Glutathione-S-transferase-oxidative stress relationship in the internal spermatic vein blood of infertile men with varicocele

Andrologia ◽  
2014 ◽  
Vol 47 (1) ◽  
pp. 47-51 ◽  
Author(s):  
T. Mostafa ◽  
L. A. Rashed ◽  
A. S. Zeidan ◽  
A. Hosni
Urology ◽  
2011 ◽  
Vol 78 (3) ◽  
pp. S232
Author(s):  
P. Sountoulides ◽  
S. Gravas ◽  
D. Kikidakis ◽  
A. Theodosiou ◽  
K. Paschalidis ◽  
...  

Andrology ◽  
2016 ◽  
Vol 4 (3) ◽  
pp. 442-446 ◽  
Author(s):  
R. Altintas ◽  
C. Ediz ◽  
H. Celik ◽  
A. Camtosun ◽  
C. Tasdemir ◽  
...  

2018 ◽  
Vol 9 (2) ◽  
pp. 287-292 ◽  
Author(s):  
M. Z. Vorobets ◽  
R. V. Fafula ◽  
A. S. Besedina ◽  
O. K. Onufrovych ◽  
D. Z. Vorobets

It is believed that the most common causes of male infertility are impairment of spermatogenesis and sperm functions. Glutathione S-transferases (EC 2.5.1.18) play an important role in sperm physiology, specifically in antioxidant protection against oxidative damage. The catalase decomposition of lipid hydro-peroxides forms as a result of oxidative stress. We used a model of superoxide anion-generating system Fe3+/ascorbate or H2O2-induced stress to study the activity of glutathione s transferase in human ejaculated spermatozoa from patients with pathospermia and products of lipid peroxidation (TBARS) as a marker of oxidative stress. In the present study, dose dependent increase in the level of lipid peroxidation was observed for treatment with Fe3+/ascorbate or H2O2. The TBARS level was higher for sperm cells incubated with superoxide anion-generating system Fe3+/ascorbate than for H2O2. GSTs activity increased in spermatozoa treated with increasing concentration of superoxide anion-generating system Fe3+/ascorbate and H2O. We found that both Fe3+/ascorbate and H2O2 displayed similar inhibitory effects on sperm GSTs activity, however H2O2 at low concentrations activated enzyme activity only in normozoospermic samples, which can be explained as a defence response to oxidative stress. The time course of incubation with 100 μM H2O2 showed a sharp decrease in the enzyme activity during the first 5 min of incubation for both normozoospermic and pathozoospermic men. Preincubation of spermatozoa with GSH completely prevented the ROS-induced inhibition on GSTs only in normozoospermic samples. On the other hand, in pathospermic samples protectory effect of GSH was observed only against non-radical (H2O) radical, but not against radical (superoxide anion-generating system Fe3+/ascorbate) species. The results of our study showed higher oxygen-free radical production, evidenced by increased TBARS level in spermatozoa obtained from infertile men than normozoospermic men. The inhibitory effect of the radical (superoxide anion-generating system Fe3+/ascorbate) species on sperm GSTs activity and products of lipid peroxidation in sperm cells of fertile and infertile men were more expressed compared to non-radical (H2O) species. Our results indicate that estimation of sperm GSTs enzyme assays can be used as a bioindicator for impaired male fertility. The obtained results argue for a biological role of sperm GSTs in susceptibility of spermatozoa to oxidative damage and maintaining sperm antioxidant status.


2006 ◽  
Vol 8 (4) ◽  
pp. 451-454 ◽  
Author(s):  
Taymour Mostafa ◽  
Tarek H. Anis ◽  
Sherif Ghazi ◽  
Abdel Rahman El-Nashar ◽  
Hager Imam ◽  
...  

1980 ◽  
Vol 52 (1) ◽  
pp. 50-56 ◽  
Author(s):  
A. V. HIRSH ◽  
K. M. CAMERON ◽  
J. P. TYLER ◽  
J. SIMPSON ◽  
J. P. PRYOR

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