Ahsan, U, Kamran, Z, Raza, I and Iqbal, Z (2014) Role of selenium in male reproduction—a review. Anim Reprod Sci 146, 55–62.
Aitken, RJ (1997) Molecular mechanisms regulating human sperm function. Mol Hum Reprod 3, 169–173.
Aitken, RJ and Baker, MA (2004) Oxidative stress and male reproductive biology. Reprod Fertil Dev 16, 581–588.
Aitken, RJ and Curry, BJ (2011) Redox regulation of human sperm function: from the physiological control of sperm capacitation to the etiology of infertility and DNA damage in the germ line. Antioxid Redox Signal 14, 367–381.
Aitken, RJ, Clarkson, JS and Fishel, S (1989) Generation of reactive oxygen species, lipid peroxidation, and human sperm function. Biol Reprod 41, 183–197.
Aitken, RJ, Jones, KT and Robertson, SA (2012) Reactive oxygen species and sperm function – in sickness and in health. J Androl 33, 1096–1106.
Aitken, RJ, Baker, MA and Nixon, B (2015) Are sperm capacitation and apoptosis the opposite ends of a continuum driven by oxidative stress? Asian J Androl 17, 633–639.
Anchordoquy, JP, Anchordoquy, JM, Pascua, AM, Nikoloff, N, Peral-García, P and Furnus, CC (2017) The copper transporter (SLC31A1/CTR1) is expressed in bovine spermatozoa and oocytes: copper in IVF medium improves sperm quality. Theriogenology 97, 124–133.
Aziz, DM (2006) Assessment of bovine sperm viability by MTT reduction assay. Anim Reprod Sci, 92(1–2), 1–8.
Barroso, G, Morshedi, M and Oehninger, S (2000) Analysis of DNA fragmentation, plasma membrane translocation of phosphatidylserine and oxidative stress in human spermatozoa. Hum Reprod 15, 1338–1344.
Basim, J Mackenzie-Bell, AM and Buhr, MM (2009) Reactive oxygen species and boar sperm function. Biol Reprod 81, 553–561.
Baumber, J, Sabeur, K, Vo, A and Ball, BA (2003) Reactive oxygen species promote tyrosine phosphorylation and capacitation in equine spermatozoa. Theriogenology 60, 1239–1247.
Cheema, RS, Bansal, AK and Bilaspuri, GS (2009) Manganese provides antioxidant protection for sperm cryopreservation that may offer new consideration for clinical fertility. Oxid Med Cell Longev 2, 152–159.
Chia, SE, Ong, CN, Chua, LH, Ho, LM and Tay, SK (2000) Comparison of zinc concentrations in blood and seminal plasma and the various sperm parameters between fertile and infertile men. J Androl 21, 53–57.
Chihuailaf, RH, Contreras, PA and Wittwer, FG (2002) Patogénesis del estrés oxidativo: Consecuencias y evaluación en salud animal pathogenesis of oxidative stress: consequences and evaluation in animal health. Vet Méx 33, 265.
Chiu, PCN, Chung, M-K, Koistinen, R and Yeung, WSB (2007) Glycodelin-A interacts with fucosyltransferase on human sperm plasma membrane to inhibit spermatozoa–zona pellucida binding. J Cell Sci 120(Pt 1), 33–44.
Coassin, M, Ursini, F and Bindoli, A (1992) Antioxidant effect of manganese. Arch Biochem Biophys 299, 330–333.
Colagar, AH, Marzony, ET and Chaichi, MJ (2009) Zinc levels in seminal plasma are associated with sperm quality in fertile and infertile men. Nutr Res 29, 82–88.
Cornwall, GA, Tulsiani, DR and Orgebin-Crist, MC (1991) Inhibition of the mouse sperm surface alpha-d-mannosidase inhibits sperm-egg binding in vitro
. Biol Reprod 44, 913–921.
Coutinho da Silva, MA, Seidel, GE, Squires, EL, Graham, JK and Carnevale, EM (2012) Effects of components of semen extenders on the binding of stallion spermatozoa to bovine or equine zonae pellucidae. Reproduction 143, 577–585.
Denizot, F and Lang, R (1986) Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. J Immunol Methods, 89, 271–277.
Dorostkar, K, Alavi-Shoushtari, SM and Mokarizadeh, A (2012) Effects of in vitro selenium addition to the semen extender on the spermatozoa characteristics before and after freezing in water buffaloes (Bubalus bubalis). Vet Res Forum 3, 263–268.
Dorostkar, K, Alavi Shoushtari, SM and Khaki, A (2014) Effects of in vitro zinc sulphate additive to the semen extender on water buffalo (Bubalus bubalis) spermatozoa before and after freezing. Int J Fertil Steril 8, 325–332.
