Volume 11, Issue 9 (12-2013)                   IJRM 2013, 11(9): 767-0 | Back to browse issues page

XML Persian Abstract Print

Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Barkhordari A, Hekmatimoghaddam S, Jebali A, Khalili M A, Talebi A, Noorani M. Effect of zinc oxide nanoparticles on viability of human spermatozoa. IJRM 2013; 11 (9) :767-0
URL: http://ijrm.ir/article-1-459-en.html
1- Department of Occupational Health, School of Health, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
2- Department of Laboratory Sciences, School of Paramedicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
3- Department of Medical Nanotechnology, Pajoohesh Lab, Yazd, Iran
4- Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
5- Department of Occupational Health, School of Paramedicine, Abarkooh, Yazd, Iran , marzieh.noorani@gmail.com
Full-Text [PDF 333 kb]   (694 Downloads)     |   Abstract (HTML)  (2791 Views)
Full-Text:   (374 Views)
There are some occupational environments which may potentially affect fertility. Previous studies showed that some toxic chemicals, heavy metals, pesticides, and radiation can lead to infertility (1). Nanoparticles (NPs), with at least one dimension at 1-100 nm range, have become much prevalent in life over the past two decades, and are now widely used in a variety of industries and medical fields. These applications have raised concerns about their biological effects.
It has previously been found that biological effects of nano-sized particles are quite different from their micro-scale particles. Interestingly, some studies have demonstrated that systemic sclerosis, rheumatoid arthritis, systemic lupus erythematous, and chronic renal disease are associated with exposure to NPs (2). Although the effects of environmental and occupational particles on human fertility are well documented, but there are few studies about the effects of NPs on sperms. For example, it has been recorded that iron oxide NPs (Fe3O4) have no effect on sperm motility (3).
According to Wiwanitkit et al study, sperm motility was decreased (25%) after exposure to gold NPs, compared with normal group (95%) (4). Ema et al revealed that titanium dioxide (TiO2) NPs decrease human sperm motility, and also silica NPs are toxic for mouse sperms (5). In 2011, a study on toxicity of TiO2 and silver NPs on reproductive system was done by Philbrook et al. Their results showed that a single oral 100 mg/kg dose of TiO2 NPs decreased mice developmental process, and increased fetal deformities and mortality (6). There are no studies on impact of Zinc oxide (ZnO) NPs on sperm. Some researchers have declared toxicity of ZnO NPs on different cells.
For example, we know that ZnO NPs can damage alveolar epithelial cells in a dose- and time-dependent manner, and may cause mitochondrial dysfunction, as they can increase intracellular reactive oxygen species (ROS) (7). Toxicity of ZnO NPs on human bronchial epithelial cells was investigated, and suggested that oxidative stress is a mechanism of toxicity (8). Also, it was demonstrated that ZnO NPs inhibit growth of Staphylococcus aureus, Pseudomonas aeruginosa, and Saccharomyces cerevisiae (9){Heng, 2010 #19}. The aim of this study was to investigate the cytotoxic effects of ZnO NPS on human spermatozoa using MTT assay.
Materials and methods
ZnO NPs were purchased from Lolitech Co., Germany. RPMI (Roswell Park Memorial Institute) 1640, 70% isopropanol, and 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl-tetrazolium bromide (MTT) were obtained from Sigma-Aldrich Chemical Co., (St Louis, MO). Hanks’ balanced salt solution (HBSS) was provided from Gibco Invitrogen, UK.
Preparation and characterization of ZnO NPS
In this laboratory trial, different concentrations of ZnO NPs (10, 100, 500, and 1000 µg/mL) were prepared in RPMI 1640, and gently shaken for 5 min. The structure of ZnO NPs w::as char::acterized by scanning electron microscopy (SEM) (Hitachi S-2400) at 15 KV as accelerating voltage, and their size distributions were analyzed by dynamic light scattering (DLS) (Malvern Instruments, Italy).
Preparation of sperms and nanoparticle exposure
For statistical testing purposes, 15 normal fresh semen samples from healthy persons were obtained and analyzed using WHO guidelines (10). They were 20-40 years old men examined by specialists in urology for being healthy regarding any disease which may affect spermatogenesis, and signed an informed consent form. All were husbands of women referred for treatment of female infertility. This study was in compliance with the ethics committee of Shahid Sadoughi University of Medical Sciences, Yazd, Iran. In the first step, 10 µL of ejaculated semen was obtained after 2-4 days of abstinence from intercourse, and washed three times with buffered normal saline. Washed sperms were resuspended in RPMI 1640 and adjusted at 5×103 cells/mL.
Then, 100 µL of each sample was added to separate wells in a 96-well microplate. In the next step, 100 µL of different concentrations of ZnO NPS was added to sperm samples, and incubated at 37oC for 45, 90, and 180 minutes. As negative control, sperms were not treated with ZnO NPs. But, as positive control, sperms were exposed to 0.1 M HCl. Same as the treated samples, both negative and positive control samples were incubated at 37oC for 45, 90, and 180 minutes, too.
MTT assay
The cytotoxicity of NPs was evaluated by MTT assay. The reduction of MTT salt to Formosan crystal by mitochondrial dehydrogenase enzymes is the mechanism of this assay (11). After incubation, sperm cells were washed three times by HBSS, and 10 µL of 5 mg/mL MTT solution was added to each well. After 3 hours incubation at 37oC, 50 µL of 70% isopropanol was added, and optical density (OD) of each well was read at 490 nm using a micro plate reader (Novin Gostar, Iran). Finally, the cell death percentage of each group was measured, according to below formula (12).

