Ultrastructural and histological characteristics of the equine endometrium at day 5 post ovulation.

Rapid endometrial adaptations occur with the embryo entering the uterus to create a receptive uterine environment, which is essential for the conceptus' development. The aim of this study was to demonstrate ultrastructural and histological changes of the endometrium at day 5 after ovulation in cyclic and inseminated mares. Mares were daily examined by transrectal palpation and ultrasonographic examination of the reproductive tract until ovulation was detected. In the first cycle, endometrial biopsies from 10 cyclic mares (Cyclic group) were collected on day 5 post-ovulation. In the second cycle, the same mares were inseminated with fresh semen from a fertile stallion (Inseminated group). Intrauterine biopsies were collected on day 5 post-ovulation, and according to sampling moment, inseminated mares were subdivided into two subgroups, those sampled at day 5-5.5 (n = 5) and those sampled at day 5.5-6 (n = 5). Biopsy samples were analyzed through scanning electron microscopy and light microscopy. Inseminated group presented an increase in glandular diameter, decrease in ciliated cell population, and an increase in lymphocyte population, compared to Cyclic group. No differences were observed between both experimental groups in number of micro-ciliated polygonal cells, percentage of flat or protruded cells in the epithelium, amount of secretion over the epithelium, glandular density, glandular luminal diameter, height of the glandular epithelium, amount of intraglandular secretion, blood vessel diameter and number of eosinophils and neutrophils. No differences in any of the variables were detected between subgroups from inseminated mares. These facts lead to the hypothesis that there is some sort of signaling to prepare and adapt the uterus to maintain pregnancy even before embryo arrival. There is also evidence to support an alternative hypothesis suggesting that all of the above mentioned are inflammatory events, resulting from a previous inflammation due to residual seminal effects. The results here presented lead to the conclusion that significant ultrastructural and histological changes of the endometrium occur on day 5 post ovulation in inseminated mares.

Uterine nitric oxide levels and isofluopredone treatment effect in mares susceptible to persistent post-breeding endometritis

Transient endometritis is a normal consequence of breeding and results from uterine contamination with both semen and bacteria. The modulation of the inflammatory response with the use of isoflupredone has been proposed as efficient for the treatment of endometritis by increasing pregnancy rates. The aim of the current study was to determine the effects of isoflupredone on nitric oxide (NO) levels in uterine samples from mares susceptible to persistent postbreeding endometritis, presenting or not the infectious process. Seven consecutive estrous cycles were induced in 11 mares, being the first one used as control (no treatment). All mares were submitted to the following four treatments: treatment 1: control, treatment 2: glucocorticoid (GC) treatment (20 mg isoflupredone acetate) every 12 h, for three consecutive days, treatment 3: infected treatment (intrauterine infusion of 1x109 CFU/ml Streptococcus equi subsp. zooepidemicus), treatment 4: combination of GC + infected treatment (infusion of bacteria 24 h after the first GC treatment). At 12 h after the end of each treatment, uterine samples were collected by flushing and NO was determined. After nitrate reduction, total nitrite was determined by spectrophotometer. No significant differences on nitric oxide concentration were verified by analysis of variance in the different experimental groups. It is concluded that the use of isoflupredone did not alter the nitric oxide concentration in uterine flushing’s from susceptible mares 12 h after treatment.

Uterine nitric oxide levels and isofluopredone treatment effect in mares susceptible to persistent post-breeding endometritis

Transient endometritis is a normal consequence of breeding and results from uterine contamination with both semen and bacteria. The modulation of the inflammatory response with the use of isoflupredone has been proposed as efficient for the treatment of endometritis by increasing pregnancy rates. The aim of the current study was to determine the effects of isoflupredone on nitric oxide (NO) levels in uterine samples from mares susceptible to persistent postbreeding endometritis, presenting or not the infectious process. Seven consecutive estrous cycles were induced in 11 mares, being the first one used as control (no treatment). All mares were submitted to the following four treatments: treatment 1: control, treatment 2: glucocorticoid (GC) treatment (20 mg isoflupredone acetate) every 12 h, for three consecutive days, treatment 3: infected treatment (intrauterine infusion of 1x109 CFU/ml Streptococcus equi subsp. zooepidemicus), treatment 4: combination of GC + infected treatment (infusion of bacteria 24 h after the first GC treatment). At 12 h after the end of each treatment, uterine samples were collected by flushing and NO was determined. After nitrate reduction, total nitrite was determined by spectrophotometer. No significant differences on nitric oxide concentration were verified by analysis of variance in the different experimental groups. It is concluded that the use of isoflupredone did not alter the nitric oxide concentration in uterine flushings from susceptible mares 12 h after treatment.(AU)

Proteomics of endometrial fluid after dexamethasone treatment in mares susceptible to endometritis.

Corticotherapy is a common treatment in mares susceptible to endometritis. Isoflupredone improves pregnancy rates and affects the protein profile of endometrial fluid in comparison to untreated mares. Dexamethasone decreases postbreeding fluid accumulation and uterine edema; however, its effects on the protein profile of the endometrial fluid have not yet been studied. The aim of the present study was to verify the effect of dexamethasone on the protein profile of endometrial fluid, in the presence or absence of infection, from mares susceptible to persistent postbreeding endometritis. Nine susceptible mares aged between 7 and 18 years were used. After checking for signs of estrus, mares were subjected to four treatments: C: mares received no treatment and served as control; D: mares received 40-mg dexamethasone at breeding, with collection of samples after 6 hours; I-6 and I-24: intrauterine infusion of 1 × 10(9)Streptococcus zooepidemicus/mL and samples collected after 6 and 24 hours; I/D-6 and I/D-24: intrauterine infusion of 1 × 10(9)S zooepidemicus/mL and 40-mg dexamethasone, collecting the sample after 6 and 24 hours. All mares were subjected to all treatments. Samples were collected and subjected to two-dimensional electrophoresis and mass spectrometry for the identification of relevant protein spots. Corticotherapy altered the protein profile of the endometrial fluid of susceptible mares, characterized by an increase and/or decrease in the optical density of inflammatory acute-phase proteins. We conclude that the use of dexamethasone in mares with and without infection alters the protein profile of endometrial fluid of susceptible mares.

Recombinant expression and purification of the bovine acidic Seminal Fluid Protein

The acidic Seminal Fluid Protein (aSFP), a 12.9 kDa protein is a maker for bovine semen freezability possibly due to its antioxidant activity and effect on sperm mitochondrial function. However, its precise function on sperm preservation during freezing thaw is poorly understood. The use of recombinant DNA technology allows new approaches on the study of function and structure of proteins, and its production in procaryote systems offers several advantages. The present work describes the recombinant expression of the bovine aSFP and its binding properties. A cDNA library from the bovine seminal vesicle was used as template for amplification of the aSFP coding region. The amplicon was cloned into a pET23a (+) vector and transformed into E.coli BL21 pLysS strain. The recombinant expression was obtained in E coli. One step ion immobilized affinity chromatography was performed, resulting in high yield of purified protein. To determine the bioactivity of the r aSFP, the protein was incubated in different concentrations with 10 7 spermtozoa at 37°C for 5 h. Western blotting and fluorescence microscopy analyses showed the ability of the recombinant aSFP to attach to the spermatozoa. Based on our results, the described method can be used to obtain mg levels of recombinant aSFP.

Effect of corticotherapy on proteomics of endometrial fluid from mares susceptible to persistent postbreeding endometritis.

The objective was to determine the effects of corticotherapy, in the presence and absence of uterine inflammation, on proteomics of endometrial fluid from mares susceptible to endometritis. In 11 mares, estrus was induced seven times with 5 mg PGF(2α) given at 14-day intervals. The first estrus was a control (no treatment). During the third estrus, mares received glucocorticoid (GC) treatment (20 mg isoflupredone acetate) every 12 h, for three consecutive days. The fifth estrus was the Infected treatment (intrauterine infusion of 1 × 10(9) colony-forming unit/mL Streptococcus equi subspecies zooepidemicus). Finally, the seventh was a combination of GC + Infected treatment (infusion of bacteria 24 h after the first GC treatment). At 12 h after the end of each treatment, uterine samples were collected and submitted to two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) for protein separation and mass spectrometry. Both GC treatment and uterine lumen infection induced proteomic alterations in the endometrial fluid of susceptible mares, characterized by an increase, decrease, or both in the relative optic density and/or frequency of inflammatory acute phase proteins (APP), with major alterations occurring when corticotherapy was applied in the presence of an infectious process. Corticotherapy in the presence of infection increased α(1)-antitrypsin (AAT), transthyretin (TT), and actin, but reduced immunoglobulin G, whereas intrauterine infection increased haptoglobin (Hp) and apolipoprotein A-1 (ApoA-1) and decreased transferrin (TF). Infection reduced levels of α(1)-antitrypsin and transthyretin, whereas corticotherapy in the presence of infection increased their frequency. We concluded that GC influenced the immune response, not only as suppressors, but also as enhancers of local defense mechanisms, through an immunomodulatory action. Short-term corticotherapy could be beneficial for treatment of uterine infectious processes in the mare.

Two-dimensional polyacrylamide gel electrophoresis of equine seminal plasma proteins and their relation with semen freezability.

