Effects of medial preoptic-anterior hypothalamic lesions on development of sociosexual behavior in dogs

Bilateral medial preoptic-anterior hypothalamic lesions in adult male dogs eliminate or impair copulatory behavior and reduce urine-marking responses but do not affect aggressive behavior. The present study examined the emergence of the adult forms of these same male sociosexual behavioral patterns when the lesions are made prior to puberty. The subjects were allowed to interact with male peers during development. Animals with lesions had reduced frequence of juvenile mounting and an almost total absence of male copulatory activity in adulthood. Urine-marking and aggressive behavior in the juvenile and adult periods were not affected by the lesions. The findings reveal a sparing of function with regard to urine-marking but not sexual behavior.     

Copulation and intermale aggression in rats

Attack behavior of reliably aggressive male Long-Evans rats against unfamiliar male intruders was observed immediately following copulation to one or more ejaculations. Compulatory series to five ejaculations did not differ from copulation to a single ejaculation or from a noncopulatory control in affecting aggressive behavior. Repetitive biting attacks occurred in all conditions, with comparable wounding. Evidently, the male postejaculatory state of insensitivity to sexual stimuli does not extend to stimuli eliciting intermale aggression. A second experiment determined the attack-eliciting capacity of foreign males placed in the home cage of an actively copulating male. As intromissions increased and the interval to ejaculation decreased, the probability of intermale aggression and interruption of copulation diminished. The results are discussed in reference to sexual and aggressive strategies of the copulating male.     

Effects of olfactory bulbectomy on social behavior of male guinea pigs (Cavia procellus)

Effects of olfactory bulbectomy on social behavior in male guinea pigs were studied. Both brief-exposure pairing techniques and a group-living observation period were employed to test for disruption. During short-term testing sessions bulbectomized animals courted females less than but mounted them as frequently as control subjects. While the groups did not differ in fighting behavior during short-term tests, control subjects scent-marked more frequently. Subsequently, animals were observed as same-treatment pairs living continuously with females, and behavior was sampled over a 3-wk period. Under these conditions bulbectomized males, unlike controls, failed to form dominance orders, exhibited virtually no intermale aggressive activity, had markedly depressed sexual activity, and scent-marked rarely. It is concluded that olfactory bulbectomy profoundly alters the behavior of male domestic guinea pigs and that hose alterations are most evident when experimental subjects are observed in a species-typical group-living environment.     

Hyperreactivity, muricide, and intraspecific aggression in the rat produced by infusion of local anesthetic into the lateral septum or surrounding areas

Intracranial infusions of a local anesthetic (lidocaine, 2%) were made bilaterally (4 microliter over 20 min) through permanently implanted cannulas ending in the lateral septum or adjacent areas. Increases in irritability and reactivity to the experimenter, muricide, and intermale aggression were produced by injections into the lateral septum and the region ventral to it. The increases in reactivity and interanimal aggresion occurred in varying degrees and were independent of one another, but intermale aggression occurred only in animals showing muricide. The most effective site for eliciting the entire spectrum of aggressive behaviors was the region ventral to the anterior septum. The region ventral to the posterior septum (medial preoptic area, anterior hypothalamic area, straia terminalis) was unique in that it tended to produce a high incidence of muricide, with only modest increases in reactivity. The lateral septum was moderately effective in producing the entire range of aggressive behaviors. No changes in behavior were noted with infusions into the medial septum or th medial forebrain bundle/lateral preoptic area ventrolateral to the septum. It is suggested that the hyperreactivity and irritability may be relat to hyperdefensiveness and that muricide and intermale aggression are points on a continuum of interanimal aggressiveness.     

The expression of the genes of aggressiveness in mice: The effect of androgen on aggression and sexual behavior in females

Female mice of strains selectively bred for aggressiveness or nonaggressiveness were injected with testosterone propionate (TF′) at the age of 2 days and as adults, or they were injected as adults only. Aggressive and sexual behavior was then tested with female, receptive female, and male partners before, during, and after the latter TP treatment. The females that had received both TP treatments displayed as much or as little aggression as males of the same strain, leading to the conclusion that aggressiveness genes are not linked with the male sex chromosome, even though they depend on it for their expression. The sexual behavior of the females of both strains that had received both TP treatments was altered to the male type. In the females of the aggressive strain even adult treatment alone was sufficient for this change. Aggressiveness and male sexual behavior would seem to be determined separately, although aggressiveness facilitates the display of male sexual behavior.     

