scholarly journals Seminal Plasma Anti-Müllerian Hormone: A Potential AI-Boar Fertility Biomarker?

Biology ◽  
2020 ◽  
Vol 9 (4) ◽  
pp. 78 ◽  
Author(s):  
Isabel Barranco ◽  
Beatriz Fernandez-Fuertes ◽  
Lorena Padilla ◽  
Ariadna Delgado-Bermúdez ◽  
Asta Tvarijonaviciute ◽  
...  
Keyword(s):  
Seminal Plasma ◽  
Sperm Quality ◽  
Sperm Concentration ◽  
Predictive Biomarker ◽  
Membrane Lipid ◽  
Enzyme Linked Immunosorbent Assay ◽  
Lipid Disorder ◽  
Size Number ◽  
Farrowing Rate

The anti-Müllerian hormone (AMH), a Sertoli cell-secreted glycoprotein that is present in seminal plasma (SP), is considered as a marker of spermatogenesis in humans. This study aimed to evaluate the presence of this hormone in boar SP, together with its putative relationship with sperm quality, function, and in vivo fertility parameters in liquid-stored semen samples. The concentration of SP-AMH was assessed in 126 ejaculates from artificial insemination (AI)-boars (n = 92) while using a commercial Enzyme-Linked ImmunoSorbent Assay (ELISA) kit with monoclonal antibodies specific for Sus scrofa AMH (CEA228Po, Cloud-clone). Sperm quality (concentration, motility, viability, and acrosome damage) and functionality (membrane lipid disorder and intracellular H2O2 generation) were assessed in semen samples at 0 and 72 h of liquid-storage. In addition, fertility parameters from 3113 sows inseminated with the AI-boars were recorded in terms of farrowing rate, litter size, number of stillbirths per litter, and the duration of pregnancy over a 12-month period. The results revealed that the SP-AMH concentration varied widely among boar ejaculates, with no differences among breeds. Moreover, the SP-AMH concentration proved to be a good predictive biomarker for sperm concentration (p ˂ 0.05), but poor for other sperm quality, functionality, and in vivo fertility parameters of liquid-stored semen samples from AI-boars.

scholarly journals Oxytocin in pig seminal plasma is positively related with in vivo fertility of inseminated sows

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Lorena Padilla ◽  
Marina López-Arjona ◽  
Silvia Martinez-Subiela ◽  
Heriberto Rodriguez-Martinez ◽  
Jordi Roca ◽  
...  
Keyword(s):  
Seminal Plasma ◽  
Sperm Quality ◽  
Sperm Count ◽  
Sperm Concentration ◽  
Reproductive Function ◽  
Peptide Hormone ◽  
Large White ◽  
Male Reproductive Function ◽  
Farrowing Rate

Abstract Background Identification of relevant in vivo biomarkers for fertility remains a challenge for the livestock industry. Concentrations of the small peptide hormone oxytocin (OXT), involved in male reproductive function and present in the seminal plasma (SP) of several species could be a robust one. This study characterized concentrations of SP-OXT in ejaculates from boars used in artificial insemination (AI) programs aiming to evaluate its relationship with sperm quality variables and in vivo fertility of their liquid-stored AI-semen. Seminal OXT concentrations (ng/mL) were measured in 169 ejaculates from 61 boars of the Duroc, Pietrain, Landrace and Large White breeds using a direct competitive immunoassay test based on AlphaLISA® technology. Ejaculate (ejaculate volume, sperm concentration, total sperm count) and sperm parameters (motility, viability, intracellular generation of reactive oxygen species, plasma membrane fluidity) were assessed at 0 h and 72 h in AI-semen samples stored at 17 °C. In vivo fertility included only 18 Large White and Landrace boars whose AI-semen was used to inseminated > 100 sows and evaluated both farrowing rate and litter size of 3,167 sows. Results The results showed that SP-OXT differed between boars and between ejaculates within boar (P < 0.05) but not between breeds (Duroc, Pietrain, Landrace and Large White). Ejaculates with higher SP-OXT concentration/mL (hierarchically grouped; P < 0.001) had larger volume and came from younger boars (P < 0.05). Ejaculates of boars showing positive farrowing rate deviation exhibited higher (P < 0.05) SP-OXT concentration/mL than those with negative farrowing rate deviation. Conclusion The SP concentrations of OXT are boar, ejaculate and age dependent, and positively related with ejaculate volume and farrowing rates of liquid-stored semen AI-doses.

