The role of mesencephalic tegmentum in regulating female rat sexual behaviors

Feminine sexual behaviors were tested in estradiol benzoate (EB) and progesterone (P) primed ovariectomized rats following four types of radiofrequency lesions in the midbrain tegmentum. The dorsomedial lesion (DML) which destroyed the ventromedial central gray including the dorsal raphe nucleus and adjacent area induced high sexual receptivity in the females primed with low dose (0.5 micrograms) of EB-P. All females with DML exhibited lordosis and ear wiggling, the mean lordosis quotient (LQ) being significantly higher than that of castrated controls or sham operated rats. Sexual receptivity in females with ventromedial tegmental lesion was not significantly different from those of the control and sham groups. In contrast to the medially lesioned groups, the mean LQ was low in the animals with bilateral lateral tegmental lesions even when the dose of EB was increased to 2 micrograms which was sufficient to induce high sexual receptivity in castrated and sham operated control females. In the animals with dorsolateral tegmental lesions (DLL), a much more severe loss of lordosis was seen than in those with ventrolateral tegmental lesions (VLL). None of the DLL females displayed sexual behavior throughout the present experiments. These results lead us to conclude that the midbrain dorsomedial tegmental area (ventral central gray and the adjacent area) is concerned with female sexual behavior inhibiting system, whereas the lateral tegmental area may be involved in the facilitatory system.     

Forebrain and lower brainstem participation in facilitatory and inhibitory regulation of the display of lordosis in female rats

Neural transection of the dorsal extrahypothalamic descending afferents by means of an L-shaped Halász knife at the anterior commissure (anterior roof deafferentation. ARD) markedly potentiated the display of lordosis and soliciting behaviors. Bilateral lesions of the ventromedial hypothalamus (VMH) attenuated lordotic activity in the ARD sham females but not in the ARD females. In contrast, the lesions in the pontine central gray concurrently with ARD effectively inhibited the display of lordosis but not soliciting behaviors. These results suggest that the VMH may not be a primary focus of the dorsal extrahypothalamic inhibitory influence on lordosis. The influence of this inhibitory system seems to be dominant in regulating the expression of lordosis behavior, compared to that of the hypothalamic lordosis facilitating system. Furthermore, the dorsal extrahypothalamic inhibitors influence which could be removed by ARD must be modified by the neural mechanism in the lower brain stem in which the pontine central gray may be actively involved.     

Sexual behavior of male and female septal lesioned rats

Gonadectomized male and female rats were given septal lesions (SL) or sham surgery at approximately 60 days of age. After 3 weeks lordosis behavior tests were initiated. Females were tested after daily injections of 2 μg estradiol benzoate (EB) for 3 days, while males were tested after EB only (2 μg×3 days), and after EB plus progesterone (Prog). The mean lordosis quotients (LQ) of septal lesioned female rats were significantly higher than those of sham operated controls. No increase in lordosis responding was seen in male rats with either EB alone or EB+Prog. Following an additional 3 week interval without steroid treatment masculine behavior tests began. All animals received a pretest and were tested again on Day 4, 7, 11 and 15 daily tesosterone propionate (150 μg/day) treatment. No alterations in masculine sexual behavior (relative to that of controls) were found in either male or female septal lesioned rats. It is concluded that the increased hormone sensitivity is specific for lordosis behavior, at least when the SL are given in adulthood.     

Lesions of the mesencephalic central gray depress ultrasound production and lordosis by female hamsters

Lesions of the mesencephalic central gray (SGC) were used to examine the role of this structure in the control of ultrasound production and lordosis by female hamsters. Rates of ultrasound production by ovariectomized, hormone-primed, females were observed in separate tests with stimulus ultrasounds and males. The postoperative ultrasound rates of females with SGC lesions were compared with preoperative rates for the same females and with postoperative call rates of females with sham lesions. SGC lesions consistently caused decreases in rates of ultrasound production. These changes were most pronounced in tests with stimulus males, and in females with extensive damage to the caudal SGC. The females also were tested for lordosis using manual stimulation and stud males. The incidence of lordosis decreased significantly following SGC lesions, though some lesioned females continued to show lordosis of normal latency and duration. These results suggest that the SGC may help to integrate ultrasound production with other hormone-dependent reproductive behaviors.     

