Printer Friendly

Combined effect of Trolox and EDTA on frozen-thawed sperm quality.


Frozen-thawed (FT) sperm have been used for artificial insemination for more than 5 decades. (1) Nowadays, the storage of frozen sperm is done in infertility clinics for various reasons, including storage and maintenance of the donor's sperm for future use and preservation of fertility following chemotherapy, radiotherapy, or various surgical procedures such as vasectomy. (2-4) Sometimes, sperm are used for artificial insemination with the husband's semen in procedures such as intracytoplasmic sperm injection, intrauterine insemination, and in vitro fertilization. (2,3) Despite the tremendous advances in cryopreservation methods during recent years, research has demonstrated that the long-term storage of semen in a frozen state leads to severe damage to sperm. (5-7) Some studies have indicated a decrease in the motility and viability of such sperm (8,9) and changes in sperm morphology such as changes in the plasma membrane and acrosomal changes (8) after thawing. It has also been reported that the freezing process increases the rate of DNA damage and DNA fragmentation, decreases the percentage of non-capacitated sperm, and increases the rate of acrosome reaction. (9) Likewise, investigations on the effect of the sperm freezing and thawing process suggest that the percentage of the production of oxygen free radicals is increased during incubation. (10,11) It has also been shown that a reduction in the content of glutathione, which plays a role in the antioxidant defense system of sperm, is induced by the freezing and thawing process. Also, in this report it was demonstrated that the addition of 1mM of glutathione to freezing medium was able to reduce free radicals and increase the motility and viability of post-thaw sperm. (11) Moreover, the addition of reduced glutathione to the fertilization medium significantly increased the rate of the in vitro fertilization of eggs by FT sperm. (12) The evaluation of intracellular antioxidants showed that the levels of antioxidants such as superoxide dismutase and glutathione were much lower in FT sperm than in fresh sperm. (13) A variety of antioxidants such as Trolox, catalase, alpha-tocopherol, and ascorbic acid have been used to improve FT sperm status in many experiments. (7,14-21)

Thermal shock, formation of intracellular ice crystals, cellular dehydration, increased concentration of salts, and osmotic shock may occur during the freezing and thawing of human spermatozoa. (5) Moreover, cryopreservation leads to structural adverse changes in the plasma membrane. (5-7,14,18) Changes in the membrane permeability to some ions such as calcium during the freezing and thawing process have also been reported. (6,22)

Calcium plays an essential role in sperm motility and also in the membrane fusion process during acrosome reaction. Binding to the zona pellucid or progesterone leads to an increase in the intracellular calcium concentration of sperm due to the opening of the calcium channel and also the releasing of calcium from intracellular stores. (23,24) The rise in the intracellular calcium concentration causes the activation of phosphatidylinositol 4,5-bisphosphate ([PIP.sub.2])-specific phospholipase C and hydrolysis of [PIP.sub.2] and production of two second messengers: diacylglycerol and inositol 1,4,5-triphosphate([IP.sub.3]). (23) [IP.sub.3] stimulates the release of calcium from intracellular stores, and diacylglycerol activates cytoplasmic protein kinase and phospholipase [A.sub.2]. (23,25) These events once again cause a rise in the intracellular calcium concentration. Eventually, a further elevation in [[[ca.sup.2+]].sub.i], which occurs prior to acrosome reaction, together with hydrolysis of [PIP.sup.2] and resulting products from phospholipase [A.sub.2] activation, leads to actin depolymerization and membrane fusion, the final event of acrosome reaction. (23,25)

On the other hand, the influx of extracellular calcium into fresh sperm leads to an increase in the production of free radicals in the cell. (26-28) Likewise, some studies have demonstrated that fresh sperm incubation in media containing calcium ionophore A23187 results in a significant increase in the production of reactive oxygen species. (26,28-30) Based on this finding, calcium chelators such as edetic acid(EDTA) have been used in some studies to improve sperm function. However, EDTA has spermicidal activity and this effect is time-dependent and dose-dependent. (22,31)

Considering the increase in intracellular calcium due to cell membrane damage in FT sperm (6,32) and with respect to the beneficial effects of antioxidants on these sperm, (7,16,17,20) we sought to examine the simultaneous effect of Trolox as an antioxidant and EDTA as a calcium chelator on FT sperm. The combination effect of an antioxidant with EDTA on the quality of fresh and FT sperm has not been investigated previously, and the results of this study may suggest a simple method to augment the quality of FT sperm.

