Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Copulation”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,495 records · Page 83Linked to original sources
PubMed1977

Protein synthesis inhibition alters Drosophila mating behavior.

Fruit fly Drosophila pseudoobscura virgin AR females mate preferentially with AR males given a choice between AR and or males. However, AR females which mated with or males when young show a significant change in sexual selection in favor of or over AR males in subsequent simultaneous choice tests. Ingestion of food moistened with 4 ml cycloheximide (400 microng/ml) produces 75% protein synthesis inhibition in the female flies. Females exposed to cycloheximide (CXM) immediately after their initial copulation with or males resemble virgin flies in their choice of mates, and mate preferentially with AR males. Females exposed to CXM before their initial copulatory experience with or males resemble or-experienced but untreated (no CXM) flies in their choice of mates, and mate preferentially with or males. The change in sexual preference shown by females with prior copulatory experience resembles learning in that it is subject to disruption by CXM in ways analogous to those reported in the literature.

Animals↗
PubMed1980

Effects of morphine, beta-endorphin and naloxone on catecholamine levels and sexual behavior in the male rat.

Intraperitoneal administration of the opiate antagonist naloxone hydrochloride (30 mg/kg) to sexually experienced male rats caused a significant reduction in mount and intromission latencies, number of mounts preceding ejaculation and ejaculation latencies. Intraperitoneal adminstration of naloxone (30 mg/kg) also stimulated persistant non-copulators to begin mating and to ejaculate within a twenty minute test period. Conversely, intraperitoneal administration of morphine sulphate (6 mg/kg) as well as intraventricular injection of the endogenous opiate beta-endorphin (6 micrograms) produced a complete loss of copulatory behavior in male rats. The deficit in sexual behavior induced by beta-endorphin was correlated with a significant increase in hypothalamic norepinephrine levels. It is suggested that the endogenous opiates may be involved in the mediation of sexual behavior via an interaction with central catecholaminergic systems.

Animals↗
PubMed1981

Effects of a new type of 5-HT receptor agonist on male rat sexual behavior.

8-Methoxy-2-(di-n-propylamino) tetralin (8-OMe-DPAT) and 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) are two new drugs exerting selective actions on brain 5-HT neurotransmission. In the present experiments we have investigated the effects of these two drugs on male rat sexual behavior. It was found that both drugs reduce the number of intromissions preceding ejaculation and shorten the ejaculation latency. These effects are extremely pronounced and several animals ejaculate at the first intromission. In addition 8-OH-DPAT produced a slight reduction of the post-ejaculatory interval. There were no significant effects on latency to initiate copulation or in the number of mounts preceding ejaculation. Finally, sexual behavior was partly or completely restored in castrated male rats after injection with 8-OMe-DPAT or 8-OH-DPAT.

DOM 2,5-Dimethoxy-4-Methylamphetamine↗
PubMed1987

Imipramine-induced erection, masturbation, and ejaculation in male horses.

Imipramine hydrochloride was administered to five male horses (400-500 kg b.wt.): one experienced young stallion, two mature normal breeding stallions, one 5-year-old stallion with erection and ejaculatory dysfunction, and one long-term castrated male horse. Oral imipramine treatment (100 to 600 mg, twice daily) led to frequent erection and masturbation while at rest in the stall in a nonsexual context. Intravenous imipramine treatment over a range of doses (50 to 1000 mg) similarly induced erection and masturbation in all animals. Erection typically occurred within 10 minutes after injection, and the erection and masturbation continued intermittently for 1 to 2 hours. These erections proceeded as during sexual excitement to a normal firmness and eventual engorgement of the glans penis. Two stallions ejaculated while masturbating. Mild ataxia and drowsiness appeared at the higher doses, but the animals remained responsive to auditory, visual, and tactile stimuli. Erection and masturbation were often interrupted by activities about the barn or the approach of the handler, suggesting cortical inhibitory control of the erection. When tested in a sexual context immediately following IV treatment (500 mg), the two mature breeding stallions bred normally. The 5-year-old stallion, which had not ejaculated over several months of breeding attempts, spontaneously ejaculated following IV imipramine treatment. Subsequently, this stallion has ejaculated during copulation while on low dose oral (100 mg. twice daily) imipramine treatment. Plasma total androgens increased during treatment in these stallions. The long-term castrate showed erection and masturbation following IV imipramine treatment, suggesting that the effect of imipramine is not testosterone dependent.

