Capacitation-like membrane changes and prolonged viability in vitro of equine spermatozoa cultured with uterine tube epithelial cells.

Reliable capacitation of equine spermatozoa has been a major obstacle in the development of equine in vitro fertilization. Experiments were done to compare in vitro capacitation of equine spermatozoa by use of heparin/caffeine, calcium ionophore, uterine tube epithelial cell (UTEC)-conditioned medium, and direct culturing of spermatozoa with UTEC (coculturing). Capacitation-like changes, as determined by chlortetracycline membrane staining patterns, developed with UTEC-conditioned medium and coculturing, equivalent to that with calcium ionophore. Both of these treatments induced more (P < 0.05) capacitation-like changes than did the control, a modified Tyrode's medium. More (P < 0.05) spermatozoa were viable after 24 hours of UTEC coculturing than in the control incubation.

Effect of pulsatile or continuous administration of GnRH on reproductive function of stallions.

Gonadotrophin-releasing hormone (GnRH) was administered subcutaneously to reproductively normal stallions, either in a pulsatile manner (10 micrograms GnRH/2 h; n = 6) or as a continuous infusion (10 micrograms GnRH/2 h; n = 6), and in a pulsatile manner to 9 reproductively abnormal stallions, from February to July, 1988. Hormonal secretion patterns, testicular parameters and semen characteristics were monitored before and during treatment. In general, pulsatile GnRH caused a significant increase (P less than 0.05) in luteinizing hormone (LH) concentrations in the peripheral blood of normal stallions. LH levels also appeared to increase in abnormal stallions but the rise was not significant (P greater than 0.05). Stallions given GnRH by continuous infusion and the untreated control stallions did not show an increase in LH concentrations during the treatment period. None of the treatments resulted in significant increases in peripheral blood concentrations of testosterone, although individual stallions that showed an increase in LH secretion appeared to show some increase in testosterone secretion rate. In general, and for individual stallions, none of the treatments resulted in increased total scrotal width, total number of spermatozoa per ejaculate or the percentage of progressively motile spermatozoa in the ejaculate. It was concluded that although pulsatile administration of GnRH may increase the secretion rate of LH and, consequently, testosterone, this adjustment does not increase testicular size or output and motility of spermatozoa.