Effects of progesterone nanoparticles on the sperm capacitation and acrosome reaction in asthenozoospermia men

Andrologia ◽  
2021 ◽  
Author(s):  
Khadijeh Baranizadeh ◽  
Mohammad Mehdi Mahboobian ◽  
Iraj Amiri ◽  
Heidar Tavilani ◽  
Gholamreza Shafiee
Keyword(s):  
Acrosome Reaction ◽  
Sperm Capacitation

scholarly journals Epidermal growth factor alleviates the negative impact of urea on frozen-thawed bovine sperm, but the subsequent developmental competence is compromised

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Rasoul Kowsar ◽  
Shahrzad Ronasi ◽  
Nima Sadeghi ◽  
Khaled Sadeghi ◽  
Akio Miyamoto
Keyword(s):  
Growth Factor ◽  
Epidermal Growth Factor ◽  
Dna Fragmentation ◽  
Acrosome Reaction ◽  
Developmental Competence ◽  
Ros Production ◽  
Sperm Capacitation ◽  
Bovine Sperm ◽  
Epidermal Growth ◽  
High Level

AbstractUpon insemination, sperm cells are exposed to components of the female reproductive tract (FRT) fluids, such as urea and epidermal growth factor (EGF). It has been shown that both urea and EGF use EGF receptor signaling and produce reactive oxygen species (ROS) that are required at certain levels for sperm capacitation and acrosome reaction. We therefore hypothesized that during bovine sperm capacitation, a high level of urea and EGF could interfere with sperm function through overproduction of ROS. High-level urea (40 mg/dl urea is equal to 18.8 mg/dl of blood urea nitrogen) significantly increased ROS production and TUNEL-positive sperm (sperm DNA fragmentation, sDF) percentage, but decreased HOS test score, progressive motility, acrosome reaction and capacitation. The EGF reversed the negative effects of urea on all sperm parameters, with the exception of ROS production and DNA fragmentation, which were higher in urea-EGF-incubated sperm than in control-sperm. The developmental competence of oocytes inseminated with urea-EGF-incubated sperm was significantly reduced compared to the control. A close association of ROS production or sDF with 0-pronuclear and sperm non-capacitation rates was found in the network analysis. In conclusion, EGF enhanced urea-reduced sperm motility; however, it failed to reduce urea-increased sperm ROS or sDF levels and to enhance subsequent oocyte competence. The data suggests that any study to improve sperm quality should be followed by a follow-up assessment of the fertilization outcome.

scholarly journals Antioxidant effect of Mn2+ on capacitation and acrosome reaction of fresh and chilled cattle bull semen

2012 ◽  
Vol 1 (1) ◽  
pp. 18
Author(s):  
Amrit Kaur Bansal ◽  
Ranjna Sundhey Cheema ◽  
Vinod Kumar Gandotra
Keyword(s):  
Reactive Oxygen Species ◽  
Lipid Peroxidation ◽  
Acrosome Reaction ◽  
Reactive Oxygen ◽  
Antioxidant Effect ◽  
Oxygen Species ◽  
Sperm Capacitation ◽  
Bull Semen

The aim of this paper was to investigate the antioxidant effect of Mn2+ (200 mM) on the sperm capacitation and acrosome reaction of fresh and chilled cattle bull semen. It has been found that Mn2+ supplementation improves (P≤0.05) the motility at 0, 2, 4 and 6 h of incubation. MDA (malondialdehyde), end product of lipid peroxidation, decreases significantly (P≤0.05) with the supplementation of manganese at 0- and 6-hr of incubation both in fresh and chilled semen. Manganese also increases acrosome reaction significantly (P≤0.05) both in fresh and chilled semen at 0, 4 and 6 h of incubation. Therefore, our findings suggest the role of Mn2+supplementation in improving the quality of cattle bull semen by its scavenging property<em> i.e.</em> reduction in the production of reactive oxygen species during its storage at 4°C or incubation at 37°C for capacitation.

scholarly journals Mechanism of sperm capacitation and the acrosome reaction: role of protein kinases

2012 ◽  
Vol 14 (6) ◽  
pp. 816-821 ◽  
Author(s):  
Debby Ickowicz ◽  
Maya Finkelstein ◽  
Haim Breitbart
Keyword(s):  
Protein Kinases ◽  
Acrosome Reaction ◽  
Sperm Capacitation

322 EFFECT OF SODIUM NITROPRUSSIDE ON BUFFALO SPERM CAPACITATION IN VITRO

2007 ◽  
Vol 19 (1) ◽  
pp. 276 ◽  
Author(s):  
L. Boccia ◽  
L. Attanasio ◽  
A. De Rosa ◽  
G. Pellerano ◽  
R. Di Palo ◽  
...  
Keyword(s):  
Sodium Nitroprusside ◽  
Acrosome Reaction ◽  
Production Efficiency ◽  
Control Group ◽  
Sperm Capacitation ◽  
Promoting Effect ◽  
Vitro Fertilization ◽  
Domestic Species ◽  
Frozen Semen