Androgens↗
PubMed1987

Naloxone inhibits mating and conditioned place preference for an estrous female in male rats soon after castration.

Three experiments were conducted to assess the role of endogenous opioids in controlling mating behavior and sexual reward in the male rat. In Experiment 1 SC administration of naloxone (0.5, 1.0, 5.0, or 10.0 mg/kg) significantly reduced mounting and ejaculation in male rats tested 14, but not 7 days, after castration. In Experiment 2 naloxone (5.0 mg/kg) administered SC to gonadally intact males, which had ejaculated repeatedly with one female until they were sexually sated, significantly inhibited the resumption of mating after the reintroduction of a female partner. One interpretation of these results is that naloxone attenuated the reward experienced by castrated and sexually sated males in the presence of an estrous female, thereby disrupting males' coital performance. This hypothesis was tested in Experiment 3 using a conditioned place preference paradigm in which males copulated with an estrous female in an initially "non-preferred" (white) compartment, whereas on alternate days they remained alone in an initially "preferred" (black) compartment. After 10 such conditioning sessions, males were either castrated or sham-operated. They later were given free access to both compartments in the absence of an estrous female. Seven days after conditioning and surgery, sham-operated, naloxone-injected males and both groups of castrates spent significantly less time than sham-operated, saline-injected controls in the initially "non-preferred" compartment. Fourteen days after conditioning and surgery castrated, naloxone-treated males spent significantly less time in the "non-preferred" compartment than males in the other three groups. Endogenous opioids may play an important role in the interpretation by males of the incentive motivational stimuli which emanate from an estrous female.

Animals↗
PubMed1988

Inhibition of sexual reflexes by lumbosacral injection of a GABAB agonist in the male rat.

The effects of gamma-aminobutyric acid (GABA) agonists on penile reflexes were investigated. An intrathecal injection of baclofen (0.2, 0.4, or 0.8 microgram), a GABAB receptor agonist, into the subarachnoid space of the lumbosacral spinal cord (L5-S1), resulted in a dose-related decrease in the number of animals responding in a penile reflex test. Doses of 0.2 and 0.4 microgram of baclofen decreased the number of erections; 0.4 microgram also increased the latency to the first glans erection. The highest dose of baclofen (0.8 microgram) completely inhibited penile responses in these tests. None of these doses, however, prevented rats from copulating to ejaculation. Antecedent ejaculation, which facilitated the onset of penile reflexes in saline controls, also blocked the inhibitory effects on penile responses by the lower doses (0.2 and 0.4 microgram) of baclofen, but was ineffective in animals treated with 0.8 microgram baclofen. In contrast to the inhibitory effects of baclofen in the lumbosacral cord, an intrathecal injection of baclofen (0.8 microgram) at thoracic segments (T8-T10) did not affect penile erections elicited following an ejaculation. The role of spinal GABAA receptors in sexual reflexes was assessed by intrathecal injection of a GABAA agonist. THIP (0.5.1. or 2 micrograms), onto the lumbosacral cord. Only at the largest dose of THIP were slight inhibitory effects on penile reflexes observed. Together, these data indicate that stimulation of GABAB receptors in the lumbosacral spinal cord inhibits erectile mechanisms ex copula.

Animals↗
PubMed1990

Facilitation of sexual behaviors in the male rat in the presence of stimuli previously paired with systemic injections of morphine.

Male rats were tested for sexual behaviors in an environment previously associated with injections of morphine. Both gonadally intact and castrated males displayed more frequent female-directed behavior, such as pursuit of the female, anogenital exploration, and partial mounts, and gonadally intact animals had shorter latencies to initiate copulation when tested for sexual behaviors in the environment previously associated with morphine. These results suggest that a conditioned state induced by stimuli previously paired with the positive incentive effects of an opiate drug can facilitate or modulate behaviors under the control of other primary positive incentives.

