Role of oxidative stress in female reproduction

Ashok Agarwal, Sajal Gupta, Rakesh K Sharma, Ashok Agarwal, Sajal Gupta, Rakesh K Sharma

Abstract

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.

Figures

Figure 1
Figure 1
Mechanisms of oxidative stress-induced cell damage.

References

    1. Pierce JD, Cackler AB, Arnett MG. Why should you care about free radicals? RN. 2004;67:38–42. quiz 43.
    1. Szczepanska M, Kozlik J, Skrzypczak J, Mikolajczyk M. Oxidative stress may be a piece in the endometriosis puzzle. Fertil Steril. 2003;79:1288–1293. doi: 10.1016/S0015-0282(03)00266-8.
    1. Van Langendonckt A, Casanas-Roux F, Donnez J. Oxidative stress and peritoneal endometriosis. Fertil Steril. 2002;77:861–870. doi: 10.1016/S0015-0282(02)02959-X.
    1. Attaran M, Pasqualotto E, Falcone T, Goldberg JM, Miller KF, Agarwal A, Sharma RK. The effect of follicular fluid reactive oxygen species on the outcome of in vitro fertilization. Int J Fertil Womens Med. 2000;45:314–320.
    1. Halliwell B, Gutteridge JM, Cross CE. Free radicals, antioxidants, and human disease: where are we now? J Lab Clin Med. 1992;119:598–620.
    1. Mello Filho AC, Hoffmann ME, Meneghini R. Cell killing and DNA damage by hydrogen peroxide are mediated by intracellular iron. Biochem J. 1984;218:273–275.
    1. Gibson GE, Huang HM. Mitochondrial enzymes and endoplasmic reticulum calcium stores as targets of oxidative stress in neurodegenerative diseases. J Bioenerg Biomembr. 2004;36:335–340. doi: 10.1023/B:JOBB.0000041764.45552.f3.
    1. Madamanchi NR, Vendrov A, Runge MS. Oxidative stress and vascular disease. Arterioscler Thromb Vasc Biol. 2005;25:29–38.
    1. Aitken RJ, Baker MA. Oxidative stress and male reproductive biology. Reprod Fertil Dev. 2004;16:581–588. doi: 10.1071/RD03089.
    1. Evans MD, Dizdaroglu M, Cooke MS. Oxidative DNA damage and disease: induction, repair and significance. Mutat Res. 2004;567:1–61. doi: 10.1016/j.mrrev.2003.11.001.
    1. Behrman HR, Kodaman PH, Preston SL, Gao S. Oxidative stress and the ovary. J Soc Gynecol Investig. 2001;8:S40–42. doi: 10.1016/S1071-5576(00)00106-4.
    1. Sabatini L, Wilson C, Lower A, Al-Shawaf T, Grudzinskas JG. Superoxide dismutase activity in human follicular fluid after controlled ovarian hyperstimulation in women undergoing in vitro fertilization. Fertil Steril. 1999;72:1027–1034. doi: 10.1016/S0015-0282(99)00411-2.
    1. Shiotani M, Noda Y, Narimoto K, Imai K, Mori T, Fujimoto K, Ogawa K. Immunohistochemical localization of superoxide dismutase in the human ovary. Hum Reprod. 1991;6:1349–1353.
    1. Suzuki T, Sugino N, Fukaya T, Sugiyama S, Uda T, Takaya R, Yajima A, Sasano H. Superoxide dismutase in normal cycling human ovaries: immunohistochemical localization and characterization. Fertil Steril. 1999;72:720–726. doi: 10.1016/S0015-0282(99)00332-5.
    1. Jozwik M, Wolczynski S, Szamatowicz M. Oxidative stress markers in preovulatory follicular fluid in humans. Mol Hum Reprod. 1999;5:409–413. doi: 10.1093/molehr/5.5.409.
    1. El Mouatassim S, Guerin P, Menezo Y. Expression of genes encoding antioxidant enzymes in human and mouse oocytes during the final stages of maturation. Mol Hum Reprod. 1999;5:720–725. doi: 10.1093/molehr/5.8.720.
    1. Guerin P, El Mouatassim S, Menezo Y. Oxidative stress and protection against reactive oxygen species in the pre-implantation embryo and its surroundings. Hum Reprod Update. 2001;7:175–189. doi: 10.1093/humupd/7.2.175.
    1. Ishikawa M. Oxygen radicals-superoxide dismutase system and reproduction medicine. Nippon Sanka Fujinka Gakkai Zasshi. 1993;45:842–848.
    1. Vega M, Johnson MC, Diaz HA, Urrutia LR, Troncoso JL, Devoto L. Regulation of human luteal steroidogenesis in vitro by nitric oxide. Endocrine. 1998;8:185–191. doi: 10.1385/ENDO:8:2:185.
    1. Dong M, Shi Y, Cheng Q, Hao M. Increased nitric oxide in peritoneal fluid from women with idiopathic infertility and endometriosis. J Reprod Med. 2001;46:887–891.
    1. Rosselli M, Keller PJ, Dubey RK. Role of nitric oxide in the biology, physiology and pathophysiology of reproduction. Hum Reprod Update. 1998;4:3–24. doi: 10.1093/humupd/4.1.3.
    1. Ohl J, Lefebvre-Maunoury C, Wittemer C, Nisand G, Laurent MC, Hoffmann P. Nitric oxide donors for patients undergoing IVF. A prospective, double-blind, randomized, placebo-controlled trial. Hum Reprod. 2002;17:2615–2620. doi: 10.1093/humrep/17.10.2615.
    1. Osborn BH, Haney AF, Misukonis MA, Weinberg JB. Inducible nitric oxide synthase expression by peritoneal macrophages in endometriosis-associated infertility. Fertil Steril. 2002;77:46–51. doi: 10.1016/S0015-0282(01)02940-5.
    1. Reynaert NL, Ckless K, Wouters EF, van der Vliet A, Janssen-Heininger YM. Nitric oxide and redox signaling in allergic airway inflammation. Antioxid Redox Signal. 2005;7:129–143. doi: 10.1089/ars.2005.7.129.
    1. Schulman IH, Zhou MS, Raij L. Nitric oxide, angiotensin II, and Reactive Oxygen Species in Hypertension and Atherogenesis. Curr Hypertens Rep. 2005;7:61–67.
    1. Hsieh YY, Chang CC, Tsai FJ, Lin CC, Chen JM, Tsai CH. Glutathione S-transferase M1*null genotype but not myeloperoxidase promoter G-463A polymorphism is associated with higher susceptibility to endometriosis. Mol Hum Reprod. 2004;10:713–717. doi: 10.1093/molehr/gah095.
    1. Schrier RW, Wang W. Acute renal failure and sepsis. N Engl J Med. 2004;351:159–169. doi: 10.1056/NEJMra032401.
    1. Ota H, Igarashi S, Hatazawa J, Tanaka T. Endothelial nitric oxide synthase in the endometrium during the menstrual cycle in patients with endometriosis and adenomyosis. Fertil Steril. 1998;69:303–308. doi: 10.1016/S0015-0282(97)00478-0.