Bulbectomy and sensitivity to estrogen: Anatomical and functional specificity

In order to clarify the influence of the olfactory system on female sexual behavior, ovariectomized rats were given sham operations (SHAM), total bilateral olfactory bulbectomy (TBULBX), partial bulbectomy (PBULBX), anterior olfactory nucleus lesions (AON) or accessory olfactory bulb lesions (AOB), and tested for lordosis behavior. Only TBULBX resulted in increased sensitivity to estradiol benzoate (EB) in that lordosis quotients (LQ) were increased and rejection behavior decreased following administration of 2, 4 or 8 μg EB/kg/day for 3 days. Only TBULBX group rats were anosmic on 2 postoperative tests. TBULBX group rats showed very mild hyperresponsiveness on an emotionality test. Effects of TBULBX on LQ are not due to general sensory hyperresponsiveness or EB-induced hyperresponsiveness since no differences in the quality of lordosis occurred, and no differences occurred in latency to paw-lift on hot plate tests with or without EB. Heightened EB sensitivity in the TBULBX group is not due to adrenal steroids since following adrenalectomy and 8 μg EB/kg treatment, TBULBX group LQ scores were still elevated relative to those of SHAM controls. The LQ scores of PBULBX group rats were intermediate to those of SHAM and TBULBX group rats. Bulbectomy-induced alterations in sensitivity to EB as measured by the LQ do not appear to be due to alterations in “arousal” mechanisms in general. While deficits in olfactory perception might exacerbate the effect, it is unlikely that anosmia per se is sufficient to induce major alterations in the degree of sexual receptivity following EB. The magnitude of behavioral effects of bulbectomy on EB sensitivity may be related, to some extent, to the amount of bulb tissue removed. It is possible that bulbectomy may enhance behavioral sensitivity to EB by disrupting biochemical responses to EB in limbic system structures which normally exert an inhibitory influence over sexual receptivity.     

Inhibitory and facilitatory neural mechanisms involved in the regulation of lordosis behavior in female rats: Effects of dual cuts in the preoptic area and hypothalamus

Two types of cuts were performed at a 4–5 week interval in the same ovariectomized rats; horizontal half-circle cut located just above the anterior commissure (ARD) and half-dome cut located anterior to the ventromedial nucleus (AD). Behavioral tests were carried out following the pretreatment with estradiol benzoate for 3 days and progesterone on the fourth day. When females received AD first (Experiment 1) the mean LQ was significantly lower than that of controls without brain surgery. Then, the AD rats were subjected to ARD or ARD sham. At the second test, the mean LQ of AD-ARD rats increased to the control level, but the LQ of AD-ARD sham rats was still low. In the experiment 2, the order of the brain surgery was just reversed. In the first test, all ARD females showed high levels of lordosis and the mean LQ was higher than that of control. Then, these ARD females receiving AD or AD sham were subjected to the second test. The mean LQ of ARD-AD rats decreased to the level of the control, but the LQ of ARD-AD sham rats was still high. Thus, dorsal neural inputs to or through the preoptic area and hypothalamus may exert inhibitory influences on a lordosis mediating system and anterolateral outputs of the medial basal hypothalamus appear to be concerned with a lordosis facilitating mechanism. These two systems seem to have a mutual correlation in regulating lordosis response. However, ARD or AD could not completely reverse the suppressive effect of AD or the facilitatory effect of ARD in the animals with dual cuts. It is suggested that the dorsal extrahypothalamic inhibitory influence and the hypothalamic facilitatory influence can regulate the display of lordosis independently in female rats.     