Animals↗
PubMed1991

Differential role of serotonin and noradrenaline on anxiety reduction after ejaculation in the rat.

As previously reported, a reduction in anxiety after ejaculation was observed. In a previous report it was demonstrated that the GABA-benzodiazepine system is involved in the mediation of this reduction in anxiety. The anxiety levels were measured using a defensive burying model. This work was performed to elucidate the serotonin and noradrenaline participation in the mediation of this phenomenon. Two experiments were made. In the first experiment the serotonergic neurotoxin 5,7-dihydroxytryptamine (5,7-DHT, 10 micrograms/10 microliters) was intracerebroventricularly injected. Five days after its administration the behavioral tests were performed. In the second experiment, the noradrenergic neurotoxin N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine (DSP4, 50 mg/kg X 2) was IP administered. The neurochemical data reveal a drastic reduction in various brain areas respective monoamine levels after these treatments. The lesion produced by 5,7-DHT was able to reverse the reduction in anxiety in copulating males, but produced no changes in noncopulating animals. This finding supports the idea that the serotonergic system is involved in the reduction of anxiety observed after ejaculation. The results of the DSP4 experiment suggest that there is not a direct participation of the noradrenergic system in the anxiety reduction observed after ejaculation.

5,7-Dihydroxytryptamine↗
PubMed1992

Effects of LY163502, a D2 dopaminergic agonist, on the sexual behavior of male rats.

LY163502, a selective D2 receptor agonist, has been reported to stimulate sexual behavior in both copulating and noncopulating male rats. Three experiments were conducted to further characterize the role of dopamine on male sexual behavior. In the first experiment, quinelorane (LY163502) was directly infused into the medial preoptic area (MPOA) of castrated males either alone or in combination with subphysiological levels of testosterone (T) exposure. The results showed that male sexual behavior was not affected by infusion of LY163502 alone, subphysiological T levels alone, or the combination of LY163502 and subphysiological T levels. For the second experiment, all animals received physiological levels of T and MPOA infusions of LY163502 or saline. The results showed an earlier restoration of male sexual behavior in the LY163502 group when compared to the T-only group. In the third study, noncopulating, gonadally intact males received SC injections of either LY163502 or saline 30 min prior to copulatory testing. The results showed that LY163502 induced a significant decrease in mount and intromission latencies after 14 days of drug exposure. From these results, we conclude a) that D2 receptors play a role in the facilitation of male sexual behavior and b) that the action of dopamine at D2 receptors requires the presence of T.

Animals↗
PubMed1994

Effects of alcohol on the sexual motivation of the male rat.

Previous research measuring the effects of alcohol on sexual behavior has primarily focused on its effects on copulation. The present experiment was designed to investigate the effects of alcohol on the sexual motivation of the male rat by requiring operant responding to gain access to a sexually receptive female. A novel apparatus was used that allowed both visual and olfactory cues from an estrous female to reach the male. Lever presses resulted in the opening of a door that permitted the male rat to enter an adjacent chamber where a receptive female was located. Treatment with low to moderate doses of alcohol (0.5 g/kg and 1.0 g/kg) resulted in increased latencies to emit the first response of the males working for access to females, but did not affect response rate or subsequent mount or ejaculation latencies, when these males were allowed access to the receptive female. Furthermore, alcohol failed to show any response-reinstating or disinhibitory effects when tested following a period of nonreinforced extinction trials. An additional experiment, in which rats received equivalent doses of alcohol, revealed no decrease in spontaneous locomotion. Taken together, these data suggest that the response-reducing effects of alcohol are probably not a result of general drug-induced reductions in activity, but rather an attenuating action of the drug on sexual motivation.

Animals↗
PubMed1979

The localization and synthesis of some collagen types in developing mouse embryos.

