Effect of tubal explants and their secretions on bovine spermatozoa: modulation of ROS production and DNA damage

2012 ◽  
Vol 24 (6) ◽  
pp. 871 ◽  
Author(s):  
Patricia Navarrete Gómez ◽  
Juan G. Alvarez ◽  
Jennie Risopatrón ◽  
Fernando Romero ◽  
Raúl Sánchez

Although low levels of reactive oxygen species (ROS) play a physiological role in maintaining sperm function, an increase in ROS generation above these levels may result in the induction of sperm membrane and DNA damage. The main objective of this study was to determine whether bovine oviducal explants (TU) and their conditioned media (CM) have a modulatory effect on the production of ROS, and consequently, on sperm DNA integrity. Thawed sperm were exposed to bovine TU and to CM obtained from the ampullar and isthmal regions after 4 and 12 h, and DNA damage and intracellular ROS production was assessed by TUNEL and DHE and SYTOX Green, respectively. Co-incubation of spermatozoa with oviducal explants from the ampullar region (TUa) for 4 h resulted in a statistically significant increase in the percentage of spermatozoa with DNA damage compared with controls (P = 0.0106), and this increase was positively correlated with ROS levels. Conversely, although the incubation of spermatozoa with explants and conditioned media from the isthmal region (TUi and CMi, respectively) for 12 h resulted in an increase of spermatozoa with DNA damage compared with controls (P < 0.0001), this increase was not correlated with ROS levels. In conclusion, significant oxidative stress may take place in the oviduct, particularly during short-term incubation, and this may be related to changes in the antioxidant factors present in the oviducal cells and secretions. A redox imbalance in pro-oxidants and antioxidants in the oviduct may lead to oxidative stress and sperm DNA damage.

2018 ◽  
Vol 58 (2) ◽  
pp. 252 ◽  
Author(s):  
L. Fraser ◽  
Ł. Zasiadczyk ◽  
C. S. Pareek

Assessment of sperm-DNA integrity is a crucial issue in male fertility. In the present study, parameters derived from the image analysis of comets after single-cell gel electrophoresis were used to analyse the types of DNA damage of frozen–thawed boar spermatozoa. Semen, frozen in a cryoprotectant-free extender or in cryoprotectant-based extenders, was analysed for DNA fragmentation and with the following comet tail measures: percentage DNA in comet tail, comet tail length and olive tail moment. The percentages of sperm DNA damage in the comet tails were classified as Type 0 (no DNA damage), Type I (very low DNA damage), Type II (light DNA damage), Type III (medium DNA damage) and Type IV (heavy DNA damage). Sperm motility characteristics and membrane integrity were assessed in the pre-freeze and frozen–thawed semen samples. Assessment of sperm DNA fragmentation and comet tail measures showed marked inter-boar variability following cryopreservation. However, consistent differences among the boars, with respect to cryo-induced sperm DNA damage, were detected by the comet tail length and olive tail moment. Besides Type IV, all types of DNA damage were detected in the cryoprotectant-based extenders. It was found that the frequency of Type II and Type III of DNA damage of frozen–thawed spermatozoa was significantly greater in the cryoprotectant-based and cryoprotectant-free extenders respectively. Deterioration in the quality of the sperm DNA integrity was concomitant with a marked decline in sperm motility characteristics, reduced plasma membrane integrity and higher lipid peroxidation and aspartate aminotransferase activity after cryopreservation. It can be suggested that the comet-assay parameters, coupled with routine laboratory tests, are useful to improve the sperm evaluations of post-thaw quality of semen from individual boars and would offer more comprehensive information for a better understanding of the degree of cryo-induced sperm-DNA damage.


2005 ◽  
Vol 21 (4) ◽  
pp. 986-993 ◽  
Author(s):  
R. Smith ◽  
H. Kaune ◽  
D. Parodi ◽  
M. Madariaga ◽  
R. Rios ◽  
...  

2016 ◽  
Vol 28 (10) ◽  
pp. 1598 ◽  
Author(s):  
Kai Zhao ◽  
Yaoping Chen ◽  
Ruifeng Yang ◽  
Yang Bai ◽  
Cuiling Li ◽  
...  

Sperm DNA integrity is an essential factor for accurate transmission of genetic information. Human sperm DNA damage is a common cause of male infertility but the exact mechanism remains poorly understood. Considering the vital role of microRNA (miRNA) in multiple pathophysiological processes, we hypothesised that testicular miRNA is involved in sperm DNA damage during spermatogenesis. Infertile patients with high sperm DNA fragment index (DFI; n = 94) were selected from 1090 infertile men and a total of 18 testis-specific seminal miRNAs previously identified from human seminal plasma were chosen and tested. miR-29c and miR-424 were downregulated in men with high DFI. The inhibition of these two miRNAs in mice confirmed the role of miR-424 (murine homologue miR-322) in sperm DNA damage during spermatogenesis; by contrast, miR-29c exhibited a negative result. Thus, miR-424/322 is involved in sperm DNA damage. Furthermore, the dysregulation of this miRNA can induce DNA double-strand breaks during spermatogenesis.


2018 ◽  
Vol 131 ◽  
pp. 162S
Author(s):  
Mai Tran ◽  
Heydy Uriondo ◽  
Florencia Nodar ◽  
Cristian Alvarez Sedó

2002 ◽  
Vol 78 ◽  
pp. S261-S262 ◽  
Author(s):  
Ramadan A Saleh ◽  
Ashok Agarwal ◽  
Essam A Nada ◽  
Mohamed H El-Tonsy ◽  
Donald P Evenson ◽  
...  

2009 ◽  
Vol 24 (9) ◽  
pp. 2061-2070 ◽  
Author(s):  
L.K. Thomson ◽  
S.D. Fleming ◽  
R.J. Aitken ◽  
G.N. De Iuliis ◽  
J.-A. Zieschang ◽  
...  

2009 ◽  
Vol 92 (3) ◽  
pp. S210
Author(s):  
R.Z. Mahfouz ◽  
A. Thiyagarajan ◽  
V. Kale ◽  
R.K. Sharma ◽  
E. Sabanegh ◽  
...  

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