Connections between the pontine central gray and the ventromedial hypothalamus are essential for lordosis in female rats

Lesions and knife cuts were used to study central gray (CG) and ventromedial hypothalamic (VMH) mediation of sexual receptivity in female rats. Lesions of the midbrain-pontine CG eliminated lordosis in female rats. Bilateral sagittal knife cuts that bracketed the rostral pontine CG also eliminated lordosis, and an experiment with the retrograde tracer Fluoro-Gold confirmed the effectiveness of these cuts in severing the lateral connections linking the VMH and the CG. Finally, females with a unilateral hypothalamic cut combined with a contralateral CG transection almost never showed lordosis. Each cut, at a different level for each side of the brain, transected axons linking the VMH and the CG. The demonstration that this combination eliminated lordosis provides new evidence that the lateral connections between the VMH and the CG are essential for the display of sexual receptivity in female rats.     

Effects of ventromedial nucleus lesions on the display of lordosis behavior in the male rat. Interactions with facilitory effects of male urine

Previous observations showed that exposure to the odor of male urine prior to mating could enhance the display of lordosis behavior in male rats feminized with ovarian hormones. This study was performed to determine in feminized male rats whether the control of lordosis behavior by the olfactory system was mediated by the ventromedial nucleus (VMN) of the hypothalamus. Male rats were orchidectomized (ORCH) as adults and primed with 25 micrograms estradiol benzoate (EB) and 150 micrograms progesterone (P) 40 hr apart. Lordosis behavior was tested 9 +/- 1 hr after P injection. VMN lesions were shown to completely suppress the display of lordosis behavior as compared to sham VMN operated and dorsomedial nucleus (DMN) lesioned animals. Exposure of feminized rats to the odor of male urine by 9 +/- 1 hr before mating significantly increased the proportion of ORCH rats that displayed lordosis behavior in response to male mounts. This effect was abolished by VMN lesions but was maintained in the sham VMN operated and DMN lesioned animals. These results were discussed in the light of the present knowledge on the neuroendocrine and olfactory structures which mediate lordosis behavior in the male rat.     

Olfactory,septal and amygdala lesions alone or in combination: Effects on lordosis behavior and emotionality

Ovariectomized female rats subjected to olfactory bulbectomy (OB) and treated with 0.5, 1.0 or 2.0 μg estradiol benzoate (EB) per day for three days showed a dose-related increase in lordosis behavior similar to that of septal lesioned (SL) rats, and relative to the response of sham operated controls. Animals with dual lesions (SL + OB) also showed increased behavioral sensitivity to estrogen, but the lesion effects were not additive. Rats given amygdala lesions (AL) showed levels of lordosis behavior comparable to that of sham animals following 2 μg EB per day for 3 days. However, AL attenuated the SL induced increase in lordosis behavior in animals given dual lesions (Sl + AL). All animals were tested for emotionality prior to surgery and on Postsurgical Days 1, 3, 7, 14, 21 and 42. Only the SL rats showed increased emotionality, and this increase was unrelated to the facilitation of lordosis behavior. It is suggested that OB and SL may exert their effects on lordosis behavior via a common neural pathway or system. Since AL reduced behavioral sensitivity to estrogen in SL rats, the amygdala may be a part of the neural system mediating the increased sensitivity to estrogen in SL rats.     

Role of the ventromedial nucleus of hypothalamus in the male-induced enhancement of lordosis in female rats.

The involvement of the ventromedial nucleus of the hypothalamus (VMH) in the mating-induced enhancement of lordosis in ovariectomized estrogen-primed rats was investigated. In the first experiment, females with bilateral VMH or sham lesions were primed with 2 micrograms estradiol benzoate, and 48 h later they were subjected to repeated-mating tests. The VMH-lesioned rats failed to exhibit lordosis during the tests; however, the sham-operated females exhibited a gradual increase in lordosis quotient (LQ) with repetitive matings. In the second experiment, ovariectomized females were bilaterally implanted with estradiol (E2) or cholesterol (C) in the VMH, 48 h prior to behavioral testing. Repeated-mating-induced elevation in LQ was observed in the females when they were bilaterally implanted with E2 in the VMH; C was ineffective. To exclude the possibility of the spread of E2 to areas adjacent to VMH, plasma-luteinizing hormone (LH) was measured. Elevation in the circulating LH levels following ovariectomy was not suppressed in the females following bilateral E2 implants in the VMH, suggesting that the effect of estrogen is localized within or immediately around the VMH. The results suggest that the integrity of the VMH is critical for the potentiation of lordosis behavior in ovariectomized estrogen-primed females by male-originating sensory cues, and that selective priming of the VMH with estrogen is sufficient for the male-induced enhancement of lordosis.     