The objective was to evaluate protein profiles of equine seminal plasma using two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and to determine whether any of these proteins were related to semen freezability. Seminal plasma was collected from 10 stallions, of high and low semen freezability, housed at the State Stud of Lower Saxony, and routinely used in AI programs. Twenty-five protein spots were identified from the two-dimensional gel (12%), seven of which were present in all samples (all proteins were identified by MALDI-MS). Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has been used to generate ion images of samples in one or more mass-to-charge (m/z) values, providing the capability of mapping specific molecules to two-dimensional coordinates of the original sample. Of the 25 proteins identified, two spots had greater relative content (P < 0.05) in seminal plasma samples collected from stallions with high semen freezability: spot 5 (80-85 kDa, isoelectric point [pI] 7.54), identified as CRISP-3; and spot 45 (18.2 kDa, pI 5.0-5.2), identified as HSP-2. Conversely, protein content was greater (P < 0.05) in seminal plasma samples from stallions with low semen freezability: spot 7 (75.4 kDa, pI 6.9-7.4), identified as lactoferrin; spot 15 (26.7 kDa, pI 5.51), identified as kallikrein; spot 25 (25 kDa, pI 7.54), identified as CRISP-3; and spot 35 (13.9 kDa, pI 3.8-4.2), identified as HSP-1. In conclusion, there were differences in the seminal plasma protein profile from stallions with high and low semen freezability. Furthermore, CRISP-3 and HSP-2 were potential seminal plasma markers of high semen freezability.

Skim milk-egg yolk based semen extender compensates for non-enzymatic antioxidant activity loss during equine semen cryopreservation

Cryopreservation exposes spermatozoa to stressful conditions, leading to reduced cell viability. Several studies propose that overproduction of reactive oxygen species and decreased antioxidant capacity of semen may increase the damaging effects of the technique. The objective of this work was to evaluate the influence of a skim milk-egg yolk based semen extender on enzymatic and non-enzymatic antioxidant activity in equine semen cryopreservation. Fifteen ejaculates from six fertile Criollo stallions were cryopreserved using a commercial citrate-Hepes, egg yolk, skim milk and glycerol extender. Activities of catalase, glutathione peroxidase and superoxide dismutase and total radical-trapping antioxidant potential were assessed in raw semen, semen diluted in extender and thawed semen. All three enzymes showed higher activities in raw semen than in diluted or in thawed semen (P 0.05). Non-enzymatic antioxidant defenses did not differ among any of the stages in the cryopreservation process (P > 0.05). In conclusion, the present study shows that dilution of semen with skim milk-egg yolk based extender after centrifugation compensates for the non-enzymatic antioxidant protection (but not enzymatic antioxidant defense) lost with seminal plasma removal. The absence of correlation between seminal and antioxidant parameters suggests that the compensation was enough for semen protection against oxidative stress, or antioxidant protection plays a minor role on semen from fertile stallions.

Skim milk-egg yolk based semen extender compensates for non-enzymatic antioxidant activity loss during equine semen cryopreservation EN

Cryopreservation exposes spermatozoa to stressful conditions, leading to reduced cell viability. Several studies propose that overproduction of reactive oxygen species and decreased antioxidant capacity of semen may increase the damaging effects of the technique. The objective of this work was to evaluate the influence of a skim milk-egg yolk based semen extender on enzymatic and non-enzymatic antioxidant activity in equine semen cryopreservation. Fifteen ejaculates from six fertile Criollo stallions were cryopreserved using a commercial citrate-Hepes, egg yolk, skim milk and glycerol extender. Activities of catalase, glutathione peroxidase and superoxide dismutase and total radical-trapping antioxidant potential were assessed in raw semen, semen diluted in extender and thawed semen. All three enzymes showed higher activities in raw semen than in diluted or in thawed semen (P < 0.01), but enzyme activities did not differ significantly between diluted and thawed semen samples (P > 0.05). Non-enzymatic antioxidant defenses did not differ among any of the stages in the cryopreservation process (P > 0.05). In conclusion, the present study shows that dilution of semen with skim milk-egg yolk based extender after centrifugation compensates for the non-enzymatic antioxidant protection (but not enzymatic antioxidant defense) lost with seminal plasma removal. The absence of correlation between seminal and antioxidant parameters suggests that the compensation was enough for semen protection against oxidative stress, or antioxidant protection plays a minor role on semen from fertile stallions.(AU)

BSP A1/A2-like proteins in ram seminal plasma.