Patients and Methods

Sample Collection and Semen Analysis

Semen samples were obtained from male volunteers (between 20 and 40 years old) who referred to the Shiraz Infertility Center to undergo routine semen analysis between 2012 and 2013. Samples were collected after 3 to 5 days of sexual abstinence. Semen volume, appearance, pH, and viscosity as well as sperm concentration, motility, and morphology were evaluated after liquefaction based on the guidelines of the World Health Organization (WHO). (2) The experiments were carried out randomly on 25 completely normal samples (table 1). These samples were transferred to the Reproductive Physiology Laboratory of the Physiology Department, Shiraz University of Medical Sciences, Shiraz, Iran. This research was approved by the local Research Ethics Committee of Shiraz University of Medical Sciences (code # EC-91-6159).

Sperm Prepration and Treatment

The samples were randomly divided into two groups (freshsperm group, n, 13; FTspermgroup, n, 12). The semen samples of the two groups were washed with Ham's F-10 medium (Sigma, N6633), centrifuged at 1,200 rpm for 10 minutes, and the supernatant was removed. Half a milliliter of Ham's F-10 was added, and the samples were incubated at 37[degrees]C under 5% C[O.sub.2]. After 60 minutes of incubation, the supernatant containing motile sperm was collected. Sperm concentration, motility, and viability were evaluated. Thirteen samples were considered as the fresh sperm group and 12 samples as the FTsperm group. A CryoSperm medium (ORIGIO11010010) was added to the samples very slowly, which was considered as the FTsperm group. The samples were loaded into straws after 10 minutes and kept at -70[degrees]C for 30 minutes and thereafter in liquid nitrogen for at least 1 month. Thawing was done at room temperature as previously described. (2,33)

The fresh and FT sperm underwent experimental procedures as follows. Each sample was divided into five groups, containing 10 x 106 sperm/mL. One group was designated the control group, and the incubation medium of the other groups contained 0.1% dimethyl sulfoxide (DMSO) (Sigma, D2650), 200 [micro]M of Trolox (Sigma, 238813), 1.1 mM of EDTA (Sigma, E6758), and 1.1 mM of EDTA + 200 [micro]M Trolox, respectively. The samples were then incubated for 60 minutes at 37[degrees]C under 5% C[O.sub.2].

Assessment of Sperm Motility and Viability

Sperm motility was assessed at 400X magnification using phase-contrast microscopy (Olympus, BX51, Tokyo, Japan). Video-recording equipment was also used for the quality control of manual motility assessment procedures according to the WHO's guideline. (2) The percentages of the progressive and nonprogressive motility and immotile sperm were assessed.

Sperm viability was evaluated by Eosin Y staining. At least 200 sperm were examined in each evaluation.

Evaluation of Acrosomal Status

Acrosomal status was evaluated with fluorescein isothiocyanate-conjugated Pisumsativum (FITC-PSA) staining according to the procedure previously reported. (34) Briefly, 10pL of the sample was smeared on glass slides and fixed by methanol for 30 seconds at room temperature. The slides were frozen at -20[degrees]C until staining. These slides were then incubated for 30 minutes with 50 pg/mL of FITC-PSA (Sigma, L0770) and, thereafter, washed with double-distilled water. Acrosomal status was assessed using fluorescence microscopy at 1000X magnification (Olympus, BX51, Tokyo, Japan). Sperm with green fluorescence in the acrosomal region were scored as acrosome intact, whereas those with no fluorescence in the acrosomal region or only fluorescence of the equatorial segment were considered acrosome-reacted.

Statistical Analysis

The statistical analyses were performed using Statistical Package for the Social Sciences (SPSS), version 16.0, for Windows. The evaluation of the differences between the experimental groups was performed using the Mann-Whitney U test. All the data are presented as mean values [+ or -] standard error (SE). A P value < 0.05 was considered statistically significant.