    1. Lee KS, Joo BS, Na YJ, Yoon MS, Choi OH, Kim WW. Relationships between concentrations of tumor necrosis factor-alpha and nitric oxide in follicular fluid and oocyte quality. J Assist Reprod Genet. 2000;17:222–228. doi: 10.1023/A:1009495913119.
    1. Agarwal A, Saleh RA, Bedaiwy MA. Role of reactive oxygen species in the pathophysiology of human reproduction. Fertil Steril. 2003;79:829–843. doi: 10.1016/S0015-0282(02)04948-8.
    1. Chan AC. Partners in defense, vitamin E and vitamin C. Can J Physiol Pharmacol. 1993;71:725–731.
    1. de Matos DG, Furnus CC. The importance of having high glutathione (GSH) level after bovine in vitro maturation on embryo development effect of beta-mercaptoethanol, cysteine and cystine. Theriogenology. 2000;53:761–771. doi: 10.1016/S0093-691X(99)00278-2.
    1. Agarwal A, Allamaneni SS. Role of free radicals in female reproductive diseases and assisted reproduction. Reprod Biomed Online. 2004;9:338–347.
    1. de Bruin JP, Dorland M, Spek ER, Posthuma G, van Haaften M, Looman CW, te Velde ER. Ultrastructure of the resting ovarian follicle pool in healthy young women. Biol Reprod. 2002;66:1151–1160.
    1. Myatt L, Cui X. Oxidative stress in the placenta. Histochem Cell Biol. 2004;122:369–382. doi: 10.1007/s00418-004-0677-x.
    1. Fainaru O, Almog B, Pinchuk I, Kupferminc MJ, Lichtenberg D, Many A. Active labour is associated with increased oxidisibility of serum lipids ex vivo. BJOG. 2002;109:938–941.
    1. Mocatta TJ, Winterbourn CC, Inder TE, Darlow BA. The effect of gestational age and labour on markers of lipid and protein oxidation in cord plasma. Free Radic Res. 2004;38:185–191. doi: 10.1080/10715760310001646048.
    1. Wall PD, Pressman EK, Woods JR., Jr Preterm premature rupture of the membranes and antioxidants: the free radical connection. J Perinat Med. 2002;30:447–457. doi: 10.1515/JPM.2002.071.
    1. Pressman EK, Cavanaugh JL, Mingione M, Norkus EP, Woods JR. Effects of maternal antioxidant supplementation on maternal and fetal antioxidant levels: a randomized, double-blind study. Am J Obstet Gynecol. 2003;189:1720–1725. doi: 10.1016/S0002-9378(03)00858-5.
    1. Ray SD, Lam TS, Rotollo JA, Phadke S, Patel C, Dontabhaktuni A, Mohammad S, Lee H, Strika S, Dobrogowska A, Bruculeri C, Chou A, Patel S, Patel R, Manolas T, Stohs S. Oxidative stress is the master operator of drug and chemically-induced programmed and unprogrammed cell death: Implications of natural antioxidants in vivo. Biofactors. 2004;21:223–232.
    1. Sugino N, Takiguchi S, Kashida S, Karube A, Nakamura Y, Kato H. Superoxide dismutase expression in the human corpus luteum during the menstrual cycle and in early pregnancy. Mol Hum Reprod. 2000;6:19–25. doi: 10.1093/molehr/6.1.19.
    1. Paszkowski T, Traub AI, Robinson SY, McMaster D. Selenium dependent glutathione peroxidase activity in human follicular fluid. Clin Chim Acta. 1995;236:173–180. doi: 10.1016/0009-8981(95)98130-9.
    1. Garcia-Pardo L, Granados MD, Gaytan F, Padilla CA, Martinez-Galisteo E, Morales C, Sanchez-Criado JE, Barcena JA. Immunolocalization of glutaredoxin in the human corpus luteum. Mol Hum Reprod. 1999;5:914–919. doi: 10.1093/molehr/5.10.914.
    1. Tranquilli AL, Bezzeccheri V, Giannubilo SR, Scagnoli C, Mazzanti L, Garzetti GG. Amniotic vascular endothelial growth factor (VEGF) and nitric oxide (NO) in women with subsequent preeclampsia. Eur J Obstet Gynecol Reprod Biol. 2004;113:17–20. doi: 10.1016/S0301-2115(03)00369-5.
    1. Takagi Y, Nikaido T, Toki T, Kita N, Kanai M, Ashida T, Ohira S, Konishi I. Levels of oxidative stress and redox-related molecules in the placenta in preeclampsia and fetal growth restriction. Virchows Arch. 2004;444:49–55. doi: 10.1007/s00428-003-0903-2.
    1. Harma M, Kocyigit A, Demir N. Role of plasma nitric oxide in complete hydatidiform mole. Eur J Gynaecol Oncol. 2004;25:333–335.
    1. Harma M, Kocyigit A. Comparison of protein carbonyl and total plasma thiol concentrations in patients with complete hydatidiform mole with those in healthy pregnant women. Acta Obstet Gynecol Scand. 2004;83:857–860. doi: 10.1111/j.0001-6349.2004.00608.x.
    1. Harma M, Erel O. Increased oxidative stress in patients with hydatidiform mole. Swiss Med Wkly. 2003;133:563–566.
    1. Loeken MR. Free radicals and birth defects. J Matern Fetal Neonatal Med. 2004;15:6–14. doi: 10.1080/14767050310001650662.
    1. Lagod L, Paszkowski T, Sikorski R, Rola R. The antioxidant-prooxidant balance in pregnancy complicated by spontaneous abortion. Ginekol Pol. 2001;72:1073–1078.
    1. Pasqualotto EB, Agarwal A, Sharma RK, Izzo VM, Pinotti JA, Joshi NJ, Rose BI. Effect of oxidative stress in follicular fluid on the outcome of assisted reproductive procedures. Fertil Steril. 2004;81:973–976. doi: 10.1016/j.fertnstert.2003.11.021.
    1. Seino T, Saito H, Kaneko T, Takahashi T, Kawachiya S, Kurachi H. Eight-hydroxy-2'-deoxyguanosine in granulosa cells is correlated with the quality of oocytes and embryos in an in vitro fertilization-embryo transfer program. Fertil Steril. 2002;77:1184–1190. doi: 10.1016/S0015-0282(02)03103-5.
    1. Vega M, Urrutia L, Iniguez G, Gabler F, Devoto L, Johnson MC. Nitric oxide induces apoptosis in the human corpus luteum in vitro. Mol Hum Reprod. 2000;6:681–687. doi: 10.1093/molehr/6.8.681.
    1. Tsafriri A, Reich R. Molecular aspects of mammalian ovulation. Exp Clin Endocrinol Diabetes. 1999;107:1–11.
    1. Van Voorhis BJ, Dunn MS, Snyder GD, Weiner CP. Nitric oxide: an autocrine regulator of human granulosa-luteal cell steroidogenesis. Endocrinology. 1994;135:1799–1806. doi: 10.1210/en.135.5.1799.