The location of type IV (basement membrane)collagen in early post-implantation mouse embryos was examined by immunoperoxidase reactions using a specific immunoglobulin raised against mouse lens capsule collagen. Reaction was positive in the earliest embryos studied--on the fifth day of gestation (the day of detection of the copulation plug is the first day). It was found only in the primitive endoderm adjacent to the blastocoelic cavity. Subsequently in development, strong staining reactions were found in the parietal endoderm, Reichert's membrane and an acellular layer which separates the visceral endoderm of the egg cylinder from the ectoderm. In tenth to eighteenth day visceral yolk sacs, the mesodermal portion was stained, which is consistent with the presence of basement membranes around blood vessels. The endodermal portion of the visceral yolk sac did not react, while small amounts were found in the amnion. By incubation of various embryonic tissues with tritiated amino acids, purification of the biosynthesized secreted collagens and their partial characterization, the differential expression of several collagen genes was detected. Identification of collagen types was made by: reaction with specific antibodies to type I and IV collagens; electrophoretic mobility; sensitivity to reduction and to collagenase; analysis of the proportions of 3-hydroxyproline, 4-hydroxyproline and hydroxylysine; and CNBr peptides. In agreement with the data of Minor et al. (1976a) for the rat, mouse parietal endoderm synthesizes large amounts of type IV collagen. In contrast to their findings, however, the 165,000 molecular weight polypeptide is not converted to one of 100,000 after reduction, alkylation and repepsinization (Dehm and Kefalides, 1978). The endoderm of the visceral yolk sac was shown to be synthesizing primarily type I collagen, while the mesoderm layer of this membrane synthesized both type I and IV collagens. Little or no type IV collagen synthesis was detected in the endoderm of the visceral yolk sac. If it is correct that the visceral endoderm of the early embryo makes a major contribution to the formation of the endoderm portion of the visceral yolk sac, then it is clear that a switch in collagen gene expression must occur as it does so.

Amnion↗
PubMed1988

A male accessory gland peptide that regulates reproductive behavior of female D. melanogaster.

The adult male accessory glands of D. melanogaster synthesize and secrete a peptide that represses female sexual receptivity and stimulates oviposition. Normally, this peptide is transferred to females during copulation; however, the peptide shows the same biological activity after purification and subsequent injection into the abdominal cavity of female virgins. Amino acid sequencing of the purified peptide and oligonucleotide-directed cDNA cloning established that the peptide consists of 36 amino acids. It appears to be synthesized as a precursor with a hydrophobic signal sequence of 19 residues at its N-terminal end. The precursor peptide is encoded by a short mRNA that accumulates exclusively in the male accessory gland. The gene has been localized by in situ hybridization to polytene chromosomes at 70A.

Amino Acid Sequence↗
PubMed1995

Superovulatory responses to eCG in llamas (Lama glama ).

Llamas are copulation-induced single-ovulators, and multiple ovulation and embryo transfer (MOET) methods have not yet been developed for this species. Superovulatory responses to eCG given during an induced (Group A) or simulated (Group B) luteal phase were investigated using ultrasound to observe ovarian follicles and corpora lutea (CLs) and plasma progesterone was used to assess luteal function. Embryos were recovered nonsurgically. Group A (n = 19): donors were given 8 microg, im GnRH analogue (Day 0) to induce ovulation of a mature follicle, 1000 IU, im eCG (Day 7), and 250 microg PGF(2alpha) analogue (Day 9). Group B (n = 17): donors were given a subcutaneous progestagen implant (3 mg Norgestomet) at Days 0 to 7) and 1000 IU, im eCG (Day 5). When most (>65%) of the follicles in both Groups A and B had matured at 5 to 11 d post eCG, the donors were given 8 microg, im GnRH and mated once (n = 26) or twice within a 24-h interval (n = 10); embryos were recovered 6 to 9 d post ovulation. More follicles and corpora lutea were induced in Group B than in Group A, but a similar mean number of embryos were recovered (1.3 vs 1.6), and a similar proportion of donors yielded multiple embryos (35 vs 32%). The embryo recovery rate was similar for Groups A and B (39 and 37%), but it was higher (P < 0.001) with 2 (72%) rather than 1 (22%) mating, and it was negatively correlated with CL number (P < 0.05). Overall, 80% of the llamas had a precocious CL and elevated plasma progesterone concentrations when multiple follicles reached maturity. This was associated with increased subsequent superovulation and embryo recovery (P < 0.01). Peak plasma progesterone was positively correlated with the CL number (P < 0.05). From these results we conclude that superovulation may be achieved with eCG given during either an induced or a simulated luteal phase, that embryo recovery is improved following 2 matings rather than 1, and that MOET may indeed be feasible for use in the llama.