At the commencement of the experiment, the total motility of the sperm chosen for the fresh and FT sperm groups was 88.7 [+ or -] 1.8 and 83.9 [+ or -] 1.3, respectively. The sperm viability of the sperm chosen for the fresh and FT sperm groups was 90.9 [+ or -] 1.4 and 88.2 [+ or -] 1.4, respectively.

The percentages of the sperm with progressive motility and the total motility of the fresh and FT sperm, after treatments, are reported in table 2. The freezing procedures decreased sperm motility significantly. The motility of the FT sperm treated with Trolox + EDTA was increased nonsignificantly. None of the treatments significantly affected the motility of the experimental groups.

The changes in the percentage of the motile sperm in each subgroup were calculated relative to their control group (table 2). This comparison showed that EDTA, especially in combination with Trolox, had the best effect on progressive motility in the FT sperm.

In the samples selected for freezing, 88% of the cells were viable but the percentage of the live sperm was decreased significantly to 44% after thawing. The incubation of the sperm in the medium containing EDTA and Trolox did not cause any significant changes in viability (table 3).

Acrosome loss was significantly greater in the FT sperm than in the fresh ones (table 4). Spontaneous acrosomal reaction in the fresh sperm was not affected by EDTA or Trolox; however, EDTA decreased acrosome loss in the FT sperm.


The long-term storage of sperm necessitates that they be maintained in a frozen state. This technique confers hope to individuals who previously had no chance of fertility. (4) Much effort has been made to improve freezing and thawing methods, and these methods have quickly evolved during the last years. Despite these improvements and the fact that we employed one of the best available standard media and methods suggested in the literature, sperm cryopreservation caused a severe decrease in sperm quality (motility and viability). Moreover, acrosome reaction was observed in almost 80% of these sperm. Such sperm are not capable of fertilizing eggs.

In the present study, 1.1 [micro]M of EDTA was used to investigate the effect of the decrement of extracellular calcium on sperm motility. Our findings revealed no effect of EDTA on sperm motility either singularly or in combination with Trolox. In physiological conditions, specific stimuli such as progesterone and zona pellucida cause the opening of membrane calcium channels, (23,24) and we suggest that the impact of extracellular calcium depletion on cellular function is observed just when the calcium channels are open. Although it has been reported that EDTA treatments 0 and 100 [micro]M/mL) improves the progressive motility of sperm, (35) in the current study, the use of EDTA in a higher concentration (more than 1.1 [micro]M) resulted in a severe decline in sperm viability (data are not shown). Many reports have mentioned that the use of Trolox (40,60, and 120 [micro]M) in a freezing extender augments the motility of FT sperm. (7,17) Moreover, the addition of Trolox (100 and 200 [micro]M) or alpha-tocopherol to freezing extenders of human (19) and bearsperm (18,20) improved motility in thawed sperm. In the current study, the addition of 200 [micro]M of Trolox to an FT sperm medium led to no change in the motility of FT sperm. We suggest that sperm are damaged during the freezing procedure and that Trolox exerts a protective effect if added to the freezing medium.

It was reported that the use of sperm-freezing extenders or thawing solutions supplemented by EDTA resulted in the improved motility of thawed sperm. (22,31) The addition of 6mM of EGTA + 6 mM of EDTA to the thawing solution enhanced sperm motility. (22) However, it was mentioned that the treatment of post-thaw sperm with any dose of ethylene glycol tetra acetic acid (EGTA) in the absence of EDTA had limited positive effects. (22) In the present study, the addition of Trolox and EDTA to the FT sperm medium (after thawing) either separately or concomitantly did not cause any significant changes in sperm motility; nevertheless, the sperm motility in the group containing Trolox + EDTA was better than that in the other groups. To compare the effects of Trolox and EDTA on progressive motility between fresh and FT sperm, we considered the percentage of progressive motility in the control group 100% and evaluated the other groups with respect to it (table 2). Our results indicated that although the addition of Trolox and EDTA to the fresh sperm medium did not cause any changes in sperm motility, the use of Trolox + EDTA caused a significant increase in the motility of the FT sperm. As has been previously mentioned, calcium channels in fresh sperm do not open without stimulation. (23,24) In this condition, the addition of a calcium chelator or antioxidant would cause no changes in sperm. Nonetheless, FT sperm membrane undergoes impairment, (7,8,36) causing an over rate of calcium influx. (6,22,32) As was mentioned earlier, the influx of extracellular calcium into fresh sperm leads to a rise in the production of free radicals in the cell. Consequently, the increased intracellular calcium either directly or due to the production of extra reactive oxygen species leads to a reduction in sperm motility. Thus, the concomitant addition of Trolox and EDTA to a thawed sperm medium can improve sperm motility. Also other studies on FT sperm have indicated that the fraction of viable cells declines and that sperm undergo early capacitation. (22) Trolox and EDTA could neither in fresh sperm nor in FT sperm significantly influence sperm viability. We suggest that the adverse effects on sperm viability occur during the freezing process. Hence, using antioxidant supplementation or extracellular calcium depletion after thawing would not work.