    1. Tamate K, Sengoku K, Ishikawa M. The role of superoxide dismutase in the human ovary and fallopian tube. J Obstet Gynaecol. 1995;21:401–409.
    1. Takayama K, Sasano H, Fukaya T, Morohashi K, Suzuki T, Tamura M, Costa MJ, Yajima A. Immunohistochemical localization of Ad4-binding protein with correlation to steroidogenic enzyme expression in cycling human ovaries and sex cord stromal tumors. J Clin Endocrinol Metab. 1995;80:2815–2821. doi: 10.1210/jc.80.9.2815.
    1. Sugino N, Takiguchi S, Ono M, Tamura H, Shimamura K, Nakamura Y, Tsuruta R, Sadamitsu D, Ueda T, Maekawa T, Kato H. Nitric oxide concentrations in the follicular fluid and apoptosis of granulosa cells in human follicles. Hum Reprod. 1996;11:2484–2487.
    1. Jauniaux E, Watson AL, Hempstock J, Bao YP, Skepper JN, Burton GJ. Onset of maternal arterial blood flow and placental oxidative stress. A possible factor in human early pregnancy failure. Am J Pathol. 2000;157:2111–2122.
    1. Wang Y, Walsh SW. Antioxidant activities and mRNA expression of superoxide dismutase, catalase, and glutathione peroxidase in normal and preeclamptic placentas. J Soc Gynecol Investig. 1996;3:179–184. doi: 10.1016/1071-5576(96)00015-9.
    1. Djordjevic A, Spasic S, Jovanovic-Galovic A, Djordjevic R, Grubor-Lajsic G. Oxidative stress in diabetic pregnancy: SOD, CAT and GSH-Px activity and lipid peroxidation products. J Matern Fetal Neonatal Med. 2004;16:367–372. doi: 10.1080/14767050400018270.
    1. Wiktor H, Kankofer M, Schmerold I, Dadak A, Lopucki M, Niedermuller H. Oxidative DNA damage in placentas from normal and pre-eclamptic pregnancies. Virchows Arch. 2004;445:74–78.
    1. Holthe MR, Staff AC, Berge LN, Lyberg T. Leukocyte adhesion molecules and reactive oxygen species in preeclampsia. Obstet Gynecol. 2004;103:913–922.
    1. Ishihara O, Hayashi M, Osawa H, Kobayashi K, Takeda S, Vessby B, Basu S. Isoprostanes, prostaglandins and tocopherols in pre-eclampsia, normal pregnancy and non-pregnancy. Free Radic Res. 2004:913–918. doi: 10.1080/10715760412331273421.
    1. Vaisanen-Tommiska M, Nuutila M, Ylikorkala O. Cervical nitric oxide release in women postterm. Obstet Gynecol. 2004;103:657–662.
    1. Buhimschi IA, Buhimschi CS, Pupkin M, Weiner CP. Beneficial impact of term labor: nonenzymatic antioxidant reserve in the human fetus. Am J Obstet Gynecol. 2003;189:181–188. doi: 10.1067/mob.2003.357.
    1. ASRM Definition of "infertility". Fertil Steril. 2004;82:S206.
    1. Yu SL, Yap C. Investigating the infertile couple. Ann Acad Med Singapore. 2003;32:611–613. quiz 614.
    1. Duckitt K. Infertility and subfertility. Clin Evid. 2003:2044–2073.
    1. DeCherney A, Nathan L, Eskandari M, Cadieux M. Current Obstetric & Gynecologic Diagnosis & Treatment McGraw Hill, New York. 2003. pp. 979–990.
    1. ASRM Guidelines for the provision of infertility services. Fertil Steril. 2004;82:S24–S25.
    1. Sharma RK, Agarwal A. Role of reactive oxygen species in gynecologic diseases. Reprod Med Bio. 2004;3:177–199. doi: 10.1111/j.1447-0578.2004.00068.x.
    1. Dennery PA. Role of redox in fetal development and neonatal diseases. Antioxid Redox Signal. 2004;6:147–53. doi: 10.1089/152308604771978453.
    1. Bedaiwy MA, Falcone T, Sharma RK, Goldberg JM, Attaran M, Nelson DR, Agarwal A. Prediction of endometriosis with serum and peritoneal fluid markers: a prospective controlled trial. Hum Reprod. 2002;17:426–431. doi: 10.1093/humrep/17.2.426.
    1. Bedaiwy MA, Falcone T. Peritoneal fluid environment in endometriosis. Clinicopathological implications. Minerva Ginecol. 2003;55:333–345.
    1. Ben-Shlomo I, Kokia E, Jackson MJ, Adashi EY, Payne DW. Interleukin-1 beta stimulates nitrite production in the rat ovary: evidence for heterologous cell-cell interaction and for insulin-mediated regulation of the inducible isoform of nitric oxide synthase. Biol Reprod. 1994;51:310–318.
    1. Malek A, Sager R, Schneider H. Effect of hypoxia, oxidative stress and lipopolysaccharides on the release of prostaglandins and cytokines from human term placental explants. Placenta. 2001;22:S45–50. doi: 10.1053/plac.2001.0635.
    1. Bilodeau JF, Hubel CA. Current concepts in the use of antioxidants for the treatment of preeclampsia. J Obstet Gynaecol Can. 2003;25:742–750.
    1. Hung TH, Charnock-Jones DS, Skepper JN, Burton GJ. Secretion of tumor necrosis factor-alpha from human placental tissues induced by hypoxia-reoxygenation causes endothelial cell activation in vitro: a potential mediator of the inflammatory response in preeclampsia. Am J Pathol. 2004;164:1049–1061.
    1. Banerjee S, Smallwood A, Moorhead J, Chambers AE, Papageorghiou A, Campbell S, Nicolaides K. Placental expression of Interferon-gamma (IFN-gamma) and its receptor (IFN-gamma) R2 fail to switch from early hypoxic to late normotensive development in pre-eclampsia. J Clin Endocrinol Metab. 2005;90:944–952. doi: 10.1210/jc.2004-1113.
    1. Oner-Iyidogan Y, Kocak H, Gurdol F, Korkmaz D, Buyru F. Indices of oxidative stress in eutopic and ectopic endometria of women with endometriosis. Gynecol Obstet Invest. 2004;57:214–217. doi: 10.1159/000076691.
    1. Sugino N, Karube-Harada A, Sakata A, Takiguchi S, Kato H. Nuclear factor-kappa B is required for tumor necrosis factor-alpha-induced manganese superoxide dismutase expression in human endometrial stromal cells. J Clin Endocrinol Metab. 2002;87:3845–3850. doi: 10.1210/jc.87.8.3845.
    1. Sugino N, Karube-Harada A, Taketani T, Sakata A, Nakamura Y. Withdrawal of ovarian steroids stimulates prostaglandin F2alpha production through nuclear factor-kappaB activation via oxygen radicals in human endometrial stromal cells: potential relevance to menstruation. J Reprod Dev. 2004;50:215–225. doi: 10.1262/jrd.50.215.