The overall in vitro embryo production efficiency in buffalo is hampered by the poor fertilization rate. It is known that the quality of the frozen semen may affect fertilization efficiency. However, it is not possible to rule out that the process of capacitation, required by spermatozoa to acquire the fertilizing ability, is impaired in the in vitro fertilization (IVF) system. Although several agents have been proven to induce sperm capacitation in vitro, heparin treatment is still the most efficient method in most of the domestic species. There is evidence that capacitation is part of an oxidative process and that nitric oxide (NO) acts as a capacitation inducer in human (Herrero et al. 1999 Biol. Reprod. 61, 575–581) and bovine (Rodriguez et al. 2005 Anim. Reprod. Sci. 85, 231–242) spermatozoa. The aim of the present study was to evaluate whether sodium nitroprusside (SNP), a well-known generator of NO in vitro, improves buffalo sperm capacitation in vitro. Frozen–thawed sperm from a bull previously tested for IVF were treated by swim-up in order to select only the motile population. Spermatozoa were incubated in the presence of 0.01 mM heparin (control group) for 1 h (n = 266), 2 h (n = 270), and 3 h (n = 306), and in the presence of 10 �M SNP for 1 h (n = 302), 2 h (n = 286), and 3 h (n = 260). The concentration of SNP was chosen on the basis of a preliminary dose-response trial (0.1 �M, 1 �M, and 10 �M). Following incubation with these agents, sperm were exposed for 15 min to 60 �g mL-1 of lysophosphatidylcholine, an agent known to induce acrosome reaction only on capacitated spermatozoa. Trypan blue was used first to differentiate live from dead spermatozoa and the dried smears were then fixed in 37% formaldehyde and stained with Giemsa for acrosome evaluation by microscopic examination. The proportion of acrosome-reacted spermatozoa in each group was used to assess the efficiency of capacitation under different incubation conditions. Differences between groups were analyzed by chi-squared test. No dead spermatozoa were found in all groups. Following 1-h sperm treatment with either heparin or SNP, the proportion of acrosome-reacted spermatozoa was similar (35.3% vs. 28.5%, respectively). However, extending the incubation time to 2 h, SNP significantly (P &lt; 0.01) increased the incidence of acrosome reaction compared to heparin (60.1% vs. 44.1%, respectively). Analogously, when the sperm treatment was prolonged to 3 h, SNP gave a significantly (P &lt; 0.01) higher percentage of acrosome reaction compared to the control (68.8% vs. 36.6%, respectively). In conclusion, sperm treatment with SNP for either 2 or 3 h significant improved the efficiency of buffalo sperm capacitation in vitro compared with heparin, that is, the capacitating agent currently used in the IVF system. The promoting effect of SNP indirectly indicates that NO acts as a capacitation inducer in buffalo spermatozoa. Finally, these results suggest the need to evaluate the effect of SNP on the fertilizing capability of buffalo spermatozoa in vitro.

Effect of estrogens on sperm capacitation and acrosome reaction in vitro

2009 ◽  
Vol 81 (2) ◽  
pp. 155
Author(s):  
L. Ded ◽  
A. Dorosh ◽  
P. Dostalova ◽  
J. Peknicova
Keyword(s):  
Acrosome Reaction ◽  
Sperm Capacitation

Effect of freezing-thawing on the expression of mannose-ligand receptors on human spermatozoa: the impact on sperm capacitation and acrosome reaction

Andrologia ◽  
2001 ◽  
Vol 33 (5) ◽  
pp. 272-276 ◽  
Author(s):  
H. Yavetz ◽  
Y. Rosenblat ◽  
L. Yogev ◽  
A. Botchan ◽  
J. B. Lessing ◽  
...  
Keyword(s):  
Acrosome Reaction ◽  
Human Spermatozoa ◽  
Sperm Capacitation ◽  
Ligand Receptors ◽  
The Impact

Potential assays for sperm capacitation in mammals

1994 ◽  
Vol 267 (5) ◽  
pp. C1167-C1176 ◽  
Author(s):  
A. Cohen-Dayag ◽  
M. Eisenbach
Keyword(s):  
Acrosome Reaction ◽  
Proteolytic Enzymes ◽  
Operational Definition ◽  
Common Denominator ◽  
Sperm Capacitation ◽  
Sperm Penetration ◽  
The Common ◽  
Definition Of ◽  
Potential Use ◽  
Egg Coat

Sperm capacitation is an essential process in fertilization. It apparently involves a large number of processes, the common denominator of which is that they donate to sperm the potential to undergo the acrosome reaction, i.e., to release proteolytic enzymes enabling sperm penetration through the egg coat. Although the phenomenon of capacitation has been known for more than 40 years, it is far from understood, and, consequently, there is, as yet, no operational definition of it. The lack of an assay to identify capacitated spermatozoa is both the cause and the effect of this situation. Here we critically review the major changes that are thought to occur during sperm capacitation, and assess their potential use as markers for the identification of capacitated spermatozoa.

scholarly journals Sperm Capacitation and the Acrosome Reaction are Compromised in Teratospermic Domestic Cats1

1996 ◽  
Vol 54 (3) ◽  
pp. 638-646 ◽  
Author(s):  
Julie A. Long ◽  
David E. Wildt ◽  
Barbara A. Wolfe ◽  
John K. Critser ◽  
Robert V. DeRossi ◽  
...  
Keyword(s):  
Acrosome Reaction ◽  
Sperm Capacitation
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