Mesencephalic mechanisms for integration of female reproductive behavior in the rat.

Placement of bilateral electrolytic lesions in the mesencephalic central gray (CG) of estrogen-primed ovariectomized female rats produced an immediate decline in performance of the lordosis reflex. Lesions that destroyed the dorsal half of the CG and the adjacent subtectal region were effective. The decrease in individual animals in terms of the lordosis reflex score ranged from 20 to 100% of the prelesion performance. Such lesions abolished the facilitation of lordosis by electrical stimulation of the ventromedial nucleus of the hypothalamus. Similar abrupt losses of lordosis followed bilateral lesions of either a) the area between CG and the cuneiform nucleus of the mesencephalic reticular formation (NCf); or b) the ventrolateral quadrant of the NCf. The difference between these two lesions was that the effect of the latter could be overridden by electrical stimulation of the CG, whereas that of the former could not. We conclude that the CG is an important supraspinal component of the circuit for lordosis behavior, constituting a link between ascending somatosensory and descending motor systems for lordosis. It probably facilitates lordosis when activated by behaviorally relevant peripheral somatosensory and/or ventromedial hypothalamic inputs.     

Effects of stimulus female on sexual behavior of male rats given olfactory tubercle and corticomedial amygdaloid lesions

Lesions of the olfactory tubercle (OT) or corticomedial amygdala (CMA) damaging projections from the main or accessory olfactory bulbs, respectively, were made in male rats. When paired with ovariectomized females treated with estradiol benzoate (EB) and progesterone (Experiment 1) sexual behavior of lesioned males did not differ from sham and unoperated controls. During Experiment 2 males were paired with females chronically treated with EB only. Lesions of the OT did not affect mating while CMA lesions produced lengthened ejaculatory latencies (EL), longer mean interintromission intervals and more intromissions per ejaculation. Lesions of the CMA produced EL which were either within a normal range or noticeably extended with ejaculatory deficits becoming more exaggerated through three ejaculatory series. Low levels of soliciting by EB treated females seemed to precipitate ejaculatory deficits.     

Lordosis in male rats: the facilitatory effect of mesencephalic dorsal raphe nucleus lesion.

The dorsal raphe nucleus was destroyed (DRL) by a radiofrequency lesion generator in castrated male rats, and lordosis behavior was observed. Five weeks after the surgery, all animals were implanted with two Silastic tubes containing estradiol (E2). Behavioral tests were started 2 days after implantation of E2 and carried out every other day for 16 days. Castrated control and sham-operated control males showed low incidence of lordosis and low lordosis quotient (LQ) throughout the tests, whereas all the DRL males displayed lordosis and the mean LQ of the group was significantly higher than that of control groups, but lower than that of an ovariectomized female group. These results suggested that the dorsal raphe nucleus plays an important role in inhibiting lordosis in male rat brain.     

Medial prefrontal cortex lesions in the female rat affect sexual and maternal behavior and their sequential organization

Temporal sequences of sexual and maternal behaviors in female rats and their correlation with each other and with performance on a sensory-motor gating response inhibition task assessed by prepulse inhibition (PPI) were investigated following medial prefrontal cortex (mPFC) lesions. Following excitotoxic mPFC (n = 10) or sham (n = 9) lesions, sexual behaviors across the ovarian cycle were scored. After mating and parturition, maternal interactions were scored until pups reached postnatal Day 10. After resumption of the ovarian cycle, the female rats were tested for PPI. Compared with sham lesions, mPFC lesions impaired proceptive behaviors and some maternal behaviors (e.g., pup retrieval, pup licking) but did not affect others (e.g., nest building, pup mouthing). Lesions disrupted temporal sequences of solicitations (number of male orientations followed, within 4 s, by a level change) and pup retrievals (number of pup retrievals followed, within 5 s, by another retrieval). These sequential behavior patterns were significantly correlated with each other and with PPI. However, when PPI effects were partialled out, group differences were less strong, but persisted. This study demonstrated that mPFC manipulations affect actions rich in sequential structure in response to biologically relevant stimuli.     