    1. Ness RB. Endometriosis and ovarian cancer: thoughts on shared pathophysiology. Am J Obstet Gynecol. 2003;189:280–294. doi: 10.1067/mob.2003.408.
    1. Murdoch WJ, Martinchick JF. Oxidative damage to DNA of ovarian surface epithelial cells affected by ovulation: carcinogenic implication and chemoprevention. Exp Biol Med (Maywood) 2004;229:546–552.
    1. Ness RB, Cottreau C. Possible role of ovarian epithelial inflammation in ovarian cancer. J Natl Cancer Inst. 1999;91:1459–1467. doi: 10.1093/jnci/91.17.1459.
    1. Modugno F, Ness RB, Allen GO, Schildkraut JM, Davis FG, Goodman MT. Oral contraceptive use, reproductive history, and risk of epithelial ovarian cancer in women with and without endometriosis. Am J Obstet Gynecol. 2004;191:733–740. doi: 10.1016/j.ajog.2004.03.035.
    1. WHO: Epithelial ovarian cancer and combined oral contraceptives. The WHO Collaborative Study of Neoplasia and Steroid Contraceptives. Int J Epidemiol. 1989;18:538–545.
    1. Young TW, Mei FC, Yang G, Thompson-Lanza JA, Liu J, Cheng X. Activation of antioxidant pathways in ras-mediated oncogenic transformation of human surface ovarian epithelial cells revealed by functional proteomics and mass spectrometry. Cancer Res. 2004;64:4577–4584. doi: 10.1158/0008-5472.CAN-04-0222.
    1. Geva E, Jaffe RB. Role of vascular endothelial growth factor in ovarian physiology and pathology. Fertil Steril. 2000;74:429–438. doi: 10.1016/S0015-0282(00)00670-1.
    1. Zbucka M, Koda M, Tomaszewski J, Przystupa W, Sulkowski S, Wolczynski S. Angiogenesis in the female reproductive processes. Ginekol Pol. 2004;75:649–657.
    1. Krussel JS, Bielfeld P, Polan ML, Simon C. Regulation of embryonic implantation. Eur J Obstet Gynecol Reprod Biol. 2003;110:S2–S9. doi: 10.1016/S0301-2115(03)00167-2.
    1. Sherer DM, Abulafia O. Angiogenesis during implantation, and placental and early embryonic development. Placenta. 2001;22:1–13. doi: 10.1053/plac.2000.0588.
    1. Choi HK, Choi BC, Lee SH, Kim JW, Cha KY, Baek KH. Expression of angiogenesis- and apoptosis-related genes in chorionic villi derived from recurrent pregnancy loss patients. Mol Reprod Dev. 2003;66:24–31. doi: 10.1002/mrd.10331.
    1. Gordon JD, Mesiano S, Zaloudek CJ, Jaffe RB. Vascular endothelial growth factor localization in human ovary and fallopian tubes: possible role in reproductive function and ovarian cyst formation. J Clin Endocrinol Metab. 1996;81:353–359. doi: 10.1210/jc.81.1.353.
    1. Bausero P, Cavaille F, Meduri G, Freitas S, Perrot-Applanat M. Paracrine action of vascular endothelial growth factor in the human endometrium: production and target sites, and hormonal regulation. Angiogenesis. 1998;2:167–182.
    1. Albrecht ED, Babischkin JS, Lidor Y, Anderson LD, Udoff LC, Pepe GJ. Effect of estrogen on angiogenesis in co-cultures of human endometrial cells and microvascular endothelial cells. Hum Reprod. 2003;18:2039–2047. doi: 10.1093/humrep/deg415.
    1. Ushio-Fukai M, Alexander RW. Reactive oxygen species as mediators of angiogenesis signaling: role of NAD(P)H oxidase. Mol Cell Biochem. 2004;264:85–97. doi: 10.1023/B:MCBI.0000044378.09409.b5.
    1. Eyries M, Collins T, Khachigian LM. Modulation of growth factor gene expression in vascular cells by oxidative stress. Endothelium. 2004;11:133–139. doi: 10.1080/10623320490482691.
    1. Sugino N, Shimamura K, Takiguchi S, Tamura H, Ono M, Nakata M, Nakamura Y, Ogino K, Uda T, Kato H. Changes in activity of superoxide dismutase in the human endometrium throughout the menstrual cycle and in early pregnancy. Hum Reprod. 1996;11:1073–1078.
    1. Sugino N, Karube-Harada A, Kashida S, Takiguchi S, Kato H. Reactive oxygen species stimulate prostaglandin F2 alpha production in human endometrial stromal cells in vitro. Hum Reprod. 2001;16:1797–1801. doi: 10.1093/humrep/16.9.1797.
    1. Zeller JM, Henig I, Radwanska E, Dmowski WP. Enhancement of human monocyte and peritoneal macrophage chemiluminescence activities in women with endometriosis. Am J Reprod Immunol Microbiol. 1987;13:78–82.
    1. Wang Y, Sharma RK, Falcone T, Goldberg J, Agarwal A. Importance of reactive oxygen species in the peritoneal fluid of women with endometriosis or idiopathic infertility. Fertil Steril. 1997;68:826–830. doi: 10.1016/S0015-0282(97)00343-9.
    1. Murphy AA, Palinski W, Rankin S, Morales AJ, Parthasarathy S. Evidence for oxidatively modified lipid-protein complexes in endometrium and endometriosis. Fertil Steril. 1998;69:1092–1094. doi: 10.1016/S0015-0282(98)00087-9.
    1. Shanti A, Santanam N, Morales AJ, Parthasarathy S, Murphy AA. Autoantibodies to markers of oxidative stress are elevated in women with endometriosis. Fertil Steril. 1999;71:1115–1118. doi: 10.1016/S0015-0282(99)00145-4.
    1. Murphy AA, Santanam N, Morales AJ, Parthasarathy S. Lysophosphatidyl choline, a chemotactic factor for monocytes/T-lymphocytes is elevated in endometriosis. J Clin Endocrinol Metab. 1998;83:2110–2113. doi: 10.1210/jc.83.6.2110.
    1. Foyouzi N, Berkkanoglu M, Arici A, Kwintkiewicz J, Izquierdo D, Duleba AJ. Effects of oxidants and antioxidants on proliferation of endometrial stromal cells. Fertil Steril. 2004;82:1019–1022. doi: 10.1016/j.fertnstert.2004.02.133.
    1. Murphy AA, Zhou MH, Malkapuram S, Santanam N, Parthasarathy S, Sidell N. RU486-induced growth inhibition of human endometrial cells. Fertil Steril. 2000;71:1014–1019. doi: 10.1016/S0015-0282(00)01606-X.
    1. Vega M, Carrasco I, Castillo T, Troncoso JL, Videla LA, Devoto L. Functional luteolysis in response to hydrogen peroxide in human luteal cells. J Endocrinol. 1995;147:177–182.