Androgens and aggressive behavior in primates: A review

This review deals with possible central and peripheral effects of androgens upon primate aggressive behavior. One problem that clouds interpretation of experimental work is that measurements of dominance have often been employed, such as competition tests for food and water. Such measures often do not correlate with those obtained by quantifying aggressive interactions. It should be remembered that very few of the 188 primate species have been studied experimentally and that great behavioral and physiological diversity occurs within the order. Therefore, generalizations about the effects of androgens upon aggressive behavior in primates (including man) should be made with caution. Testosterone has an organizing influence upon the foetal brain of rhesus monkeys and may affect the development of neural mechanisms which govern aggression in males. More data are required on primates, however, since rhesus monkeys show some important differences from rodents as regards the effects of androgen upon sexual differentiation of the hypothalamus. In future, marmosets may provide a suitable model for such studies, because there is evidence that sexual differentiation of brain by androgen occurs postnatally in these monkeys. At puberty, male primates show a variety of behavioral changes and, during adulthood, males of seasonally breeding species may be more aggressive during the mating season, when testosterone levels are maximal. This does not indicate a causative relationship between testosterone and aggressive responses, because castration and androgen treatments have little effect upon aggression in prepubertal or adult males of several primate species. Androgens have pronounced effects on sexual responses in adult male monkeys, but their central effects upon aggression are much less important than among rodents. Elec trical stimulation of hypothalamic pathways has been employed to evoke aggressive behavior in marmosets and rhesus monkeys. In the rhesus, preliminary evidence indicates that such pathways show some sensitivity to androgens. In rodents it is known that these areas are richly supplied with monoaminergic neurons, which play an important role in aggressive behavior. There is little evidence on primates, however, and this remains a crucial topic for future research. Peripheral effects of androgens should also be considered. Many prosimians and New World monkeys use scent-marking behaviors and, in males, androgen-dependent chemical cues may be involved in sexual recognition and territorial behavior. This possibility awaits investigation. Finally, plasma testosterone levels may alter as a function of aggression itself; thus levels decrease if male rhesus monkeys are defeated by conspecifics. This might occur because neural events associated with giving (or receiving) aggression also influence pituitary function and hence alter gonadal testosterone secretion. Theoretically, it is possible that such changes in circulating testosterone might affect aggressive behavior via a feedback action on the brain, but the experimental evidence does not support such a view.     

The ventromedial hypothalamus and aggressive behaviour in rats

Male rats were given bilateral lesions in either the anterior or posterior ventromedial hypothalamus (VMH). The intermale aggressive behaviour of these animals within their own territory was observed before and after the surgical procedure and compared with the behaviour of sham-operated animals. The effects of anterior VMH lesions include an increased tendency to respond with frontal threatening upon approach of a conspecific male. This behaviour closely resembles the aggressive responses described in “shock-induced aggression” tests. Posterior VMH lesions facilitate territorial aggressive behaviour characterized by approaching the opponent followed by lateral threatening and fighting. It is suggested that 2 distinct neural substrates exist, which serve to inhibit defensive (anterior-VMH) and offensive (posterior-VMH) intermale aggression, respectively.     

Effects of early exposure to mating on adult sexual behavior in male mice varying in their genetic disposition for aggressive behavior

This study examined whether the sexual behavior of adult male mice is influenced by exposure in early postnatal life to brief episodes of mating. Another focus of interest was the interplay between a genetic disposition for aggressive behavior and the early exposure experiences. The subjects used in the study were male mice of the fiftysixth generation of selection for high (Turku aggressive, TA) and low (Turku non-aggressive, TNA) levels of aggressiveness. Moderately aggressive males of the parental strain (normal, N) were also used. Subjects of each strain were exposed from 21 to 32 days of age to mating mice behind a wire mesh screen. Control subjects were placed in a comparable enclosure, but were exposed to nothing. The results showed that male mice exposed to mating early in life showed a higher rate of activities in the sexuality tests, including aggressive responses. A genetic potential for aggressive behavior was related to a higher degree of sexual activity, and the early exposures optimized the hereditary attributes. The relation between sexual and aggressive behavior is discussed. © 1994 Wiley-Liss, Inc.     

The relationship between aggressive and sexual behavior in male mice: Effects of testosterone and parachlorophenylalanine

The purpose of this study was to clarify the connection between aggressive and sexual behavior with the aid of testosterone propionate (TP) and parachlorophenylalanine (PCPA). Previous studies have indicated that aggressive and sexual behavior are positively correlated, and it has been suggested that both behaviors are related to the level of general arousal. Testosterone has documented effects on both aggressive and sexual behavior. It has been hypothesized that these effects are due to an increased level of general arousal. If this is the case, aggressive and sexual behavior could be restored by administration of drugs excitating the central nervous system, e.g., PCPA. The present study examined the effects of TP and PCPA on aggressive and sexual behavior in gonadectomized male mice. Control animals were injected with sesame seed oil or saline. The level of aggressiveness was assessed by means of dyadic tests with gonad-intact male opponents. For the sexuality tests, a receptive female was placed in the home cage of the experimental male. The results showed that male mice injected with PCPA were more aggressive than the males of the other groups, while the TP-exposed males expressed the most sexual activity. Compared to the control group, the PCPA and TP groups were more active in both the aggression and the sexuality tests. These findings lend support to the hypothesis that the earlier documented correlations between aggressive and sexual behavior could be due to both behaviors being dependent on a certain level of general activation. Aggr. Behav. 24:367–377, 1998. © 1998 Wiley-Liss, Inc.     