scholarly journals Exploring Seminal Plasma GSTM3 as a Quality and In Vivo Fertility Biomarker in Pigs—Relationship with Sperm Morphology

Antioxidants ◽  
2020 ◽  
Vol 9 (8) ◽  
pp. 741
Author(s):  
Marc Llavanera ◽  
Ariadna Delgado-Bermúdez ◽  
Yentel Mateo-Otero ◽  
Lorena Padilla ◽  
Xavier Romeu ◽  
...  
Keyword(s):  
Antioxidant Enzyme ◽  
Seminal Plasma ◽  
Cell Biology ◽  
Sperm Morphology ◽  
Sperm Quality ◽  
Mammalian Species ◽  
Enzyme Linked Immunosorbent Assay ◽  
Epididymal Maturation

Glutathione S-transferases Mu 3 (GSTM3) is an essential antioxidant enzyme whose presence in sperm has recently been related to sperm cryotolerance, quality and fertility. However, its role in seminal plasma (SP) as a predictor of the same sperm parameters has never been investigated. Herein, cell biology and proteomic approaches were performed to explore the presence, origin and role of SP-GSTM3 as a sperm quality and in vivo fertility biomarker. GSTM3 in SP was quantified using a commercial Enzyme-Linked Immunosorbent Assay (ELISA) kit specific for Sus scrofa, whereas the presence of GSTM3 in testis, epididymis and accessory sex glands was assessed through immunoblotting analysis. Sperm quality and functionality parameters were evaluated in semen samples at 0 and 72 h of liquid-storage, whereas fertility parameters were recorded over a 12-months as farrowing rate and litter size. The presence and concentration of GSTM3 in SP was established for the first time in mammalian species, predominantly synthesized in the epididymis. The present study also evidenced a relationship between SP-GSTM3 and sperm morphology and suggested it is involved in epididymal maturation rather than in ejaculated sperm physiology. Finally, the data reported herein ruled out the role of this antioxidant enzyme as a quality and in vivo fertility biomarker of pig sperm.

294 EFFECT OF SPERMATOZOA MOTILITY ON TRANSFERABLE EMBRYO RATE OF SUPEROVULATED JAPANESE BLACK CATTLE

2009 ◽  
Vol 21 (1) ◽  
pp. 244
Author(s):  
K. Hayama ◽  
M. Takeuchi ◽  
A. Ideta ◽  
M. Urakawa ◽  
M. Sasatani ◽  
...  
Keyword(s):  
Sperm Motility ◽  
Sperm Quality ◽  
Sperm Concentration ◽  
Electronic Systems ◽  
Embryo Production ◽  
Spermatozoa Motility ◽  
Multiple Comparison Test ◽  
Medical Electronic ◽  
D 20

Sperm motility is known to affect fertilization; however, little is known about the relationship between frozen–thawed sperm motility and in vivo fertilization following superovulatory treatment. The objective of this study was to evaluate a sperm function test as potential predictors of embryo production following superovulatory treatment in cattle. Two to five batches of semen (Japanese black bull, n = 4, A to D) were diluted with egg york-citrate-glycerol in 0.5 mL plastic straws, and they were stored in liquid nitrogen until analyzed. Frozen–thawed spermatozoa were evaluated for motility {motile sperm concentration (MSC, million mL–1), progressive MSC (PMSC, million mL–1) and velocity (μm s–1)} using a sperm quality analyzer for bulls (SQA-Vb, Medical Electronic Systems, Caesarea, Israel). Each sample of 20 μL aspirated into the disposable capillary, was inserted into SQA-Vb. Measurements were displayed within 75 s. Intra-assay CVs of MSC, PMSC, and velocity were 14.2, 7.3 and 7.5%, respectively. Inter-assey CVs of them were 13.5, 3.9 and 4.3% respectively. Superstimulated donors (Japanese black cows, n = 161) were artificially inseminated with one dose of frozen–thawed semen (bull A = 74, B = 46, C = 21 and D = 20). The proportion of transferable embryo (IETS grade 1 to 3) was examined on day 7 (day 0 = estrus). Data were analyzed using ANOVA followed by Scheffe multiple comparison test, and Fisher’s z-transformation. MSC, PMSC and velocity values differed significantly among each bull. The values of bull A were much lower than those of the other bulls. The proportion of transferable embryos produced by bull A was significantly lower than that of other bulls (P < 0.05, Table 1). Correlations showed significant association between MSC and proportion of transferable embryos (r = 0.99, P < 0.01). We conclude that bovine sperm motility using a SQA-Vb is a useful predictor of embryo production following superovulatory treatment. Table 1.Relationship between sperm motility and proportion of transferable embryo

