Life-span changes in the copulatory behavior of male rats (Rattus norvegicus).

Studied the copulatory behavior of 36 5-, 10-, 15-, and 20-mo old sexually naive male Long-Evans rats during 2-hr tests with receptive females. There was no apparent change in sexual arousal as measured by latency to initiate copulation across age, with Ss from all groups exhibiting comparable latencies to 1st mount and 1st mount with intromission. The numbers of ejaculations achieved were also similar across ages. Significant age differences were found for frequency of mounts, with 20-mo olds having the highest mean frequency. The persistent mounting by older Ss appeared to account for significant group differences in interintromission interval and ejaculation latency. It is suggested that motor deficits may impair the ability of older Ss to achieve intromission, increasing the number of mount bouts as well as the number of mounts for each bout, thus extending the length of each copulatory series. (31 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region

The influence of the nitric oxide synthase inhibitor N-nitro-L-arginine methyl ester (L-NAME) on the copulatory behavior of sexually experienced male Wistar rats was investigated. L-NAME was injected i.p. 10 min before the onset of a session using a dose of 30 mg/kg (L-NAME 30 group), or 60 mg/kg (L-NAME 60 group). The copulatory sessions were terminated after the third ejaculation in the control group or after 1500 s in the L-NAME 30 and L-NAME 60 groups. L-NAME administration reduced the number of rats that achieved ejaculation by 43% and 86% in the L-NAME 30 and 60 groups, respectively. In both experimental groups only a few intromissions and an increased number of mountings were observed. An increase in the number of ultrasonic vocalizations in the 50 kHz band, a dose-dependent effect, was observed. The level of sexual motivation evaluated by mount latency was not influenced by inhibition of NO synthesis.     

Copulatory behavior of male rats given intermittent electric shocks: Theoretical implications.

Results of 3 experiments show that mildly painful .5-sec shocks, delivered to the skin of 17 Long-Evans and 6 Sprague-Dawley male rats every 30 sec in the presence of a receptive female, reduced the intervals between intromissions and the latencies to resume mounts and intromissions after ejaculation, but did not affect the number of intromissions preceding ejaculation. The effects of shock on postejaculatory intromission and mount latencies support F. A. Beach and A. M. Holz-Tucker's concept of the postejaculatory period consisting of absolute and relative phases. The pattern of results led to the development of a model of the fluctuation in sexual arousal during copulation and to a modification of existing theories of the accumulation of ejaculatory potential. (29 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of ibotenic acid lesions of the nucleus accumbens on paced mating behavior in the female rat.

The present study investigated the role of the nucleus accumbens (NAcc) in paced mating behavior in female rats. A sexually receptive female rat will approach and withdraw from a sexually active male, thereby controlling the timing of the receipt of sexual stimulation (e.g., mounts, intromissions, ejaculations). In this study, ibotenic acid lesions in the NAcc core increased the likelihood that a female rat would withdraw from a male rat after a mount but did not affect contact return latency or sexual receptivity. lbotenic acid lesions in the NAcc shell did not affect paced mating behavior or sexual receptivity. The results suggest that the NAcc core plays a role in suppressing withdrawal behavior in response to less intense mating stimulation. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of prenatal exposure to low concentrations of carbon monoxide on sexual behaviour and mesolimbic dopaminergic function in rat offspring

1. Inhalation of low concentrations of carbon monoxide (CO) by pregnant rats (75 and 150 p.p.m. from day 0 to day 20 of gestation) leads to changes in mesolimbic dopaminergic transmission associated with an impairment of sexual behaviour in male offspring. 2. Eighty day old males exposed in utero to CO (150 p.p.m.) exhibited a significant increase in mount/ intromission latency as well as a significant decrease in mount/intromission frequency. A significant decrease in ejaculation frequency was also found in CO (150 p.p.m.)-exposed animals. 3. The acute administration of amphetamine, at a dose (0.5 mg kg(-1) s.c.) stimulating copulatory activity in control rats, failed to reduce mount/intromission latency and did not increase mount frequency in 80-day offspring exposed to CO (150 p.p.m.) during gestation. 4. These behavioural alterations were paralleled by neurochemical changes (in vivo microdialysis) showing that prenatal CO exposure, at concentrations (150 p.p.m.) that did not affect basal extracellular levels of dopamine in the nucleus accumbens, blunted the amphetamine (0.5 mg kg(-1) s.c.)-induced increase in dopamine release in 80-day old male rats. 5. No significant changes in either behavioural or neurochemical parameters were observed in 10-month old rats exposed prenatally to CO. 6. Since the alterations in sexual behaviour and dopaminergic transmission have been produced by prenatal exposure to CO levels resulting in maternal blood carboxyhaemoglobin concentrations equivalent to those maintained by human cigarette smokers, the present data further point out the large risk that the smoking mother poses for her offspring.     

