scholarly journals THE EFFECT OF FERTILIZATION MEDIA pH ON SPERMATOZOA FERTILIZATION PROCESS AS THE RESULTS OF SEXING ON PANGASIUS (PANGASIONODON HYPOPHTHALMUS)

2021 ◽  
Vol 110 (2) ◽  
pp. 41-49
Author(s):  
Y. Adhitomo ◽  
I. Astuti ◽  
A. Laishevtcev
2009 ◽  
Vol 35 (12) ◽  
pp. 2234-2242
Author(s):  
Ran-Li LI ◽  
Jia-Heng SHEN ◽  
Yuan JIA ◽  
Wei LI ◽  
Li-Ming WANG

2020 ◽  
Vol 158 ◽  
pp. 104951 ◽  
Author(s):  
Nunzia Limatola ◽  
Iacopo Bertocci ◽  
Jong Tai Chun ◽  
Luigi Musco ◽  
Marco Munari ◽  
...  

2000 ◽  
Vol 71 (1-2) ◽  
pp. 381-386 ◽  
Author(s):  
Cinzia Allegrucci ◽  
Lavinia Liguori ◽  
Isabella Mezzasoma ◽  
Alba Minelli

2021 ◽  
Vol 36 (Supplement_1) ◽  
Author(s):  
R Rahban ◽  
A Rehfeld ◽  
C Schiffer ◽  
C Brenker ◽  
D. Louise Egeberg Palme ◽  
...  

Abstract Study question Do Selective Serotonin Reuptake Inhibitor (SSRI) antidepressants affect the function of human sperm? Summary answer The SSRI-antidepressant Sertraline (e.g. Zoloft) inhibits the sperm-specific Ca2+ channel CatSper and affects human sperm function in vitro. What is known already In human sperm, CatSper translates changes of the chemical microenvironment into changes of the intracellular Ca2+ concentration ([Ca2+]i) and swimming behavior. CatSper is promiscuously activated by oviductal ligands, but also by synthetic chemicals that might disturb the fertilization process. It is well known that SSRIs have off-target actions on Ca2+, Na+, and K+ channels in somatic cells. Whether SSRIs affect the activity of CatSper is, however, unknown. Study design, size, duration We studied the action of the seven drugs belonging to the most commonly prescribed class of antidepressants, SSRIs, on resting [Ca2+]i and Ca2+ influx via CatSper in human sperm. The SSRI Sertraline was selected for in-depth analysis of its action on steroid-, prostaglandin-, pH-, and voltage-activation of human CatSper. Moreover, the action of Sertraline on sperm acrosomal exocytosis and penetration into viscous media was evaluated. Participants/materials, setting, methods The activity of CatSper was investigated in sperm of healthy volunteers, using kinetic Ca2+ fluorimetry and patch-clamp recordings. Acrosomal exocytosis was investigated using Pisum sativum agglutinin (PSA) and image cytometry. Sperm penetration in viscous media was evaluated using the Kremer test. Main results and the role of chance Four SSRIs increased [Ca2+]i, two out of which also attenuated ligand-induced Ca2+ influx via CatSper. In contrast, Sertraline decreased [Ca2+]i and almost completely suppressed ligand-induced Ca2+ influx via CatSper. Remarkably, the drug was about four-fold more potent to suppress prostaglandin- versus steroid-induced Ca2+ influx. Sertraline also suppressed alkaline- and voltage-activation of CatSper, indicating that the drug directly inhibits human CatSper. Finally, Sertraline suppressed ligand-induced acrosome reaction and sperm penetration into viscous media. Limitations, reasons for caution This is an in vitro study. Future studies have to assess the physiological relevance in vivo. Wider implications of the findings The off-target action of Sertraline on CatSper in human sperm might impair the fertilization process. In a research setting, Sertraline may be used to selectively inhibit prostaglandin-induced Ca2+ influx. Trial registration number CRU326


2002 ◽  
Vol 56 (1-2) ◽  
pp. 105-110
Author(s):  
Radoslav Dosen ◽  
Mladen Gagrcin ◽  
Jasna Prodanov