Preoptic lesions, sexual behavior, and spontaneous ejaculation in the rat

Abstract.— A possible relation between sexual behavior and spontaneous ejaculation was studied in the male rat. Electrolytic lesions in the preoptic area completely abolished sexual behavior without affecting the frequency of spontaneous ejaculation. It is therefore suggested that this latter process is controlled independently of sexual behavior and sexual excitability.     

Sexual arousal,situational restrictiveness,and aggressive behavior

Eighty male college freshmen participated in an experiment designed to investigate the hypotheses that enhanced arousal will facilitate subsequent aggressive behavior and that an increase in aggressive behavior will be more likely to occur in a setting of situational permissiveness rather than situational restrictiveness. Subjects were either angered or not angered by a same-sex confederate, then told to imagine either a sexually arousing or a nonarousing situation during relaxation, and finally provided with an opportunity to aggress against this person by means of electric shocks. For half of the subjects, a setting of permissiveness was created, while for the other half the setting was one of situational restrictiveness. The results indicated that, even in a permissive setting, sexual arousal may inhibit aggressive behavior mediated by self-consciousness or anxiety. For nonaroused men, however, situational permissiveness tended to facilitate subsequent aggression. The investigation was considered a replication and an extension of the Baron (1974) study on the aggression-inhibiting influence of heightened sexual arousal.     

Genotype modulates prenatal stress effects on aggression in male and female mice

Prenatal stress (heat and restraint) significantly increased postpartum aggression (proportion of animals fighting and/or the intensity of the behavior) in C57BL/6J female mice and reduced the behavior in DBA/2J females. For intermale aggression, prenatal stress increased the behavior (intensity of aggression) in C57BL/6J males but did not affect aggressive behavior in DBA/2J animals. Infanticidal behavior (the killing of young) exhibited by male mice was not influenced by prenatal stress in either strain. Relative anogenital distance measurements in neonates at birth did not serve as a reliable predictor of strain variation in prenatal stress effects. Prenatal stress did not influence this measure of prenatal androgen exposure in DBA/2J or C57BL/6J females. For males, prenatal stress elevated relative anogenital distance in C57BL/6J mice and decreased this measure in DBA/2J animals. Prenatal stress effects on aggressive behavior in male and female mice therefore depend upon genotype. Strain-dependent differences may be modulated by differences in endocrine reactivity to prenatal stress/and or differential central neural tissue sensitivity to hormones.     

Intermale fighting and predatory behavior in house mice: An analysis of behavioral content

Two forms of aggression, intermale and predatory, wwere compared on the basis of behavioral content. Male wild mice were presented with opponents of two types, nonaggressive male mice and crickets, and the amounts of time spent in each of 18 behaviors were recorded. Results from analyses of variance and principal components analyses indicated that the structure of behavioral content differs greatly for intermale fighting and predatory behavior. It was, therefore, concluded that the integrated patterns of beahvior were controlled by separate mechanisms for predatory versus intermale aggression.     

Effect of anosmia on the behavior of standard non-aggressive male mice opponents during agonistic encounters

This study assessed whether the differences observed in a previous experiment [Martinez M, Salvador A, Simon VM (1994): Aggressive Behavior 20:441–451] in the behavior of isolated male mice over several agonistic encounters in which they confronted either an “anosmic” or an “intact” non-aggressive “standard opponent” were due to the differences in the behavior of the opponents themselves. Ethologically-inspired analysis was used to assess the behavior of the opponents during the first agonistic encounter. Anosmic opponents spent less time in social investigation and defense and more time in immobility than intact ones. These results suggest that the differences in the behavior of the opponents could be one of the causes of the differences observed in the behavior of the aggressive males confronting them. However, more research is needed to study if other variables, such as the production of odors, are also affected by the state (deprived or intact) of the olfactory sense. These findings provide additional support for the view that the type of opponent used in studies on intermale aggression is of paramount importance.Aggr. Behav. 23:179–181, 1997.© 1997 Wiley-Liss, Inc.     