Although some investigators have reported that the use of EDTA has no effect on acrosome reaction, (35) there are studies indicating that EDTA supplementation reduces acrosome reaction through the calcium omission of the sperm medium. (31,37) However, in the present research, EDTA supplementation had no effect on the acrosomal status of the fresh sperm. Perhaps the most interesting observation in this study was that the lowest rate of acrosome reaction was observed in the groups containing EDTA (with or without Trolox), and this decline was significant compared to all the groups lacking EDTA. EDTA considerably reduced the rate of acrosome reaction through the omission of extracellular calcium. The difference in the effect of EDTA on the fresh and FT sperm may have been due to the membrane impairment in the FT sperm.

The effect of other antioxidants and calcium chelators should be examined to achieve the best incubation extender for FT sperm.


The findings of this study indicated that the freezing and thawing process of sperm caused severe irreversible damage to the sperm and that the antioxidant supplementation or omission of extracellular calcium might partly improve motility and reduce acrosomal damage.

What's Known

* Cryopreservation of sperms is associated with serious damage to these cells such as damage to plasma and acrosomal membrane and changes inmembrane permeability to some ions, including calcium. Generation of oxygen-free radicals increases during the freezing-thawing process.

* These events lead to a decrement in sperm motility and viability.

What's New

* We, for the first time, investigated the effects of Trolox as an antioxidant and Edetic Acid (EDTA) as a calcium chelator on fresh and frozen-thawed sperm.

* Combination of Trolox and EDTA partly improved frozen-thawed sperm motility and reduced the spontaneous acrosomal reaction of sperm.


This work was supported by the Deputyship of Research, Shiraz University of Medical Sciences, Shiraz, Iran (Grant # 91-6159). This manuscript is part of an M.S. thesis by Farideh Iravanpour. We specially thank the staff of the Shiraz Infertility Center for technical support.

Conflict of Interest: None declared.


(1.) Day JG, Stacey G. Cryopreservation and freeze-drying protocols. 2nd ed. New Jersey: Humana Press; 2007. 347 p.

(2.) World Health Organization. WHO laboratory manual for the examination and processing of human semen. 5th ed. Geneva: World Health Organization; 2010. 271 p.

(3.) Abdel Hafez F, Bedaiwy M, El-Nashar SA, Sabanegh E, Desai N. Techniques for cryopreservation of individual or small numbers of human spermatozoa: a systematic review. Hum Reprod Update. 2009;15:153-64. doi: 10.1093/humupd/ dmn061. PubMed PMID: 19109313.

(4.) Di Santo M, Tarozzi N, Nadalini M, Borini A. Human Sperm Cryopreservation: Update on Techniques, Effect on DNA Integrity, and Implications for ART. Adv Urol. 2012;2012:854837. doi: 10.1155/2012/854837. PubMed PMID: 22194740; PubMed Central PMCID: PMC3238352.

(5.) Martinez-Soto JC, Garcia-Vazquez FA, Gumbao D, Landeras J, Gadea J. Assessment of two thawing processes of cryopreserved human sperm in pellets. Cryobiology. 2011;63:131-6. doi: 10.1016/j. cryobiol.2011.08.001. PubMed PMID: 21884688.

(6.) Kadirvel G, Kumar S, Kumaresan A, Kathiravan P. Capacitation status of fresh and frozen-thawed buffalo spermatozoa in relation to cholesterol level, membrane fluidity and intracellular calcium. Anim Reprod Sci. 2009;116:244-53. doi: 10.1016/j. anireprosci.2009.02.003. PubMed PMID: 19261396.