Ecroyd, HW, Jones, RC and Aitken, RJ (2003) Endogenous redox activity in mouse spermatozoa and its role in regulating the tyrosine phosphorylation events associated with sperm capacitation. Biol Reprod 69, 347–354.
El-Sharawy, M, Eid, E, Darwish, S, Abdel-Razek, I, Islam, MR, Kubota, K, Yamauchi, N and El-Shamaa, I (2017) Effect of organic and inorganic selenium supplementation on semen quality and blood enzymes in buffalo bulls: selenium effects on buffalo semen quality. Anim Sci J 88, 999–1005.
Fazeli, AR, Steenweg, W, Bevers Mvan den Broek, J, Bracher, V, Parlevliet, J and Colenbrander, B (1995) Relation between stallion sperm binding to homologous hemizonae and fertility. Theriogenology 44, 751–760.
Gavella, M and Lipovac, V (1998)
In vitro effect of zinc on oxidative changes in human semen. Andrologia, 30, 317–323.
Gil-Guzman, E, Ollero, M, Lopez, MC, Sharma, RK, Alvarez, JG, Thomas, AJ Jr and Agarwal, A (2001) Differential production of reactive oxygen species by subsets of human spermatozoa at different stages of maturation. Hum Reprod 16, 1922–1930.
Gonçalves, FS, Barretto, LS, Arruda, RP, Perri, SH and Mingoti, GZ (2010) Effect of antioxidants during bovine in vitro fertilization procedures on spermatozoa and embryo development. Reprod Domest Anim, 45, 129–135.
Gong, X, Dubois, DH, Miller, DJ and Shur, BD (1995) Activation of a G protein complex by aggregation of beta-1,4-galactosyltransferase on the surface of sperm. Science 269(5231), 1718–1721.
Hoodbhoy, T and Dean, J (2004) Insights into the molecular basis of sperm-egg recognition in mammals. Reproduction 127, 417–422.
Ivanova, M and Mollova, M (1993) Zona-penetration in vitro test for evaluating boar sperm fertility. Theriogenology 40 397–410.
Jones, R, Mann, T and Sherins, R (1979) Peroxidative breakdown of phospholipids in human spermatozoa, spermicidal properties of fatty acid peroxides, and protective action of seminal plasma. Fertil Steril 31, 531–537.
Kasimanickam, R, Kasimanickam, V, Thatcher, CD, Nebel, RL and Cassell, BG (2007) Relationships among lipid peroxidation, glutathione peroxidase, superoxide dismutase, sperm parameters, and competitive index in dairy bulls. Theriogenology 67, 1004–1012.
Kaushik, K, Mittal, PK and Kalla, NR (2015) Antioxidant potential of Mn2+ in the human ejaculated spermatozoa under oxidative stress. Int J Pharm Sci Res 42, 2153–2162.
Kincaid, RL (1999) Assessment of trace mineral status of ruminants: a review.
J Anim Sci 77(E-Suppl), 1–10.
Kiziler, AR, Aydemir, B, Onaran, I, Alici, B, Ozkara, H, Gulyasar, T and Akyolcu, MC (2007) High levels of cadmium and lead in seminal fluid and blood of smoking men are associated with high oxidative stress and damage in infertile subjects. Biol Trace Elem Res 120(1–3), 82–91.
Kodama, H, Kuribayashi, Y and Gagnon, C (1996) Effect of sperm lipid peroxidation on fertilization. J Androl 17, 151–157.
Lapointe, S, Ahmad, I, Buhr, MM and Sirard, MA (1996) Modulation of postthaw motility, survival, calcium uptake, and fertility of bovine sperm by magnesium and manganese. J Dairy Sci 79, 2163–2169.
Liu, D-Y, Sie, B-S, Liu, M-L, Agresta, F and Baker, HWG (2009) Relationship between seminal plasma zinc concentration and spermatozoa–zona pellucida binding and the ZP-induced acrosome reaction in subfertile men. Asian J Androl 11, 499–507.
Marai, IFM, El-Darawany, A-HA, Ismail, E-SA-F and Abdel-Hafez, MAM (2009) Reproductive and physiological traits of Egyptian Suffolk rams as affected by selenium dietary supplementation and housing heat radiation effects during winter of the sub-tropical environment of Egypt. Arch Anim Breed 52, 402–409.
Mendoza, C, Carreras, A, Moos, J and Tesarik, J (1992) Distinction between true acrosome reaction and degenerative acrosome loss by a one-step staining method using Pisum sativum agglutinin. J Reprod Fertil 95, 755–763.
Michailov, Y, Ickowicz, D and Breitbart, H (2014) Zn2+-stimulation of sperm capacitation and of the acrosome reaction is mediated by EGFR activation. Dev Biol 396, 246–255.
Miller, DJ, Macek, MB and Shur, BD (1992) Complementarity between sperm surface beta-1,4-galactosyltransferase and egg-coat ZP3 mediates sperm-egg binding. Nature 357(6379), 589–593.
