Tactile stimulation prevents disruptions in male rat copulatory behavior induced by artificial rearing.

Early life social interactions in gregarious mammals provide an important source of stimulation required for the development of species-typical behaviors. In the present study, complete deprivation of maternal and littermate contact through artificial rearing was used to examine the role of early social stimulation on copulatory behavior and the ejaculate in adult rats. We found that artificially reared naïve male rats were sexually motivated; nevertheless, they did not acquire the level of sexual experience that typically occurs during copulatory training. Disrupted expression of sexual experience of artificially reared rats was demonstrated by an inconsistent pattern of ejaculatory behavior across training tests. Artificial tactile stimulation applied during isolation prevented this disruption and rats achieved ejaculation in most copulatory tests. Despite the irregularity of ejaculatory behavior in isolated rats, their sperm count and seminal plug were similar to control maternally reared (sexually experienced) and artificially-reared rats that received tactile stimulation. These results suggest that tactile sensory information provided by the mother and/or littermates to the offspring is crucial for the development of copulatory behavior. The absence of social and/or tactile stimulation during early life compromises the ability of male rats to gain sexual experience in adulthood.

Threshold for copulation-induced analgesia varies according to the ejaculatory endophenotypes in rats.

Analgesia may be modulated by multiple internal and external factors. In prior studies, copulatory-induced analgesia was demonstrated using the vocalization threshold to tail shock (VTTS) in male and female rats. Three ejaculatory endophenotypes have been characterized in male Wistar rats based upon their ejaculation latency (EL). Since intromissions and ejaculations produce analgesia, and these copulatory patterns are performed with different frequency depending on the male's ejaculatory endophenotype, we hypothesized that copulation-induced analgesia would vary in relation to these endophenotypes. In the present study, we used three groups according to the EL (medians): rapid ejaculators (236 s; n = 21), intermediate ejaculators (663.2 s; n = 20) and sluggish ejaculators (1582.2 s; n = 8). Our aim was to evaluate whether copulation-induced analgesia is related to the ejaculatory endophenotypes during two consecutive ejaculatory series (EJS). In the first EJS, the VTTS of the rapid ejaculators was significantly higher than that of intermediate and sluggish rats. At the onset of the second EJS, the VTTS of the rapid and intermediate ejaculators was significantly higher than that of the sluggish rats. No differences in VTTS were observed during the first or second post-ejaculatory intervals among the three groups. These findings provide evidence that the more intromissions that occurred per unit time, the higher was the level of analgesia.

Anatomical organization and somatic axonal components of the lumbosacral nerves in female rabbits.

AIM: To determine the anatomical organization and somatic axonal components of the lumbosacral nerves in female rabbits. METHODS: Chinchilla adult anesthetized female rabbits were used. Anatomical, electrophysiological, and histological studies were performed. RESULTS: L7, S1, and some fibers from S2 and S3 form the lumbosacral trunk, which gives origin to the sciatic nerve and innervation to the gluteal region. From S2 to S3 originates the pudendal nerve, whose branches innervates the striated anal and urethra sphincters, as well as the bulbospongiosus, ischiocavernosus, and constrictor vulvae muscles. The sensory field of the pudendal nerve is ∼1800 mm2 and is localized in the clitoral sheath and perineal and perigenital skin. The organization of the pudendal nerve varies between individuals, three patterns were identified, and one of them was present in 50% of the animals. From S3 emerge the pelvic nerve, which anastomoses to form a plexus localized between the vagina and the rectum. The innervation of the pelvic floor originates from S3 to S4 fibers. CONCLUSIONS: Most of the sacral spinal nerves of rabbit are mixed, carrying sensory, and motor information. Sacral nerves innervate the hind limbs, pelvic viscera, clitoris, perineal muscles, inguinal and anal glands and perineal, perigenital, and rump skin. The detailed description of the sacral nerves organization, topography, and axonal components further the knowledge of the innervation in pelvic and perinal structures of the female rabbit. This information will be useful in future studies about the physiology and physiopathology of urinary, fecal, reproductive, and sexual functions.

