Estradiol and progesterone in the control of sexual receptivity in female rats

Estradiol (E₂) and progesterone (P) are both required for induction of sexual behavior in female rats under physiological conditions. Administration of E₂ in brief pulses can induce the behavior in ovariectomized rats. P does not normally exert inhibitory or anti-estrogenic effects on the behavior. The decline of sexual receptivity in ovariectomized E₂+P-treated rats is dependent upon the amount of E₂ and P given but independent on the continued presence of either hormone. Ovariectomized animals treated with a constant amount of E₂ show a behavioral rhythm which is disrupted by hypothalamic lesions and it is suggested that peptidergic neurons in the suprachiasmatic nuclei of the hypothalamus rhythmically inhibit the behavior of ovariectomized E₂-treated rats.     

Male-related chemical cues promote sexual receptivity in the female musk shrew

The role of conspecific chemical cues in the activation of sexual behavior was investigated in the female musk shrew (Suncus murinus). In Experiment 1, virgin female musk shrews were exposed to either clean cages or cages recently vacated by an adult male. Regardless of whether the male used for the sexual behavior test was "familiar" to the female (having spent the 24 h exposure in his vacant cage) or "unfamiliar," females exposed to male-related cues received mounts from males significantly sooner than females exposed to clean cages. In Experiment 2, females housed for 24 h in a cage soiled by an adult male allowed males to mount significantly sooner than females housed in a cage soiled by a castrated male, another female, or a clean cage. These results demonstrate that chemical cues, produced exclusively by adult males, promote sexual receptivity in female musk shrews.     

Effect of novel and familiar mating partners on the duration of sexual receptivity in the female hamster

The lordosis duration of the female golden hamster (Mesocricetus auratus) in response to novel and familiar mating partners was examined. In Experiment 1, females mated to the point of sexual satiation with one male hamster, and following its removal, showed renewed receptivity in response to the introduction of a second male. Upon sexual satiation with the second male, females either received a novel third male or were reexposed to the original male. Total lordosis duration in the third bout in the group receiving a novel male was significantly greater than in the group reexposed to the original male. In Experiment 2, the insertion of a 1-h delay between the second and the third mating partner had no effect on the female's responsiveness, regardless of whether the third male was the original male or a novel male. In Experiment 3, removal of the ovaries followed by hormone replacement treatment (40 micrograms estradiol benzoate, 72 h prior to testing, and 500 micrograms progesterone, 4 h prior to testing) failed to alter the females' ability to discriminate between novel and familiar mating partners. These results demonstrate that females make clear discriminations among individual mating partners, that this can affect sexual receptivity and will continue to do so following a delay of at least 1 h, and that the effect is not mediated by the release of ovarian steroids.     

Role of monoamines in the control by hormones of sexual receptivity in the female rat.

The involvement of indole- and catecholamines in the hormonal regulation of sexual receptivity has been investigated in ovariectomized female rats. Drugs that reduce 5-hydroxytryptamine, dopamine, and adrenaline or increase noradrenaline neurotransmission tended to facilitate the occurrence of estrous behavior in estrogen-treated females, and drugs having opposite effects tended to inhibit receptivity induced by estrogen and progesterone. Estrogen decreased noradrenaline turnover in cortex and brain stem; progesterone enhanced this effect in brain stem but prevented it in cortex. Both hormones tended to block noradrenaline uptake in hypothalamus in vitro. In a schedule used to induce receptivity, estrogen accelerated serotonin turnover, an effect prevented by progesterone. Thus a number of monoamines may be involved in the control by hormones of estrous behavior. Furthermore, hormones affect both amine turnover and uptake mechanisms.     

Central progesterone induces female sexual behavior in estrogen-primed intact males rats

Progesterone induced high levels of female lordotic behavior in 10 of 17 intact, estrogen-primed male rats when it was applied directly to the medial preoptic-anterior hypothalamic area. All 17 males previously had shown lordosis when the serotonergic antagonist methysergide was applied to the same central sites. Few males responded to systemic progesterone and none to intracralial cholesterol. Intradiencephalic Metycaine, a local anesthetic, induced lordosis in eight male that previously had responded to central progesterone. These data indicate that estrogen and progesterone act synergistically to induce lordosis in male rats when progesterone is administered directly to sensitive brain sites.     

Mating-induced inhibition of receptivity in the female golden hamster. I. Short-term and long-term effects

Female golden hamsters (Mesocricetus auratus) which have actively terminated mating with one male will respond in succession to two or more novel males. However, mating with the first male results in a reduction in receptivity shown toward a second male, with the size of the decrease being proportional to the amount of copulatory stimuli provided by the first male. Furthermore, the decreased receptivity shown toward the second male results in his achieving fewer ejaculations. These effects are more pronounced when the second mating occurs 5 min or 8 h after the first mating than when it occurs 1 or 4 h later, suggesting both short-term and long-term inhibitory effects. Copulation with a single male also effects a 40% shortening of behavioral receptivity. In a promiscuous species such as the hamster, prolonged copulation by the male may enhance the short-term inhibition of female receptivity, thereby reducing the risk of subsequent sperm displacement. The long-term effect occurs too late to affect sperm competition and may, instead, function to reduce the risk of predation as a result of unnecessary further mating.     