A diallel cross analysis of genetic determinants of copulatory behavior in rats.

Conducted a diallel cross analysis aimed at obtaining information regarding genetic influences on the copulatory behavior of rats, and permitting considerations of adaptive significance. A total of 1,073 rats of 4 inbred strains-ACI, F344, LEW, and WF-and all possible F1 crosses were used. Of 385 males tested, 73 failed to mate. The F1 Ss were more likely to mate than were Ss with inbred genotypes. Overdominance was generally apparent for low frequencies of mounts and intromissions preceding ejaculation across 5 series and 3 tests. A trend for directional dominance toward low scores on various latency measures of copulatory behavior also was apparent. According to the theory relating directional dominance to adaptation, it would appear generally adaptive for rats to copulate rapidly and to ejaculate after relatively few mounts and intromissions. (42 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Monoaminergic influences on temporal patterning of sexual behavior in male rats

We evaluated the effects of the serotonin (5-HT) presynaptic uptake blocker fluoxetine (FLX) and the dopamine (DA)/noradrenaline (NE) releaser amantadine (AMA), separately and in combination, on the temporal patterning of male rat sexual behavior. FLX alone increased intermount-bout intervals, time-outs, grooming time, ejaculation latency, number of mounts per mount bout, and number of mount bouts per ejaculation. AMA alone had the opposite effect on these measures. Additionally, AMA, when given in combination with FLX, completely reversed the FLX-induced deficits in copulatory behavior. We interpret our results as suggesting an interaction between 5-HT and catecholamines in the temporal patterning of male rat copulatory behavior.     

Treatment with a serotonin-depleting regimen of MDMA prevents conditioned place preference to sex in male rats.

Among young adults, 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy") is a popular drug of abuse, and anecdotal evidence indicates that repeated use of MDMA may result in impairments in sexual function and decreased sex drive in human users. There has been little investigation of the effects of MDMA on sexual function in rodents. In the present study, the authors determined that in male rats (Rattus novegicus) tested in a sexually na?ve or a sexually experienced state, administration of a serotonin (5-HT)-depleting regimen of MDMA did not produce a change in mount, intromission, and ejaculation latency or in mount and intromission frequency compared with such latency and frequency in vehicle-treated control rats. In contrast to vehicle-treated rats, MDMA-treated rats did not form a conditioned place preference (CPP) to sex. Failure of MDMA-treated rats to form CPP to sex may be due to MDMA-induced impairments in circuits mediating sexual reward. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

MPOA lesions affect female pacing of copulation in rats.

This study examined the effects of electrolytic and ibotenic acid (IA) lesions of the medial preoptic area (MPOA) on the temporal pattern of female sexual behavior in the laboratory rat. Both electrolytic and IA MPOA lesions significantly increased the female's latency to return to the male after an intromission or an ejaculation, thereby decreasing the percentage of time spent with a male. Both types of MPOA lesions significantly increased the percentage of times the female left the male's chamber following intromissions. These results demonstrate that neurons in the MPOA regulate the female's temporal copulatory behavior, and the authors suggest that they do so by virtue of their response to vaginocervical stimulation. Studies of female pacing draw attention to parallels between male and female sexual behaviors, including the possibility that they are regulated by similar neural substrates in the MPOA. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of losartan on the sexual behavior of male rats