Activity of the external urethral sphincter evoked by genital stimulation in male rats.

AIMS: To determine whether the external urethral sphincter (EUS) fasciculi of male rats respond to the mechanical stimulation of genital structures and to characterize the pattern of the electromyographic (EMG) activity of the three regions of the EUS: the cranial (CrEUS), the medial (MeEUS) and the caudal (CaEUS). METHODS: Electromyographic signals were recorded from the CrEUS, MeEUS and CaEUS regions of the male rat's EUS, before, during and after the mechanical stimulation of the urogenital structures. RESULTS: The CrEUS, MeEUS and CaEUS regions responded when brushing and squeezing the foreskin and glans as well as to penile and prostatic urethral distension. The CaEUS EMG amplitude (P < 0.01) and frequency (P < 0.05) were lower in comparison to the CrEUS and MeEUS responses to the mechanical stimulation. In addition, the CaEUS was characterized by a short or no afterdischarge. In contrast, the CrEUS and MeEUS responded by presenting a long discharge after the penile or prostatic urethral distension. CONCLUSIONS: The activity of the EUS is modulated by both, cutaneous and visceral genitourinary stimuli, with motor units being activated by mechanoreceptors located in the foreskin, glans, bladder, and urethra. The CrEUS, MeEUS and CaEUS have differential EMG patterns, indicating that the EUS consists of three anatomically and functionally different regions. Precise coordination in the muscular activity of these regions may be crucial for the control of male expulsive urethral functions, i.e., during voiding and ejaculation. Neurourol. Urodynam. 35:914-919, 2016. © 2015 Wiley Periodicals, Inc.

Sperm count and sperm motility decrease in old rats.

Sexual behavior declines with age in male rats. The rate and magnitude of this decline may depend on the amount of prior sexual experience and a number of other, unidentified factors. Age-dependent changes in the characteristics of ejaculate quality in rats have not been described earlier, and the relationship between such changes and modifications of sexual behavior is likewise unknown. We have recently developed a technique for the detailed analysis of parameters of ejaculate in rats, and this technique was used for the determination of semen and seminal plug characteristics in rats of different ages. Sexually experienced Wistar rats were tested for sex behavior at the ages of 3, 12 and 24 months. Semen was obtained from the female partner immediately after ejaculation at these tests. Between tests, the males were offered the opportunity to copulate once every 3-4 weeks. The behavioral data showed that the latency to ejaculation was increased only at 24 months. Concerning the characteristics of semen, there was a substantial increase in the proportion of immobile spermatozoa and motility of those moving was much reduced, both at 12 and 24 months of age. There was no relationship between parameters of sexual behavior and those of the ejaculate. Likewise, the size of the seminal plug did not affect the amount of intrauterine spermatozoa. The reduced sperm number together with the increased sperm immobility diminishes the ejaculate quality of old males, which could influence fertility.

Copulation and ejaculation in male rats under sexual satiety and the Coolidge effect.

Sexually satiated males cease copulating after several ejaculations with the same female; and the presence of an unknown receptive female renews copulation including ejaculation, a process named the Coolidge effect. It is believed that the Coolidge effect has the aim to impregnate another female, although it is known that the sperm count gradually decreases after consecutive ejaculations. The main goal was to investigate if sexually satiated males during the Coolidge effect can reestablish seminal expulsion associated to the ejaculation behavior and/or penile erection associated to the intromission behavior. The results show that during the Coolidge effect, most of the sexually satiated males showed the motor ejaculatory behavior, however, no sperm in the uterine horns or seminal plug in the vagina were detected. Such lack of sperm was not related with the number of ejaculations required to achieve sexual satiety nor with the number of intromissions needed for ejaculating (experiment 1: 2.4.1.). After the behavioral ejaculation, during the Coolidge effect, there was a 44% decrease in sperm count in the epididymal caudae (experiment 1: 2.4.2.). Males that mated for 8 behavioral ejaculations (close to sexual satiety) deposited tiny seminal plugs but no sperm in the female reproductive tract (experiment 1: 2.4.3.). Interestingly, sexually satiated and non-satiated-animals displayed similar number of intromissions and spent a similar time in dislodging the seminal plug from the vagina deposited by other males (experiment 2). These results suggest that sexually satiated males during the Coolidge effect have the capacity for penile erection and vaginal insertion, because they are able to dislodge seminal plugs; but are unable to expel seminal fluid, because neither form seminal plugs nor deposit sperm in the female genital tract.

