen species are unstable and highly reactive molecules.”
BackgroundIron, Oxidative Stress and Health
Udipi, S., Ghugre, P., & Gokhale, C. (2012) · Oxidative Stress - Molecular Mechanisms and Biological Effects · doi:10.5772/34975 · Cited by 17
“Also, higher levels of 8-hydroxy2-deoxyguanosine, an indicator of DNA damage caused by oxidative stress, have been observed in granulosa cells of patients with endometriosis and were associated with lower fertilization rates and poor embryo quality (Agarwal et al., 2005).”
BackgroundInfluentialKanney, N., Patki, A., Chandler-Laney, P., Garvey, W. T., & Hidalgo, B. A. (2022) · Metabolites · doi:10.3390/metabo12121226 · Cited by 10
Ferreira, S. R., Goyeneche, A. A., Heber, M. F., Abruzzese, G. A., Ferrer, M. J., Telleria, C. M., & Motta, A. B. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2020.111045 · Cited by 8
Metadata
- Authors
- Agarwal, A., Gupta, S., & Sharma, R. K.
- Affiliations
- Cleveland Clinic (US)
- Corresponding author
- Agarwal, Ashok
- Venue
- Reproductive Biology and Endocrinology
- Published
- 2005-07-14
- Volume
- 3
- Issue
- 1
- Pages
- 28-28
- ISSN
- 1477-7827 (ISSN-L)
- PMC
- PMC1215514
- OpenAlex
- W2135935849
- Cited by
- 1,729
- References
- 218
- Citations by year
- 2026: 82 · 2025: 106 · 2024: 121 · 2023: 114 · 2022: 140 · 2021: 118 · 2020: 109 · 2019: 101 · 2018: 93 · 2017: 84 · 2016: 85 · 2015: 90 · 2014: 85 · 2013: 72 · 2012: 69
- FWCI
- 5.18
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Reproductive Biology and Endocrinology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Biology and Fertility
- Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- oxidative stress, reactive oxygen species, female reproduction, female infertility, antioxidants, nitric oxide, endometriosis, preeclampsia, hydatidiform mole, preterm labour, gestational diabetes mellitus, assisted reproduction, folliculogenesis, oocyte maturation, embryonic development, pregnancy, abortion, angiogenesis, cytokines, ovarian cancer, menopause, unexplained infertility
- MeSH terms
- Aging, Animals, Antioxidants, Female, Humans, Infertility, Female, Menopause, Pregnancy, Pregnancy Complications, Reproduction, Reactive Oxygen Species, Oxidative Stress, Nitric Oxide Synthase, Reproductive Techniques, Assisted, Embryonic Development
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