Evidence that a factor besides progesterone, prolactin, or plasma-estradiol-binding protein inhibits estrogen-induced sexual receptivity in pregnant rats.

Daily administration of estradiol benzoate stimulated significantly less lordotic behavior in rats during the second half of pregnancy than in ovariectomized females that received subcutaneous progesterone implants, pituitary grafts that raised plasma prolactin, or both treatments combined. Following an initial facilitation of receptivity, females with progesterone implants showed only moderate reductions in lordosis quotients over 3 test days. The capacity of plasma from pregnant rats to bind estradiol was found to increase significantly during the second half of pregnancy. However, daily administration to pregnant rats of a synthetic estrogen, R 2858, which is not bound by plasma protein, was no more effective than estradiol benzoate in stimulating receptive behavior. Administration of estradiol benzoate also stimulated significantly lower levels of sexual behavior in pregnant females than in females in which pseudopregnancy had been prolonged by previous hysterectomy or induction of uterine decidualization. These findings suggest that some endocrine factor other than progesterone, prolactin, or estradiol-binding protein is primarily responsible for the potent suppression of behavioral responsiveness to estrogen which occurs in pregnant rats. It is suggested that 5 alpha-reduced androgens may cause these behavioral effects.     

Initial psychological effects of sexual abuse on female children as reflected in the Hand Test

Previous research regarding the initial effects of sexual abuse on children has varied in terms of methodologies, measurement instruments, and reported findings. Recent studies, however, suggest that projective techniques may be useful in resolving some of these inconsistencies. This study utilized the Hand Test to investigate the initial effects of sexual abuse on female children. Authenticated cases of sexually abused children were compared to a matched sample of presumably nonabused children. Significant differences on six variables were obtained between the groups but, more important, Hand Test patterns emerged which appeared to distinguish among those victims who: (a) were severely traumatized by the abuse, (b) displayed neurotic tendencies, and (c) did not seem to have suffered measurable detrimental effects. It was suggested that these findings may help reconcile conflicting views that have appeared in the literature.     

Perinatal bromopride treatment: effects on sexual behavior of male and female rats

Effects of different perinatal bromopride treatments on sexual behavior were examined in adult male and female rats of Wistar origin. Female rats of mothers treated with bromopride (BRO) during lactation (VB group) and during pregnancy and lactation (BB group) showed lower lordosis quotients than those of controls (VV group). Females of mothers treated with BRO only during pregnancy (BV group) showed no differences in lordosis quotient when compared to the VV group. There were no significant differences in male sexual behavior between experimental and control groups. The effect of bromopride on the control of sexual behavior is discussed.     

Peer victimization in adolescence has different effects on the sexual behavior of male and female college students

We studied levels of peer victimization from an evolutionary perspective by investigating self-reported victimization during adolescence in relation to sexual behavior in college students. One-hundred and twelve (47 female) undergraduates completed self-report measures of victimization during middle and high school, onset of sexual activity, and number of sexual partners. Nearly 85% of victimization during adolescence was perpetrated by members of the same sex. Furthermore, results show that this intrasexual victimization (particularly indirect forms) was negatively correlated with reproductive opportunities in males, but positively correlated in females. Males who were frequently victimized had fewer total sexual partners and partners per year on average, while females who were often victims of aggression reported having more sexual partners and an earlier onset of sexual activity. Regression analysis revealed that demeaning, diminishing and embarrassing was the most significant predictor of the rate of sexual activity in both sexes (although this relationship was inverted between them), while teasing was the best predictor of total sexual partners in females. This evidence is consistent with evolutionary interpretations regarding human aggression and competition, as well as with recent findings suggesting that indirect victimization during adolescence is a form of intrasexual competition associated with reproductive opportunities.     

Evaluation of prenatal androgen and ovarian secretions on receptivity in female and male rats

Offspring of rats infected daily from Day 16 through Day 20 of gestation with either 2 mg of testosterone propionate (TP) in .1 ml of sesame oil or oil alone were tested for sexual receptivity following injections of 3.3 microgram of estradiol benzoate (EB) and .5 mg of progesterone (P) beginning at 40, 80, or 120 days of age. At each age, neonatally gonadectomized males and females from TP-injected litters exhibited less receptivity than corresponding oil-injected controls. Prenatally androgenized females were similar to neonatally castrated oil-injected males at all ages. Ovarian implants from birth to 35 days of age significantly increased receptivity in neonatally castrated males and androgenized females. Increasing the age at which testing was initiated systematically reduced receptivity in all groups.