8 research outputs found

    Type III antifreeze protein (AFP) improves the post-thaw quality and in vivo fertility of rooster spermatozoa

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    [EN] Antifreeze proteins (AFP) have the potential for improving sperm cryopreservation. We have applied Type III antifreeze protein (AFP3) on the cryopreservation of spermatozoa from broiler breeder roosters, aiming to enhance post-thawing quality and fertility. Semen was extended at 37°C in Lake's extender containing AFP3 at 0.01, 0.1, 1, 5, and 10 ”g/mL (no AFP3 as control). Post-thawing sperm assessment included sperm motility (CASA), morphology, membrane functionality by hypoosmotic swelling test (HOST), lipoperoxidation as malondialdehyde (MDA) production, and sperm viability, early apoptosis (phosphatidylserine exposure as annexin V-positive staining in viable spermatozoa), and mitochondrial activity by flow cytometry. Fertility was assessed after artificial insemination (30 hens/treatment). Total and progressive motility, membrane functionality, and mitochondrial activity increased in 0.1 and 1 ”g/mL AFP, compared to control and other concentrations, whereas apoptosis was significantly lower. VAP, VSL, and viability were significantly higher for 1 ”g/mL AFP3 than with the other treatments except for 0.1 ”g/mL (which was not always significantly different from the control or other concentrations), and with abnormal forms being significantly lower. The proportion of fertilized and hatched eggs was also higher for 1 ”g/mL AFP3, with 0.1 ”g/mL also showing significantly higher results than the control, and no differences with other concentrations). In conclusion, 1 ”g/mL AFP3 could improve the post-thawing results of rooster spermatozoa frozen in Lake's extender. According to our results, concentrations between 1 and 0.1 ”g/mL could be similarly efficientSIThis research was supported by a research grant from the University of Tabriz (number 5782

    Explaining Positive Couple Interactions after Myocardial Infarction: A Qualitative Study

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    Background: The quality of marital relationships can impact couples’ cardiovascular health directly and indirectly. Given that communication is essential for a happy marriage and plays an important role in health, this study aimed to explain the positive interactions of couples after myocardial infarction.Methods: The current study was conducted qualitatively with the participation of seven couples (patient and his or her spouse) in teaching hospitals affiliated with Zahedan University of Medical Sciences. Purposive sampling was used to select participants. Then, unstructured in-depth interviews were conducted after obtaining informed consent. The interviews were immediately transcribed and analyzed. MAXQDA 2020 was used to categorize the data, and the method proposed by Elo and Kingas was used for data analysis.Results: The analysis of the data revealed that myocardial infarction could affect the way couples interact through two main themes including empathetic union (acceptance of each other’s true selves, mutual understanding, adjusting expectations, increase in cooperation and joint activities) and optimizing couples’ interactions (mutual care and attention, increase in intimacy, mutual reliance).Conclusion: This study indicated that positive couple interactions affected not only marital relationships but also health status, both directly and indirectly. Therefore, the findings of this study can be used to improve nursing student education and nursing care, and would help to develop educational and supportive interventions for patients and their spouses

    Improvement of post-thawed sperm quality in broiler breeder roosters by ellagic acid-loaded liposomes

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    P. 440–446Liposomes could improve the delivery of substances to sperm. This study was conducted to investigate the effect of the antioxidant ellagic acid and ellagic acid-loaded liposomes on post-thawed sperm quality in broiler breeder roosters. Semen was diluted in Beltsville extender containing ellagic acid or ellagic acid-loaded liposomes (ellagic acid at 0 (control), 0.5, 1, and 2 mM) and cryopreserved. Sperm quality was evaluated post-thawing: motility characteristics (Computer-Assisted Semen Analysis), membrane functionality (HOS test), abnormal morphology, mitochondrial activity (Rhodamine 123), apoptotic status (Annexin V/Propidium iodide), malondialdehyde, and antioxidant activities (glutathione peroxidase (GPx), superoxide dismutase (SOD), and total antioxidant capacity (TAC)). The results showed that 1 mM ellagic acid-loaded liposomes improved total motility, membrane functionality, and viability comparing to 0.5 and 2 mM ellagic acid, 2 mM ellagic acid-loaded liposomes, and control group. Mitochondrial activity was significantly higher for 1 mM ellagic acid-loaded liposomes compared to the rest of the treatments, except 1 mM ellagic acid. Ellagic acid at 1 mM in both forms significantly increased GPx and TAC after freeze-thawing (no significant variation for SOD), and also yielded the lower proportion of apoptotic and dead cells. In conclusion, ellagic acid improved post-thawed sperm quality in broiler breeder roosters. The use of liposomes could further enhance the effects of ellagic acid.S