Mosmann, T (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 65(1–2), 55–63.
Nair, SJ, Brar, AS, Ahuja, CS, Sangha, SP and Chaudhary, KC (2006) A comparative study on lipid peroxidation, activities of antioxidant enzymes and viability of cattle and buffalo bull spermatozoa during storage at refrigeration temperature. Anim Reprod Sci 96(1–2), 21–29.
Oehninger, S, Mahony, M, Ozgür, K, Kolm, P, Kruger, T and Franken, D (1997) Clinical significance of human sperm–zona pellucida binding. Fertil Steril 67, 1121–1127.
Overstreet, JW, Yanagimachi, R, Katz, DF, Hayashi, K and Hanson, FW (1980) Penetration of human spermatozoa into the human zona pellucida and the zona-free hamster egg: a study of fertile donors and infertile patients. Fertil Steril 33, 534–542.
Parrish, JJ, Susko-Parrish, JL, Leibfried-Rutledge, ML, Critser, ES, Eyestone, WH and First, NL (1986) Bovine in vitro fertilization with frozen–thawed semen. Theriogenology 25, 591–600.
Reid, AT, Redgrove, K, Aitken, RJ and Nixon, B (2011) Cellular mechanisms regulating sperm–zona pellucida interaction. Asian J Androl 13, 88–96.
Reis, LSLS, Ramos, AA, Camargos, AS and Oba, E (2014) Effect of manganese supplementation on the membrane integrity and the mitochondrial potential of the sperm of grazing Nellore bulls. Anim Reprod Sci 150(1–2), 1–6.
Revell, SG and Mrode, RA (1994) An osmotic resistance test for bovine semen. Anim Reprod Sci 36, 77–86.
Rivlin, J, Mendel, J, Rubinstein, S, Etkovitz, N and Breitbart, H (2004) Role of hydrogen peroxide in sperm capacitation and acrosome reaction. Biol Reprod 70, 518–522.
Roblero, L, Guadarrama, A, Lopez, T and Zegers-Hochschild, F (1996) Effect of copper ion on the motility, viability, acrosome reaction and fertilizing capacity of human spermatozoa in vitro
. Reprod Fertil Dev 8, 871–874.
Roy, SC and Atreja, SK (2008) Effect of reactive oxygen species on capacitation and associated protein tyrosine phosphorylation in buffalo (Bubalus bubalis) spermatozoa. Anim Reprod Sci 107(1–2), 68–84.
Shamsi, MB, Kumar, R and Dada, R (2008) Evaluation of nuclear DNA damage in human spermatozoa in men opting for assisted reproduction. Indian J Med Res 127, 115–123.
Shur, BD and Neely, CA (1988) Plasma membrane association, purification, and partial characterization of mouse sperm beta-1,4-galactosyltransferase. J Biol Chem 263(33), 17706–17714.
Sikka, SC (1996) Oxidative stress and role of antioxidants in normal and abnormal sperm function. Front Biosci 1, e78–e86.
Sinowatz, F, Töpfer‐Petersen, E, Kölle, S and Palma, G (2001) Functional morphology of the zona pellucida. Anat Histol Embryol 30, 257–263.
Slater, TF, Sawyer, B and Sträuli, U (1963) Studies on succinate-tetrazolium reductase systems. Biochim Biophys Acta 77, 383–393.
Storey, BT (2008) Mammalian sperm metabolism: oxygen and sugar, friend and foe. Int J Dev Biol 52(5–6), 427–437.
Tosic, J and Walton, A (1946) Formation of hydrogen peroxide by spermatozoa and its inhibitory effect of respiration. Nature 158, 485.
Underwood, EJ and Suttle, NF (1999) The Mineral Nutrition of Livestock, 3rd edn. Wallingford: CABI.
Ursini, F, Heim, S, Kiess, M and Flohé, L (1999) Dual function of the selenoprotein PHGPx during sperm maturation. Science 285(5432), 1393–1396.
Varghese, AC Sinha, B and Bhattacharyya, AK (2005) Current trends in evaluation of sperm function: in vitro selection and manipulation of male gametes for assisted conception. Indian J Exp Biol 43, 1023–1031.
Wassarman, PM (1990) Regulation of mammalian fertilization by zona pellucida glycoproteins. J Reprod Fertil Suppl 42, 79–87.
Wassarman, PM and Litscher, ES (2008) Mammalian fertilization: the egg’s multifunctional zona pellucida. Int J Dev Biol 52(5–6), 665–676.
Zhang, BR, Larsson, B, Lundeheim, N, Håård, MG and Rodriguez-Martinez, H (1999) Prediction of bull fertility by combined in vitro assessments of frozen–thawed semen from young dairy bulls entering an AI-programme. Int J Androl 22, 253–260.