Journal Article↗
PubMed1996

Luteolytic effects of prostaglandin F2alpha on day 8 to 19 corpora lutea in the bitch.

Luteolysis was induced in 5 experimental Beagle (8 cycles) and 7 client-owned bitches treated with 150 to 200 microg/kg, sc of prostaglandin F2alpha administered twice daily for 4 d, starting on Days 8 to 19 after the onset of cytological diestrus. Five experimental Beagle bitches had been mated during the estrus preceding treatment, and copulation had been confirmed in 2/7 client-owned bitches presented for termination of unwanted pregnancy. Serum progesterone concentration (mean +/- SD) declined from 26.1 +/- 66 ng/ml before treatment to 0.3 +/- 0.4 ng/ml on the fourth day of treatment One of the 7 client-owned bitches maintained her pregnancy even though serum progesterone concentrations were less than 0.5 ng/ml on the third and fourth day of treatment. Mean (+/- SEM) inter-estrous intervals before and following prostaglandin-induced luteolysis were 207.3 +/- 12.4 (n = 11 cycles in 6 bitches) and 95.5 +/- 20.0 d (n = 6 cycles in the same 6 bitches; P < 0.0001), respectively These results suggest that effective prostaglandin-induced luteolysis can be achieved with administration of 180 microg/kg during the third week of diestrus in pregnant and nonpregnant bitches.

Journal Article↗
PubMed1993

Substance P and neurokinin A are colocalized in the central chemosensory pathway of the male golden hamster.

The medial nucleus of the amygdala, bed nucleus of the stria terminalis and medial preoptic area play critical roles in the regulation of mating behavior in the male hamster. Destruction of these nuclei or the pathways that connect them severely disrupt copulation. We have begun identifying the neuropeptides contained in these neurons as a prelude to determining the role of peptide neurotransmitters in the regulation of male copulatory behavior. We have found that substance P is localized within these neurons and is regulated by gonadal steroids. In this study we report 1) that a closely related peptide, NKA (substance K), is also present in the medial nucleus of the amygdala, the bed nucleus of the stria terminalis and the medial preoptic area; 2) that all those neurons which contain SP also contain NKA and 3) testosterone also regulates the production of NKA. Thus, NKA may also play a role in the regulation of male copulatory behavior.

Amygdala↗
PubMed1995

Dopamine and sexual behavior.

Among central neurotransmitters involved in the control of sexual behavior, dopamine is certainly one of the most extensively studied. Our attempt to review old and recent neuropharmacological, biochemical, electrophysiological, and psychobiological studies performed so far only in rats, monkeys, and humans, provides evidence that dopamine through its different neuronal systems and receptor subtypes plays different roles in the control of several aspects of sexual behavior. In fact, while the nigrostriatal system is necessary for the control of the sensory-motor coordination required for copulation, the mesolimbic-mesocortical system plays a key role in the preparatory phase of the behavior, mainly in sexual arousal, motivation and possibly reward. Conversely, the incertohypothalamic system plays a major role in the consummation of the behavior, mainly in seminal emission and erectile performance, but evidence for its involvement in sexual motivation also exists. The dopaminergic receptors playing the major role in the control of male sexual behavior belong to the D2 receptor subtype. However a D1/D2 receptor interaction is well established and an opposite role for D1 and D2 receptors in the preoptic area suggested. Despite some differences, most studies show that treatments that increase or decrease, respectively, brain dopaminergic activity improve or worsen, respectively, several parameters of copulatory activity, supporting a facilitatory role of dopamine in male sexual behavior. In contrast, no conclusion can be deduced from the available studies on the role of central dopaminergic systems in the control of proceptivity and receptivity, the two main components of female sexual behavior.

