M. Kaabi

Effect of epididymis handling conditions on the quality of ram spermatozoa recovered post-mortem

Post-mortem spermatozoa recovery is an important technique for obtaining germplasm reserves from genetically valuable animals or endangered species. However, there are many factors that influence the outcome of this technique. We have studied the effect of the interval between animals death and sperm recovery (0, 24 or 48 h) on the quality and freezability of ram spermatozoa from cauda epididymidis. Storage temperature of epididymis (room temperature or 5 degrees C) was also analysed. Spermatozoa were diluted with Tes-Tris-Fructose solution supplemented with egg yolk (10%) and glycerol (4%), and frozen using a programmable biofreezer (-20 degrees C/min). Pre-freeze and post-thaw sperm samples showed viable spermatozoa up to 48 h after the animals death, although their quality declined significantly as post-mortem storage time increased. Epididymis sperm stored at 5 degrees C showed better motility and a lower percentage of abnormal forms than epididymis stored at room temperature after 24 and 48 h. The fertilizing ability of cauda epididymis ram spermatozoa obtained at 0 and 24h after the animals death is similar to that of ejaculated spermatozoa. Therefore, a good protocol for post-mortem semen collection in rams when epididymal spermatozoa cannot be collected immediately, is to preserve the epididymis at 5 degrees C and process the samples in the first 24h after the animals death.

Field and in vitro assay of three methods for freezing ram semen

Glycerol has been the most widely used cryopreservation agent for spermatozoa and a wide range of factors affect its action on sperm viability and fertilizing capacity. We tested three methods for freezing ram semen packed in 0.25 ml straws (final cellular concentration: 100 x 10(6) spz/ml). Method M1: Two-thirds of the final volume of diluent was added as solution A (without glycerol) to the pure semen at 35 degrees C. The sample was cooled to 5 degrees C (-0.30 degrees C/min), one-third of final diluent volume was added as solution B (final concentration of glycerol 4%) and the sample was maintained at 5 degrees C for 2h. It was then frozen in a programmable biofreezer (-20 degrees C/min down to -100 degrees C). Method M2: The sample was diluted with a specific solution at 35 degrees C (final concentration of glycerol 3%), cooled to 5 degrees C (-0.20 degrees C/min) and left for 2h. After that, it was frozen in nitrogen vapours. Method M3: Semen was diluted 1:1 in a specific solution (concentration of glycerol 2%) and cooled to 5 degrees C (-0.25 degrees C/min). The sample was then diluted again in the same solution to the final cellular concentration (final concentration of glycerol 4%). It was left for 1h at 5 degrees C and then frozen in a programmable biofreezer (-20 degrees C/min down to -100 degrees C). Best total motility (TM) and progressive motility (PM) (75.8 and 55.18%) were obtained using Method M3. Methods M1 and M3 gave significantly higher values (P<0.05) for kinetic parameters: average path velocity (VAP) (81.3 and 85.2 microm/s), straight-line velocity (VSL) (72.8 and 77.3 microm/s) and linearity (LIN) (66.6 and 68.8%). Method M2 showed the lowest kinetic parameters of motility (VAP 74.4, VSL 67.3 and LIN 62.5) and the highest percentage of cells with damaged plasma membrane (53.8%). Method M1 gave the worst results in viability and acrosome status assessed using fluorescence probes (31.3%-dead cells with damaged acrosomes-versus 25.4% in M2 and 23.3% in M3). A field trial carried out on fertility showed a significantly higher percentage of pregnant or lambing ewes (P<0.05) with Method M3 (67.3% versus 51.1% for M1 and 58.8% for M2). We concluded that the use of a simple dilution medium (test-fructose-glycerol-egg yolk) with the addition of glycerol (to 2% at 35 degrees C and to 4% at 5 degrees C) in two steps together with a programmable biofreezer was a productive method for freezing ram semen.

POST-MORTEM SPERMATOZOA RECOVERY AND FREEZING IN A CANTABRIC BROWN BEAR (URSUS ARCTOS) : A PRELIMINARY REPORT

At present the Cantabric Brown Bear (Ursus arctos), which probably constitutes the last pure breed aggregate of brown bear in the world, is a seriously endangered population (~80 animals are living in a fragmentary area in the North of Spain). The harvesting of gametes obtained post-mortem could be a useful tool in creating a genetic resource bank. The present work is a preliminary report about post-mortem spermatozoa (spz) recovery in a Cantabric Brown Bear (7 years old, 170 kg), died 8 days after an accident in the wilds (3 rd May 1998). The testis was extracted 70 min post-mortem and the epididymis was dissected at 5°C. A sample of gametes was obtained from each epididymis region and deferens ductus (reference of the preejaculatory spermatic cells). The percentage and position of the cytoplasmic droplets (CD) were evaluated as a gamete maturity index (viability prediction).

Design and “in vivo” evaluation of two adapted catheters for intrauterine transcervical insemination in sheep

In order to obtain better fertility, we evaluated two ovine artificial insemination (AI) catheters that were manufactured according to the anatomical structure of the ewe cervix. Morphometric data of the cervix in Churra and Assaf breeds were used to design two types of curved catheters: CAT06 with one curvature and ZIGZAG with five curvatures in a zigzag shape. Two commercial catheters (IMV(®) and Minitüb(®)) were used as controls. In experiment 1, cervical penetration and the degree of reflux were measured in a Cervical AI simulated assay both Churra (n=28) and Assaf ewes (n=28). In experiment 2, a fertility study was performed with three catheters (only one commercial control catheter - IMV) in 465 inseminations (Assaf); and a second study analyzed only the top two catheters (IMV and CAT06) in 428 inseminations (210 Assaf and 218 Churra). The ewes were synchronized using intravaginal sponges (40 FGA mg during 14 days) and 500 IU of eCG. Deeper penetration of the cervix was obtained with the new catheters compared with the commercial ones (1.5, 1.3, 3.5 and 3.2 cm for the IMV, Minitüb, CAT06 and ZIGZAG catheters, respectively). The cervical penetration and the reflux grade of each catheter showed no differences between breeds. In experiment 2, the degree of penetration had no correlation with fertility of different catheters. The best percentage of lambing ewes was obtained with the IMV and CAT06 catheters (39.5 and 48.1%, respectively. vs 27.2% for ZIGZAG catheter, in the Assaf breed). Regarding effect of breed, Assaf (39.3% and 49.5 for IMV and CAT06, respectively) showed better lambing rates than Churra (29.0% and 39.0%, respectively), and the CAT06 catheter showed significantly higher rates for each breed.