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Published in: Archives of Gynecology and Obstetrics 1/2013

01-07-2013 | Reproductive Medicine

Influence of reactive oxygen species on human sperm functions and fertilizing capacity including therapeutical approaches

Authors: Shu-jian Chen, Jean-Pierre Allam, Yong-gang Duan, Gerhard Haidl

Published in: Archives of Gynecology and Obstetrics | Issue 1/2013

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Abstract

Background

Reactive oxygen species (ROS) are an array of molecules including oxygen-centered radicals, which are endowed with one or more unpaired electrons and non-radical oxygen derivatives such as hydrogen peroxide, which behave, to a large extent, like a double-edged sword in human sperm biology. This study aimed to overview the current knowledge of ROS in sperm physiology and pathology, as well as related therapies in spermatozoal dysfunction.

Methods

We performed this study by searching for keywords from PUBMED, including reactive oxygen species, oxidative stress, sperm function, and antioxidant therapy.

Results and conclusions

Low levels of ROS exert critical function in normal sperm physiology, such as fertilizing ability (acrosome reaction, hyperactivation, capacitation, and chemotaxis) and sperm motility; while increased ROS generation and/or decreased antioxidant capacity leads to the imbalance between oxidation and reduction in living systems, which is called sperm oxidative stress. This condition was widely considered to be a significant contributory factor to sperm DNA damage/apoptosis, lipid peroxidation, and reduced motility, which in turn, increased risk of male factor infertility/subfertility and birth defects. Under the current status quo, numerous subsequent studies have concentrated on antioxidant therapy. Although utility of such a therapeutic strategy significantly improved sperm function and motility in a myriad of experimental and clinical reports, the overall effectiveness still remains controversial mainly due to non-standardized assay to measure the level of ROS and sperm DNA damage, various antioxidant supplementation strategies, and inadequate fertilization and pregnancy data after clinical treatment. Therefore, standardized assessment and evaluation of ROS and total antioxidant capacity in semen should be established to keep ROS in a physiological level and prevent over-treatment of antioxidants toward reductive stress, which should be kept in mind, especially in assisted reproductive procedure. Moreover, the significance of large sample size populations, double-blind randomized, placebo-controlled clinical trials of antioxidant therapies is emphasized in this review to achieve optimal ingredients and dosage of antioxidants for patients with reactive oxygen-induced male fertility/subfertility.
Literature
1.
go back to reference Gharagozloo P, Aitken RJ (2011) The role of sperm oxidative stress in male infertility and the significance of oral antioxidant therapy. Hum Reprod 26(7):1628–1640PubMedCrossRef Gharagozloo P, Aitken RJ (2011) The role of sperm oxidative stress in male infertility and the significance of oral antioxidant therapy. Hum Reprod 26(7):1628–1640PubMedCrossRef
2.
go back to reference Agarwal A, Sharma RK, Nallella KP, Thomas AJ Jr, Alvarez JG, Sikka SC (2006) Reactive oxygen species as an independent marker of male factor infertility. Fertil Steril 86(4):878–885PubMedCrossRef Agarwal A, Sharma RK, Nallella KP, Thomas AJ Jr, Alvarez JG, Sikka SC (2006) Reactive oxygen species as an independent marker of male factor infertility. Fertil Steril 86(4):878–885PubMedCrossRef
3.
go back to reference MacLeod J (1943) The role of oxygen in the metabolism and motility of human spermatozoa. Am J Physiol 138(3):512–518 MacLeod J (1943) The role of oxygen in the metabolism and motility of human spermatozoa. Am J Physiol 138(3):512–518
4.
go back to reference Sawyer DE, Mercer BG, Wiklendt AM, Aitken RJ (2003) Quantitative analysis of gene-specific DNA damage in human spermatozoa. Mutat Res 529(1–2):21–34PubMed Sawyer DE, Mercer BG, Wiklendt AM, Aitken RJ (2003) Quantitative analysis of gene-specific DNA damage in human spermatozoa. Mutat Res 529(1–2):21–34PubMed
5.
go back to reference Suresh S, Prithiviraj E, Prakash S (2010) Effect of Mucuna pruriens on oxidative stress mediated damage in aged rat sperm. Int J Androl 33(1):22–32PubMedCrossRef Suresh S, Prithiviraj E, Prakash S (2010) Effect of Mucuna pruriens on oxidative stress mediated damage in aged rat sperm. Int J Androl 33(1):22–32PubMedCrossRef
6.
go back to reference Rajesh Kumar T, Doreswamy K, Shrilatha B, Muralidhara (2002) Oxidative stress associated DNA damage in testis of mice: induction of abnormal sperms and effects on fertility. Mutat Res 513(1–2):103–111PubMed Rajesh Kumar T, Doreswamy K, Shrilatha B, Muralidhara (2002) Oxidative stress associated DNA damage in testis of mice: induction of abnormal sperms and effects on fertility. Mutat Res 513(1–2):103–111PubMed
7.
go back to reference Guthrie HD, Welch GR (2012) Effects of reactive oxygen species on sperm function. Theriogenology 78(8):1700–1708 Guthrie HD, Welch GR (2012) Effects of reactive oxygen species on sperm function. Theriogenology 78(8):1700–1708
8.
go back to reference Agarwal A, Allamaneni SS, Nallella KP, George AT, Mascha E (2005) Correlation of reactive oxygen species levels with the fertilization rate after in vitro fertilization: a qualified meta-analysis. Fertil Steril 84(1):228–231PubMedCrossRef Agarwal A, Allamaneni SS, Nallella KP, George AT, Mascha E (2005) Correlation of reactive oxygen species levels with the fertilization rate after in vitro fertilization: a qualified meta-analysis. Fertil Steril 84(1):228–231PubMedCrossRef
9.
go back to reference Gupta MK, Uhm SJ, Lee HT (2010) Effect of vitrification and beta-mercaptoethanol on reactive oxygen species activity and in vitro development of oocytes vitrified before or after in vitro fertilization. Fertil Steril 93(8):2602–2607PubMedCrossRef Gupta MK, Uhm SJ, Lee HT (2010) Effect of vitrification and beta-mercaptoethanol on reactive oxygen species activity and in vitro development of oocytes vitrified before or after in vitro fertilization. Fertil Steril 93(8):2602–2607PubMedCrossRef
10.
go back to reference de Lamirande E, Jiang H, Zini A, Kodama H, Gagnon C (1997) Reactive oxygen species and sperm physiology. Rev Reprod 2(1):48–54PubMedCrossRef de Lamirande E, Jiang H, Zini A, Kodama H, Gagnon C (1997) Reactive oxygen species and sperm physiology. Rev Reprod 2(1):48–54PubMedCrossRef
11.
go back to reference Ford WC (2004) Regulation of sperm function by reactive oxygen species. Hum Reprod Update 10(5):387–399PubMedCrossRef Ford WC (2004) Regulation of sperm function by reactive oxygen species. Hum Reprod Update 10(5):387–399PubMedCrossRef
12.
go back to reference de Lamirande E, Gagnon C (1993) Human sperm hyperactivation and capacitation as parts of an oxidative process. Free Radic Biol Med 14(2):157–166PubMedCrossRef de Lamirande E, Gagnon C (1993) Human sperm hyperactivation and capacitation as parts of an oxidative process. Free Radic Biol Med 14(2):157–166PubMedCrossRef
13.