scholarly journals Validation of the Turkey Semen Cryopreservation by Evaluating the Effect of Two Diluents and the Inseminating Doses

Animals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 1329
Author(s):  
Michele Di Iorio ◽  
Giusy Rusco ◽  
Roberta Iampietro ◽  
Lucia Maiuro ◽  
Achille Schiavone ◽  
...  
Keyword(s):  
Sperm Quality ◽  
Sperm Concentration ◽  
Membrane Integrity ◽  
In Vivo Test ◽  
Sperm Analysis ◽  
Fertilizing Ability ◽  
Vitro Analysis ◽  
Hatching Rates

This study was designed to test the fertilizing ability of cryopreserved turkey semen, and here, two experiments were performed: an in vitro analysis to assess the effects of Tselutin and Lake diluents and an in vivo test to determine the fertility and hatching rates by also studying the feat of three insemination doses (250, 400 and 600 × 106 sperm/hen). Pooled semen samples were diluted with Tselutin or Lake extender which contained 20% of dimethylsulfoxide and 1 mM of Ficoll at final sperm concentration of 3 × 109 sperm/mL. Thereafter, semen was packaged into straws and frozen on liquid nitrogen. The post-thaw sperm quality was evaluated considering motility (computer-aided sperm analysis—CASA system) and membrane integrity (flow cytometry). Significantly higher values of progressive motility and some kinetic parameters in semen frozen with Lake were found. When we compared the extenders in vivo, no significant effects were detected, whilst sperm concentration significantly affected both fertility and hatching rates, with the best results obtained with the sperm concentration of 400 × 106 sperm/hen. From the results obtained, it emerged that the extender type only affected sperm motility characteristics, not the fertilizing ability of frozen-thawed semen, while inseminating dose markedly affected fertility and hatching rates.

scholarly journals Increased F2-Isoprostane Levels in Semen and Immunolocalization of the 8-Iso Prostaglandin F2α in Spermatozoa from Infertile Patients with Varicocele

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Giulia Collodel ◽  
Elena Moretti ◽  
Mariangela Longini ◽  
Nicola Antonio Pascarelli ◽  
Cinzia Signorini
Keyword(s):  
Fatty Acid ◽  
Sperm Quality ◽  
Sperm Concentration ◽  
Prostaglandin F2α ◽  
Fertility Index ◽  
Idiopathic Infertility ◽  
Prostaglandin F ◽  
Sperm Midpiece ◽  
Infertile Patients

Polyunsaturated fatty acid damages lead to alterations in sperm function. This study aimed to investigate the involvement of F2-isoprostanes (F2-IsoPs), oxidized lipid products from arachidonic acid, in sperm quality impairment. For this purpose, F2-IsoP levels in semen and F2-IsoP localization in spermatozoa were explored in infertile subjects affected by idiopathic infertility or varicocele, as well as in fertile men. As compared to fertile men, in the idiopathic infertility and varicocele groups, sperm concentration, motility, morphology, viability, and fertility index were significantly lower and the mean scores concerning sperm apoptosis, necrosis, and immaturity were significantly higher. The idiopathic infertile group showed a reduction in sperm motility and fertility index, as well as an increase of apoptosis and necrosis percentages, in comparison to the varicocele group. The varicocele group showed the highest levels of F2-IsoPs, a significant increase of sperm immaturity, and a significant correlation between F2-IsoP levels and sperm immaturity. 8-Iso Prostaglandin F2α, biomarker of in vivo F2-IsoP, was clearly localized in sperm midpiece and cytoplasmic residues. Data show that F2-IsoP formation is relevant in semen and sperm from infertile patients with varicocele and high percentage of immaturity, suggesting that a correct fatty acid integrity is needed for sperm maturation.