GABA(A) receptor regulation of kyphotic nursing and female sexual behavior in the caudal ventrolateral periaqueductal gray of postpartum rats

Bilateral lesions of the ventrolateral caudal periaqueductal gray inhibit lordosis and kyphosis, the postures of female sexual receptivity and maternal nursing that are characterized respectively by dorsoflexion and ventroflexion of the spinal column. These lesions also inhibit the solicitation behaviors that accompany lordosis, but they do not impair retrieval or licking of pups. We tested the hypothesis that reproductive behaviors affected by these lesions are tonically inhibited by activity of the GABA(A) receptor via site-specific manipulations of receptor activity. Rats were bilaterally implanted during pregnancy with guide cannulae aimed at the caudal periaqueductal gray and ovariectomized on day 1 postpartum. Microinfusions (0.25 microl/side) of saline or drug took place on days 5 and 7 postpartum into the dorsolateral column and on days 9 and 11 into the ventrolateral column. Five minutes post-infusion dams were reunited with their pups and their maternal behavior was observed for 30 min. Feminine sexual behaviors were evaluated post-weaning after another set of microinfusions in the ventrolateral caudal periaqueductal gray. Potential facilitation of kyphosis and lordosis was tested with the GABA(A) antagonist bicuculline (15 ng/side) during sub-threshold conditions, i.e., non-suckling pups or sub-threshold ovarian hormone dosages; potential inhibition of these postures was tested with the GABA(A) agonist muscimol (125 ng/side) during optimal conditions, i.e., suckling pups or supra-threshold ovarian hormone treatments. Dorsolateral drug manipulations were ineffective. In the ventrolateral periaqueductal gray bicuculline significantly increased and muscimol significantly decreased kyphosis, lordosis, and sexual solicitations compared with saline. Retrieval and licking of pups were not altered by GABA(A) manipulations. These findings suggest that the reproductive postures of female rats, lordosis and kyphosis, as well as sexual solicitations, are tonically inhibited by the neurotransmitter GABA within the ventrolateral caudal periaqueductal gray in the midbrain. In contrast, retrieval and licking of pups appear to be under separate neurochemical or neuroanatomical control, or both. Further, this tonic inhibition is likely relieved by excitatory somatosensory inputs to this site, from mounting and suckling respectively.     

Sexual behavior in aged, noncycling female rats

Sexual behavior of 19 month old, noncycling, female rats was evaluated for a period of 8 days. The sexual behavior of 11 aged females revealing constant vaginal cornification (CVC) for 30 days prior to, and during the observation period was variable. Eight of the CVC females showed consistently high lordosis quotients (LQ), whereas 3 showed no lordosis. A significant negative correlation was found between food intake and LQ over the 8 day period. In 8 other aged females, the vaginal smear was characterized by a mixture of both leucocytes and cornified cells, each day, for a period of 30 days prior to, and during the observation period. Lordosis behavior was absent in all females revealing this mixed type (MX) smear when they were tested. At random times after the test period, 3 CVC and 2 MX females showed a vaginal cycle. As the vaginal cycle was observed each female was again tested for sexual behavior. All 5 females were highly receptive when placed with the male during the evening of vaginal proestrus, but not at other times. It is concluded that despite disruptions of regular ovarian cyclicity, aged female rats are still capable of showing a lordosis response.     