Many commonly used antihypertensive drugs such as diuretics and beta-blockers can interfere with sexual function in both sexes, causing loss of libido, impairment of erectile function and ejaculation in men, and delay or prevent orgasm in women. Newly developed antihypertensive drugs should ideally not interfere with the patients' quality of life including sexual function. This study examined the effects of losartan, a nonpeptide, specific antagonist for type I angiotensin II receptors, on the male sexual behavior of rats. Spontaneously hypertensive rats (SHRs) and normotensive Wistar-Kyoto (WKY) rats were treated with losartan 30 mg/ kg/day or saline control for 7, 30 and 90 days. Dark-cycle video recording was used to analyze the male sexual activities of the rats. No significant alteration in male sexual performance was observed after 7 and 30 days of treatment with losartan. In contrast, SHRs treated with propranolol 5 mg/kg/day showed increases in intromission latency, ejaculation latency and postejaculatory period indicating decreased libido and erectile and ejaculatory function. Upon completion of 90 days of losartan administration, the mount latency of the SHR was significantly increased, suggesting a decrease in libido although other parameters were unchanged and there was no effect in WKY rats. It is therefore concluded that losartan may have an advantage in preservation of sexual function when used clinically for the treatment of hypertensive disorders.     

Effects of intrathecal administration of adrenergic agonists on the frequency of copulatory pelvic thrusting of the male rat

The effects of the intrathecal perispinal administration of adrenergic agonists on the characteristics of frequency, duration, and vigor of pelvic thrusting displayed by male rats during copulation was assessed by an accelerometric technique. A different dose of one drug (noradrenaline, clonidine or isoproterenol) and saline as control was administered at the lumbosacral level of the spinal cord to sexually active male rats in tests of sexual behavior performed at weekly intervals. The intrathecal administration of noradrenaline (alpha-adrenoceptor agonist) increased the frequency of pelvic thrusting in mount and intromission responses, whereas both the alpha 2-adrenoceptor agonist clonidine (25 micrograms) and the beta-adrenoceptor agonist isoproterenol (40 micrograms) reduced the frequency of pelvic thrusting in these responses as compared to values obtained under the intrathecal administration of saline. On the other hand, the duration of the thrusting trains and the potency or vigor of pelvic thrusting in mounts and intromissions did not differ from values obtained under saline treatment. These findings indicate a possible participation of noradrenaline in the modulation of the spinal mechanisms involved in the generation of rhythmic pelvic thrusting performed by the male rat during copulation.     

Postpartum sexual behavior of the corn mouse (Calomys musculinus): Repertoire, measurements, and effects of removal of pups.

The patterns of sexual behavior of the South American cricetid Calomys musculinus, the corn mouse, were observed in 36 pairs of laboratory-reared mice during the postpartum estrus. Copulatory behavior was displayed by 26 of these pairs, 15 of which were observed with their litter in the arena. The other 11 pairs had their litters removed immediately after parturition. The behavioral elements were classified in 21 mutually exclusive categories. Seven categories were noninteractive (the animals performed them by themselves). Agonistic behaviors were predominant in male–female encounters in this species, accounting for 6 of the interactive categories. A kind of fighting, probably a ritualized one, usually precedes copulation. Removal of the litter decreases the incidence of aggression by females and increases the incidence of other interactive behaviors by males (e.g., grooming or sniffing the female, especially the genitals). The incidence of precopulatory fighting is not modified by the presence or absence of the litter, however. The copulatory behavior of this species has a general pattern of no lock, intravaginal thrusting, a single intromission per ejaculation, and multiple ejaculations. Copulation started after a short latency. Most pairs performed only two ejaculatory series. The ejaculation latency was shorter than those of other South American species. When compared with other cricetids displaying intravaginal thrusting, the corn mouse performs a high number of thrusts in the intromission with ejaculation. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Involvement of dopamine D2 receptors in the effect of cocaine on sexual behaviour and stretching-yawning of male rats