A is the OD of negative control,
B is the OD of sample after exposure to ZnO NPs
Statistical analysis
Toxicity of each concentration of ZnO NPs was evaluated twice, and its average was calculated. Statistical analysis was performed by SPSS v.16 software (SPSS Inc, Chicago, USA). Mann-Whitney test was used for detection of significant differences. Any P-value less than 0.05 were considered as statistically significant difference.
The SEM image of ZnO NPs is shown in figure 1a. This image shows that the structure of ZnO NPs is amorphous, and their sizes are about 50 nm. As shown in figure 1b, the size distribution of ZnO NPs is about 30-70 nm. The relationships between different concentrations of ZnO NPs and cell death percentage after 45, 90, and 180 minutes are presented in figure 2a, figure 2b, and figure 2c, respectively.
According to these figures, the maximum cell death after 45, 90, and 180 minutes was 20.86%, 21.2%, and 33.26%, respectively. In all incubation times, the highest cell death was observed at concentration of 1000 µg/mL, and the lowest one at 10 µg/mL. Based on figures 2a, 2b and 2c, with increase in incubation time from 45-90 min, no significant change was observed in cell death, but after 180 minutes exposure, the percentage of cell death was increased at all concentrations. This research showed that at all incubation times, there are significant differences between cell death related to ZnO NPs at concentration of 500 µg/mL and 1000 µg/mL vs. control group (p=0.001). On the other hand, significant differences were shown between cell death percentage after 180 minutes vs. 45 and 90 minutes (p=0.001) at concentration of 100, 500, and 1000 µg/mL. However, there was no such difference between cell death at 45 min and 90 minutes (p=0.08).

Figure 1. The SEM image of ZnO NPs (a), and the size distribution of ZnO NPs (b), obtained by DLS method.

Figure 2. The cell death percentage after treatment with ZnO NPs.
At first, 100 µL of spermatozoa suspension was separately incubated with different concentrations of ZnO NPs at 37ºC for 45 (a), 90 (b), and 180 (c) minutes. Then, spermatozoa were washed by HBSS, and 10 µL of 5 mg/mL MTT solution was added. After 3 hours incubation, OD of each well was read at 490 nm. Finally, the cell death percentage of each sample was calculated, according to formula 1. All data are shown as mean±SD. *p<0.05 compared with control.

To evaluate spermatotoxicity of ZnO NPs, different concentrations of these NPs (10,100, 500 and 1000 µg/mL) were prepared and added to sperm cells for 45, 90, and 180 minutes. In this study, the percentage of cell death was measured by MTT assay. According to our results, when cells were treated with higher concentrations of ZnO NPs, their toxicity was increased. This means that ZnO NPs affect sperm cells in a dose-dependent manner.
Also, this research showed that the maximum cell death was 20.86%, 21.2%, and 33.26% after 45, 90, and 180 minutes, respectively. As shown in figure 2a, 2b and 2c, the toxicity to sperms is increased with increase in incubation times. This clearly suggests a time-dependent process of toxicity. Dose-dependent and time-dependent toxicity of NPs are commonly seen in nanotoxicological studies (3-5). As an important finding extracted from the present study, although there were little increments in cell death after 90 minutes, but a high rise (33.26%) was observed after 180 minutes. Compared with silver and TiO2 NPs which have high toxicity, ZnO NPs have moderate toxicity on sperms.
Although there is no study on toxic effect of ZnO NPs on human sperm cells, but toxicity of other NPs were investigated in previous studies. For example, Ema et al showed that silica NPs are toxic for spermatozoa at high concentrations (5). In a recent study, it was shown that gold NPs decrease sperm motility, and TiO2 NPs are more cytotoxic for Leyding cells than other NPs (4, 12). In addition, previous studies have mainly focused on changes in the motility of sperm cells (13-15). According to previous researches, ZnO NPs damage alveolar epithelial cells in a dose- and time-dependent manner (7). Also, ZnO NPs can affect human bronchial epithelial cells (8). The toxicity mechanisms of ZnO NPs have not been well defined. Mitochondrial dysfunction, ion release, binding to membrane or cytosol protein, and generation of intracellular ROS are some of proposed mechanisms of toxicity (8).
In this study, MTT assay was used to evaluate cytotoxicity. The MTT assay is a simple, rapid and reliable method for estimation of percentage of cell viability, depending on accumulation of Formosan crystals (16, 17). As noted before, mitochondrial dehydrogenase enzymes reduce MTT salt to Formosan. We used only MTT test, and this is the main limitation of this study. Other tests such as release of lactate dehydrogenase, generation of ROS, annexin dye binding, and investigation of involved genes should be used in future studies. Toxicity of ZnO NPs would also be investigated in actual conditions. The authors suggest an in vivo study (both in animal models and exposed patients) for toxicity evaluation of ZnO NPs. Taken together; ZnO NPs have spermatotoxicity, and may lead to infertility after exposure. Toxicity of ZnO NPs is dependent on both concentration and exposure time.
This study was financially supported by Shahid Sadoughi University of Medical Sciences, Yazd, Iran. The authors thank the laboratory staff of the Yazd Pajoohesh Medical Lab, and also the Cellular and Molecular Biology Research Center in Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Conflict of interest
There was no conflict of interest in this study.
Type of Study: Original Article |

1. Jungwirth A, Giwercman A, Tournaye H, Diemer T, Kopa Z, Dohle G, et al. European Association of Urology Guidelines on Male Infertility: The 2012 Update. Eur Urol 2012; 62: 324-332. [DOI:10.1016/j.eururo.2012.04.048]
2. Peters K, Unger RE, Kirkpatrick CJ, Gatti AM, Monari E. Effects of nano-scaled particles on endothelial cell function in vitro: studies on viability, proliferation and inflammation. J Mater Sci Mater Med 2004; 15: 321-325. [DOI:10.1023/B:JMSM.0000021095.36878.1b]
3. Makhluf SBD, Qasem R, Rubinstein S, Gedanken A, Breitbart H. Loading magnetic nanoparticles into sperm cells does not affect their functionality. Langmuir 2006; 22: 9480-9482. [DOI:10.1021/la061988z]
4. Wiwanitkit V, Sereemaspun A, Rojanathanes R. Effect of gold nanoparticles on spermatozoa: the first world report. Fertil Steril 2009; 91: 7-8. [DOI:10.1016/j.fertnstert.2007.08.021]
5. Ema M, Kobayashi N, Naya M, Hanai S, Nakanishi J. Reproductive and developmental toxicity studies of manufactured nanomaterials. Reprod Toxicol 2010; 30: 343-352. [DOI:10.1016/j.reprotox.2010.06.002]
6. Philbrook NA, Winn LM, Afrooz AR, Saleh NB, Walker VK. The effect of TiO2 and Ag nanoparticles on reproduction and development of Drosophila melanogaster and CD-1 mice. Toxicol Appl Pharmacol 2011; 257: 429-436. [DOI:10.1016/j.taap.2011.09.027]
7. Kim YH, Fazlollahi F, Kennedy IM, Yacobi NR, Hamm-Alvarez SF, Borok Z, et al. Alveolar epithelial cell injury due to zinc oxide nanoparticle exposure. Am J Respir Crit Care Med 2010; 182: 1398-1409. [DOI:10.1164/rccm.201002-0185OC]
8. Heng BC, Zhao X, Xiong S, Ng KW, Boey FY, Loo JS. Toxicity of zinc oxide (ZnO) nanoparticles on human bronchial epithelial cells (BEAS-2B) is accentuated by oxidative stress. Food Chem Toxicol 2010; 48: 1762-1766. [DOI:10.1016/j.fct.2010.04.023]
9. Zvekić D, Srdić VV, Karaman MA, Matavulj MN. Antimicrobial properties of ZnO nanoparticles incorporated in polyurethane varnish. Proc Appl Ceram 2011; 5: 41-45. [DOI:10.2298/PAC1101041Z]
10. World Health Organization. WHO laboratory manual for the examination and processing of human semen: World Health Organization; 2010.
11. Slater TF, Sawyer B, Sträeuli U. Studies on succinate-tetrazolium reductase systems. III. Points of coupling of four different tetrazolium salts. Biochim Biophys Acta 1963; 77: 383-393. [DOI:10.1016/0006-3002(63)90513-4]
12. Iqbal M, Ijaz A, Aleem M, Rehman H, Yousaf MS. Assessment of Nili-Ravi buffalo (Bubalus bubalis) semen by MTT reduction assay. South Afr J Anim Sci 2009; 39: 294-300.
13. Sahoo SK, Parveen S, Panda JJ. The present and future of nanotechnology in human health care. Nanomedicine 2007; 3: 20-31. [DOI:10.1016/j.nano.2006.11.008]
14. Anerao AM, Sharma RC, Rathore Mansee, Gangawane AK. Studies on human sperm motility and viability when treatment with rock salt. J Pathol Res 2010; 1: 1-10.
15. Rurangw E, Kime DE, Ollevier F, Nash JP. The measurement of sperm motility and factors affecting sperm quality in cultured fish. Aquaculture 2004; 234: 1-28. [DOI:10.1016/j.aquaculture.2003.12.006]
16. Nasr-Esfahani MH, Aboutorabi R, Esfandiari E, Mardani M. Sperm MTT viability assay: a new method for evaluation of human sperm viability. J Assist Reprod Genet 2002; 19: 477-482. [DOI:10.1023/A:1020310503143]
17. Gaczarzewicz D, Piasecka M, Udala J, Blaszczyk B, Laszczynska M, Kram A. Oxidoreductive capability of boar sperm mitochondria in fresh semen and during their preservation in BTS extender. Reprod Biol 2003; 3: 161-172.

Send email to the article author

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb