9% physiological saline solution), and the physiologic parameters were monitored. The animals were kept in lateral recumbency, and semen was http://www.selleckchem.com/products/LBH-589.html collected using an electroejaculator (Autojac®, Neovet, Campinas, SP, Brazil) connected to a 12 V source. The stimulatory cycle included 10 stimuli in each voltage, starting from 5 V, and followed by a voltage increase in steps of 1 V up to 12 V. Each electrical stimulus lasted for 3 s, with intermittent breaks of 2 s. The stimuli cycle was maintained for a duration of 10 min from the beginning of the procedure. The electroejaculator probe measured 15 cm in length and 1.3 cm in diameter; a length of 12 cm was inserted into the rectum of the male [7] and [8]. The semen

was collected in plastic tubes and immediately evaluated. The semen volume was measured by micropipettes, and the color of the semen was

noted. Sperm motility and kinetic rating (0–5) were assessed immediately by evaluating a sample (5 μL) under light microscopy at 100× and 400× magnification. Brome-phenol blue-stained smears [12] were prepared with 5 μL of semen for evaluating the sperm viability and morphology, using light microscopy (1000×), counting 100 cells per slide. The sperm morphologic defects were classified as primary, when derived from the sperm production in the testes; or secondary, 3-Methyladenine datasheet when originated from the sperm maturation in the epididymis or from the sample manipulation. The same smears were used for acrosome integrity evaluation under phase-contrast

microscopy (400×). Following the initial assessment, a 5 μL semen aliquot was diluted in 10% buffered formalin (1 mL) and the sperm concentration was determined using a Neubauer counting chamber. The functional integrity of the sperm membrane was evaluated by a hypo-osmotic swelling (HOST) test, using distilled water (0 mOsm/L) as the hypo-osmotic solution [28]. Briefly, semen (0.01 mL) was diluted in 0.09 mL hypo-osmotic solution and kept in a water bath at 38 °C. After 45 min, an aliquot of semen was placed on a glass slide, covered by a coverslip, and evaluated by phase-contrast microscopy (400×), counting 100 cells. Sperm with swollen coiled Morin Hydrate tails were considered to have a functional membrane. The ACP® used in the experiment was registered as ACP-116c® for use in the cryopreservation of the collared peccary semen. ACP-116c® is composed of dehydrated coconut water and pH regulators. A vial of ACP-116c® contains 12 g of the product, which must be diluted with 50 mL of distilled water, according to the fabricant’s recommendation (ACP-Biotecnologia, Fortaleza, Brazil). After reconstitution, the extender pH was 7.4 with an osmolarity of 307 mOsm/kg. The semen samples were diluted in ACP-116c® extender with 20% egg yolk, evaluated for motility and kinetic rating, and divided in two aliquots that were equilibrated following different freezing curves. A two-step dilution was conducted and the glycerol was only added to the samples at 5 °C.