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.     

Effects of early exposure to intermale aggression on the aggressiveness of adult male mice varying in their genetic disposition for aggressive behavior

This study examined whether adult male aggression is influenced by either visual or olfactory exposure in early postnatal life to brief episodes of aggression. Another focus of interest was the interplay between a genetic disposition for aggressive behavior and early exposure experiences. The subjects used in the study were male mice of the 49th 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 fighting males either behind a wire mesh or glass screen. Control subjects were isolated during the entire experimental period. At 90–100 days of age, each subjects was tested three times for its aggressiveness. Exposure to fighting males behind a wire mesh screen enhanced later aggressiveness of juvenile male mice. Juveniles exposed solely to visual cues were comparable to isolates, both groups showing less adult aggression. Early experience and the genetic disposition for aggression were correlated; TA males showing the greatest increase in aggressive behavior. The role of early olfactory learning is discussed. © 1993 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.     

Effects of alpha and beta adrenergic antagonists on aggressive behavior in male mice

The effects of a variety of alpha and beta adrenergic antagonists were examined on the social encounters of isolated male mice with anosmic male partners. A range of alpha antagonists, including phentolamine, prazosin, and yohimbine, all suppressed social aggression. A range of beta antagonists, including propranolol, atenolol, metaprolol, and ICI 118, 551, also reduced this type of attack. Ethological assessment of the lowest effective dose of these adrenergic antagonists revealed a marked inhibitor action on offensive, social, and nonsocial behavior, while defensive responses and immobility were enhanced. It is concluded that the noradrenergic system has a significant non-specific role in mediating intermale aggression via both alpha and beta adrenergic receptor subtypes. © 1993 Wiley-Liss, Inc.     

Stages in the development of aggressive behavior in early childhood

Primary manifestations of aggression appear in the behavior of children in the second half of the first year of life. The frequency of Occurrence of interpeer aggression increases with age, and reaches its maximum in the third year. The frequency of aggression may later decrease, but there are considerable individual differences. Changes a h Occur in the form in which aggression is manifested; its motivational background and associated elicitors; its direction, duration, timing, and other operational characteristics, and in the modes of its acquisition. A certain continuity may be traced, however, in any of these features and the development of aggression may be perhaps more adequately represented by the following sequence of developmental stage:

• 1 Stage of preaggressive behavior;
• 2 Stage of primary differentiation;
• 3 Stage of the appearance of the individual pattern of aggressive behavior;
• 4 Stage of secondary differentiation of aggression;
• 5 Stage of the beginning of the transition into covert behavior—internalization of aggression

These stages represent certain facets of the interaction between the changing behavioral performance of the child and herlhis social environment, and may be used for evaluating aggressive behavior in young children.     

Strain‐specific aggressive behavior of male mice submitted to different husbandry procedures

Severe aggression within groups of male laboratory mice can cause serious welfare problems. Previous experiments have shown that the transfer of specific olfactory cues during cage cleaning and the provision of nesting material decrease aggression and stress in group‐housed male mice. In this study, the combined effect of these husbandry procedures was tested for their long‐term effect on aggression in two strains of male mice (BALB/c and CD‐1). We used postcleaning aggressive behavior, wound counts, and testosterone levels as indicators of aggressiveness. Physiological responses to social challenge were investigated through urinary corticosterone and adrenal tyrosine‐hydroxylase measurements. Furthermore, the aggression‐modulating effects of two enrichment items (ShepherdShack/DesRes and PVC tube) were explored. Marked differences were found between the two strains. CD‐1 mice were more aggressive, had higher testosterone levels but lower corticosterone levels, and had fewer wounds than BALB/c mice. However, in neither of the two strains was long‐term enrichment with nesting material and its transfer after cage cleaning effective in lasting reduction of intermale aggression. This may be explained by the fact that aggression levels were generally low. It seems that housing mice in small, socially stable groups or keeping social disturbances to a minimum considerably modulates aggression in group‐housed male mice. Mice of both strains housed in cages enriched with nesting material had lower urinary corticosterone levels than standard‐housed mice. We therefore conclude that the long‐term provision of nesting material, including the transfer of nesting material during cage cleaning, may enhance the welfare of laboratory mice. Aggr. Behav. 29:69–80, 2003. © 2002 Wiley‐Liss, Inc.     