(7.) Silva SV, Soares AT, Batista AM, Almeida FC, Nunes JF, Peixoto CA, et al. Vitamin E (Trolox) addition to Tris-egg yolk extender preserves ram spermatozoon structure and kinematics after cryopreservation. Anim Reprod Sci. 2013;137:37-44. doi: 10.1016/j. anireprosci.2012.12.002. PubMed PMID: 23280096.

(8.) Ozkavukcu S, Erdemli E, Isik A, Oztuna D, Karahuseyinoglu S. Effects of cryopreservation on sperm parameters and ultrastructural morphology of human spermatozoa. J Assist Reprod Genet. 2008;25:403-11. doi: 10.1007/s10815-0089232-3. PubMed PMID: 18704674; PubMed Central PMCID: PMC2582121.

(9.) Peris SI, Bilodeau JF, Dufour M, Bailey JL. Impact of cryopreservation and reactive oxygen species on DNA integrity, lipid peroxidation, and functional parameters in ram sperm. Mol Reprod Dev. 2007;74:878-92. doi: 10.1002/mrd.20686. PubMed PMID: 17186553.

(10.) Chatterjee S, Gagnon C. Production of reactive oxygen species by spermatozoa undergoing cooling, freezing, and thawing. Mol Reprod Dev. 2001;59:451-8. doi: 10.1002/mrd.1052. PubMed PMID: 11468782.

(11.) Gadea J, Molla M, Selles E, Marco MA, Garcia-Vazquez FA, Gardon JC. Reduced glutathione content in human sperm is decreased after cryopreservation: Effect of the addition of reduced glutathione to the freezing and thawing extenders. Cryobiology. 2011;62:40-6. doi: 10.1016/j. cryobiol.2010.12.001. PubMed PMID: 21156167.

(12.) Bath ML. Inhibition of in vitro fertilizing capacity of cryopreserved mouse sperm by factors released by damaged sperm, and stimulation by glutathione. PLoS One. 2010;5:e9387. doi: 10.1371/journal. pone.0009387. PubMed PMID: 20195370; PubMed Central PMCID: PMC2827551.

(13.) Bilodeau JF, Chatterjee S, Sirard MA, Gagnon C. Levels of antioxidant defenses are decreased in bovine spermatozoa after a cycle of freezing and thawing. Mol Reprod Dev. 2000;55:282-8. doi: 10.1002/ (SICI)1098-2795(200003)55:3<282:AIDMRD6>3.0.CO;2-7. PubMed PMID: 10657047.

(14.) Maia Mda S, Bicudo SD, Sicherle CC, Rodello L, Gallego IC. Lipid peroxidation and generation of hydrogen peroxide in frozen-thawed ram semen cryopreserved in extenders with antioxidants. Anim Reprod Sci. 2010;122:118-23. doi: 10.1016/j. anireprosci.2010.08.004. PubMed PMID: 20813469.

(15.) da Silva Maia M, Bicudo SD, Azevedo HC, Sicherle CC, de Sousa DB, Rodello L. Motility and viability of ram sperm cryopreserved in a Tris-egg yolk extender supplemented with anti-oxidants. Small Ruminant Research. 2009;85:85-90. doi: 10.1016/j.smallrumres.2009.07.001.

(16.) Martinez-Pastor F, Aisen E, Fernandez Santos MR, Esteso MC, Maroto-Morales A, Garcia-Alvarez O, et al. Reactive oxygen species generators affect quality parameters and apoptosis markers differently in red deer spermatozoa. Reproduction. 2009;137:225-35. doi: 10.1530/REP-08 0357. PubMed PMID: 19028926.

(17.) Minaei MB, Barbarestani M, Nekoonam S, Abdolvahabi MA, Takzare N, Asadi MH, et al. Effect of Trolox addition to cryopreservation media on human sperm motility. Iran J Reprod Med. 2012;10:99-104. PubMed PMID: 25242981; PubMed Central PMCID: PMC4163270.