The objective of this study was to assess the protein profile of ovine seminal plasma using 2D-PAGE and verify if BSP A1/A2 are present in ovine seminal plasma. Seminal plasma was collected from three mature rams and pooled to eliminate individual differences. Seminal plasma samples were submitted to 2D-PAGE using 12% acrylamide gels. The image analysis software identified 21 protein spots on the air-dried gel, with molecular weight ranging from 15 to 115 kDa and pI 3.2 to 8.7. The most prominent spots were those <30 kDa. The most intensely stained spots were: 3 (18-19 kDa, pI 4.8-5.0), 5 (17-18 kDa, pI 5.0-5.2), 7 (15-16 kDa, pI 6.2-6.4), and 23 (105-108 kDa, pI 6.8-7.0). Three of these spots (spots 3, 5 and 7, respectively) accounted for 41.1% of the relative intensity of the spots of the gels, based on the intensity of the Comassie blue staining. Western blot analysis indicated that spots 3 and 5 were similar to BSP A1/A2 (16.5, pI 4.7-5.0 and 16 kDa, pI 4.9-5.2) identified in Manjunath's studies [Manjunath P, Sairam MR. Purification and biochimical characterization of three major acid proteins (BSP A1, BSP A2 and BSP A3) from bovine seminal plasma. Biochem J 7 (1987) 685-92.], based on the specific reaction of the polyclonal antibody to those spots.

Two-dimensional polyacrylamide gel electrophoresis of bovine seminal plasma proteins and their relation with semen freezability.

The objective of this study was to evaluate the low weight (10-30 kDa) protein profile of bovine seminal plasma using two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and to determine if any of these proteins was associated with semen freezability. Seminal plasma was collected from 16 bulls of high or low semen freezability. Twelve protein spots were identified from the 2D gel (15%); six of these were present in all samples. Of the 12 proteins found, three spots, present in all samples, 3 (15-16 kDa), 5 (16-17 kDa), and 7 (10-12 kDa) had nonsignificant variation among bulls, regardless of their freezability classification. Four proteins were more abundant (P<0.05) in seminal plasma samples collected from bulls with high semen freezability than in samples of bulls with low semen freezability: the spots 3 (15-16 kDa, pI 4.7-5.2), 7 (11-12 kDa, pI 4.8-4.9), 11 (13-14 kDa, pI 4.0-4.5), and 23 (20-22 kDa, pI 4.8-5.2). On the other hand, spot 25 (25-26 kDa, pI 6.0-6.5) was more abundant (P<0.05) on seminal plasma samples from bulls with low semen freezability. The N-terminus sequence of protein 7 was identical to the acidic seminal fluid protein (aSFP). Protein 23 (after trypsin digestion) had structural similarity to bovine clusterin. We concluded that there were differences in the seminal plasma protein profile from bulls with low and high semen freezability; aSFP, clusterin, proteins 3 and 11 may be used as semen freezability markers; and protein 25 was related to low semen freezability.

Incidência de mortalidade embrionária em ovelhas submetidas à inseminaçäo artificial / Embryonic mortality in sheep inseminated artificially

A pesquisa incidiu sobre 170 ovelhas adultas da raça Corriedale, criadas em regime extensivo, sob moderadas condiçöes de nutriçäo, com peso médio de 35-40 kg, divididas em cinco grupos, sendo dois com estro induzido hormonalmente. O trabalho foi efetuado durante as estaçöes reprodutivas de 1986 e 1988, e os animais foram inseminados com sêmen fresco e congelado, pelas vias cervical e intra-uterina, esta mediante laparoscopia. A mortalidade embrionária foi medida indiretamente, pela relaçäo entre o número de fetos e o número de corpos lúteos encontrados nas ovelhas abatidas e que näo retornaram ao estro no prazo de 20 dias. A incidência da mortalidade embrionária mostrou-se equivalente quando se empregou o sêmen congelado pelas vias cervical e intra-uterina. O mesmo ocorreu com o uso do sêmen fresco e congelado pela via cervical, quando se utilizou o estro espontâneo. A mortalidade embrionária foi significativamente maior quando se aplicou sêmen congelado, tanto pela via cervical como intra-uterina, no estro induzido. O tratamento hormonal apesar de lograr aumento da taxa ovulatória näo influiu favoravelmente na prolificidade das ovelhas tratadas näo sendo por isso indicado para rebanhos que näo estejam em condiçöes nutritivas favoráveis

Biometria testicular em ovinos de raças de corte. I. Reprodutores racionados / Scrotal circumference in meat sheep. I. Concentrate suplemented rams

Foram obtidos dados de perímetro escrotal e peso corporal de 666 carneiros apresentados em exposiçöes feiras realizadas nos anos de 1985, 1986 e 1987, das raças Suffolk, Hampshire Down, Ile de France e Texel, com diferentes idades. Os resultados mostraram diferença no perímetro escrotal quanto à idade apenas na raça Hampshire Down. Para todas as raças observou-se correlaçäo significativa entre peso corporal e perímetro escrotal. Os baixos coeficientes de determinaçäo no entanto, näo recomendam o peso corporal como único estimador do perímetro escrotal