Development of sperm sexing and associated assisted reproductive technology for sex preselection of captive bottlenose dolphins (Tursiops truncatus)

2006 ◽  
Vol 18 (3) ◽  
pp. 319 ◽  
Author(s):  
J. K. O'Brien ◽  
T. R. Robeck
Keyword(s):  
Tursiops Truncatus ◽  
Sperm Quality ◽  
Bottlenose Dolphins ◽  
Sperm Concentration ◽  
Motility Index ◽  
Liquid Storage ◽  
Directional Freezing

Research was conducted to develop sperm sorting and novel sperm preservation methodologies for sex predetermination in the bottlenose dolphin (Tursiops truncatus) using artificial insemination. In Study 1, the effect of seminal plasma (SP), sperm concentration and freezing rate (FR) on in vitro sperm quality of liquid-stored, non-sorted spermatozoa was examined. There was no effect (P > 0.05) of prefreeze SP addition on post-thaw quality (progressive motility, kinetic rating, sperm motility index (SMI), viability and acrosome integrity). Post-thaw motility parameters and viability were higher (P < 0.05) for slow FR than fast FR samples. In Study 2 investigating the effects of liquid storage and sorting on sperm quality, motility and SMI after sorting and centrifugation were lower (P < 0.05) than those of the initial ejaculate. The sort rate for enrichment (91 ± 4% purity) of X- and Y-bearing spermatozoa was 3400 ± 850 spermatozoa sex−1 s−1. In Study 3, compared with a modified straw method, directional freezing resulted in enhanced in vitro quality of sorted and non-sorted spermatozoa derived from liquid-stored semen (P < 0.05). In Study 4, endoscopic insemination of three dolphins with sorted, frozen–thawed X-bearing spermatozoa resulted in one conception and the birth of a female calf. High-purity sorting of dolphin spermatozoa, derived from liquid-stored semen, can be achieved with minimal loss of in vitro sperm quality and samples are functional in vivo.

scholarly journals The Association between Bisphenol A, Steroid Hormones, and Selected MicroRNAs Levels in Seminal Plasma of Men with Infertility

2021 ◽  
Vol 10 (24) ◽  
pp. 5945
Author(s):  
Ewelina Palak ◽  
Weronika Lebiedzińska ◽  
Sławomir Anisimowicz ◽  
Maria Sztachelska ◽  
Piotr Pierzyński ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Seminal Plasma ◽  
Sperm Quality ◽  
Sperm Concentration ◽  
Circulating Mirnas ◽  
Endocrine Disrupting Chemical ◽  
Endocrine Disrupting ◽  
Healthy Control ◽  
Mirnas Expression ◽  
Semen Morphology

Bisphenol A (BPA), the most common endocrine-disrupting chemical, has been associated with male reproductive dysfunctions. Recently, it has been shown that BPA may also affect miRNAs expression. Herein, we aimed to evaluate the association of BPA levels with steroid hormone concentration and circulating miRNAs levels to investigate the potential direct effect of BPA on homeostasis in the testis environment. The level of BPA in the seminal plasma of azoospermic men was significantly higher compared to the healthy control. The concentrations of estradiol (E2) and androstenedione (A) were significantly decreased in the seminal plasma of azoospermic men compared to the normospermic men. The levels of miR-let-7a, miR-let-7b, and miR-let-7c were significantly up-regulated, and the level of miR-518f was significantly down-regulated in the seminal plasma of the azoospermic men compared to the healthy control. The level of BPA correlated negatively with sperm concentration and normal semen morphology. A significant positive correlation was found between BPA levels and miR-let-7a and miR-let-7c levels, whereas BPA negatively correlated with miR-518f levels. Our results suggest that BPA may negatively affect sperm quality. Moreover, BPA correlated with the miR-let-7a, miR-let-7c, and miR-518f levels in seminal plasma, which suggests that BPA may act directly in seminal plasma, affecting the testicular environment.

326 COMPARING CHANGES IN MEMBRANE LIPID ORDER IN EPIDIDYMAL AND EJACULATED BOAR SPERMATOZOA

2007 ◽  
Vol 19 (1) ◽  
pp. 277
Author(s):  
C. Matas ◽  
F. Garcia-Vazquez, ◽  
M. Sansegundo ◽  
S. Ruiz ◽  
J. Gadea
Keyword(s):  
Plasma Membrane ◽  
Seminal Plasma ◽  
Lipid Membrane ◽  
Calcium Influx ◽  
Membrane Lipid ◽  
Treatment Groups ◽  
Lipid Disorder ◽  
Lipid Order ◽  
Merocyanine 540 ◽  
Boar Spermatozoa

The diffusion of lipids in the plasma membrane of ejaculated spermatozoa is influenced by seminal plasma proteins and the composition of the suspending medium (Wolfe et al. 2001 Mol. Reprod. Dev. 59, 306–313). Merocyanine 540 (M540) is a hydrophobic dye that has been shown to stain cell membranes more intensely if their lipid components are in a higher state of disorder, as is the case of capacitated spermatozoa. It is believed that the membrane fluidity changes detected by M540 precede the calcium influx, making M540 a method for evaluating the early events of capacitation. The aim of this study was to determine if there are differences in the dynamics of lipid disorder in the plasma membrane of ejaculated and epididymal boar spermatozoa under different conditions of capacitation. The sperm capacitation treatments were: washed in Delbucco's PBS supplemented with 0.1 % BSA (PBS-BSA), washed on a Percoll gradient (PG), and unwashed (UW: Control). During measurement, the samples were kept at 38�C and 5 % CO2 to maintain constant incubation conditions. Membrane lipid order and sperm viability were determined by flow cytometry with M540 (2.7 �M) and Yo-Pro-1 (25 nM), respectively. Samples were analyzed on a Coulter Epics XL flow cytometer (Beckman Coulter Co., Inc., Fullerton, CA, USA). A total of 10 000 gated events were collected per sample, with sample running rates of approximately 600 events/s. Data were analyzed by analysis of variance (ANOVA). For the epidydimal vs. ejaculated results, the percentage of low lipid disorder spermatozoa was higher in the epididymal (19.23%) than in the ejaculated (5.84%) groups, and the proportion of high disorder (42.85%) and dead cells (48.59%) was higher in the ejaculated group. In relation to sperm treatment (UW, PBS-BSA, and PG), the percentage of high disorder was similar in all of the treatment groups (UW: 44.62 %; PBS-BSA: 43.08%; PG: 43.41%). Finally, the percentage of low disorder was lower in the PBS-BSA and PERCOLL (10.68% and 12.83%, respectively) groups, and the highest was obtained for the UW group (14.09%). In conclusion, the staining with M540 revealed that the lipid disorder was affected by the source of the sperm and the sperm treatment. A significant increase in membrane lipid low disorder and decrease in high disorder and dead cells were detected when epididymal sperm were compared with ejaculated sperm, so the seminal plasma and the sperm treatment to eliminate disorder have an important effect in the lipid membrane order. Supported by MEC (AGL2006-03495/GAN) and Fundaci�n S�neca (03018/PI/05).