(18.) Breininger E, Beorlegui NB, O'Flaherty CM, Beconi MT. Alpha-tocopherol improves biochemical and dynamic parameters in cryopreserved boar semen. Theriogenology. 2005;63:2126-35. doi: 10.1016/j. theriogenology.2004.08.016. PubMed PMID: 15826678.

(19.) Kalthur G, Raj S, Thiyagarajan A, Kumar S, Kumar P, Adiga SK. Vitamin E supplementation in semen-freezing medium improves the motility and protects sperm from freeze-thaw-induced DNA damage. Fertil Steril. 2011;95:1149-51. doi: 10.1016/j. fertnstert.2010.10.005. PubMed PMID: 21067726.

(20.) Pena FJ, Johannisson A, Wallgren M, Rodriguez Martinez H. Antioxidant supplementation in vitro improves boar sperm motility and mitochondrial membrane potential after cryopreservation of different fractions of the ejaculate. Anim Reprod Sci. 2003;78:85-98. PubMed PMID: 12753785.

(21.) Yoshimoto T, Nakamura S, Yamauchi S, Muto N, Nakada T, Ashizawa K, et al. Improvement of the post-thaw qualities of Okinawan native pig spermatozoa frozen in an extender supplemented with ascorbic acid 2-O-alpha-glucoside. Cryobiology. 2008;57:30-6. doi: 10.1016/j. cryobiol.2008.05.002. PubMed PMID: 18589410.

(22.) Okazaki T, Yoshida S, Teshima H, Shimada M. The addition of calcium ion chelator, EGTA to thawing solution improves fertilizing ability in frozen-thawed boar sperm. Anim Sci J. 2011;82:412-9. doi: 10.1111/j.1740-0929.2010.00856.x. PubMed PMID: 21615834.

(23.) Patrat C, Serres C, Jouannet P. The acrosome reaction in human spermatozoa. Biol Cell. 2000;92:255-66. doi: 10.1016/ S0248-4900(00)01072-8. PubMed PMID: 11043413.

(24.) O'Toole CM, Arnoult C, Darszon A, Steinhardt RA, Florman HM. Ca(2+) entry through store-operated channels in mouse sperm is initiated by egg ZP3 and drives the acrosome reaction. Mol Biol Cell. 2000;11:1571-84. PubMed PMID: 10793136; PubMed Central PMCID: PMC14868.

(25.) Kalive M, Faust JJ, Koeneman BA, Capco DG. Involvement of the PKC family in regulation of early development. Mol Reprod Dev. 2010;77:95-104. doi: 10.1002/ mrd.21112. PubMed PMID: 19777543.

(26.) Aitken RJ, Clarkson JS. Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. J Reprod Fertil. 1987;81:459-69. PubMed PMID: 2828610.

(27.) Baker MA, Aitken RJ. The importance of redox regulated pathways in sperm cell biology. Mol Cell Endocrinol. 2004;216:47-54. doi: 10.1016/j.mce.2003.10.068. PubMed PMID: 15109744.

(28.) Burnaugh L, Sabeur K, Ball BA. Generation of superoxide anion by equine spermatozoa as detected by dihydroethidium. Theriogenology. 2007;67:580-9. doi: 10.1016/j.theriogenology.2006.07.021. PubMed PMID: 17045638.

(29.) Aitken RJ, Clarkson JS, Fishel S. Generation of reactive oxygen species, lipid peroxidation, and human sperm function. Biol Reprod. 1989;41:183-97. doi: 10.1095/ biolreprod41.1.183. PubMed PMID: 2553141.

(30.) Aitken RJ, Clarkson JS, Hargreave TB, Irvine DS, Wu FC. Analysis of the relationship between defective sperm function and the generation of reactive oxygen species in cases of oligozoospermia. J Androl. 1989;10:214-20. doi: 10.1002/j.1939 4640.1989.tb00091 .x. PubMed PMID: 2501260.

(31.) Anel L, Gomes-Alves S, Alvarez M, Borragan S, Anel E, Nicolas M, et al. Effect of basic factors of extender composition on post-thawing quality of brown bear electroejaculated spermatozoa. Theriogenology. 2010;74:643-51. doi: 10.1016/j.theriogenology.2010.03.004. PubMed PMID: 20494423.