In this paper we examined the effects of certain pathological conditions on the sterility of breeding sows. Pathomorphological investigations were performed on 185 reproductive organs. We analyzed the reasons for elimination from local records. The biggest number of sows with pathological changes on reproductive organs were in the group of barren sows, 48.68% followed by anestric sows, 30.26%, and the smallest number in sows with failed fertilizations, 21.05%. Cysts in ovaries, ovarian tubes, oviducts and ?the mesosalpinx were found in 23.77% of the examined sows. Lutein cysts were found in a significantly higher percentage in sows which fail to be fertilized than in barren or anestric animals. Small granular degeneration of the ovaries was determined in barren sows and those which cannot be fertilized, while it was not determined in anestric sows. Cysts on uterus ligaments and ovaries and on ovarian tubes and oviducts were found in significantly higher numbers in sows which fail be fertilized than in barren or anestric sows. Their presence can be connected to obstructions in the transport process of spermatozoa, eggs, and the fertilization process in sows which fail to be fertilized, especially in cases of cysts located on the very serosa of ovarian tubes which we found in these sows. We determined small granular degeneration of the ovaries in barren sows and those which fail to fertilized, but not in anestric sows. Ovarian insufficiency was mostly connected to anestric sows. Vaginitis, endometritis, periometritis and oocytis present an important factor in the occurrence of sterility primarily in sows which are barren or which fail to be fertilized.


2010 ◽  
Vol 5 (2) ◽  
pp. 182-187
Author(s):  
Edwin Widodo ◽  
Aulanni’am Aulanni’am

Zonna pellucidae can be develop as antigen potential candidates based on reversible immunocontraceptive vaccines. Immunogenic sites of bovine zonna pellucidae 3 (bZP3) could stimulated the presence of anti-bZP3 which be located on rabbit ZP and inhibit sperm-egg interaction on fertilization process. Purpose of this research is to detect spesific binding anti-bZP3 to rabbit oocytes using dot blotting and ELISA method. Sub cutan induction of bZP3 with Freund's adjuvant, CFA (Complete Freund's Adjuvant) for initial immunization and following by IFA (Incomplete Freund's Adjuvant) at the 14th day and 39th day. Control female rabbit injected by Tris-Cl buffer diluted in Freund's adjuvant without bZP3 antigen. Rabbit serum injected to rat for producing Rat Anti Rabbit Anti-bZP3. This research concludes spesific binding of anti-bZP3 with increasing purple colour on dot blotting methods. Anti-bZP3 increasing on 24th day and 31th day and still until 48th day. Measurement with ELISA methods showed increased titer on OD405. Highest titer showed on 31th day post immunization. Anti-bZP3 synthetized by bZP3 induced on rabbit detectable by immunohistochemistry methods on late primary oocytes, early secondary oocytes, growing secondary oocytes, and oocytes on de Graaf folicular phase. Keywords: Dot blotting, ELISA, bZP3, anti-bZP3


Genes ◽  
2019 ◽  
Vol 10 (7) ◽  
pp. 522 ◽  
Author(s):  
Selvam ◽  
Agarwal ◽  
Pushparaj ◽  
Baskaran ◽  
Bendou

Up to 30% of men with normal semen parameters suffer from infertility and the reason for this is unknown. Altered expression of sperm proteins may be a major cause of infertility in these men. Proteomic profiling was performed on pooled semen samples from eight normozoospermic fertile men and nine normozoospermic infertile men using LC-MS/MS. Furthermore, key differentially expressed proteins (DEPs) related to the fertilization process were selected for validation using Western blotting. A total of 1139 and 1095 proteins were identified in normozoospermic fertile and infertile men, respectively. Of these, 162 proteins were identified as DEPs. The canonical pathway related to free radical scavenging was enriched with upregulated DEPs in normozoospermic infertile men. The proteins associated with reproductive system development and function, and the ubiquitination pathway were underexpressed in normozoospermic infertile men. Western blot analysis revealed the overexpression of annexin A2 (ANXA2) (2.03 fold change; P = 0.0243), and underexpression of sperm surface protein Sp17 (SPA17) (0.37 fold change; P = 0.0205) and serine protease inhibitor (SERPINA5) (0.32 fold change; P = 0.0073) in men with unexplained male infertility (UMI). The global proteomic profile of normozoospermic infertile men is different from that of normozoospermic fertile men. Our data suggests that SPA17, ANXA2, and SERPINA5 may potentially serve as non-invasive protein biomarkers associated with the fertilization process of the spermatozoa in UMI.


2019 ◽  
Vol 381 (2) ◽  
pp. 179-190 ◽  
Author(s):  
Nunzia Limatola ◽  
Filip Vasilev ◽  
Jong Tai Chun ◽  
Luigia Santella

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