    1. LaPolt PS, Leung K, Ishimaru R, Tafoya MA, You-hsin Chen J. Roles of cyclic GMP in modulating ovarian functions. Reprod Biomed Online. 2003;6:15–23.
    1. Hanafy KA, Krumenacker JS, Murad F. NO, nitrotyrosine, and cyclic GMP in signal transduction. Med Sci Monit. 2001;7:801–819.
    1. Ekerhovd E, Brannstrom M, Alexandersson M, Norstrom A. Evidence for nitric oxide mediation of contractile activity in isolated strips of the human Fallopian tube. Hum Reprod. 1997;12:301–305. doi: 10.1093/humrep/12.2.301.
    1. Rosselli M, Dubey RK, Rosselli MA, Macas E, Fink D, Lauper U, Keller PJ, Imthurn B. Identification of nitric oxide synthase in human and bovine oviduct. Mol Hum Reprod. 1996;2:607–612.
    1. Rosselli M, Dubey RK, Imthurn B, Macas E, Keller PJ. Effects of nitric oxide on human spermatozoa: evidence that nitric oxide decreases sperm motility and induces sperm toxicity. Hum Reprod. 1995;10:1786–1790.
    1. Tseng L, Zhang J, Peresleni T, Goligorsky MS. Cyclic expression of endothelial nitric oxide synthase mRNA in the epithelial glands of human endometrium. J Soc Gynecol Investig. 1996;3:33–38. doi: 10.1016/1071-5576(95)00039-9.
    1. Taguchi M, Alfer J, Chwalisz K, Beier HM, Classen-Linke I. Endothelial nitric oxide synthase is differently expressed in human endometrial vessels during the menstrual cycle. Mol Hum Reprod. 2000;6:185–190. doi: 10.1093/molehr/6.2.185.
    1. Telfer JF, Lyall F, Norman JE, Cameron IT. Identification of nitric oxide synthase in human uterus. Hum Reprod. 1995;10:19–23.
    1. Norman JE, Thompson AJ, Telfer JF, Young A, Greer IA, Cameron IT. Myometrial constitutive nitric oxide synthase expression is increased during human pregnancy. Mol Hum Reprod. 1999;5:175–181. doi: 10.1093/molehr/5.2.175.
    1. Sun X, Qiu X, Gemzell-Danielsson K. Effects of mifepristone on expression of endothelial nitric oxide synthase in human endometrium during the implantation phase. Fertil Steril. 2003;80:1454–60. doi: 10.1016/j.fertnstert.2003.05.001.
    1. Shaamash AH, Zakhari MM. Increased serum levels of nitric oxide metabolites among users: a possible role in progestin-induced bleeding. Hum Reprod. 2005;20:302–306. doi: 10.1093/humrep/deh541.
    1. Bansal RK, Goldsmith PC, He Y, Zaloudek CJ, Ecker JL, Riemer RK. A decline in myometrial nitric oxide synthase expression is associated with labor and delivery. J Clin Invest. 1997;99:2502–2508.
    1. Seyffarth G, Nelson PN, Dunmore SJ, Rodrigo N, Murphy DJ, Carson RJ. Lipopolysaccharide induces nitric oxide synthase expression and platelet-activating factor increases nitric oxide production in human fetal membranes in culture. Reprod Biol Endocrinol. 2004;2:29. doi: 10.1186/1477-7827-2-29.
    1. Marinoni E, Di Iorio R, Villaccio B, Alberini A, Rota F, Cosmi EV. Amniotic fluid nitric oxide metabolite levels and nitric oxide synthase localization in feto-placental tissues are modified in association with human labor. Eur J Obstet Gynecol Reprod Biol. 2000;89:47–54. doi: 10.1016/S0301-2115(99)00186-4.
    1. Lee TH, Wu MY, Chen MJ, Chao KH, Ho HN, Yang YS. Nitric oxide is associated with poor embryo quality and pregnancy outcome in in vitro fertilization cycles. Fertil Steril. 2004;82:126–131. doi: 10.1016/j.fertnstert.2004.02.097.
    1. Oztezcan S, Turkoglu UM, Kervancioglu E, Kocak T, Kocak-Toker N, Aykac-Toker G. In vitro effects of peroxynitrite on human spermatozoa. Andrologia. 1999;31:195–198. doi: 10.1046/j.1439-0272.1999.00279.x.
    1. Chung HT, Pae HO, Choi BM, Billiar TR, Kim YM. Nitric oxide as a bioregulator of apoptosis. Biochem Biophys Res Commun. 2001;282:1075–1079. doi: 10.1006/bbrc.2001.4670.
    1. Polak G, Koziol-Montewka M, Gogacz M, Blaszkowska I, Kotarski J. Total antioxidant status of peritoneal fluid in infertile women. Eur J Obstet Gynecol Reprod Biol. 2001;94:261–263. doi: 10.1016/S0301-2115(00)00352-3.
    1. Arumugam K, Dip YC. Endometriosis and infertility: the role of exogenous lipid peroxides in the peritoneal fluid. Fertil Steril. 1995;63:198–199.
    1. Ho HN, Wu MY, Chen SU, Chao KH, Chen CD, Yang YS. Total antioxidant status and nitric oxide do not increase in peritoneal fluids from women with endometriosis. Hum Reprod. 1997;12:2810–2815. doi: 10.1093/humrep/12.12.2810.
    1. Khorram O, Lessey BA. Alterations in expression of endometrial endothelial nitric oxide synthase and alpha(v)beta(3) integrin in women with endometriosis. Fertil Steril. 2002;78:860–864. doi: 10.1016/S0015-0282(02)03347-2.
    1. Wu MY, Chao KH, Yang JH, Lee TH, Yang YS, Ho HN. Nitric oxide synthesis is increased in the endometrial tissue of women with endometriosis. Hum Reprod. 2003;18:2668–2671. doi: 10.1093/humrep/deg484.
    1. Kamada Y, Nakatsuka M, Asagiri K, Noguchi S, Habara T, Takata M, Kudo T. GnRH agonist-suppressed expression of nitric oxide synthases and generation of peroxynitrite in adenomyosis. Hum Reprod. 2000;15:2512–2519. doi: 10.1093/humrep/15.12.2512.
    1. Ekerhovd E, Enskog A, Caidahl K, Klintland N, Nilsson L, Brannstrom M, Norstrom A. Plasma concentrations of nitrate during the menstrual cycle, ovarian stimulation and ovarian hyperstimulation syndrome. Hum Reprod. 2001;16:1334–1339. doi: 10.1093/humrep/16.7.1334.
    1. Portz DM, Elkins TE, White R, Warren J, Adadevoh S, Randolph J. Oxygen free radicals and pelvic adhesion formation: I. Blocking oxygen free radical toxicity to prevent adhesion formation in an endometriosis model. Int J Fertil. 1991;36:39–42.
