Several studies have reported that the plasma testosterone (T) level and semen volume are compensated after hemicastration (HEC) in adult dogs, but that the sperm count is not. Nevertheless, the effects of HEC in prepubertal dogs have not been reported. In this study, HEC was performed at 16 weeks of age in 8 male beagles, and the function of the residual testis was investigated until 48 weeks of age. The testis volume was consistently higher in the HEC group than the control (CON) group. After 40 weeks of age, compensatory hypertrophy was observed, with a mean testis volume of 125% of that in the CON group (p<0.05). Furthermore, the semen volume and plasma testosterone (T) level were similar to those in the CON group, suggesting functional compensation, but the sperm count was not compensated. These results showed that the testis volume, semen volume, and plasma T level were compensated after HEC in prepubertal dogs, but the spermatogenic function was not.

In the present study, we investigated the effect of various carbohydrates on the ability of bovine spermatozoa to bind to the bovine oviduct epithelial cells (OECs). We also examined the fertilization competence and motility of spermatozoa that bind to OECs in the presence of carbohydrates. Frozen-thawed spermatozoa were incubated with OECs, with and without various carbohydrates. The sperms were then divided into two fractions: OEC-binding sperms (B-sperm) and non-OEC binding sperms (NB-sperm). The fertilization rate, ability to bind the zona pellucida, and membrane integrity of the spermatozoa as determined using a hypo-osmotic-swelling test (HOST) were lower in NB-sperm than in the unseparated spermatozoa (control). The motility of the B-sperm was maintained for a longer time than that of the control spermatozoa. The addition of N-acetyl-d-glucosamine (GlcNAc, 5 mm) to the sperm-OEC mixture increased the number of B-sperm. D-mannose (5 mm) and D-fucose (5 mm) had no effect on the number of B-sperm. The motility of B-sperm, which bound to OECs in the presence of GlcNAc, however, was not maintained. When either OECs or the spermatozoa were treated with GlcNAc prior to sperm-OEC co-incubation, only sperm-side treatment enhanced sperm-OEC binding, but B-sperm motility was not maintained. The motility of spermatozoa incubated with GlcNAc was lower than that of controls. These results indicate that GlcNAc enhances sperm binding to OECs, probably via sperm surface modification, but does not promote increased sperm survival.