Brain transections differentially alter lordosis and ear wiggling of 6-day-old rats

Six-day-old male and female rats display lordosis and ear wiggling in response to tactile stimulation of the flanks and rump, without priming by exogenous estrogen. The involvement of various brain regions in these behaviors, which resemble components of adult female sexual behavior, was examined by making acute transections along the neuraxis from the olfactory tract to the medulla in 6-day-old rats. Four to 5 hr after the transection procedure, pups were tested for lordosis and ear wiggling. Lordosis was severely reduced or eliminated in pups with cuts through the hindbrain or diencephalon (above the level of the mammillary bodies) but was relatively unaffected by cuts through the posterior hypothalamus and rostral tegmentum and by cuts rostral to the anterior hypothalamus. Ear wiggling was disrupted by transections throughout the hindbrain and was facilitated only in females by transections throughout the forebrain (anterior to the mammillary bodies). These data suggest that facilitation from the hypothalamus is required for lordosis in the infant rat and the forebrain inhibitory systems for ear wiggling are functional in female infants by 6 days of age. Similarities and differences between the neural control of lordosis and ear wiggling in infant and adult rats suggest that the infant sex-like behaviors may be precursors of adult female sexual behavior.     

Effects of potassium chloride on sexual behavior and the cortical EEG in the ovariectomized rat

The facilitation of lordosis behavior by the cortical application of KCl has been confirmed. Ovariectomized female rats were injected with estradiol benzoate (EB) for 3 days and then a 15% KCl solution was put into permanent cannulae resting on the cortical dura. Sexual behavior tests were performed 15, 30, 60 and 90 min and 24 hr after KCl application and a lordosis quotient (LQ) was obtained from each 10-mount test. There was a significant increase in the LQ 15 min after KCl application to levels which approached those seen after priming with both EB and progesterone. Although lordosis behavior was facilitated, no EEG changes were found following KCl application in 7 of 9 rats, but there was marked depression of the amplitude of the cortical EEG in the remaining 2. It is concluded that KCl application, a treatment which produces functional decortication by inducing spreading depression, suppresses a cortical inhibitory system for lordosis behavior.     

Area postrema lesions produce feeding deficits in the rat: Effects of preoperative dieting and 2-deoxy-D-glucose

To investigate the possible role of the area postrema (AP) in the control of food intake and body weight, male albino rats were divided into four groups: (a) animals dieted to 80% of their original body weights prior to receiving AP lesions, (b) nondieted animals with AP lesions, (c) animals dieted to 80% prior to receiving sham lesions, and (d) nondieted animals with sham lesions. Lesions of the AP in nondieted rats resulted in hypophagia, hypodipsia and body weight loss followed by recovery of normal intake and maintenance of body weight at a fixed percentage of the sham operated animals' weight. Reducing body weight prior to surgery led to body weight maintenance levels equivalent to those of the nondieted groups. We also tested the animals for sensitivity to glucoprivation caused by intraperitoneal injections of 2-deoxy-D-glucose (2-DG). Injections of 2-DG produced hyperphagia in sham lesioned rats, but not in rats with AP lesions. Our data suggest that the effects of AP lesions on intake and body weight are similar, in several important respects, to the lateral hypothalamic feeding syndrome and to the effects of subdiaphragmatic vagotomy. We discuss the results with respect to hierarchical levels of neural circuitry involved in controlling feeding behavior.     

Effects of REM deprivation on the lordosis response induced by gonadal steroids in ovariectomized rats

Ovariectomized rats were submitted to REM sleep deprivation (REMd) using the water tank technique and their behavioral responsiveness (lordosis) to gonadal steroids was tested. In Experiment 1, animals received 2 micrograms of estradiol benzoate (EB) followed by 2 mg of progesterone (P) 44 hours later. Several REMd periods (12, 72, 96 and 120 hr) were applied, all ending four hr after P. REMd animals showed significantly lower lordosis quotients (LQ) than undisturbed sleep animals regardless of the duration of the deprivation period. In Experiment 2, animals received a single dose of EB (2 micrograms) and were REMd for 120 hours. Animals were tested daily to evaluate their LQ. EB, at this dose level, failed to elicit significant lordosis behavior in undisturbed sleep rats. REMd rats gradually increased their LQ values reaching maximal levels at 72 hours. Adrenalectomized control groups receiving the same hormonal treatment responded similarly to the experimental groups, thus discarding the participation of adrenal steroids in these effects. The present results show that REMd differentially affects the response to E and P in ovariectomized rats, enhancing the former and inhibiting the latter.