    1. Zervou S, Karteris E, Goumenou AG, Vatish M, Koumantakis EE, Hillhouse EW. The Glu298-->Asp polymorphism of the endothelial nitric oxide synthase gene is associated with endometriosis. Fertil Steril. 2003;80:1524–1525. doi: 10.1016/S0015-0282(03)02204-0.
    1. Ota H, Igarashi S, Hatazawa J, Tanaka T. Endometriosis and free radicals. Gynecol Obstet Invest. 1999;48:29–35. doi: 10.1159/000052866.
    1. Leyendecker G, Kunz G, Wildt L, Beil D, Deininger H. Uterine hyperperistalsis and dysperistalsis as dysfunctions of the mechanism of rapid sperm transport in patients with endometriosis and infertility. Hum Reprod. 1996;11:1542–1551.
    1. Kim KH, Oh DS, Jeong JH, Shin BS, Joo BS, Lee KS. Follicular blood flow is a better predictor of the outcome of in vitro fertilization-embryo transfer than follicular fluid vascular endothelial growth factor and nitric oxide concentrations. Fertil Steril. 2004;82:586–592. doi: 10.1016/j.fertnstert.2004.02.120.
    1. Song IO, Huh Y, Yoo KJ, Choi BC, Paik EC, Son IP. Increased expression of endothelial nitric oxide synthase in endometrium of infertile women with endometriosis or hydrosalpinx during the window of implantation. Abstract of the 15th Annual Meeting of the ESHRE Tours, France. June 14–17, 2000, Abstract No. O-035.
    1. Cicinelli E, Ignarro LJ, Lograno M, Galantino P, Balzano G, Schonauer LM. Circulating levels of nitric oxide in fertile women in relation to the menstrual cycle. Fertil Steril. 1996:1036–1038.
    1. Friden BE, Runesson E, Hahlin M, Brannstrom M. Evidence for nitric oxide acting as a luteolytic factor in the human corpus luteum. Mol Hum Reprod. 2000;6:397–403. doi: 10.1093/molehr/6.5.397.
    1. Anteby EY, Hurwitz A, Korach O, Revel A, Simon A, Finci-Yeheskel Z, Mayer M, Laufer N. Human follicular nitric oxide pathway: relationship to follicular size, oestradiol concentrations and ovarian blood flow. Hum Reprod. 1996;11:1947–1951.
    1. Manau D, Balasch J, Jimenez W, Fabregues F, Casamitjana R, Creus M, Arroyo V, Vanrell JA. Adrenomedullin and nitric oxide in menstrual and in vitro fertilization cycles. Relationship to estradiol. Acta Obstet Gynecol Scand. 1999;78:626–631. doi: 10.1034/j.1600-0412.1999.780711.x.
    1. Fabregues F, Balasch J, Manau D, Creus M, Jimenez W, Carmona F, Casamit J, Vanrell JA. Circulating levels of nitric oxide in successful and unsuccessful implantation after in vitro fertilization and embryo transfer. Relationship to estradiol and progesterone. Acta Obstet Gynecol Scand. 2000;79:564–569. doi: 10.1034/j.1600-0412.2000.079007564.x.
    1. Manau D, Balasch J, Jimenez W, Fabregues F, Civico S, Casamitjana R, Creus M, Vanrell JA. Follicular fluid concentrations of adrenomedullin, vascular endothelial growth factor and nitric oxide in IVF cycles: relationship to ovarian response. Hum Reprod. 2000;15:1295–1299. doi: 10.1093/humrep/15.6.1295.
    1. Battaglia C, Salvatori M, Maxia N, Petraglia F, Facchinetti F, Volpe A. Adjuvant L-arginine treatment for in-vitro fertilization in poor responder patients. Hum Reprod. 1999;14:1690–1697. doi: 10.1093/humrep/14.7.1690.
    1. Battaglia C, Regnani G, Marsella T, Facchinetti F, Volpe A, Venturoli S, Flamigni C. Adjuvant L-arginine treatment in controlled ovarian hyperstimulation: a double-blind, randomized study. Hum Reprod. 2002;17:659–665. doi: 10.1093/humrep/17.3.659.
    1. Barrionuevo MJ, Schwandt RA, Rao PS, Graham LB, Maisel LP, Yeko TR. Nitric oxide (NO) and interleukin-1beta (IL-1beta) in follicular fluid and their correlation with fertilization and embryo cleavage. Am J Reprod Immunol. 2000;44:359–364. doi: 10.1111/j.8755-8920.2000.440607.x.
    1. Hata T, Hashimoto M, Manabe A, Aoki S, Iida K, Masumura S, Miyazaki K. Maternal and fetal nitric oxide synthesis is decreased in pregnancies with small for gestational age infants. Hum Reprod. 1998;13:1070–1073. doi: 10.1093/humrep/13.4.1070.
    1. Lees C, Campbell S, Jauniaux E, Brown R, Ramsay B, Gibb D, Moncada S, Martin JF. Arrest of preterm labour and prolongation of gestation with glyceryl trinitrate, a nitric oxide donor. Lancet. 1994;343:1325–1326. doi: 10.1016/S0140-6736(94)92468-6.
    1. Braude P, Rowell P. Assisted conception. II – in vitro fertilisation and intracytoplasmic sperm injection. BMJ. 2003;327:852–855. doi: 10.1136/bmj.327.7419.852.
    1. Isaksson R, Tiitinen A. Present concept of unexplained infertility. Gynecol Endocrinol. 2004;18:278–290. doi: 10.1080/0951359042000199878.
    1. Bedaiwy MA, Falcone T, Mohamed MS, Aleem AA, Sharma RK, Worley SE, Thornton J, Agarwal A. Differential growth of human embryos in vitro: role of reactive oxygen species. Fertil Steril. 2004;82:593–600. doi: 10.1016/j.fertnstert.2004.02.121.
    1. Oyawoye O, Abdel Gadir A, Garner A, Constantinovici N, Perrett C, Hardiman P. Antioxidants and reactive oxygen species in follicular fluid of women undergoing IVF: relationship to outcome. Hum Reprod. 2003;18:2270–2274. doi: 10.1093/humrep/deg450.
    1. Paszkowski T, Clarke RN, Hornstein MD. Smoking induces oxidative stress inside the Graafian follicle. Hum Reprod. 2002;17:921–925. doi: 10.1093/humrep/17.4.921.
    1. Van Blerkom J, Antczak M, Schrader R. The developmental potential of the human oocyte is related to the dissolved oxygen content of follicular fluid: association with vascular endothelial growth factor levels and perifollicular blood flow characteristics. Hum Reprod. 1997;12:1047–1055. doi: 10.1093/humrep/12.5.1047.
    1. Yang HW, Hwang KJ, Kwon HC, Kim HS, Choi KW, Oh KS. Detection of reactive oxygen species (ROS) and apoptosis in human fragmented embryos. Hum Reprod. 1998;13:998–1002. doi: 10.1093/humrep/13.4.998.