The effect of cocaine (7.5, 15 and 30 mg/kg) administered in acute or subchronic mode, on the mating behaviour of sexually active male rats varied in a dose- and mode-dependent manner. Regardless of mode of treatment, 30 mg/kg markedly impaired the rats copulatory ability and impairment continued for a week after suspension of subchronic treatment. An acute dose of 15 mg/kg reduced intromission frequency, while in subchronic mode it also reduced ejaculation latency. Mount frequency was increased by 7.5 and 15 mg/kg, but only on first injection. In the case of sexually-naive male rats, acute administration of cocaine (3-30 mg/kg) stimulated penile erections at 7.5 mg/kg and motor hyperactivity at all doses. (-) Eticlopride (0.025 and 0.05 mg/kg), a DA D2 antagonist, counteracted cocaine-induced motor hyperactivity but not penile erection, which it enhanced. (-) Eticlopride at the same doses also antagonized cocaine potentiation of lisuride (0.2 mg/kg)-induced behavioural effects. When male rats treated with subchronic cocaine (15 mg/kg) were injected with the DA D2 agonist SND 919 (0.1 mg/kg), they displayed a more marked stretching-yawning behaviour than control animals receiving SND 919 at the same dose. The involvement of DA D2 receptors in cocaine-induced effects is suggested.     

Differential behavioral response to dopamine D? agonists by sexually naive, sexually active, and sexually inactive male rats.

This study was performed with male rats categorized as sexually active (SN), sexually active (SA). or sexually inactive (SI). In a first experiment the effects of the dopamine (DA) D? agonist SND 919 (0.05, 1, and 10 mg/kg) on the copulatory behavior of SN, SA. and SI rats were assessed. In a second experiment the DA D? agonist B-HT 920 (0.2 mg/kg) was used, and examination was limited to SN and SA rats. The effects exerted on stretching-yawning, penile erection, and sedation by the same compounds at the same doses in these three rat categories were also investigated. The main findings were that SND 919 and B-HT 920 facilitated ejaculation in SA rats, and that the rats that were different as regards level of sexual activity exhibited different behavioral responses to the two DA agonists. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of sequential preoptic and mammillary lesions on male rat sexual behavior.

Observed the sexual behavior of 52 male Sprague-Dawley rats prior to and following bilateral medial preoptic, unilateral medial preoptic, bilateral posterior preoptic, bilateral mammillary, and sham lesions. Bilateral medial preoptic lesions and mammillary lesions were made either simultaneously or sequentially within the same Ss in separate groups. Mammillary lesions had no effect on sexual behavior. Complete destruction of the medial preoptic area made prior to, simultaneous with, and following mammillary lesions completely abolished mating behavior. Partial destruction of the medial preoptic area increased mount and intromission latencies and slightly increased ejaculation latency. Results suggest that since there was no change in the postejaculatory-refractory interval, the medial preoptic area mediates sexual arousal but apparently is not involved in a copulatory-ejaculatory mechanism. (32 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Relation of Fos-IR expression in the pelvic ganglion to sexual behavior in laboratory rats.

The pelvic ganglion (PG) provides both sympathetic and parasympathetic innervation to the genitalia and other pelvic structures. To determine whether neuronal activity of the PG, as detected by Fos-like immunoreactivity (Fos-IR), is related to sexual stimulation, male and female rats were tested under a variety of conditions. In males, Fos-IR expression in the PG was positively correlated with the amount of both genital and noncontact stimulation. In females, only ejaculation preceded by multiple intromissions induced a significant increase in Fos-IR; multiple intromissions or ejaculation preceded by only 0–1 intromission did not affect Fos-IR. Additional experiments comparing Fos-IR expression, in which some females were allowed to pace their sexual contact and others were not, revealed that ejaculation duration was the key factor in the induction of Fos-IR in female rats. Because the conditions under which Fos-IR expression occurred in females are identical to those required for sperm transport, we suggest that, in the female, sperm transport is regulated in part by autonomic outflow from the PG after copulation. These relations between sexual behavior and measures of PG activity are consistent with the idea that the sexually dimorphic organization of the peripheral nervous system plays a major role in mediating the gender-specific outcome of copulation: ejaculation in the male and sperm transport in the female. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Precontact 50-kHz vocalizations in male rats during acquisition of sexual experience.