    Lycopene-loaded nanoliposomes improve the performance of a modified Beltsville extender broiler breeder roosters

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    P. 168-175Antioxidants may ameliorate the effects of the freeze-thawing stress on cryopreserved spermatozoa. Lycopene is an effective antioxidant yet to be tested for rooster sperm cryopreservation and nanoliposomes, a technology recently applied to sperm cryopreservation, could improve conservation and antioxidant delivery to spermatozoa. Therefore, we evaluated the effect of 0.1, 0.2, and 0.3 mM lycopene and lycopene-loaded nanoliposomes (LnL) on the cryopreservation of rooster sperm in Beltsville extender. Post-thawing evaluation included sperm motility, membrane integrity, abnormal morphology, mitochondria activity, apoptotic status, malondialdehyde (MDA) and antioxidant activities: Glutathione peroxidase (GPx), superoxide dismutase (SOD) and total antioxidant capacity (TAC). Total and progressive motility, membrane integrity and mitochondria activity were higher with 0.2 mM lycopene and LnL (P < 0.05), compared to 0.1 and 0.3 mM (lycopene and LnL) and the control group. The 0.2 mM lycopene and LnL showed a lower percentage of apoptotic sperm and increased GPx activity and TAC when compared with the other treatments, and reduced MDA levels when compared to 0.3 mM (lycopene and LnL) and control. Supplementation did not significantly affect activities of SOD or the proportion of abnormal spermatozoa. A fertility trial showed that 0.2 mM lycopene increased the proportion of fertile and hatched eggs in comparison to the control, especially when using nanoliposomes. Therefore, the supplementation of the Beltsville extender with 0.2 mM lycopene could improve the quality of rooster spermatozoa after freeze-thawing, and the combination with nanoliposomes seems promising in order to improve the performance of existing approaches

    Effect of crocin and naringenin supplementation in cryopreservation medium on post-thaw rooster sperm quality and expression of apoptosis associated genes

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    The aim of our study was to examine the effects of crocin (0.5 (C0.5), 1 (C1) and 1.5 (C1.5) mM) and naringenin (50 (N50), 100 (N100) and 150 (N150) mu M) in cryopreservation extender for freezing rooster semen. Sperm motility, viability, abnormalities, membrane functionality, active mitochondria, apoptosis status, lipid peroxidation (LP), GPX, SOD, TAC, the mRNA expression of pro-apoptotic (CASPASE 3) and anti-apoptotic (Bcl-2) genes, fertile eggs, hatched eggs and hatching rate were investigated following freeze-thawing. C1 and N100 resulted in higher (P &amp;lt; 0.05) total motility and progressive motility in comparison to the control group. The C1 and N100 groups improved viability, membrane functionality and reduced lipid peroxidation. We found higher values for active mitochondria with C1 and N100 compared to control group. The C1 and N100 groups showed lower percentages of early apoptosis when compared with control group. Also, C1 and N100 had higher TAC, compared to the control group. The mRNA expressions of BCL-2 in the C1 and N100 groups were significantly higher than that of other treatments. The expression of CASPASES 3 was significantly reduced in C1 and N100 group (P &amp;lt; 0.05) when compared to control group. Significantly higher percentages of fertile eggs, hatched eggs and hatching rate were observed in C1 and N100 compared to the control group. In conclusion, crocin at 1 mM and naringenin at 100 mu M seem to improve the post-thawing rooster semen quality, fertility and could protect the sperm by reducing the pro-apoptotic (CASPASE 3) and increasing anti-apoptotic (Bcl-2) genes
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