    1. Kurzawa R, Glabowski W, Baczkowski T, Wiszniewska B, Marchlewicz M. Growth factors protect in vitro cultured embryos from the consequences of oxidative stress. Zygote. 2004;12:231–240. doi: 10.1017/S0967199404002783.
    1. Reubinoff BE, Har-El R, Kitrossky N, Friedler S, Levi R, Lewin A, Chevion M. Increased levels of redox-active iron in follicular fluid: a possible cause of free radical-mediated infertility in beta-thalassemia major. Am J Obstet Gynecol. 1996;174:914–918.
    1. Wiener-Megnazi Z, Vardi L, Lissak A, Shnizer S, Zeev Reznick A, Ishai D, Lahav-Baratz S, Shiloh H, Koifman M, Dirnfeld M. Oxidative stress indices in follicular fluid as measured by the thermochemiluminescence assay correlate with outcome parameters in in vitro fertilization. Fertil Steril. 2004;82:1171–1176. doi: 10.1016/j.fertnstert.2004.06.013.
    1. Torok A, Nemeth P, Torok B, Berki T, Tinneberg HR, Bodis J. Organic hydroperoxide-induced chemiluminescence of follicular fluid and blood serum samples obtained from women pretreated for in vitro fertilization. Gynecol Obstet Invest. 2004;57:72–79. doi: 10.1159/000075381.
    1. Shiverick KT, Salafia C. Cigarette smoking and pregnancy I: ovarian, uterine and placental effects. Placenta. 1999;20:265–272. doi: 10.1053/plac.1998.0377.
    1. Schweigert FJ, Steinhagen B, Raila J, Siemann A, Peet D, Buscher U. Concentrations of carotenoids, retinol and alpha-tocopherol in plasma and follicular fluid of women undergoing IVF. Hum Reprod. 2003;18:1259–1264. doi: 10.1093/humrep/deg249.
    1. Takasaki A, Nakamura Y, Tamura H, Shimamura K, Morioka H. Melatonin as a new drug for improving oocyte quality. Reprod Med Biol. 2003;2:139–144. doi: 10.1111/j.1447-0578.2003.00035.x.
    1. Harvey AJ, Kind KL, Thompson JG. REDOX regulation of early embryo development. Reproduction. 2002;123:479–486. doi: 10.1530/rep.0.1230479.
    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. doi: 10.1290/1543-706X(2003)039<0098:HOAAAP>;2.
    1. Parman T, Wiley MJ, Wells PG. Free radical-mediated oxidative DNA damage in the mechanism of thalidomide teratogenicity. Nat Med. 1999;5:582–585. doi: 10.1038/8466.
    1. Burton GJ, Hempstock J, Jauniaux E. Oxygen, early embryonic metabolism and free radical-mediated embryopathies. Reprod Biomed Online. 2003;6:84–96.
    1. Wentzel P, Welsh N, Eriksson UJ. Developmental damage, increased lipid peroxidation, diminished cyclooxygenase-2 gene expression, and lowered prostaglandin E2 levels in rat embryos exposed to a diabetic environment. Diabetes. 1999;48:813–820.
    1. Nicol CJ, Zielenski J, Tsui LC, Wells PG. An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis. Faseb J. 2000;14:111–127.
    1. Dumoulin JC, Meijers CJ, Bras M, Coonen E, Geraedts JP, Evers JL. Effect of oxygen concentration on human in-vitro fertilization and embryo culture. Hum Reprod. 1999;14:465–469. doi: 10.1093/humrep/14.2.465.
    1. Kitagawa Y, Suzuki K, Yoneda A, Watanabe T. Effects of oxygen concentration and antioxidants on the in vitro developmental ability, production of reactive oxygen species (ROS), and DNA fragmentation in porcine embryos. Theriogenology. 2004;62:1186–1197. doi: 10.1016/j.theriogenology.2004.01.011.
    1. Paszkowski T, Clarke RN. Antioxidative capacity of preimplantation embryo culture medium declines following the incubation of poor quality embryos. Hum Reprod. 1996;11:2493–2495.
    1. Ermilov A, Diamond MP, Sacco AG, Dozortsev DD. Culture media and their components differ in their ability to scavenge reactive oxygen species in the plasmid relaxation assay. Fertil Steril. 1999;72:154–157. doi: 10.1016/S0015-0282(99)00204-6.
    1. Agarwal A, Nallella KP, Allamaneni SS, Said TM. Role of antioxidants in treatment of male infertility: an overview of the literature. Reprod Biomed Online. 2004;8:616–627.
    1. Henmi H, Endo T, Kitajima Y, Manase K, Hata H, Kudo R. Effects of ascorbic acid supplementation on serum progesterone levels in patients with a luteal phase defect. Fertil Steril. 2003;80:459–461. doi: 10.1016/S0015-0282(03)00657-5.
    1. Vural P, Akgul C, Yildirim A, Canbaz M. Antioxidant defence in recurrent abortion. Clin Chim Acta. 2000;295:169–177. doi: 10.1016/S0009-8981(99)00255-7.
    1. Crha I, Hruba D, Ventruba P, Fiala J, Totusek J, Visnova H. Ascorbic acid and infertility treatment. Cent Eur J Public Health. 2003;11:63–67.
    1. Westphal LM, Polan ML, Trant AS, Mooney SB. A nutritional supplement for improving fertility in women: a pilot study. J Reprod Med. 2004;49:289–293.
    1. Griesinger G, Franke K, Kinast C, Kutzelnigg A, Riedinger S, Kulin S, Kaali SG, Feichtinger W. Ascorbic acid supplement during luteal phase in IVF. J Assist Reprod Genet. 2002;19:164–168. doi: 10.1023/A:1014837811353.
    1. Catt JW, Henman M. Toxic effects of oxygen on human embryo development. Hum Reprod. 2000;15:199–206.
    1. Lane M, Maybach JM, Gardner DK. Addition of ascorbate during cryopreservation stimulates subsequent embryo development. Hum Reprod. 2002;17:2686–2693. doi: 10.1093/humrep/17.10.2686.
    1. Chui DK, Pugh ND, Walker SM, Gregory L, Shaw RW. Follicular vascularity – the predictive value of transvaginal power Doppler ultrasonography in an in-vitro fertilization programme: a preliminary study. Hum Reprod. 1997;12:191–196. doi: 10.1093/humrep/12.1.191.
    1. Sher G, Fisch JD. Vaginal sildenafil (Viagra): a preliminary report of a novel method to improve uterine artery blood flow and endometrial development in patients undergoing IVF. Hum Reprod. 2000;15:806–809. doi: 10.1093/humrep/15.4.806.
    1. Sher G, Fisch JD. Effect of vaginal sildenafil on the outcome of in vitro fertilization (IVF) after multiple IVF failures attributed to poor endometrial development. Fertil Steril. 2002;78:1073–1076. doi: 10.1016/S0015-0282(02)03375-7.
    1. Lornage J. Biological aspects of endometriosis in vitro fertilization. J Gynecol Obstet Biol Reprod (Paris) 2003;32:S48–50.
    1. Tarin JJ. Potential effects of age-associated oxidative stress on mammalian oocytes/embryos. Mol Hum Reprod. 1996;2:717–724.
    1. Tarin JJ, Perez-Albala S, Cano A. Consequences on offspring of abnormal function in ageing gametes. Hum Reprod Update. 2000;6:532–549. doi: 10.1093/humupd/6.6.532.
    1. Arteaga E, Villaseca P, Rojas A, Arteaga A, Bianchi M. Comparison of the antioxidant effect of estriol and estradiol on low density lipoproteins in post-menopausal women. Rev Med Chil. 1998;126:481–487.
    1. Tamir S, Izrael S, Vaya J. The effect of oxidative stress on ERalpha and ERbeta expression. J Steroid Biochem Mol Biol. 2002;81:327–232. doi: 10.1016/S0960-0760(02)00115-2.
    1. Villar J, Say L, Shennan A, Lindheimer M, Duley L, Conde-Agudelo A, Merialdi M. Methodological and technical issues related to the diagnosis, screening, prevention, and treatment of pre-eclampsia and eclampsia. Int J Gynaecol Obstet. 2004;85:S28–S41. doi: 10.1016/j.ijgo.2004.03.009.
    1. Harma M, Erel O. Measurement of the total antioxidant response in preeclampsia with a novel automated method. Eur J Obstet Gynecol Reprod Biol. 2005;118:47–51. doi: 10.1016/j.ejogrb.2004.04.012.
    1. Aydin S, Benian A, Madazli R, Uludag S, Uzun H, Kaya S. Plasma malondialdehyde, superoxide dismutase, sE-selectin, fibronectin, endothelin-1 and nitric oxide levels in women with preeclampsia. Eur J Obstet Gynecol Reprod Biol. 2004;113:21–25. doi: 10.1016/S0301-2115(03)00368-3.
    1. Mikhail MS, Anyaegbunam A, Garfinkel D, Palan PR, Basu J, Romney SL. Preeclampsia and antioxidant nutrients: decreased plasma levels of reduced ascorbic acid, alpha-tocopherol, and beta-carotene in women with preeclampsia. Am J Obstet Gynecol. 1994;171:150–157.
    1. Pijnenborg R, Dixon G, Robertson WB, Brosens I. Trophoblastic invasion of human decidua from 8 to 18 weeks of pregnancy. Placenta. 1980;1:3–19.
    1. Chappell LC, Seed PT, Briley AL, Kelly FJ, Lee R, Hunt BJ, Parmar K, Bewley SJ, Shennan AH, Steer PJ, Poston L. Effect of antioxidants on the occurrence of pre-eclampsia in women at increased risk: a randomised trial. Lancet. 1999;354:810–816.
    1. Gulmezoglu AM, Hofmeyr GJ, Oosthuisen MM. Antioxidants in the treatment of severe pre-eclampsia: an explanatory randomised controlled trial. Br J Obstet Gynaecol. 1997;104:689–696.
    1. Beazley D, Ahokas R, Livingston J, Griggs M, Sibai BM. Vitamin C and E supplementation in women at high risk for preeclampsia: a double-blind, placebo-controlled trial. Am J Obstet Gynecol. 2005;192:520–521. doi: 10.1016/j.ajog.2004.09.005.
    1. Jauniaux E, Hempstock J, Greenwold N, Burton GJ. Trophoblastic oxidative stress in relation to temporal and regional differences in maternal placental blood flow in normal and abnormal early pregnancies. Am J Pathol. 2003;162:115–125.
    1. Jauniaux E, Cindrova-Davies T, Johns J, Dunster C, Hempstock J, Kelly FJ, Burton GJ. Distribution and transfer pathways of antioxidant molecules inside the first trimester human gestational sac. J Clin Endocrinol Metab. 2004;89:1452–1458. doi: 10.1210/jc.2003-031332.
    1. Miller H, Wilson R, Jenkins C, MacLean MA, Roberts J, Walker JJ. Glutathione levels and miscarriage. Fertil Steril. 2000;74:1257–1258. doi: 10.1016/S0015-0282(00)01585-5.
    1. Sata F, Yamada H, Kondo T, Gong Y, Tozaki S, Kobashi G, Kato EH, Fujimoto S, Kishi R. Glutathione S-transferase M1 and T1 polymorphisms and the risk of recurrent pregnancy loss. Mol Hum Reprod. 2003;9:165–169. doi: 10.1093/molehr/gag021.
    1. Cramer DW, Wise LA. The epidemiology of recurrent pregnancy loss. Semin Reprod Med. 2000;18:331–339. doi: 10.1055/s-2000-13722.
    1. Comporti M, Signorini C, Leoncini S, Buonocore G, Rossi V, Ciccoli L. Plasma F2-isoprostanes are elevated in newborns and inversely correlated to gestational age. Free Radic Biol Med. 2004;37:724–732. doi: 10.1016/j.freeradbiomed.2004.06.007.
    1. Ekerhovd E, Weijdegard B, Brannstrom M, Mattsby-Baltzer I, Norstrom A. Nitric oxide induced cervical ripening in the human: Involvement of cyclic guanosine monophosphate, prostaglandin F(2 alpha), and prostaglandin E(2) Am J Obstet Gynecol. 2002;186:745–750. doi: 10.1067/mob.2002.121327.
    1. Plessinger MA, Woods JR, Jr, Miller RK. Pretreatment of human amnion-chorion with vitamins C and E prevents hypochlorous acid-induced damage. Am J Obstet Gynecol. 2000;183:979–985. doi: 10.1067/mob.2000.106676.
    1. Siega-Riz AM, Promislow JH, Savitz DA, Thorp JM, Jr, McDonald T. Vitamin C intake and the risk of preterm delivery. Am J Obstet Gynecol. 2003;189:519–525. doi: 10.1067/S0002-9378(03)00363-6.
    1. Holmes VA, Young IS, Maresh MJ, Pearson DW, Walker JD, McCance DR. The Diabetes and Pre-eclampsia Intervention Trial. Int J Gynaecol Obstet. 2004;87:66–71. doi: 10.1016/j.ijgo.2004.06.015.
    1. Mayne ST, Wright ME, Cartmel B. Assessment of antioxidant nutrient intake and status for epidemiologic research. J Nutr. 2004;134:3199S–3200S.
    1. Kupka R, Msamanga GI, Spiegelman D, Morris S, Mugusi F, Hunter DJ, Fawzi WW. Selenium status is associated with accelerated HIV disease progression among HIV-1-infected pregnant women in Tanzania. J Nutr. 2004;134:2556–2560.
    1. Fawzi W, Msamanga G. Micronutrients and adverse pregnancy outcomes in the context of HIV infection. Nutr Rev. 2004;62:269–275. doi: 10.1301/nr.2004.jul.269-275.
    1. Mates M. Effects of antioxidant enzymes in the molecular control of reactive oxygen species toxicology. Toxicology. 2000;153:83–104. doi: 10.1016/S0300-483X(00)00306-1.

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