(32.) Hossain MS, Johannisson A, Siqueira AP, Wallgren M, Rodriguez-Martinez H. Spermatozoa in the sperm-peak-fraction of the boar ejaculate show a lower flow of Ca(2+) under capacitation conditions post-thaw which might account for their higher membrane stability after cryopreservation. Anim Reprod Sci. 2011;128:37-44. doi: 10.1016/j.anireprosci.2011.08.006. PubMed PMID: 21962836.

(33.) Donnelly ET, McClure N, Lewis SE. Cryopreservation of human semen and prepared sperm: effects on motility parameters and DNA integrity. Fertil Steril. 2001;76:892-900. doi: 10.1016/S0015 0282(01)02834-5. PubMed PMID: 11704107.

(34.) Mendoza C, Carreras A, Moos J, Tesarik J. Distinction between true acrosome reaction and degenerative acrosome loss by a onestep staining method using Pisum sativum agglutinin. J Reprod Fertil. 1992;95:755-63. doi: 10.1530/jrf.0.0950755. PubMed PMID: 1383539.

(35.) Chi HJ, Kim JH, Ryu CS, Lee JY, Park JS, Chung DY, et al. Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa. Hum Reprod. 2008;23:1023-8. doi: 10.1093/humrep/ den060. PubMed PMID: 18325884.

(36.) Bailey JL, Bilodeau JF, Cormier N. Semen cryopreservation in domestic animals: a damaging and capacitating phenomenon. J Androl. 2000;21:1-7. PubMed PMID: 10670514.

(37.) Aisen EG, Alvarez HL, Venturino A, Garde JJ. Effect of trehalose and EDTA on cryoprotective action of ram semen diluents. Theriogenology. 2000;53:1053-61. doi: 10.1016/S0093-691X(00)00251-X. PubMed PMID: 10798483.

Sara Keshtgar [1], PhD; Farideh Iravanpour [2], MS; Behrooz Gharesi-Fard [3,4], PhD; Marjaneh Kazerooni [5], MS

[1] Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran;

[2] Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran;

[3] Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran;

[4] Infertility Research Center, Shiraz University of Medical Sciences, Shiraz, Iran;

[5] Shiraz Infertility Center, Shiraz, Iran


Sara Keshtgar, PhD; Department of Physiology, School of Medicine, Zand St, Postal code: 71348-45794, Shiraz, Iran

Tel/Fax: +98 71 32302026


Received: 06 July 2014

Revised: 16 September 2014

Accepted: 12 October 2014
Table 1: Analysis of the selected semen samples

Semen characteristics   Mean [+ or -] standard error

                        Fresh group           Frozen-thawed
                        (n, 13)               group (n, 12)

Semen volume (mL)       4.0 [+ or -] 0.4      3.2 [+ or -] 0.3
pH                      7.8 [+ or -] 0.07     7.8 [+ or -] 0.07
Sperm concentration     107.6 [+ or -] 12.6   125 [+ or -] 12
(x [10.sup.6]/mL)
Total sperm count       438.6 [+ or -] 74.7   374.5 [+ or -] 38.7
  (x [10.sup.6])
Progressive             41.8 [+ or -] 3.1     40.7 [+ or -] 3.4
  motility (%)
Nonprogressive          14.8 [+ or -] 1.8     12.9 [+ or -] 1.6
  motility (%)
Immotile sperm (%)      43.4 [+ or -] 3.2     46.4 [+ or -] 2.3
Abnormal sperm          52.1 [+ or -] 1.4     48.7 [+ or -] 2.1
  morphology (%)
Viability (%)           57.1 [+ or -] 1.2     57.9 [+ or -] 1.9
Viscosity               Normal                Normal

Table 2: Motility of the fresh and FT sperm in different
experimental subgroups after 1 hour's incubation andchanges
(%) in progressive motility relative to the control group
under treatment with Trolox and EDTA