Hydroxy-selenomethionine as an organic source of selenium in the diet improves boar reproductive performance in artificial insemination programs

2021 ◽  
Author(s):  
Ana Paula P Pavaneli ◽  
Cristian H G Martinez ◽  
Denis H Nakasone ◽  
Ana Carolina Pedrosa ◽  
Maitê V Mendonça ◽  
...  
Keyword(s):  
Seminal Plasma ◽  
Reproductive Performance ◽  
Artificial Insemination ◽  
Semen Quality ◽  
Sperm Quality ◽  
Sperm Count ◽  
Dietary Treatments ◽  
Gpx Activity ◽  
Organic Source

Abstract This study aimed to compare different selenium (Se) sources in the diet on boar's semen quality and fertility. For this, 28 boars aged 8 to 28 months were fed with the following dietary treatments for 95 days: 0.3 mg Se/kg as sodium selenite (SS, n = 14) and 0.3 mg Se/kg as hydroxy-selenomethionine (OH-SeMet, n = 14). During this period, two experiments were carried out. In experiment 1, the semen of all boars was evaluated every 2 weeks. Raw semen was initially evaluated for the processing of seminal doses, which were stored at 17 °C for 72 h, followed by sperm quality assessments. Furthermore, Se concentration and glutathione peroxidase (GPx) activity were measured in the seminal plasma. In experiment 2, 728 females were inseminated weekly with seminal doses from boars of the different experimental groups to further assess in vivo fertility and litter characteristics. Results demonstrated that boars fed OH-SeMet had more Se in their seminal plasma (p &lt; 0.05), showing the greater bioavailability of the organic source in the male reproductive system. Moreover, boars fed OH-SeMet tended (p &lt; 0.10) towards a higher total sperm count in the ejaculate (66.60 vs. 56.57 × 10 9 sperm), and the number of seminal doses (22.11 vs. 18.86; 3 × 10 9 sperm/dose) when compared to those fed SS. No effect of the dietary treatments was observed on GPx activity in seminal plasma (p &gt; 0.05), as well as on raw and stored semen quality (p &gt; 0.05). Under in vivo conditions, seminal doses from boars fed OH-SeMet tended (p &lt; 0.10) towards a higher pregnancy rate at weeks 3, 5, and 8, and also resulted in a higher (p &lt; 0.05) percentage of pregnant females in the overall period (99.30 vs. 97.00). In conclusion, the replacement of SS with OH-SeMet in boars' diet can improve sperm production and results in better reproductive performance for them, bringing greater productivity and profitability to artificial insemination centers and commercial pig farms.

scholarly journals HVCN1 but Not Potassium Channels Are Related to Mammalian Sperm Cryotolerance

2021 ◽  
Vol 22 (4) ◽  
pp. 1646
Author(s):  
Ariadna Delgado-Bermúdez ◽  
Yentel Mateo-Otero ◽  
Marc Llavanera ◽  
Sergi Bonet ◽  
Marc Yeste ◽  
...  
Keyword(s):  
Potassium Channels ◽  
Sperm Quality ◽  
Membrane Integrity ◽  
Physiological Role ◽  
Membrane Lipid ◽  
Proton Channels ◽  
Lipid Disorder ◽  
Mammalian Sperm

Little data exist about the physiological role of ion channels during the freeze–thaw process in mammalian sperm. Herein, we determined the relevance of potassium channels, including SLO1, and of voltage-gated proton channels (HVCN1) during mammalian sperm cryopreservation, using the pig as a model and through the addition of specific blockers (TEA: tetraethyl ammonium chloride, PAX: paxilline or 2-GBI: 2-guanidino benzimidazole) to the cryoprotective media at either 15 °C or 5 °C. Sperm quality of the control and blocked samples was performed at 30- and 240-min post-thaw, by assessing sperm motility and kinematics, plasma and acrosome membrane integrity, membrane lipid disorder, intracellular calcium levels, mitochondrial membrane potential, and intracellular O2−⁻ and H2O2 levels. General blockade of K+ channels by TEA and specific blockade of SLO1 channels by PAX did not result in alterations in sperm quality after thawing as compared to control samples. In contrast, HVCN1-blocking with 2-GBI led to a significant decrease in post-thaw sperm quality as compared to the control, despite intracellular O2−⁻ and H2O2 levels in 2-GBI blocked samples being lower than in the control and in TEA- and PAX-blocked samples. We can thus conclude that HVCN1 channels are related to mammalian sperm cryotolerance and have an essential role during cryopreservation. In contrast, potassium channels do not seem to play such an instrumental role.

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