RESUMEN
Supplementing bovine serum albumin-containing medium with phosphatidylcholine (PC) accelerated the in vitro development of human sperm acrosomal responsiveness. Responsiveness was assessed by exposing the sperm to progesterone. The maximum effect was produced by incubation with 100 micrograms PC/ml, which resulted in 40% (23-56%) (mean, 95% confidence limits) of the sperm becoming responsive to progesterone at 24 hours, compared to 23% (10-40%) of control sperm. Enhancement was apparent after as little as 6 hours of incubation in vitro, and the number of responsive sperm was still increasing at the last time point tested (30 hours). PC had no apparent ill effects; it did not alter the percentage of motile sperm or the percentage of sperm stained with the supravital stain, Hoechst 33258. Enhanced responsiveness required prolonged incubation in PC, because PC was not effective when it was only applied at the same time as progesterone. Lysophosphatidylcholine did not enhance acrosomal responsiveness when used at concentrations from 10 ng/ml to 100 micrograms/ml, indicating that the effect of PC was not due to trace amounts of lysophosphatidylcholine. PC also increased the response of sperm to the Ca2+/H(+)-exchanging ionophore, ionomycin, suggesting that PC modifies an event that is coincident with or subsequent to the rise in intracellular free Ca2+ that is triggered by progesterone.
Asunto(s)
Acrosoma/efectos de los fármacos , Fosfatidilcolinas/farmacología , Análisis de Varianza , Medios de Cultivo , Humanos , MasculinoRESUMEN
Mammalian sperm must be acrosome reacted before penetrating the zona pellucida. In some species the sperm undergo the acrosome reaction before binding to the zona pellucida and in other species only acrosome intact sperm can initiate binding to the zona. In this study we addressed the question of acrosomal status and sperm-zona binding with human gametes. Sperm acrosome reactions were induced by treatment with human follicular fluid or N-(6-amino-hexyl)-5-chloro-naphthalene sulfonamide (W-7). The sperm suspensions, containing various percentages of acrosome-reacted sperm, were then incubated with human oocytes for 1 min. The acrosomal status of the sperm population bound to the zona was similar to the acrosomal status of the population of sperm in suspension (R2 = 0.77), regardless of the treatment to induce acrosome reactions. Our interpretation of these results is that both acrosome intact and acrosome-reacted human sperm can initiate binding to the zona pellucida. However, we reported earlier (N. L. Cross, P. Morales, J. W. Overstreet, and F. W. Hanson, 1988, Biol. Reprod. 38, 235-244) that the human zona pellucida is able to induce acrosome reactions. Thus, to exclude the possibility that sperm had undergone the acrosome reaction on the zona within 1 min of binding, sperm were suspended in a nominally calcium-free Tyrode's medium (0 Ca-mTyr) before incubation with oocytes (this medium was supplemented with SrCl2 and spermine to support sperm motility and zona binding). In 0 Ca-mTyr, the proportion of acrosome-reacted sperm on the zona was still highly correlated with the proportion of reacted sperm in suspension, indicating that the sperm were reacted before binding. Evidence that 0 Ca-mTyr effectively inhibited acrosome reactions induced by the zona pellucida was derived from experiments in which sperm were treated with human follicular fluid or control medium and the suspensions were diluted with either 0 Ca-mTyr or control medium.4+ Human oocytes were added for 1 min (pulse) at which time some oocytes were fixed and other oocytes were transferred to sperm-free medium and incubated for 35 min (chase) before fixation. Sperm diluted in control medium, pretreated with either human follicular fluid or control medium, showed a similar increase (40%) in the percentage of acrosome reactions among the zona-bound sperm after the chase. Sperm diluted in 0 Ca-mTyr did not show an increase in the percentage of acrosome-reacted sperm on the zona pellucida after the chase.(ABSTRACT TRUNCATED AT 400 WORDS)
Asunto(s)
Acrosoma/fisiología , Óvulo/metabolismo , Interacciones Espermatozoide-Óvulo , Espermatozoides/fisiología , Zona Pelúcida/metabolismo , Líquidos Corporales/fisiología , Calcio/farmacología , Femenino , Humanos , Masculino , Folículo Ovárico , Motilidad Espermática , Espermatozoides/efectos de los fármacos , Espermatozoides/ultraestructura , Sulfonamidas/farmacologíaRESUMEN
Mice, rats and guinea pigs were exposed to the smoke produced by ignition of a zinc oxide/hexachloroethane pyrotechnic composition, 1 h/day, 5 days/week, at three different dose levels, together with controls. The animals received 100 exposures except for the high dose guinea pigs, which underwent 15 exposures, because of high death rate during the first few days of exposure. The test material had very little effect on weight gain, but there was a high rate of early deaths in the top dose of mice. A variety of incidental findings was seen in both decedents and survivors, but organ specific toxicity was, with one exception, confined to the respiratory tract. The most important of these findings was a statistically significant increase in the frequency of alveologenic carcinoma in the high dose group mice (p less than 0.01) and a statistically significant trend in the prevalence of the same tumour over all dose groups and the controls. A variety of inflammatory changes was seen in the lungs of all species and some appeared to be treatment-related. Fatty change in the mouse liver was more common in the middle and high dose groups than the controls. The aetiology of the tumour incidence is discussed and it is pointed out that hexachloroethane and zinc, as well as carbon tetrachloride, which may be present in the smoke, may be animal carcinogens in appropriate circumstances. Carbon tetrachloride is a known human carcinogen.