Group Motility(%)   Mean [+ or -] standard error

                    Control         DMSO             Trolox

Fresh (N, 13)
  Progressive       77.0 [+ or -]   75.3 [+ or -]    78.6 [+ or -]
    motility          2.9             3.6              2.7
  Total motility    92.8 [+ or -]   91.8 [+ or -]    93.5 [+ or -]
                      1.1             1.5              1.3
  Change in         100             98.4 [+ or -]    102.6 [+ or -]
    motility (%)                      3.9              2.9
FT (N, 12)
  Progressive       16.5 [+ or -]   14.3 [+ or -]    17.8 [+ or -]
    motility          2.2 (a)         2.8 (a)          2.6 (a)
  Total motility    38.4 [+ or -]   39.8 [+ or -]    42.4 [+ or -]
                      3.9 (a)         5.3 (a)          4.6 (a)
  Change in         100             108.6 [+ or -]   115.6 [+ or -]
    progressive                       28.2             16.2
    motility (%)

Group Motility(%)   Mean [+ or -] standard error

                    EDTA             Trolox+EDTA

Fresh (N, 13)
  Progressive       76.3 [+ or -]    76.3 [+ or -]
    motility          2.6              2.0
  Total motility    91.7 [+ or -]    90.1 [+ or -]
                      0.9              1.3
  Change in         100.4 [+ or -]   100.3 [+ or -]
    motility (%)      4.4              4.2
FT (N, 12)
  Progressive       21.4 [+ or -]    23.4 [+ or -]
    motility          2.8 (a)          2.3 (a)
  Total motility    41.3 [+ or -]    44.6 [+ or -]
                      3.5 (a)          3 (a)
  Change in         157 [+ or -]     184.5 [+ or -]
    progressive       29.6             37 (a)
    motility (%)

(a) Significant difference relative to fresh sperm
under similar treatment (P<0.005); FT: Frozen-thawed;
EDTA: Edetic acid; DMSO: Dimethyl sulfoxide

Table 3: Viability of the fresh and FT sperm under treatment with
EDTA and Trolox

Subgroups             Mean [+ or -] standard error
Live sperm (%)

                      Control                 DMSO

Fresh sperm (N, 13)   91.8 [+ or -] 1.2       91 [+ or -] 1.3
FT sperm (N, 12)      44.0 [+ or -] 3.4 (a)   47.6 [+ or -] 2.6 (a)

Subgroups             Mean [+ or -] standard error
Live sperm (%)

                      Trolox                  EDTA

Fresh sperm (N, 13)   94.4 [+ or -] 1         91 [+ or -] 0.8
FT sperm (N, 12)      44.4 [+ or -] 4.7 (a)   45.9 [+ or -] 4.0 (a)

Subgroups             Mean [+ or -] standard
Live sperm (%)        error


Fresh sperm (N, 13)   90.1 [+ or -] 1.4
FT sperm (N, 12)      47.4 [+ or -] 3.3 (a)

(a) Significant difference relative to fresh sperm under similar
treatment (P<0.005); FT: Frozen-thawed; EDTA: Edetic acid;
DMSO: Dimethyl sulfoxide

Table 4: Acrosomal reaction in the fresh and FT sperm
under treatment with EDTA and Troloxt

Groups         Mean [+ or -] standard error (N, 5)
reaction (%)

               Control                  Trolox

Fresh          8.3 [+ or -] 1.9         5.7 [+ or -] 0.6
FT             83.4 [+ or -] 3.2 (ab)   80.08 [+ or -] 3.3 (ab)

Groups         Mean [+ or -] standard error (N, 5)
reaction (%)

               EDTA                    Trolox+

Fresh          5.4 [+ or -] 0.6        5.6 [+ or -] 1.4
FT             64.6 [+ or -] 2.7 (a)   63.9 [+ or -] 4 (a)

(a) Significant difference relative to fresh sperm under
similar treatment (P < 0.005); (b) Significant difference
relative to EDTA-containing groups (P<0.02); FT:
Frozen-thawed; EDTA: Edetic acid
COPYRIGHT 2016 Shiraz University of Medical Sciences
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2016 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Brief Report
Author:Keshtgar, Sara; Iravanpour, Farideh; Gharesi-Fard, Behrooz; Kazerooni, Marjaneh
Publication:Iranian Journal of Medical Sciences
Article Type:Report
Geographic Code:7IRAN
Date:May 1, 2016
Previous Article:Ileoileal knot as a content of obstructed hernia: what are the odds?
Next Article:Diagnostic value of the urine mucus test in childhood masturbation among children below 12 years of age: a cross-sectional study from Iran.

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters