Volume 14, Issue 2 (2-2016)                   IJRM 2016, 14(2): 141-144 | Back to browse issues page


XML Persian Abstract Print


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

Golshan Iranpour F, Kheiri S. Coadministration of calcium chloride with lead acetate can improve motility of cauda epididymal spermatozoa in Swiss white mice. IJRM. 2016; 14 (2) :141-144
URL: http://journals.ssu.ac.ir/ijrmnew/article-1-718-en.html
1- Department of Anatomical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran , fgolshaniranpour@yahoo.com
2- Herbal Medicine Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran
Full-Text [PDF 97 kb]   (33 Downloads)     |   Abstract (HTML)  (72 Views)
Full-Text:   (8 Views)
Introduction
 
Lead, mercury, chromium, nickel and cadmium are examples of heavy metals. Among these metals lead is the most famous one. In addition to workers who deal with lead, other people are also exposed to lead pollution daily. Lead excretion is slow in the body and biological half-life of it is 24-40 days (1). In recent years, the negative effects of environmental substances on male genitalia have been received considerable interest. Lead could reduce the number of sperms and decrease follicle stimulating hormone (FSH), but the amount of luteinizing hormone (LH) was not changed (2).
The effects of low or moderate doses of lead acetate were investigated on rats for 24 wk. The results showed that there was no change in body weight and weight of testes and epididymides (3). Ca²+ has an important role in many cellular functions of sperm such as flagellar beating, movement velocity and acrosome reaction. For appropriate function, motile sperm maintains intracellular free calcium concentration (4). Because of the crucial role of calcium in sperm cell function and motility, it may protect sperm against environmental factors. So the aim of this study was to investigate the protective effect of calcium against lead on motility of cauda epididymal spermatozoa of mouse.
 
Materials and methods
 
Animals
In this prospective study, 40 healthy Swiss white male mice obtained from Pasteur’s Institute (Tehran, Iran) were used. Their weights were between 25-40 gr. Every five mice were kept in a cage for two weeks in animal house to acclimate to laboratory conditions. Food and water was provided ad libitum. All animal procedures were approved by Shahrekord University of Medical Sciences Ethical Committee, Shahrekord, Iran.
 
Chemicals
Purified lead acetate and calcium chloride were purchased from Merck (Merck Company, Germany). Also Ham’s F10 was purchased from Gibco (Gibco Company, England). Lead acetate and calcium chloride doses of 200 mg/kg and 80 mg/kg were selected according to the previous studies of Achyra et al and Aboul-Ela (5, 6). Both of them were dissolved in distilled water and injected intraperitoneally.
 
Experimental design
40 adult male Swiss white mice were randomly selected and divided into 5 groups (control, lead of 1st wk, lead of 2nd wk, lead/calcium of 1st wk and lead/calcium of 2nd wk). Lead groups were injected by a single dose of 200 mg/kg of lead acetate. Lead/calcium groups were injected by a single dose of 200 mg/kg lead acetate followed by three injections of 80 mg/kg calcium chloride. Calcium chloride injection was done one time immediately after injection of lead acetate and two times in two days following the first injection.
Mice of the 1st and 2nd wk groups were sacrificed through cervical dislocation one and two weeks after lead injection respectively. The control group was also injected with the same volume of distilled water. This group was sacrificed one week after the injection of distilled water. All injections in all groups were intraperitoneally.
 
Weighing of testes and epididymides
Right side testes and epididymides of the mice were removed, cleaned of accessory tissues and weighed in grams.
 
Sperm motility
Sperm suspension was prepared by squeezing of the tail part of epididymides in Ham’s F10 medium. After putting one drop of sperm suspension on a slide, a cover slip was placed on it to assess percentage of progressive motile spermatozoa. Then the slides were examined under the 40× objective lens of light microscope. Three slide replicates were assessed and at least 200 sperms were counted and the percentage of progressive motile sperms was calculated for each slide.
 
Statistical analysis
The data was analyzed using Statistical Package for Social Studies (SPSS) software. Testes and epididymides weight and sperm motility were reported as mean±SD for each group. An analysis of the variance was performed for weight. One way ANOVA and post hoc analysis were carried out by LSD for motility of spermatozoa. A comparison is considered significantly different when p<0.05.
 
Results
 
Weight of testes and epididymides
Statistical analysis of the results obtained from weighing of the testes and epididymides showed that there is no significant difference among various groups of study (respectively p=0.11, p=0.31, Table I).
 
Sperm motility
The mean percentages of progressive motile sperms were measured in each group. In order to ensure the normal distribution of data, primarily Kolmogorov-Smironov test was performed. Based on this test the distribution of sperm motility percentages were normal in different groups (p=0.2). Therefore, these variables were compared in groups of one-way ANOVA with LSD post hoc test. The results for motility are given in table I. As it can be seen in the table I, the mean percentages of progressive motile sperms in lead and lead/calcium groups were significantly lower than the control group (for all of them p<0.001).
Also the mean percentage of progressive motile spermatozoa in lead /calcium group of the first week was higher than the lead group of the first week and this difference was significant (p=0.04). Moreover, the results indicated that there was no significant difference between the percentages of motility in the lead/calcium group of the second week and the lead group of the second week (p=0.46).

Table I. Percentage of motile spermatozoa of cauda epididymis and weight of right testis and epididymis in control, lead and lead/calcium groups
Data are presented as mean±SD.
  1. Significant comparing to the control group. p<0.001
  2. Significant comparing to the lead group of first week. p<0.05
  3. No significant comparing to the lead group of second week
 

Discussion
 
In our preceding report, we demonstrated that lead reduces motility and viability of spermatozoa but this effect will disappear up to three weeks after the injection. In contrast to motility and viability, lead does not denature DNA of sperms (7). Because the effects of lead will disappear three weeks after the lead injection, in the present study the results were followed for two weeks. Significant changes were not seen in the weight of testes and epididymides of mice of lead group in the present study. These results are in accordance with those of some researchers who did not find any significant changes in the weight of testis and seminal vesicle after administration of lead in rats (2, 3). Nevertheless, some researchers reported that lead administration could reduce weight of mice testes (6). It seems that lead dosage and route of administration are the main reasons for the difference in the results.
Our results show that mean percentage of progressive motile spermatozoa in lead/calcium group of the first week was significantly higher than the lead group of the first week and this difference was significant. It has been shown that certain vitamins like vitamin C and E have the ability to decrease the toxic effects of lead on sperm count and morphology in Swiss white mice (8). Moreover, the protective function of zirconium against the clastogenic effects of lead has been reported (9). Prescribed calcium supplementation during pregnancy reduces the amount of lead in the blood and may decrease it in maternal and subsequently fetal blood (10). Rising of dietary calcium decreases lead absorption (11). A number of studies have revealed that intracellular calcium plays an important role in sperm motility and different steps of fertilization, such as, capacitation, acrosome reaction and zona penetration (12, 13). However, the exact role of intracellular calcium in spermatogenesis is unclear (13).
It has been illustrated that calcium at lower concentrations (lower than 10 µg) promoted motility and velocity of spermatozoa (14). Aboul- Ela demonstrated the protective effect of calcium against genotoxicity of lead in somatic and germ cells (6). These findings are consistent with those of Weber et al study. They found that verapamil, that is a calcium antagonist, increases DNA damage which is induced by Bleomicin (15). To our knowledge, our results are the first ones that indicate co-administration of calcium with lead could reduce the effects of lead on the sperm motility up to one week. However, this effect is temporary and did not continue in the second week. The results of this study complete the results of Aboul-Ela that indicate co-administration of calcium with lead reduces chromosomal changes of spermatocytes (6). It seems that re-injection of calcium after one week can avoid the toxic effects of lead even in the second week. This issue needs further research.
It can be concluded that calcium can decrease the potential effects of lead on reducing sperm motility in caudal part of epididymis of mouse.
 
Acknowledgments
 
This study was sponsored by the Research Deputy of Shahrekord University of Medical Sciences and its Ethics Committee has approved this work. The authors would like to extend their gratitude towards The Cell and Molecular Research Center and its stuff for their assistance.
 
Conflict of interest
 
There is no conflict of interest in this research.

 
Type of Study: Original Article |
Received: 2017/10/1 | Accepted: 2017/10/4 | Published: 2017/10/4

References
1. Vincoli JW. Lead chloride. In: Risk management for hazardous chemicals. Boca Raton: Lewis Publisher. 1997; 2005-2010.
2. Sokol RZ, Madding CE, Swerdloff RS. Lead toxicity and the hypothalamic-pituitary-testicular axis. Biol Reprod 1985; 33: 722-728. [DOI:10.1095/biolreprod33.3.722]
3. Allouche L, Hamadouche M, Touabti A. Chronic effects of low lead levels on sperm quality, gonadotropins and testosterone in albino rats. Exp Toxicol Pathol 2009; 61: 503-510. [DOI:10.1016/j.etp.2008.12.003]
4. Krasznai Z, Márián T, Izumi H, Damjanovich S, Balkay L, Trón L, Morisawa M. Membrane hyperpolarization removes inactivation of Ca2+ channels, leading to Ca2+ influx and subsequent initiation of sperm motility in the common carp. Proc Nat Acad Sci 2000; 97: 2052-2057. [DOI:10.1073/pnas.040558097]
5. Acharya UR, Acharya S, Mishra M. Lead acetate induced cytotoxicity in male germinal cells of Swiss mice. Industrial Health 2003; 41: 291-294. [DOI:10.2486/indhealth.41.291]
6. Aboul-Ela EI. The protective effect of calcium against genotoxicity of lead acetate administration on bone marrow and spermatocyte cells of mice in vivo. Mutat Res 2002; 516: 1-9. [DOI:10.1016/S1383-5718(01)00332-1]
7. Golshan-Iranpour F, Emami E. The effects of lead on motility, viability and DNA denaturation of cauda epididymal spermatozoa of mouse. J Shahrekord Univ Med Sci 2011; 13:1-8.
8. Mishra M, Acharya UR. Protective action of vitamins on the spermatogenesis in lead-treated Swiss mice. J Trace Elem Med Biol 2004; 18: 173-178. [DOI:10.1016/j.jtemb.2004.03.007]
9. Dhir H, Ghosh S, Sharma A, Talukder G. Interaction between two group IV metals-lead and zirconium-in bone marrow cells of Mus musculus in vivo. Biometals 1992; 5: 81-86. [DOI:10.1007/BF01062218]
10. Lamadrid-Figueroa H, Téllez-Rojo MM, Mercado-García A, Hu H, Hernández-Avila M, Ettinger AS, et al. Effect of calcium supplementation on blood lead levels in pregnancy: a randomized placebo-controlled trial. Environ Health Perspect 2008; 117: 26-31.
11. Meredith PA, Moore MR, Goldberg A. The effect of calcium on lead absorption in rats. Biochem J 1977; 166: 531-537. [DOI:10.1042/bj1660531]
12. Marín-Briggiler CI, Gonzalez-Echeverría F, Buffone M, Calamera JC, Tezón JG, Vazquez-Levin MH.Calcium requirements for human sperm function in vitro. Fertil Steril 2003; 79: 1396-1403. [DOI:10.1016/S0015-0282(03)00267-X]
13. Darszon A, Nishigaki T, Beltran C, Trevi-o CL. Calcium channels in the development, maturation, and function of spermatozoa. Physiol Rev 2011; 91: 1305-1355. [DOI:10.1152/physrev.00028.2010]
14. Bhoumik A, Saha S, Majumder GC, Dungdung SR. Optimum calcium concentration: a crucial factor in regulating sperm motility in vitro. Cell Biochem Biophys 2014; 70:1177-1183. [DOI:10.1007/s12013-014-0038-x]
15. Weber J, Scheid W, Traut H. Enhancement of bleomycin-induced DNA damage by exposing isolated DNA to high concentrations of the calcium antagonist verapamil. Arzneimittel-Forschung 1989; 39: 1550-1554.

Add your comments about this article : Your username or Email:
Write the security code in the box

Send email to the article author


© 2018 All Rights Reserved | International Journal of Reproductive Biomedicine

Designed & Developed by : Yektaweb