go back to reference de Lamirande E, Gagnon C (1993) A positive role for the superoxide anion in triggering hyperactivation and capacitation of human spermatozoa. Int J Androl 16(1):21–25PubMedCrossRef de Lamirande E, Gagnon C (1993) A positive role for the superoxide anion in triggering hyperactivation and capacitation of human spermatozoa. Int J Androl 16(1):21–25PubMedCrossRef
14.
go back to reference Griveau JF, Le Lannou D (1997) Reactive oxygen species and human spermatozoa: physiology and pathology. Int J Androl 20(2):61–69PubMedCrossRef Griveau JF, Le Lannou D (1997) Reactive oxygen species and human spermatozoa: physiology and pathology. Int J Androl 20(2):61–69PubMedCrossRef
15.
go back to reference Parks JE, Lynch DV (1992) Lipid composition and thermotropic phase behavior of boar, bull, stallion, and rooster sperm membranes. Cryobiology 29(2):255–266PubMedCrossRef Parks JE, Lynch DV (1992) Lipid composition and thermotropic phase behavior of boar, bull, stallion, and rooster sperm membranes. Cryobiology 29(2):255–266PubMedCrossRef
16.
go back to reference Zalata AA, Christophe AB, Depuydt CE, Schoonjans F, Comhaire FH (1998) The fatty acid composition of phospholipids of spermatozoa from infertile patients. Mol Hum Reprod 4(2):111–118PubMedCrossRef Zalata AA, Christophe AB, Depuydt CE, Schoonjans F, Comhaire FH (1998) The fatty acid composition of phospholipids of spermatozoa from infertile patients. Mol Hum Reprod 4(2):111–118PubMedCrossRef
17.
18.
go back to reference Henkel RR (2011) Leukocytes and oxidative stress: dilemma for sperm function and male fertility. Asian J Androl 13(1):43–52PubMedCrossRef Henkel RR (2011) Leukocytes and oxidative stress: dilemma for sperm function and male fertility. Asian J Androl 13(1):43–52PubMedCrossRef
19.
go back to reference Tavilani H, Goodarzi MT, Doosti M, Vaisi-Raygani A, Hassanzadeh T, Salimi S, Joshaghani HR (2008) Relationship between seminal antioxidant enzymes and the phospholipid and fatty acid composition of spermatozoa. Reprod Biomed Online 16(5):649–656PubMedCrossRef Tavilani H, Goodarzi MT, Doosti M, Vaisi-Raygani A, Hassanzadeh T, Salimi S, Joshaghani HR (2008) Relationship between seminal antioxidant enzymes and the phospholipid and fatty acid composition of spermatozoa. Reprod Biomed Online 16(5):649–656PubMedCrossRef
20.
go back to reference Sies H, Stahl W, Sundquist AR (1992) Antioxidant functions of vitamins. Vitamins E and C, beta-carotene, and other carotenoids. Ann NY Acad Sci 669:7–20PubMedCrossRef Sies H, Stahl W, Sundquist AR (1992) Antioxidant functions of vitamins. Vitamins E and C, beta-carotene, and other carotenoids. Ann NY Acad Sci 669:7–20PubMedCrossRef
21.
go back to reference Sies H (1985) Oxidative stress: introductory remarks. In: Sies H (ed) Oxidative stress. Academic Press, London, pp 1–8 Sies H (1985) Oxidative stress: introductory remarks. In: Sies H (ed) Oxidative stress. Academic Press, London, pp 1–8
22.
go back to reference Aitken RJ, Roman SD (2008) Antioxidant systems and oxidative stress in the testes. Oxid Med Cell Longev 1(9):15–24PubMedCrossRef Aitken RJ, Roman SD (2008) Antioxidant systems and oxidative stress in the testes. Oxid Med Cell Longev 1(9):15–24PubMedCrossRef
23.
go back to reference Tunc O, Thompson J, Tremellen K (2009) Improvement in sperm DNA quality using an oral antioxidant therapy. Reprod Biomed Online 18(6):761–768PubMedCrossRef Tunc O, Thompson J, Tremellen K (2009) Improvement in sperm DNA quality using an oral antioxidant therapy. Reprod Biomed Online 18(6):761–768PubMedCrossRef
24.
go back to reference Gil-Villa AM, Cardona-Maya W, Agarwal A, Sharma R, Cadavid A (2009) Role of male factor in early recurrent embryo loss: do antioxidants have any effect? Fertil Steril 92(2):565–571PubMedCrossRef Gil-Villa AM, Cardona-Maya W, Agarwal A, Sharma R, Cadavid A (2009) Role of male factor in early recurrent embryo loss: do antioxidants have any effect? Fertil Steril 92(2):565–571PubMedCrossRef
25.
go back to reference Chi HJ, Kim JH, Ryu CS, Lee JY, Park JS, Chung DY, Choi SY, Kim MH, Chun EK, Roh SI (2008) Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa. Hum Reprod 23(5):1023–1028PubMedCrossRef Chi HJ, Kim JH, Ryu CS, Lee JY, Park JS, Chung DY, Choi SY, Kim MH, Chun EK, Roh SI (2008) Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa. Hum Reprod 23(5):1023–1028PubMedCrossRef
26.
go back to reference Greco E, Romano S, Iacobelli M, Ferrero S, Baroni E, Minasi MG, Ubaldi F, Rienzi L, Tesarik J (2005) ICSI in cases of sperm DNA damage: beneficial effect of oral antioxidant treatment. Hum Reprod 20(9):2590–2594PubMedCrossRef Greco E, Romano S, Iacobelli M, Ferrero S, Baroni E, Minasi MG, Ubaldi F, Rienzi L, Tesarik J (2005) ICSI in cases of sperm DNA damage: beneficial effect of oral antioxidant treatment. Hum Reprod 20(9):2590–2594PubMedCrossRef
27.
go back to reference Donnelly ET, McClure N, Lewis SE (1999) Antioxidant supplementation in vitro does not improve human sperm motility. Fertil Steril 72(3):484–495PubMedCrossRef Donnelly ET, McClure N, Lewis SE (1999) Antioxidant supplementation in vitro does not improve human sperm motility. Fertil Steril 72(3):484–495PubMedCrossRef
28.
go back to reference Akmal M, Qadri JQ, Al-Waili NS, Thangal S, Haq A, Saloom KY (2006) Improvement in human semen quality after oral supplementation of vitamin C. J Med Food 9(3):440–442PubMedCrossRef Akmal M, Qadri JQ, Al-Waili NS, Thangal S, Haq A, Saloom KY (2006) Improvement in human semen quality after oral supplementation of vitamin C. J Med Food 9(3):440–442PubMedCrossRef
29.
go back to reference Ménézo YJ, Hazout A, Panteix G, Robert F, Rollet J, Cohen-Bacrie P, Chapuis F, Clément P, Benkhalifa M (2007) Antioxidants to reduce sperm DNA fragmentation: an unexpected adverse effect. Reprod Biomed Online 14(4):418–421PubMedCrossRef Ménézo YJ, Hazout A, Panteix G, Robert F, Rollet J, Cohen-Bacrie P, Chapuis F, Clément P, Benkhalifa M (2007) Antioxidants to reduce sperm DNA fragmentation: an unexpected adverse effect. Reprod Biomed Online 14(4):418–421PubMedCrossRef
30.
go back to reference Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C (2008) Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases. Cochrane Database Syst Rev (2):CD007176. doi:10.1002/14651858 Bjelakovic G, Nikolova D, Gluud LL, Simonetti RG, Gluud C (2008) Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases. Cochrane Database Syst Rev (2):CD007176. doi:10.​1002/​14651858
31.
go back to reference Verma A, Kanwar KC (1998) Human sperm motility and lipid peroxidation in different ascorbic acid concentrations: an in vitro analysis. Andrologia 30(6):325–329PubMedCrossRef Verma A, Kanwar KC (1998) Human sperm motility and lipid peroxidation in different ascorbic acid concentrations: an in vitro analysis. Andrologia 30(6):325–329PubMedCrossRef
32.
go back to reference Safarinejad MR, Safarinejad S (2009) Efficacy of selenium and/or N-acetyl-cysteine for improving semen parameters in infertile men: a double-blind, placebo controlled, randomized study. J Urol 181(2):741–751PubMedCrossRef Safarinejad MR, Safarinejad S (2009) Efficacy of selenium and/or N-acetyl-cysteine for improving semen parameters in infertile men: a double-blind, placebo controlled, randomized study. J Urol 181(2):741–751PubMedCrossRef
33.
go back to reference Deepinder F, Cocuzza M, Agarwal A (2008) Should seminal oxidative stress measurement be offered routinely to men presenting for infertility evaluation? Endocr Pract 14(4):484–491PubMedCrossRef Deepinder F, Cocuzza M, Agarwal A (2008) Should seminal oxidative stress measurement be offered routinely to men presenting for infertility evaluation? Endocr Pract 14(4):484–491PubMedCrossRef
34.
go back to reference World Health Organization (2010) WHO laboratory manual for the examination and processing of human semen, 5th edn. World Health Organization, Geneva World Health Organization (2010) WHO laboratory manual for the examination and processing of human semen, 5th edn. World Health Organization, Geneva
35.
go back to reference Athayde KS, Cocuzza M, Agarwal A, Krajcir N, Lucon AM, Srougi M, Hallak J (2007) Development of normal reference values for seminal reactive oxygen species and their correlation with leukocytes and semen parameters in a fertile population. J Androl 28(4):613–620PubMedCrossRef Athayde KS, Cocuzza M, Agarwal A, Krajcir N, Lucon AM, Srougi M, Hallak J (2007) Development of normal reference values for seminal reactive oxygen species and their correlation with leukocytes and semen parameters in a fertile population. J Androl 28(4):613–620PubMedCrossRef
36.
go back to reference Desai N, Sharma R, Makker K, Sabanegh E, Agarwal A (2009) Physiologic and pathologic levels of reactive oxygen species in neat semen of infertile men. Fertil Steril 92(5):1626–1631PubMedCrossRef Desai N, Sharma R, Makker K, Sabanegh E, Agarwal A (2009) Physiologic and pathologic levels of reactive oxygen species in neat semen of infertile men. Fertil Steril 92(5):1626–1631PubMedCrossRef
37.
go back to reference Aitken RJ, Buckingham DW, West KM (1992) Reactive oxygen species and human spermatozoa: analysis of the cellular mechanisms involved in luminol- and lucigenin-dependent chemiluminescence. J Cell Physiol 151(3):466–477PubMedCrossRef Aitken RJ, Buckingham DW, West KM (1992) Reactive oxygen species and human spermatozoa: analysis of the cellular mechanisms involved in luminol- and lucigenin-dependent chemiluminescence. J Cell Physiol 151(3):466–477PubMedCrossRef
38.
go back to reference Aitken RJ, Baker MA, O’Bryan M (2004) Shedding light on chemiluminescence: the application of chemiluminescence in diagnostic andrology. J Androl 25(4):455–465PubMed Aitken RJ, Baker MA, O’Bryan M (2004) Shedding light on chemiluminescence: the application of chemiluminescence in diagnostic andrology. J Androl 25(4):455–465PubMed
39.
go back to reference Sharma RK, Pasqualotto FF, Nelson DR, Thomas AJ Jr, Agarwal A (1999) The reactive oxygen species-total antioxidant capacity score is a new measure of oxidative stress to predict male infertility. Hum Reprod 14(11):2801–2807PubMedCrossRef Sharma RK, Pasqualotto FF, Nelson DR, Thomas AJ Jr, Agarwal A (1999) The reactive oxygen species-total antioxidant capacity score is a new measure of oxidative stress to predict male infertility. Hum Reprod 14(11):2801–2807PubMedCrossRef
40.
go back to reference Pasqualotto FF, Sundaram A, Sharma RK, Borges E Jr, Pasqualotto EB, Agarwal A (2008) Semen quality and oxidative stress scores in fertile and infertile patients with varicocele. Fertil Steril 89(3):602–607PubMedCrossRef Pasqualotto FF, Sundaram A, Sharma RK, Borges E Jr, Pasqualotto EB, Agarwal A (2008) Semen quality and oxidative stress scores in fertile and infertile patients with varicocele. Fertil Steril 89(3):602–607PubMedCrossRef
41.
go back to reference Mahfouz R, Sharma R, Sharma D, Sabanegh E, Agarwal A (2009) Diagnostic value of the total antioxidant capacity (TAC) in human seminal plasma. Fertil Steril 91(3):805–811PubMedCrossRef Mahfouz R, Sharma R, Sharma D, Sabanegh E, Agarwal A (2009) Diagnostic value of the total antioxidant capacity (TAC) in human seminal plasma. Fertil Steril 91(3):805–811PubMedCrossRef
42.
go back to reference Smith DC, Barratt CL, Williams MA (1989) The characterization of non-sperm cells in the ejaculates of fertile men using transmission electron microscopy. Andrologia 21(4):319–333PubMedCrossRef Smith DC, Barratt CL, Williams MA (1989) The characterization of non-sperm cells in the ejaculates of fertile men using transmission electron microscopy. Andrologia 21(4):319–333PubMedCrossRef
43.
go back to reference Garrido N, Meseguer M, Simon C, Pellicer A, Remohi J (2004) Pro-oxidative and anti-oxidative imbalance in human semen and its relation with male fertility. Asian J Androl 6(1):59–65PubMed Garrido N, Meseguer M, Simon C, Pellicer A, Remohi J (2004) Pro-oxidative and anti-oxidative imbalance in human semen and its relation with male fertility. Asian J Androl 6(1):59–65PubMed
44.
go back to reference Hipler UC, Görnig M, Hipler B, Römer W, Schreiber G (2000) Stimulation and scavestrogen-induced inhibition of reactive oxygen species generated by rat Sertoli cells. Arch Androl 44(2):147–154PubMedCrossRef Hipler UC, Görnig M, Hipler B, Römer W, Schreiber G (2000) Stimulation and scavestrogen-induced inhibition of reactive oxygen species generated by rat Sertoli cells. Arch Androl 44(2):147–154PubMedCrossRef
45.
go back to reference Gomez E, Buckingham DW, Brindle J, Lanzafame F, Irvine DS, Aitken RJ (1996) Development of an image analysis system to monitor the retention of residual cytoplasm by human spermatozoa: correlation with biochemical markers of the cytoplasmic space, oxidative stress, and sperm function. J Androl 17(3):276–287PubMed Gomez E, Buckingham DW, Brindle J, Lanzafame F, Irvine DS, Aitken RJ (1996) Development of an image analysis system to monitor the retention of residual cytoplasm by human spermatozoa: correlation with biochemical markers of the cytoplasmic space, oxidative stress, and sperm function. J Androl 17(3):276–287PubMed
46.
go back to reference Aitken RJ (1999) The Amoroso Lecture. The human spermatozoon—a cell in crisis? J Reprod Fertil 115(1):1–7PubMedCrossRef Aitken RJ (1999) The Amoroso Lecture. The human spermatozoon—a cell in crisis? J Reprod Fertil 115(1):1–7PubMedCrossRef
47.
go back to reference Koppers AJ, De Iuliis GN, Finnie JM, McLaughlin EA, Aitken RJ (2008) Significance of mitochondrial reactive oxygen species in the generation of oxidative stress in spermatozoa. J Clin Endocrinol Metab 93(8):3199–3207PubMedCrossRef Koppers AJ, De Iuliis GN, Finnie JM, McLaughlin EA, Aitken RJ (2008) Significance of mitochondrial reactive oxygen species in the generation of oxidative stress in spermatozoa. J Clin Endocrinol Metab 93(8):3199–3207PubMedCrossRef
48.
go back to reference Bánfi B, Molnár G, Maturana A, Steger K, Hegedûs B, Demaurex N, Krause KH (2001) A Ca(2 +)-activated NADPH oxidase in testis, spleen, and lymph nodes. J Biol Chem 276(40):37594–37601PubMedCrossRef Bánfi B, Molnár G, Maturana A, Steger K, Hegedûs B, Demaurex N, Krause KH (2001) A Ca(2 +)-activated NADPH oxidase in testis, spleen, and lymph nodes. J Biol Chem 276(40):37594–37601PubMedCrossRef
49.
go back to reference Musset B, Clark RA, Decoursey TE, Petheo GL, Geiszt M, Chen Y, Cornell JE, Eddy CA, Brzyski RG, El Jamali A (2012) NOX5 in human spermatozoa: expression, function and regulation. J Biol Chem 287(12):9376–9388PubMedCrossRef Musset B, Clark RA, Decoursey TE, Petheo GL, Geiszt M, Chen Y, Cornell JE, Eddy CA, Brzyski RG, El Jamali A (2012) NOX5 in human spermatozoa: expression, function and regulation. J Biol Chem 287(12):9376–9388PubMedCrossRef
50.
go back to reference Henkel R, Kierspel E, Stalf T, Mehnert C, Menkveld R, Tinneberg HR, Schill WB, Kruger TF (2005) Effect of reactive oxygen species produced by spermatozoa and leukocytes on sperm functions in non-leukocytospermic patients. Fertil Steril 83(3):635–642PubMedCrossRef Henkel R, Kierspel E, Stalf T, Mehnert C, Menkveld R, Tinneberg HR, Schill WB, Kruger TF (2005) Effect of reactive oxygen species produced by spermatozoa and leukocytes on sperm functions in non-leukocytospermic patients. Fertil Steril 83(3):635–642PubMedCrossRef
51.
go back to reference Plante M, de Lamirande E, Gagnon C (1994) Reactive oxygen species released by activated neutrophils, but not by deficient spermatozoa, are sufficient to affect normal sperm motility. Fertil Steril 62(2):387–393PubMed Plante M, de Lamirande E, Gagnon C (1994) Reactive oxygen species released by activated neutrophils, but not by deficient spermatozoa, are sufficient to affect normal sperm motility. Fertil Steril 62(2):387–393PubMed
52.
go back to reference Sharma RK, Pasqualotto AE, Nelson DR, Thomas AJ Jr, Agarwal A (2001) Relationship between seminal white blood cell counts and oxidative stress in men treated at an infertility clinic. J Androl 22(4):575–583PubMed Sharma RK, Pasqualotto AE, Nelson DR, Thomas AJ Jr, Agarwal A (2001) Relationship between seminal white blood cell counts and oxidative stress in men treated at an infertility clinic. J Androl 22(4):575–583PubMed
53.
go back to reference Lavranos G, Balla M, Tzortzopoulou A, Syriou V, Angelopoulou R (2012) Investigating ROS sources in male infertility: a common end for numerous pathways. Reprod Toxicol 34(3):298–307 Lavranos G, Balla M, Tzortzopoulou A, Syriou V, Angelopoulou R (2012) Investigating ROS sources in male infertility: a common end for numerous pathways. Reprod Toxicol 34(3):298–307
54.
go back to reference Wolff H (1995) The biologic significance of white blood cells in semen. Fertil Steril 63(6):1143–1157PubMed Wolff H (1995) The biologic significance of white blood cells in semen. Fertil Steril 63(6):1143–1157PubMed
55.
go back to reference Tremellen K, Tunc O (2010) Macrophage activity in semen is significantly correlated with sperm quality in infertile men. Int J Androl 33(6):823–831PubMedCrossRef Tremellen K, Tunc O (2010) Macrophage activity in semen is significantly correlated with sperm quality in infertile men. Int J Androl 33(6):823–831PubMedCrossRef
56.
go back to reference Morgan MJ, Liu ZG (2011) Crosstalk of reactive oxygen species and NF-κB signaling. Cell Res 21(1):103–115PubMedCrossRef Morgan MJ, Liu ZG (2011) Crosstalk of reactive oxygen species and NF-κB signaling. Cell Res 21(1):103–115PubMedCrossRef
57.
go back to reference Galli SJ, Borregaard N, Wynn TA (2011) Phenotypic and functional plasticity of cells of innate immunity: macrophages, mast cells and neutrophils. Nat Immunol 12(11):1035–1044PubMedCrossRef Galli SJ, Borregaard N, Wynn TA (2011) Phenotypic and functional plasticity of cells of innate immunity: macrophages, mast cells and neutrophils. Nat Immunol 12(11):1035–1044PubMedCrossRef
58.
go back to reference Ochsendorf FR (1999) Infections in the male genital tract and reactive oxygen species. Hum Reprod Update 5(5):399–420PubMedCrossRef Ochsendorf FR (1999) Infections in the male genital tract and reactive oxygen species. Hum Reprod Update 5(5):399–420PubMedCrossRef
59.
go back to reference Allam JP, Langer M, Fathy A, Oltermann I, Bieber T, Novak N, Haidl G (2009) Mast cells in the seminal plasma of infertile men as detected by flow cytometry. Andrologia 41(1):1–6PubMedCrossRef Allam JP, Langer M, Fathy A, Oltermann I, Bieber T, Novak N, Haidl G (2009) Mast cells in the seminal plasma of infertile men as detected by flow cytometry. Andrologia 41(1):1–6PubMedCrossRef
60.
go back to reference Haidl G, Duan YG, Chen SJ, Kohn FM, Schuppe HC, Allam JP (2011) The role of mast cells in male infertility. Expert Rev Clin Immunol 7(5):627–634PubMedCrossRef Haidl G, Duan YG, Chen SJ, Kohn FM, Schuppe HC, Allam JP (2011) The role of mast cells in male infertility. Expert Rev Clin Immunol 7(5):627–634PubMedCrossRef
61.
go back to reference Swindle EJ, Metcalfe DD, Coleman JW (2004) Rodent and human mast cells produce functionally significant intracellular reactive oxygen species but not nitric oxide. J Biol Chem 279(47):48751–48759PubMedCrossRef Swindle EJ, Metcalfe DD, Coleman JW (2004) Rodent and human mast cells produce functionally significant intracellular reactive oxygen species but not nitric oxide. J Biol Chem 279(47):48751–48759PubMedCrossRef
62.
go back to reference Suzuki Y, Yoshimaru T, Matsui T, Inoue T, Niide O, Nunomura S, Ra C (2003) Fc epsilon RI signaling of mast cells activates intracellular production of hydrogen peroxide: role in the regulation of calcium signals. J Immunol 171(11):6119–6127PubMed Suzuki Y, Yoshimaru T, Matsui T, Inoue T, Niide O, Nunomura S, Ra C (2003) Fc epsilon RI signaling of mast cells activates intracellular production of hydrogen peroxide: role in the regulation of calcium signals. J Immunol 171(11):6119–6127PubMed
63.
go back to reference Swindle EJ, Metcalfe DD (2007) The role of reactive oxygen species and nitric oxide in mast cell-dependent inflammatory processes. Immunol Rev 217:186–205PubMedCrossRef Swindle EJ, Metcalfe DD (2007) The role of reactive oxygen species and nitric oxide in mast cell-dependent inflammatory processes. Immunol Rev 217:186–205PubMedCrossRef
64.
go back to reference Sly LM, Kalesnikoff J, Lam V, Wong D, Song C, Omeis S, Chan K, Lee CW, Siraganian RP, Rivera J, Krystal G (2008) IgE-induced mast cell survival requires the prolonged generation of reactive oxygen species. J Immunol 181(6):3850–3860PubMed Sly LM, Kalesnikoff J, Lam V, Wong D, Song C, Omeis S, Chan K, Lee CW, Siraganian RP, Rivera J, Krystal G (2008) IgE-induced mast cell survival requires the prolonged generation of reactive oxygen species. J Immunol 181(6):3850–3860PubMed
65.
go back to reference Suzuki Y, Yoshimaru T, Inoue T, Niide O, Ra C (2005) Role of oxidants in mast cell activation. Chem Immunol Allergy 87:32–42PubMedCrossRef Suzuki Y, Yoshimaru T, Inoue T, Niide O, Ra C (2005) Role of oxidants in mast cell activation. Chem Immunol Allergy 87:32–42PubMedCrossRef
66.
go back to reference Wolff H, Anderson DJ (1988) Immunohistologic characterization and quantitation of leukocyte subpopulations in human semen. Fertil Steril 49(3):497–504PubMed Wolff H, Anderson DJ (1988) Immunohistologic characterization and quantitation of leukocyte subpopulations in human semen. Fertil Steril 49(3):497–504PubMed
67.
go back to reference Aitken RJ, Buckingham DW, West K, Brindle J (1996) On the use of paramagnetic beads and ferrofluids to assess and eliminate the leukocytic contribution to oxygen radical generation by human sperm suspensions. Am J Reprod Immunol 35(6):541–551PubMedCrossRef Aitken RJ, Buckingham DW, West K, Brindle J (1996) On the use of paramagnetic beads and ferrofluids to assess and eliminate the leukocytic contribution to oxygen radical generation by human sperm suspensions. Am J Reprod Immunol 35(6):541–551PubMedCrossRef
68.
go back to reference Barraud-Lange V, Pont JC, Ziyyat A, Pocate K, Sifer C, Cedrin-Durnerin I, Fechtali B, Ducot B, Wolf JP (2011) Seminal leukocytes are Good Samaritans for spermatozoa. Fertil Steril 96(6):1315–1319PubMedCrossRef Barraud-Lange V, Pont JC, Ziyyat A, Pocate K, Sifer C, Cedrin-Durnerin I, Fechtali B, Ducot B, Wolf JP (2011) Seminal leukocytes are Good Samaritans for spermatozoa. Fertil Steril 96(6):1315–1319PubMedCrossRef
69.
go back to reference Yanushpolsky EH, Politch JA, Hill JA, Anderson DJ (1996) Is leukocytospermia clinically relevant? Fertil Steril 66(5):822–825PubMed Yanushpolsky EH, Politch JA, Hill JA, Anderson DJ (1996) Is leukocytospermia clinically relevant? Fertil Steril 66(5):822–825PubMed
70.
go back to reference Kaleli S, Oçer F, Irez T, Budak E, Aksu MF (2000) Does leukocytospermia associate with poor semen parameters and sperm functions in male infertility? The role of different seminal leukocyte concentrations. Eur J Obstet Gynecol Reprod Biol 89(2):185–191PubMedCrossRef Kaleli S, Oçer F, Irez T, Budak E, Aksu MF (2000) Does leukocytospermia associate with poor semen parameters and sperm functions in male infertility? The role of different seminal leukocyte concentrations. Eur J Obstet Gynecol Reprod Biol 89(2):185–191PubMedCrossRef
72.
go back to reference Zini A, Al-Hathal N (2011) Antioxidant therapy in male infertility: fact or fiction? Asian J Androl 13(3):374–381PubMedCrossRef Zini A, Al-Hathal N (2011) Antioxidant therapy in male infertility: fact or fiction? Asian J Androl 13(3):374–381PubMedCrossRef
73.
go back to reference Henkel R (2012) Sperm preparation: state-of-the-art—physiological aspects and application of advanced sperm preparation methods. Asian J Androl 14(2):260–269PubMedCrossRef Henkel R (2012) Sperm preparation: state-of-the-art—physiological aspects and application of advanced sperm preparation methods. Asian J Androl 14(2):260–269PubMedCrossRef
74.
go back to reference de Lamirande E, Lamothe G, Villemure M (2009) Control of superoxide and nitric oxide formation during human sperm capacitation. Free Radic Biol Med 46(10):1420–1427PubMedCrossRef de Lamirande E, Lamothe G, Villemure M (2009) Control of superoxide and nitric oxide formation during human sperm capacitation. Free Radic Biol Med 46(10):1420–1427PubMedCrossRef
75.
go back to reference Aitken RJ, Irvine DS, Wu FC (1991) Prospective analysis of sperm–oocyte fusion and reactive oxygen species generation as criteria for the diagnosis of infertility. Am J Obstet Gynecol 164(2):542–551PubMedCrossRef Aitken RJ, Irvine DS, Wu FC (1991) Prospective analysis of sperm–oocyte fusion and reactive oxygen species generation as criteria for the diagnosis of infertility. Am J Obstet Gynecol 164(2):542–551PubMedCrossRef
76.
go back to reference Sánchez R, Sepúlveda C, Risopatrón J, Villegas J, Giojalas LC (2010) Human sperm chemotaxis depends on critical levels of reactive oxygen species. Fertil Steril 93(1):150–153PubMedCrossRef Sánchez R, Sepúlveda C, Risopatrón J, Villegas J, Giojalas LC (2010) Human sperm chemotaxis depends on critical levels of reactive oxygen species. Fertil Steril 93(1):150–153PubMedCrossRef
77.
go back to reference Aitken RJ, Clarkson JS (1987) Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. J Reprod Fertil 81(2):459–469PubMedCrossRef Aitken RJ, Clarkson JS (1987) Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. J Reprod Fertil 81(2):459–469PubMedCrossRef
78.
go back to reference Gil-Guzman E, Ollero M, Lopez MC, Sharma RK, Alvarez JG, Thomas AJ Jr, Agarwal A (2001) Differential production of reactive oxygen species by subsets of human spermatozoa at different stages of maturation. Hum Reprod 16(9):1922–1930PubMedCrossRef Gil-Guzman E, Ollero M, Lopez MC, Sharma RK, Alvarez JG, Thomas AJ Jr, Agarwal A (2001) Differential production of reactive oxygen species by subsets of human spermatozoa at different stages of maturation. Hum Reprod 16(9):1922–1930PubMedCrossRef
79.
go back to reference Donà G, Fiore C, Tibaldi E, Frezzato F, Andrisani A, Ambrosini G, Fiorentin D, Armanini D, Bordin L, Clari G (2011) Endogenous reactive oxygen species content and modulation of tyrosine phosphorylation during sperm capacitation. Int J Androl 34(5 Pt 1):411–419PubMedCrossRef Donà G, Fiore C, Tibaldi E, Frezzato F, Andrisani A, Ambrosini G, Fiorentin D, Armanini D, Bordin L, Clari G (2011) Endogenous reactive oxygen species content and modulation of tyrosine phosphorylation during sperm capacitation. Int J Androl 34(5 Pt 1):411–419PubMedCrossRef
80.
go back to reference Awda BJ, Buhr MM (2010) Extracellular signal-regulated kinases (ERKs) pathway and reactive oxygen species regulate tyrosine phosphorylation in capacitating boar spermatozoa. Biol Reprod 83(5):750–758PubMedCrossRef Awda BJ, Buhr MM (2010) Extracellular signal-regulated kinases (ERKs) pathway and reactive oxygen species regulate tyrosine phosphorylation in capacitating boar spermatozoa. Biol Reprod 83(5):750–758PubMedCrossRef
81.
go back to reference de Lamirande E, Lamothe G (2009) Reactive oxygen-induced reactive oxygen formation during human sperm capacitation. Free Radic Biol Med 46(4):502–510PubMedCrossRef de Lamirande E, Lamothe G (2009) Reactive oxygen-induced reactive oxygen formation during human sperm capacitation. Free Radic Biol Med 46(4):502–510PubMedCrossRef
82.
go back to reference de Lamirande E, O’Flaherty C (2008) Sperm activation: role of reactive oxygen species and kinases. Biochim Biophys Acta 1784(1):106–115PubMedCrossRef de Lamirande E, O’Flaherty C (2008) Sperm activation: role of reactive oxygen species and kinases. Biochim Biophys Acta 1784(1):106–115PubMedCrossRef
83.
go back to reference Teves ME, Guidobaldi HA, Uñates DR, Sanchez R, Miska W, Publicover SJ, Morales Garcia AA, Giojalas LC (2009) Molecular mechanism for human sperm chemotaxis mediated by progesterone. PLoS ONE 4(12):e8211PubMedCrossRef Teves ME, Guidobaldi HA, Uñates DR, Sanchez R, Miska W, Publicover SJ, Morales Garcia AA, Giojalas LC (2009) Molecular mechanism for human sperm chemotaxis mediated by progesterone. PLoS ONE 4(12):e8211PubMedCrossRef
84.
go back to reference Kaupp UB, Kashikar ND, Weyand I (2008) Mechanisms of sperm chemotaxis. Annu Rev Physiol 70:93–117PubMedCrossRef Kaupp UB, Kashikar ND, Weyand I (2008) Mechanisms of sperm chemotaxis. Annu Rev Physiol 70:93–117PubMedCrossRef
86.
go back to reference Chang H, Suarez SS (2010) Rethinking the relationship between hyperactivation and chemotaxis in mammalian sperm. Biol Reprod 83(4):507–513PubMedCrossRef Chang H, Suarez SS (2010) Rethinking the relationship between hyperactivation and chemotaxis in mammalian sperm. Biol Reprod 83(4):507–513PubMedCrossRef
87.
go back to reference Velando A, Torres R, Alonso-Alvarez C (2008) Avoiding bad genes: oxidatively damaged DNA in germ line and mate choice. BioEssays 30(11–12):1212–1219PubMedCrossRef Velando A, Torres R, Alonso-Alvarez C (2008) Avoiding bad genes: oxidatively damaged DNA in germ line and mate choice. BioEssays 30(11–12):1212–1219PubMedCrossRef
88.
go back to reference Flesch FM, Gadella BM (2000) Dynamics of the mammalian sperm plasma membrane in the process of fertilization. Biochim Biophys Acta 1469(3):197–235PubMedCrossRef Flesch FM, Gadella BM (2000) Dynamics of the mammalian sperm plasma membrane in the process of fertilization. Biochim Biophys Acta 1469(3):197–235PubMedCrossRef
90.
go back to reference Whittington K, Harrison SC, Williams KM, Day JL, McLaughlin EA, Hull MG, Ford WC (1999) Reactive oxygen species (ROS) production and the outcome of diagnostic tests of sperm function. Int J Androl 22(4):236–242PubMedCrossRef Whittington K, Harrison SC, Williams KM, Day JL, McLaughlin EA, Hull MG, Ford WC (1999) Reactive oxygen species (ROS) production and the outcome of diagnostic tests of sperm function. Int J Androl 22(4):236–242PubMedCrossRef
91.
go back to reference Shi TY, Chen G, Huang X, Yuan Y, Wu X, Wu B, Li Z, Shun F, Chen H, Shi H (2012) Effects of reactive oxygen species from activated leucocytes on human sperm motility, viability and morphology. Andrologia 44(Suppl 1):696–703PubMedCrossRef Shi TY, Chen G, Huang X, Yuan Y, Wu X, Wu B, Li Z, Shun F, Chen H, Shi H (2012) Effects of reactive oxygen species from activated leucocytes on human sperm motility, viability and morphology. Andrologia 44(Suppl 1):696–703PubMedCrossRef
92.
go back to reference Armstrong JS, Rajasekaran M, Chamulitrat W, Gatti P, Hellstrom WJ, Sikka SC (1999) Characterization of reactive oxygen species induced effects on human spermatozoa movement and energy metabolism. Free Radic Biol Med 26(7–8):869–880PubMedCrossRef Armstrong JS, Rajasekaran M, Chamulitrat W, Gatti P, Hellstrom WJ, Sikka SC (1999) Characterization of reactive oxygen species induced effects on human spermatozoa movement and energy metabolism. Free Radic Biol Med 26(7–8):869–880PubMedCrossRef
93.
go back to reference Aitken RJ, Clarkson JS, Fishel S (1989) Generation of reactive oxygen species, lipid peroxidation, and human sperm function. Biol Reprod 41(1):183–197PubMedCrossRef Aitken RJ, Clarkson JS, Fishel S (1989) Generation of reactive oxygen species, lipid peroxidation, and human sperm function. Biol Reprod 41(1):183–197PubMedCrossRef
94.
go back to reference Łuczaj W, Skrzydlewska E (2003) DNA damage caused by lipid peroxidation products. Cell Mol Biol Lett 8(2):391–413PubMed Łuczaj W, Skrzydlewska E (2003) DNA damage caused by lipid peroxidation products. Cell Mol Biol Lett 8(2):391–413PubMed
95.
go back to reference Esterbauer H (1993) Cytotoxicity and genotoxicity of lipid-oxidation products. Am J Clin Nutr 57(5 Suppl):779S–785S (discussion 785S–786S)PubMed Esterbauer H (1993) Cytotoxicity and genotoxicity of lipid-oxidation products. Am J Clin Nutr 57(5 Suppl):779S–785S (discussion 785S–786S)PubMed
96.
go back to reference Wang X, Sharma RK, Sikka SC, Thomas AJ Jr, Falcone T, Agarwal A (2003) Oxidative stress is associated with increased apoptosis leading to spermatozoa DNA damage in patients with male factor infertility. Fertil Steril 80(3):531–535PubMedCrossRef Wang X, Sharma RK, Sikka SC, Thomas AJ Jr, Falcone T, Agarwal A (2003) Oxidative stress is associated with increased apoptosis leading to spermatozoa DNA damage in patients with male factor infertility. Fertil Steril 80(3):531–535PubMedCrossRef
97.
go back to reference Aitken RJ, Koppers AJ (2011) Apoptosis and DNA damage in human spermatozoa. Asian J Androl 13(1):36–42PubMedCrossRef Aitken RJ, Koppers AJ (2011) Apoptosis and DNA damage in human spermatozoa. Asian J Androl 13(1):36–42PubMedCrossRef
98.
go back to reference Alvarez JG (2005) The predictive value of sperm chromatin structure assay. Hum Reprod 20(8):2365–2367PubMedCrossRef Alvarez JG (2005) The predictive value of sperm chromatin structure assay. Hum Reprod 20(8):2365–2367PubMedCrossRef
99.
go back to reference Matés JM, Segura JA, Alonso FJ, Márquez J (2012) Oxidative stress in apoptosis and cancer: an update. Arch Toxicol 86(11):1649–1665 Matés JM, Segura JA, Alonso FJ, Márquez J (2012) Oxidative stress in apoptosis and cancer: an update. Arch Toxicol 86(11):1649–1665
100.
go back to reference Aitken RJ, Krausz C (2001) Oxidative stress, DNA damage and the Y chromosome. Reproduction 122(4):497–506PubMedCrossRef Aitken RJ, Krausz C (2001) Oxidative stress, DNA damage and the Y chromosome. Reproduction 122(4):497–506PubMedCrossRef
101.
go back to reference Greco E, Iacobelli M, Rienzi L, Ubaldi F, Ferrero S, Tesarik J (2005) Reduction of the incidence of sperm DNA fragmentation by oral antioxidant treatment. J Androl 26(3):349–353PubMedCrossRef Greco E, Iacobelli M, Rienzi L, Ubaldi F, Ferrero S, Tesarik J (2005) Reduction of the incidence of sperm DNA fragmentation by oral antioxidant treatment. J Androl 26(3):349–353PubMedCrossRef
102.
go back to reference Gorczyca W, Gong J, Darzynkiewicz Z (1993) Detection of DNA strand breaks in individual apoptotic cells by the in situ terminal deoxynucleotidyl transferase and nick translation assays. Cancer Res 53(8):1945–1951PubMed Gorczyca W, Gong J, Darzynkiewicz Z (1993) Detection of DNA strand breaks in individual apoptotic cells by the in situ terminal deoxynucleotidyl transferase and nick translation assays. Cancer Res 53(8):1945–1951PubMed
103.
go back to reference Henkel R, Hoogendijk CF, Bouic PJ, Kruger TF (2010) TUNEL assay and SCSA determine different aspects of sperm DNA damage. Andrologia 42(5):305–313PubMedCrossRef Henkel R, Hoogendijk CF, Bouic PJ, Kruger TF (2010) TUNEL assay and SCSA determine different aspects of sperm DNA damage. Andrologia 42(5):305–313PubMedCrossRef
104.
go back to reference Sakkas D, Alvarez JG (2010) Sperm DNA fragmentation: mechanisms of origin, impact on reproductive outcome, and analysis. Fertil Steril 93(4):1027–1036PubMedCrossRef Sakkas D, Alvarez JG (2010) Sperm DNA fragmentation: mechanisms of origin, impact on reproductive outcome, and analysis. Fertil Steril 93(4):1027–1036PubMedCrossRef
105.
go back to reference Ws O, Chen H, Chow PH (2006) Male genital tract antioxidant enzymes—their ability to preserve sperm DNA integrity. Mol Cell Endocrinol 250(1–2):80–83 Ws O, Chen H, Chow PH (2006) Male genital tract antioxidant enzymes—their ability to preserve sperm DNA integrity. Mol Cell Endocrinol 250(1–2):80–83
106.
go back to reference Smith R, Vantman D, Ponce J, Escobar J, Lissi E (1996) Total antioxidant capacity of human seminal plasma. Hum Reprod 11(8):1655–1660PubMedCrossRef Smith R, Vantman D, Ponce J, Escobar J, Lissi E (1996) Total antioxidant capacity of human seminal plasma. Hum Reprod 11(8):1655–1660PubMedCrossRef
107.
go back to reference Crisol L, Matorras R, Aspichueta F, Expósito A, Hernández ML, Ruiz-Larrea MB, Mendoza R, Ruiz-Sanz JI (2012) Glutathione peroxidase activity in seminal plasma and its relationship with classical sperm parameters and in vitro fertilization-intracytoplasmic sperm injection outcome. Fertil Steril 97(4):852–857PubMedCrossRef Crisol L, Matorras R, Aspichueta F, Expósito A, Hernández ML, Ruiz-Larrea MB, Mendoza R, Ruiz-Sanz JI (2012) Glutathione peroxidase activity in seminal plasma and its relationship with classical sperm parameters and in vitro fertilization-intracytoplasmic sperm injection outcome. Fertil Steril 97(4):852–857PubMedCrossRef
108.
go back to reference Almbro M, Dowling DK, Simmons LW (2011) Effects of vitamin E and beta-carotene on sperm competitiveness. Ecol Lett 14(9):891–895PubMedCrossRef Almbro M, Dowling DK, Simmons LW (2011) Effects of vitamin E and beta-carotene on sperm competitiveness. Ecol Lett 14(9):891–895PubMedCrossRef
109.
go back to reference Moilanen J, Hovatta O (1995) Excretion of alpha-tocopherol into human seminal plasma after oral administration. Andrologia 27(3):133–136PubMedCrossRef Moilanen J, Hovatta O (1995) Excretion of alpha-tocopherol into human seminal plasma after oral administration. Andrologia 27(3):133–136PubMedCrossRef
110.
go back to reference Sikka SC (2004) Role of oxidative stress and antioxidants in andrology and assisted reproductive technology. J Androl 25(1):5–18PubMed Sikka SC (2004) Role of oxidative stress and antioxidants in andrology and assisted reproductive technology. J Androl 25(1):5–18PubMed
111.
go back to reference Greco E, Romano S, Iacobelli M, Ferrero S, Baroni E, Minasi MG, Ubaldi F, Rienzi L, Tesarik J (2005) ICSI in cases of sperm DNA damage: beneficial effect of oral antioxidant treatment. Hum Reprod 20(9):2590–2594PubMedCrossRef Greco E, Romano S, Iacobelli M, Ferrero S, Baroni E, Minasi MG, Ubaldi F, Rienzi L, Tesarik J (2005) ICSI in cases of sperm DNA damage: beneficial effect of oral antioxidant treatment. Hum Reprod 20(9):2590–2594PubMedCrossRef
112.
go back to reference Comhaire F, Decleer W (2011) Quantifying the effectiveness and cost-efficiency of food supplementation with antioxidants for male infertility. Reprod Biomed Online 23(3):361–362PubMedCrossRef Comhaire F, Decleer W (2011) Quantifying the effectiveness and cost-efficiency of food supplementation with antioxidants for male infertility. Reprod Biomed Online 23(3):361–362PubMedCrossRef
113.
go back to reference Ramasamy R, Stahl PJ, Schlegel PN (2012) Medical therapy for spermatogenic failure. Asian J Androl 14(1):57–60PubMedCrossRef Ramasamy R, Stahl PJ, Schlegel PN (2012) Medical therapy for spermatogenic failure. Asian J Androl 14(1):57–60PubMedCrossRef
114.
go back to reference Gomes Sobrinho DB, Oliveira JB, Petersen CG, Mauri AL, Silva LF, Massaro FC, Baruffi RL, Cavagna M, Franco JG Jr (2011) IVF/ICSI outcomes after culture of human embryos at low oxygen tension: a meta-analysis. Reprod Biol Endocrinol 9:143PubMedCrossRef Gomes Sobrinho DB, Oliveira JB, Petersen CG, Mauri AL, Silva LF, Massaro FC, Baruffi RL, Cavagna M, Franco JG Jr (2011) IVF/ICSI outcomes after culture of human embryos at low oxygen tension: a meta-analysis. Reprod Biol Endocrinol 9:143PubMedCrossRef
115.
go back to reference Chi HJ, Kim JH, Ryu CS, Lee JY, Park JS, Chung DY, Choi SY, Kim MH, Chun EK, Roh SI (2008) Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa. Hum Reprod 23(5):1023–1028PubMedCrossRef Chi HJ, Kim JH, Ryu CS, Lee JY, Park JS, Chung DY, Choi SY, Kim MH, Chun EK, Roh SI (2008) Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa. Hum Reprod 23(5):1023–1028PubMedCrossRef
116.
go back to reference Zini A, San Gabriel M, Baazeem A (2009) Antioxidants and sperm DNA damage: a clinical perspective. J Assist Reprod Genet 26(8):427–432PubMedCrossRef Zini A, San Gabriel M, Baazeem A (2009) Antioxidants and sperm DNA damage: a clinical perspective. J Assist Reprod Genet 26(8):427–432PubMedCrossRef
117.
go back to reference Giustarini D, Dalle-Donne I, Colombo R, Milzani A, Rossi R (2008) Is ascorbate able to reduce disulfide bridges? A cautionary note. Nitric Oxide 19(3):252–258PubMedCrossRef Giustarini D, Dalle-Donne I, Colombo R, Milzani A, Rossi R (2008) Is ascorbate able to reduce disulfide bridges? A cautionary note. Nitric Oxide 19(3):252–258PubMedCrossRef
118.
go back to reference Ross C, Morriss A, Khairy M, Khalaf Y, Braude P, Coomarasamy A, El-Toukhy T (2010) A systematic review of the effect of oral antioxidants on male infertility. Reprod Biomed Online 20(6):711–723PubMedCrossRef Ross C, Morriss A, Khairy M, Khalaf Y, Braude P, Coomarasamy A, El-Toukhy T (2010) A systematic review of the effect of oral antioxidants on male infertility. Reprod Biomed Online 20(6):711–723PubMedCrossRef
119.
go back to reference Agarwal A, Sekhon LH (2011) Oxidative stress and antioxidants for idiopathic oligoasthenoteratospermia: is it justified? Indian J Urol 27(1):74–85PubMedCrossRef Agarwal A, Sekhon LH (2011) Oxidative stress and antioxidants for idiopathic oligoasthenoteratospermia: is it justified? Indian J Urol 27(1):74–85PubMedCrossRef
120.
go back to reference Lombardo F, Sansone A, Romanelli F, Paoli D, Gandini L, Lenzi A (2011) The role of antioxidant therapy in the treatment of male infertility: an overview. Asian J Androl 13(5):690–697PubMedCrossRef Lombardo F, Sansone A, Romanelli F, Paoli D, Gandini L, Lenzi A (2011) The role of antioxidant therapy in the treatment of male infertility: an overview. Asian J Androl 13(5):690–697PubMedCrossRef
121.
go back to reference Showell MG, Brown J, Yazdani A, Stankiewicz MT, Hart RJ (2011) Antioxidants for male subfertility. Cochrane Database Syst Rev (1):CD007411 Showell MG, Brown J, Yazdani A, Stankiewicz MT, Hart RJ (2011) Antioxidants for male subfertility. Cochrane Database Syst Rev (1):CD007411
122.
go back to reference Eunice M, Ammini AC (2010) Genomics revolution on andrology: genetic testing for male infertility. Asian J Androl 12(3):449–450PubMedCrossRef Eunice M, Ammini AC (2010) Genomics revolution on andrology: genetic testing for male infertility. Asian J Androl 12(3):449–450PubMedCrossRef
123.
go back to reference Azadi L, Abbasi H, Deemeh MR, Tavalaee M, Arbabian M, Pilevarian AA, Nasr-Esfahani MH (2011) Zaditen (Ketotifen), as mast cell blocker, improves sperm quality, chromatin integrity and pregnancy rate after varicocelectomy. Int J Androl 34(5 Pt 1):446–452PubMedCrossRef Azadi L, Abbasi H, Deemeh MR, Tavalaee M, Arbabian M, Pilevarian AA, Nasr-Esfahani MH (2011) Zaditen (Ketotifen), as mast cell blocker, improves sperm quality, chromatin integrity and pregnancy rate after varicocelectomy. Int J Androl 34(5 Pt 1):446–452PubMedCrossRef
Metadata
Title
Influence of reactive oxygen species on human sperm functions and fertilizing capacity including therapeutical approaches
Authors
Shu-jian Chen
Jean-Pierre Allam
Yong-gang Duan
Gerhard Haidl
Publication date
01-07-2013
Publisher
Springer-Verlag
Published in
Archives of Gynecology and Obstetrics / Issue 1/2013
Print ISSN: 0932-0067
Electronic ISSN: 1432-0711
DOI
https://doi.org/10.1007/s00404-013-2801-4

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