Animals↗
PubMed1995

Placing erection in context: the reflexogenic-psychogenic dichotomy reconsidered.

Penile erections are usually classified as arising from "reflexogenic" or "psychogenic" causes. In practice this dichotomy has translated, somewhat circularly, to a distinction between spinal vs. supraspinal mediation, pelvic vs. hypogastric neural mediation, and perineal somesthetic stimulation vs. stimulation of receptors innervated by the cranial nerves. Evidence for differential regulation of erection in different contexts is reviewed. Research ascribing a physiological role to the hypogastric nerves in psychogenic erection, exemplified by classic studies of cats and spinally injured men, is suggestive but not compelling. Somewhat stronger is evidence that erection in some contexts (e.g., nocturnal penile tumescence (NPT) in humans or touch-stimulated erection in rats) is more sensitive to androgen levels than in other contexts (e.g., visual erotic stimuli in men or copulation in rats). However, some of these differences may arise from the relative erectogenic strength of the stimuli, rather than from qualitative differences in androgen sensitivity of different contexts. More compelling is the possibility that conflicting interpretations of the role of dopamine in erection may stem in large part from differences among laboratories in the context in which erection is evoked. In light of the evidence reviewed, it seems unlikely that the conventional reflexogenic-psychogenic dichotomy should be retained, at least in its present form. As a first step, it may be worth considering that reflexive erections may not be limited to somesthetic perineal stimulation, but rather may also include stimuli received via the cranial nerves. Two alternatives to the standard reflexogenic-psychogenic dichotomy are proposed. The first is a minor revision in which two senses of psychogenic erection are distinguished: the weak, commonly used, sense would include erection resulting from any extrinsic nonsomesthetic stimulation, whether visual, auditory, or chemosensory. In this sense, reflexive erections and psychogenic erections may not be mutually exclusive. The strong sense of psychogenic erection would be limited to memory and fantasy. The origins of psychogenic erection in both senses need not be available to consciousness, which may account for apparently spontaneous erections. In the second alternative taxonomy, erectogenic stimuli are classified as contact (somesthetic) or noncontact, and their action in evoking erection is placed on a continuum of reflexivity. Erectile contexts could then be considered as orthogonal to the other two dimensions. Even without a change in taxonomy, the conduct and interpretation of research into erectile function may be expected to benefit from closer attention to differences and similarities between contexts and species, and to context-sensitive differences in the regulation of erection.

Animals↗
PubMed1991

Sensory cues that elicit ultrasonic vocalizations in female rats (Rattus norvegicus).

Female rats emit ultrasonic vocalizations during copulation. Female vocalizations are associated with darting and other proceptive behavior. In addition, females frequently call while approaching the male. A series of experiments was undertaken to determine whether female rats emit ultrasonic vocalizations in response to other rats or to their odors. Females were exposed either to bedding soiled by males or females or to devocalized conspecifics separated from the subject by a barrier. Females vocalized more to male cues than to female cues, regardless of whether the odor cues were from soiled bedding or from a devocalized conspecific. In addition, subjects vocalized more when presented with a devocalized female rather than a neutral stimulus. Furthermore, devocalized adult males, separated by a barrier, were more effective than either devocalized castrated or juvenile males in eliciting vocalizations; in turn, castrates and juveniles were more effective than neutral stimuli. Female calling was likely induced by odors from the male. In one experiment, the female subject was positioned in such a way that she could neither see or touch the stimulus male. Presentation of tape-recorded male vocalizations did not affect calling by the female. Vocalizations emitted by females in response to male odors may attract males or may facilitate subsequent copulatory behavior by the male.

Animals↗