Differential effects of progesterone and genital stimulation on sequential inhibition of estrous behavior and progesterone receptor expression in the rat brain.

The effect of genital stimulation, either by vaginocervical stimulation (VCS) using a calibrated vaginal probe combined with manual flank stimulation (FS), or by mounts performed by the male, on the hypothalamus and preoptic area concentration of the progesterone receptors A (PR-A) and B (PR-B) was assessed in ovariectomized (ovx) estrogen-primed rats. VCS/FS or stimulation provided by male mounts, even without intromission, significantly decreased PR-B concentration in the hypoythalamus. Down regulation of PR produced by genital stimulation was quantitatively similar to that elicited by progesterone (P) administration. Bilateral or unilateral transection of the pelvic or the pudendal nerves prevented down regulation elicited by VCS/FS. Repeated VCS/FS elicited lordosis behavior in most ovx estrogen primed rats, but the lordosis intensity was lower than that observed in response to P. P administered to ovx estrogen primed rats, induced sequential inhibition, i.e., failure to display estrous behavior in response to a second P injection (24h after the initial P injection). VCS/FS failed to elicit sequential inhibition, since rats responded with normal estrous behavior to the second injection of P. This suggests that down regulation by VCS, by contrast with P, failed to inhibit the subpopulation of PR involved in the facilitation of estrous behavior by P.

Rat dorsal prostate is necessary for vaginal adhesion of the seminal plug and sperm motility in the uterine horns.

The rat prostate comprises dorsal, ventral and lateral lobes that are morphologically and biochemically distinct. Lesions to these structures are expected to affect the quality of the ejaculate and male fertility. In experiment 1, we analyzed ejaculate parameters of males that had chemical lesions of the dorsal or ventral lobes. At pre-lesion and at 5 and 20 days post-lesion males were mated, and after ejaculation, seminal fluid and seminal plug were obtained from the mated females. In experiment 2, the ventral lobes were ablated, and the ejaculate was analyzed. In experiment 3, the fertility of males with chemically-lesioned dorsal lobes or ablation of the ventral lobes was evaluated. Chemical lesion of the dorsal lobe prevented the adhesion of the seminal plug to vaginal walls. When these males were tested at 5-days postlesion, no sperm were found in uterus, and at 20-days post-lesion, the few sperm encountered showed slow progressive motility. None of the females that mated with dorsal lobe-lesioned males became pregnant. However, chemical lesion or ablation of the ventral lobes did not affect ejaculate or fertility. Our results indicate that the dorsal prostatic lobes are indispensable for reproductive success in males, and define parameters of ejaculate with which fertility can be estimated.

Rat dorsal prostate is necessary for vaginal adhesion of the seminal plug and sperm motility in the uterine horns

The rat prostate comprises dorsal, ventral and lateral lobes that are morphologically and biochemically distinct. Lesions to these structures are expected to affect the quality of the ejaculate and male fertility. In experiment 1, we analyzed ejaculate parameters of males that had chemical lesions of the dorsal or ventral lobes. At pre-lesion and at 5 and 20 days post-lesion males were mated, and after ejaculation, seminal fluid and seminal plug were obtained from the mated females. In experiment 2, the ventral lobes were ablated, and the ejaculate was analyzed. In experiment 3, the fertility of males with chemically-lesioned dorsal lobes or ablation of the ventral lobes was evaluated. Chemical lesion of the dorsal lobe prevented the adhesion of the seminal plug to vaginal walls. When these males were tested at 5-days postlesion, no sperm were found in uterus, and at 20-days post-lesion, the few sperm encountered showed slow progressive motility. None of the females that mated with dorsal lobe-lesioned males became pregnant. However, chemical lesion or ablation of the ventral lobes did not affect ejaculate or fertility. Our results indicate that the dorsal prostatic lobes are indispensable for reproductive success in males, and define parameters of ejaculate with which fertility can be estimated.