Gender-specific social experiences and the development of aggressive and sexual behavior in male mice

This study examined influences of gender-specific social experiences on the development of aggressive and sexual behavior in male mice. To determine the effects of gender-specific social experience three different types of groups were constituted after the animals had been weaned. The subjects were randomly assigned to different treatments. Female groups were composed of one experimental male and three female cohabitants. Male groups were composed of five experimental males each, and the mixed-sex groups were composed of two experimental males and of two females. The experimental subjects stayed in these groups until the age of approximately three months, when the testing for sexual and aggressive behavior commenced. For the sexuality tests, a receptive female was placed in the home cage of the experimental male for ten minutes. A nonaggressive male was placed in the home cage of the experimental male for seven minutes for the aggression tests. The experimental males were administered both sexuality and aggression tests, the sequence of testing sexual and aggressive behavior was systematically varied in order to control the influence of the two different types of behavioral tests. The results showed that males with only male social experiences showed fewer responses and were less active in both the aggression and sexuality tests than the males from the two other types of groups. Significant positive correlations between activity during aggression and sexual tests were obtained for all three groups. © 1994 Wiley-Liss, Inc.     

THE EFFECT OF PRIOR AGGRESSIVE OR SEXUAL AROUSAL ON SUBSEQUENT AGGRESSIVE OR SEXUAL REACTIONS IN MALE MICE

Previous aggressive behaviour towards a male mouse was found to decrease sexual behaviour of inexperienced male mice towards a female in heat, mainly due to aggressive behaviour occurring in the sexual situation. Sexual behaviour decreased the aggression displayed in a subsequent encounter with a male. Instead, homosexual behaviour occurred in the situation with the male. After either sexual or aggressive behaviour had been practised, it was no longer influenced by practice of the other activity. Inhibition of aggressive behaviour by successive defeats did not affect sexual performance.     

Aggressive behavior induced by electrical stimulation in the midbrain central gray of male rats

Electrical stimulation via electrodes implanted in the lateral hypothalamus may induce intraspecific aggressive behavior. Small electrolytic lesions placed via these electrodes resulted in a five– to tenfold increase in the current threshold for aggression. Degenerating fibers were stained by means of the Fink-Heimer method and could be followed caudally to the dorsal midbrain central gray and to the mammillary bodies. A few axons could be traced rostrally to the medial septum. Aggression could be induced from 10 of 112 electrodes implanted in the central gray; the other electrodes elicited either locomotion, vocalization, jump, or “alarm-like reactions.” The morphology of the induced aggression was similar to the morphology of the hypothalamically induced aggression, though it was often accompanied with motor disturbances and was less intense. Hypothalamic stimulation was combined with simultaneous central gray stimulation in rats with electrodes both in the hypothalamus and in the central gray. Hypothalamic thresholds for aggression could be lowered by this stimulation of the central gray, even when no aggressive responses were observed during central gray stimulation alone. This suggests that, although aggression is not manifest, electrical stimulation may activate neural tissue involved in aggressive behavior. It is concluded that in rats central gray and hypothalamus are part of the same neural network mediating intraspecific aggression.     

The effects of ethnicity and perceived power on women's sexual behavior

To aid development of programs to prevent HIV transmission in women, differences in sexual attitudes and behavior were examined among women who described themselves as dominant in their relationship with a male partner, sharing dominance equally with a male partner, or being dominated by a male partner. Ethnic differences were also examined among these three groups. Results indicated that perceived dominance was a significant predictor of women's personal empowerment (self-efficacy and outcome expectancies) with regard to sexual decision-making in their current relationship and safer sex behaviors. Ethnic differences were found between African American and White women in personal empowerment and safer sex behavior. Perceived dominance did not appear to affect African American and White women differently.     

The effects of reward and punishment in violent video games on aggressive affect, cognition, and behavior

Three experiments examined the effects of rewarding and punishing violent actions in video games on later aggression-related variables. Participants played one of three versions of the same race-car video game: (a) a version in which all violence was rewarded, (b) a version in which all violence was punished, and (c) a nonviolent version. Participants were then measured for aggressive affect (Experiment 1), aggressive cognition (Experiment 2), and aggressive behavior (Experiment 3). Rewarding violent game actions increased hostile emotion, aggressive thinking, and aggressive behavior. Punishing violent actions increased hostile emotion, but did not increase aggressive thinking or aggressive behavior. Results suggest that games that reward violent actions can increase aggressive behavior by increasing aggressive thinking.     

Functional organization of the rat amygdala with respect to avoidance behavior.

Bilateral electrolytic lesions in the periamygdaloid piriform cortex of female albino rats produced marked disruptive effects on the acquisition of active avoidance responses in a 1-way as well as a 2-way test situation, significantly impaired passive avoidance behavior, and inhibited feeding in a novel environment. Lesions in each of the 6 major subdivisions of the amygdala (cortical, medial, central, intercalated, lateral, and basolateral nuclei) consistently produced facilitatory effects on active avoidance behavior in 1-way as 2-way situations. Passive avoidance behavior was impaired in animals with lesions in the central, intercalated, and basolateral nuclei. Damage to the anterior amygdaloid area or the the nuclei of the lateral olfactory tract did not reliably affect active or passive avoidance behavior.