Abstract:Reactive oxygen species (ROS) are generated by sperm metabolism. While, ROS are required for maturation, capacitation and acrosome reaction, they also modify many peroxidable cellular compounds. There is production of ROS during cryopreservation and frozen spermatozoa are highly sensitive to lipid peroxidation (LPO). Antioxidants exert a protective effect on the plasma membrane of frozen bovine sperm preserving both metabolic activity and cellular viability. Manganese (Mn++) is proved to be a chain breaking an… Show more
“…The current results also agreed with Cheema et al [22] who found that the addition of Mn +2 (150 µM) to egg-yolkcitrate extender increased PC individual motility (58.3%) in comparison with those of control group (45%). Similar authors found that the addition of Mn +2 to Tris extender improved PC plasma membrane integrity (30.1%) in comparison with the control group (19.7%).…”
Section: Sajeda Mahdi Eidan Et Al: Influence Of Adding Manganese To supporting
Abstract:This study was conducted to explore the adding effect of manganese (Mn +2 ) to Tris extender on post cooling and cryopreservation semen attributes of Holstein bulls for different periods. Seven Holstein bulls of 3.5-4.5 years old were used in this study. Pooled semen was divided into three groups. The first group was diluted with Tris only (control group, G1). While the 2 nd (G2) and 3 rd (G3) groups were added 0.7 and 0.9 mM Mn +2 respectively. The effect of these additions on Holstein bulls semen quality was studied during different periods (cooling at 5 Celsius, 72 hrs.,1 st , 2 nd and 3 rd post cryopreservation, PC). Addition of Mn +2 led to significant increases of total ( ×10 6 ) plasma membrane integrity of sperms and total function sperm fraction as compared with control groups during cooling and PC periods. It can be concluded that the addition two levels of acid Mn +2 led to enhanced PC semen quality of bulls. This will in turn improved fertility rate of cows and owner's economic income.
“…The current results also agreed with Cheema et al [22] who found that the addition of Mn +2 (150 µM) to egg-yolkcitrate extender increased PC individual motility (58.3%) in comparison with those of control group (45%). Similar authors found that the addition of Mn +2 to Tris extender improved PC plasma membrane integrity (30.1%) in comparison with the control group (19.7%).…”
Section: Sajeda Mahdi Eidan Et Al: Influence Of Adding Manganese To supporting
Abstract:This study was conducted to explore the adding effect of manganese (Mn +2 ) to Tris extender on post cooling and cryopreservation semen attributes of Holstein bulls for different periods. Seven Holstein bulls of 3.5-4.5 years old were used in this study. Pooled semen was divided into three groups. The first group was diluted with Tris only (control group, G1). While the 2 nd (G2) and 3 rd (G3) groups were added 0.7 and 0.9 mM Mn +2 respectively. The effect of these additions on Holstein bulls semen quality was studied during different periods (cooling at 5 Celsius, 72 hrs.,1 st , 2 nd and 3 rd post cryopreservation, PC). Addition of Mn +2 led to significant increases of total ( ×10 6 ) plasma membrane integrity of sperms and total function sperm fraction as compared with control groups during cooling and PC periods. It can be concluded that the addition two levels of acid Mn +2 led to enhanced PC semen quality of bulls. This will in turn improved fertility rate of cows and owner's economic income.
“…Elegant work by Daly and colleagues has shown that tolerance to radiation and oxidative stress in a variety of bacterial species is due to accumulation of high levels of intracellular Mn, but low Fe (Daly 2006(Daly , 2009Daly et al 2007Daly et al , 2010Gross 2007;Granger et al 2011). In higher organisms, Mn treatment can prolong the life span and oxidative stress resistance in the simple metazoan, Caenorhabditis elegans, and also defend against reactive oxygen species (ROS) in the cryopreservation of sperm (Lin et al 2006;Bansal and Kaur 2009;Cheema et al 2009). …”
In aerobic organisms, protection from oxidative damage involves the combined action of enzymatic and nonproteinaceous cellular factors that collectively remove harmful reactive oxygen species. One class of nonproteinaceous antioxidants includes small molecule complexes of manganese (Mn) that can scavenge superoxide anion radicals and provide a backup for superoxide dismutase enzymes. Such Mn antioxidants have been identified in diverse organisms; however, nothing regarding their physiology in the context of cellular adaptation to stress was known. Using a molecular genetic approach in Bakers' yeast, Saccharomyces cerevisiae, we report that the Mn antioxidants can fall under control of the same pathways used for nutrient sensing and stress responses. Specifically, a serine/threonine PASkinase, Rim15p, that is known to integrate phosphate, nitrogen, and carbon sensing, can also control Mn antioxidant activity in yeast. Rim15p is negatively regulated by the phosphate-sensing kinase complex Pho80p/Pho85p and by the nitrogen-sensing Akt/S6 kinase homolog, Sch9p. We observed that loss of either of these upstream kinase sensors dramatically inhibited the potency of Mn as an antioxidant. Downstream of Rim15p are transcription factors Gis1p and the redundant Msn2/Msn4p pair that typically respond to nutrient and stress signals. Both transcription factors were found to modulate the potency of the Mn antioxidant but in opposing fashions: loss of Gis1p was seen to enhance Mn antioxidant activity whereas loss of Msn2/4p greatly suppressed it. Our observed roles for nutrient and stress response kinases and transcription factors in regulating the Mn antioxidant underscore its physiological importance in aerobic fitness.
“…The remainder are common signal transduction and receptor activities. Manganese is an anti-oxidant that prevents the damaging effects of oxidative stress (OS) and has been used to improve the in vitro environment to aid successful IVF or ICSI (Intra Cytoplasmic Sperm Injection) [Cheema et al 2009]. Our results show that the manganese ion transport activity is an important molecular function for sperm-egg interaction that if supressed finally leads to infertility.…”
Elucidation of the sperm-egg interaction at the molecular level is one of the unresolved problems in sexual reproduction, and understanding the molecular mechanism is crucial in solving problems in infertility and failed in vitro fertilization (IVF). Many molecular interactions in the form of protein-protein interactions (PPIs) mediate the sperm-egg membrane interaction. Due to the complexity of the problem such as difficulties in analyzing in vivo membrane PPIs, many efforts have failed to comprehensively elucidate the fusion mechanism and the molecular interactions that mediate sperm-egg membrane fusion. The main purpose of this study was to reveal possible protein interactions and associated molecular function during sperm-egg interaction using a protein interaction network approach. Different databases have been used to construct the human sperm-egg interaction network. The constructed network revealed new interactions. These included CD151 and CD9 in human oocyte that interact with CD49 in sperm, and CD49 and ITGA4 in sperm that interact with CD63 and CD81, respectively, in the oocyte. These results showed that the different integrins in sperm may be involved in human spermegg interaction. It was also suggested that sperm ADAM2 plays a role as a protein candidate involved in sperm-egg membrane interaction by interacting with CD9 in the oocyte. Interleukin-4 receptor activity, receptor signaling protein tyrosine kinase activity, and manganese ion transmembrane transport activity are the major molecular functions in sperm-egg interaction protein network. The disease association analysis indicated that spermegg interaction defects are also reflected in other disease networks such as cardiovascular, hematological, and breast cancer diseases. By analyzing the network, we identified the major molecular functions and disease association genes in sperm-egg interaction protein. Further experimental studies will be required to confirm the significance of these new computationally resolved interactions and the genetic links between sperm-egg interaction abnormalities and the associated disease.
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