Components of the neural circuitry of the vaginocavernosus reflex in rabbits.

In mammals the mechanisms underlying female sexual and reproductive biology are poorly understood. Little attention has been paid to striated muscles and their neural regulation. The aim of the present study was to describe the components of the vaginocavernosus reflex in adult rabbits. It was found that mechanical stimulation of the glans of the clitoris and the perineal vagina induced electromyographic (EMG) responses in bulbocavernosus (Bcm) and ischiocavernosus (Icm) muscles. Unilateral and bilateral nerve transection indicated that the clitoral nerve is the main afferent path of the reflex and that it recruits ipsilateral and contralateral perineal motoneurons. Injection of horseradish peroxides-wheat germ agglutinin (HRP-WGA) into the Bcm and Icm labeled spinal motoneurons scattered in L7 and S1 segments. According to the results of this study and previous work, the elements of the vaginocavernosus reflex may be described as follows. Mechanical receptors are located in the glans clitoris and in the wall of the perineal vagina. The main afferent pathway is the clitoral nerve. It activates ipsilateral and contralateral Bcm and Icm motoneurons in lumbosacral segments. Axons of efferent neurons travel through the clitoral and ischiocavernosus nerves, and the effectors are the Bcm and Icm perineal muscles. Identification of neural components of the vaginocavernosus reflex in rabbits will allow the use of this animal as a model to assess the physiological characteristics of the perineal motoneurons as well as the contribution of the Bcm and Icm in female urogenital functions.

Análisis de los parámetros del eyaculado en la rata Wistar de laboratorio: descripción de la técnica / Analysis of the parameters of the ejaculate in the laboratory Wistar rat: technical description

The number of spermatozoa, weight and size of the seminal plug has been quantified in the ejaculate of the laboratory rat and sperm viability, sperm mobility and sperm concentration in samples obtained from the epididymis. The reference values for the rat ejaculate have not been determined maybe due to the difficulty to obtain it directly from the male. Nevertheless, an approach can be obtained analyzing the ejaculate collected from the inseminated female. The objective of this study was to evaluate and propose the values of the macroscospic and microscopic parameters of the semen and seminal plug obtained from the female. The seminal analysis of the Wistar rats was performed adapting the methods used for other species. After one ejaculatory series, semen contained in the uterine horns was obtained, as well as the seminal plug from the vagina. In more than one hundred ejaculates, 94.54% were off-white with 2.35 ± 0.06 mm of viscosity and 8.13 ± 0.02 of pH. The sperm concentration was 16.3 ± 0.59 millions of spermatozoa per mL, 0.72 ± 0.01 mobility index, 64.4 ± 0.7% viability and 99.11 ± 0.20% normal morphology. From 99% of seminal plugs, 92.7% were hardened, they weighed 115.63 ± 1.54 mg, measured 12.41 ± 0.13 and 5.31 ± 0.05 mm of length and width respectively, and volume 87.70 ± 1.74 mm3 . In conclusion, the used method to obtain and to evaluate the parameters of the ejaculate is reliable, for that reason, it is suggested that the results obtained could be considered as indicative values for semen and seminal plug for the Wistar rat.

Se ha cuantificado en el eyaculado de la rata de laboratorio, el número de espermatozoides, peso y tamaño del tapón seminal, y en muestras obtenidas de epidídimo, la viabilidad, movilidad y concentración espermáticas. Los valores de referencia para el eyaculado de la rata no se han determinado quizá por la dificultad para obtenerlo directamente del macho. No obstante, puede obtenerse una aproximación al analizar el eyaculado recolectado de una hembra recién inseminada. El objetivo de este estudio fue evaluar y proponer los valores de los parámetros macroscópicos y microscópicos del semen y tapón seminal obtenidos de la hembra. El análisis del semen de ratas Wistar se realizó adecuando los métodos usados para otras especies. Después de una serie eyaculatoria, se obtuvo el semen contenido en los cuernos uterinos y el tapón seminal de la vagina. En más de 100 eyaculados, 94.54% fueron blanquecinos, con 2.35 ± 0.06 mm de viscosidad y 8.13 ± 0.02 de pH. La concentración espermática fue de 16.3 ± 0.59 millones de espermatozoides por mL, 0.72 ± 0.01 de índice de movilidad, 64.4 ± 0.7% de viabilidad y 99.11 ± 0.20% de morfología normal. Del 99% de los tapones seminales, 92.7% fueron endurecidos, pesaron 115.63 ± 1.54 mg, midieron 12.41 ± 0.13 y 5.31 ± 0.05 mm de largo y ancho, respectivamente, y de volumen 87.70 ± 1.74 mm³. En conclusión, el método utilizado para obtener y evaluar los parámetros del eyaculado es confiable, por ello se sugiere que los resultados obtenidos podrían considerarse como valores indicativos para el semen y tapón seminal de la rata Wistar.

An anatomical and electrophysiological study of the genitofemoral nerve and some of its targets in the male rat.

Anatomical descriptions of the genitofemoral nerve (GFn) innervating the lower pelvic area are contradictory. Here we re-examine its origin and innervation by its various branches of principal target organs in the male rat. Using gross dissection, electrophysiological techniques and retrograde tracing of motoneurones with horseradish peroxidase, we confirm that the GFn originates from lumbar spinal nerves 1 and 2, and that at the level of the common iliac artery it divides into a lateral femoral and a medial genital branch. In contrast to previous studies, we report that the genital and not the femoral branch innervates the abdominal-inguinal skin, and not only the genital but also the femoral branch innervates the cremaster muscle (Cm) surrounding the testes. Motoneurones innervating the Cm proper are located in the ventral nucleus of L1 and L2, and those innervating the muscular transition region of the rostral Cm are located in the ventral nucleus in L1 and the ventrolateral nucleus in L2. The GFn may contribute to male reproductive performance by transmitting cutaneous information during copulation and, via contraction of the Cm to promote ejaculation, the protective displacement of the testes into the abdominal cavity during fighting and as a sperm-protecting thermoregulatory measure.

Anatomical and physiological characteristics of perineal muscles in the female rabbit.

Little information is available on the participation of the perineal striated muscles in female reproductive processes. Here, we describe the gross anatomy and innervation of two striated perineal muscles in the female rabbit, the bulbospongiosus (BSM) and ischiocavernosus (ISM), and analyze their reflex electromyographic (EMG) activity in response to stimulation of the perigenital skin and vaginal tract. Twenty-four mature chinchilla-breed rabbit does were used: 12 to describe the anatomy and innervation of the muscles, 9 to determine reflex EMG activity of the muscles in response to stimulation of the perigenital skin and specific levels of the vaginal tract and 3 to analyze the effect of contraction of the muscles on intravaginal pressure. Both muscles were well developed, with their fibers originating at the ischiadic arch and inserting onto the ligamentum suspensorium clitoridis. Branches of the clitoral and perineal nerves innervated the BSM and ISM, respectively. Bilateral electrical stimulation of these nerves provoked retraction of the clitoral sheath and an increase in intravaginal pressure at the level of the perineal vagina. Whereas neither muscle responded to stimulation of the perigenital skin, both were reflexively activated during mechanical stimulation of the inner walls of the perineal vagina. Prolonged cervical stimulation inhibited this reflex. Thus, in reproductive processes such as copulation and/or parturition, the contraction of these muscles may be induced during stimulation of the perineal vagina.