50-kHz ultrasonic vocalizations emitted by male rats during a 5-min period before introduction of a female (precontact vocalizations [PVs]) were analyzed in the context of acquisition of sexual experience. Changes in the main copulatory parameters and their N-methyl-D-aspartate (NMDA) receptor dependence, the role of contact with either anestrous or estrous females, and conditioning to odor and background cues were also investigated. Mount latency (ML) and intromission latency (IL) decreased after the 1st copulatory session, but ejaculation latency (EL) changed significantly only starting from the 4th session onward. The number of PVs gradually increased during the first 3–4 sessions. Blocking of NMDA receptors affected PVs and EL but not ML or IL. After a 5-month break in copulatory sessions, ML remained unchanged, whereas EL increased and the number of PVs decreased significantly. PVs were most robustly elevated by contact with estrous females. Exposure to background cues resulted in a linear decrease in number of PVs during 10 subsequent sessions without exposure to a female. The results suggest that, in the course of acquisition of a sexual experience, PVs reflect a learning process that depends on a rewarding value of sociosexual contact. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of morphiceptin in the medial preoptic area on male sexual behavior

Morphiceptin, a selective mu opioid agonist, injected into the medial preoptic area (MPOA), delayed the onset of copulation in male rats, but did not affect genital reflexes, sexual motivation or general motor activity. In a dose-dependent manner, morphiceptin (100 ng and 1000 ng) injected into the MPOA increased mount and intromission latencies. Similar injections of morphiceptin into the ventromedial hypothalamus had no effect on any parameter of copulation. The increase in copulatory latencies following the injection of the highest dose of morphiceptin was blocked by pretreatment with the opioid antagonist naloxone. In the X-maze task, morphiceptin had no effect on sexual motivation, as measured by the percentage of trials on which the male chose the female's chamber, but it increased the number of trials in which the subject did not select a chamber within 60 s and the latency to the female the first time he chose her chamber. Similar to the copulation task, the mount and intromission latencies were also increased in the X-maze, after the male reached the female. Morphiceptin in the MPOA had no effect on ex copula genital reflexes, tested in restrained supine males, or on motor activity, tested in a grid box. These results suggest that morphiceptin disrupts either the specific copulatory somatomotor pattern or a more general motivational component.     

Influence of gonadal hormones and sexual behavior on ultrasonic vocalization in rats: II. Treatment of males.

Male Long-Evans rats were tested with estrous female rats in a divided cage to determine whether ultrasonic vocalizing varies as a function of recent sexual behavior or hormonal condition. In Exp I, when males were tested after 3 intromissions, a short latency to vocalization and a high rate of 50-kHz pulses occurred. 40% of the males changed their vocalization to 22-kHz pulses. With sexually fatigued males, long vocalization latencies and low vocalization rates were observed, and no males shifted to 22 kHz. Rates were intermediate with control males. In Exp II, a decline in vocalization rate occurred following castration of male rats compared with sham-operated controls. In both experiments the male nosed the screen divider during high-rate ultrasound production, maximizing contact with the female. Darting by females appeared only when ultrasonic pulse rates were high. The abrupt shift from 50- to 22-kHz vocalizing was characteristic of males with short intromission latencies. Data suggest that gradation of vocalization is correlated with the sexual readiness of the male and that vocalization may facilitate female darting behavior. (25 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Pacing of copulatory behavior in the male rat: Effects of receptive females and intermittent shocks.

Describes 2 experiments with 7 male hooded Long-Evans rats. In Exp I, Ss were tested with females continuously present and with the presence of the female after each sex act contingent upon a barpress. The sole effect of the barpress requirement was to increase the intervals between copulations before ejaculation. In Exp II, intermittent shocks were superimposed upon the conditions of Exp I. Shocks were followed with short latency by mounts in the ad-lib condition and by barpress and mounts in the operant condition. The pacing of copulatory acts before ejaculation is inferred to result from an interaction of stimuli from the female and feedback from the copulatory acts; after ejaculation, factors primarily endogenous to the male govern the timing of resumption of copulation. (18 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)