Pain‐induced aggression and changes in social behavior in mice

The effects of neuropathic, formalin, and acetic acid‐induced visceral pain were investigated on the social and aggressive behaviors in the Swiss male mice. Neuropathic pain was induced by tibial nerve transection (TNT). Also, somatic and visceral pain was conducted by intraplantar injection of diluted formalin (1%, 20 μl) and intraperitoneal administration of acetic acid (0.6%, 200 μl), respectively. Fourteen and twenty one days after the TNT surgery, and also, 1 and 7 days following formalin and acetic acid administration, the three‐chambered test was used to determine sociability and preference for social novelty and resident/intruder test was used for the evaluation of the aggressive behaviors. In the sociability phase of the three‐chambered test, all the three models of pain did not change the animal's sociability. However, in the social novelty preference phase, the animals in pain showed deficits in social novelty preference by a significant increase in the time spent with the familiar mice compared to the control groups. Also, animals in pain significantly showed more aggressive behaviors like biting and clinching and have much less attack latency in comparison to the control groups. Pain‐induced changes in the social novelty preference and aggressive behaviors continued in the neuropathic group until the end of the experiment. However, 7 days following the induction of both formalin and visceral pain, animals' social memory, and aggression almost returned to the standard value. These results suggest that long‐lasting pain could lead to social memory impairment and increase aggressive behaviors in mice.     

Female behavior in populations of mice in the presence and absence of male hierarchy

Female aggression may be the regulator of population size in small mammals. Freely growing populations of house mice showed several differences in aggressive female behavior in the presence and the absence of a male hierarchy. Territoriality in females and not in males appeared to maintain social order and regulate population density. Certain females were seen patrolling and guarding the territory and chasing and fighting with both male and female intruders. These females did not fight amongst themselves, suggesting that they were not fighting for rank (as do the males) but for territory. Although these aggressive females produced young, the pups were neglected, and few were weaned. The non-aggressive females were the successful breeders. Aggression by the females only occurred when there was reproduction and increased densities. Assembled females with no males present never show this aggression. The occurrence of “male-type” behavior became most apparent when the males were removed at peak population densities. The removed males were then castrated and injected with testosterone cyprionate. Doses were increased by population cage, and therefore all males returned to each freely growing population were given the same dose. The males given oil placebo injections showed no return of a male hierarchy and the females showed high levels of aggression toward them. Males injected with testosterone cyprionate showed return of male aggression and fighting and mounting of females. But the new “dominant” females continued their patrols and chased males away from their territories and did not permit these males to mount. Male-male fighting consisted primarily of frontal attacks to the face and roll and tumble fights. Female-male aggression consisted primarily of attacks to the posterior region targeted at the base of the tail and the genitals of the male. The males were rarely seen attacking females and then only during mating. Females only attacked each other in defense of their territories.     

The reinforcing properties of aggressive vs nonaggressive social interactions in isolated male ICR mice (Mus musculus)

Isolated male ICR mice in a T-maze consistently selected the goal box which enabled them to fight another mouse if the alternative goal box allowed no social interaction (Experiment 1). However, if the alternative choice enabled the isolated mice to interact with another mouse through a mesh screen which prevented fighting, the preference for the opportunity to fight did not appear (Experiment 2). Because the visual, olfactory, and auditory stimuli available through the screen appeared to be as attractive as the stimuli provided by the additional opportunity to fight, it is not necessary to conclude that the stimuli reinforcing the choice behavior in Experiment 1 were provided by fighting. Since there is no compelling reason to conclude that fighting is a primary reinforcer for these isolated mice, it is not necessary to argue that the high incidence of isolation-induced fighting is the reflection of a primary aggressive motive.     

Relationship between sexual activity and intraspecific fighting in male mice

Significantly more male mice having cohabited and mated with intact females subsequently displayed intraspecific fighting behavior after castration than males having cohabited with noncycling (ovariectomized) females. Also, intact males that failed to achieve a criterion for aggression during three screening tests subsequently showed a marked increase in fighting after having had copulatory experience relative to males that lived with ovariectomized females. Lastly, spontaneously aggressive males copulated more frequently than nonfighters.     

Habituation of aggressive behavior in mice: A parametric study

The decline of aggression as a result of repeated episodes of fighting may represent a habituation phenomenon. The frequency of biting and sideways threat by male mice toward conspecific intruders declined over ten 5-min confrontations. Aggression returned to about 50% of original levels when a new intruder was introduced. Variations in length or frequency of confrontation indicated that the rate of decline of attack bites and sideways threats depended on these confrontation parameters. The condition that provided the fewest opportunities to fight provided the least decline in the frequency of attack and threat. The frequency of attack bites and sideways threats elicited by the presentation of a new intruder after repeated confrontations was greater than the frequency of attack bite and sideways threat in the last confrontation with the original intruder, when the resident and intruder were relatively inexperienced. Spontaneous recovery of attack and threat occurred but rate of recovery did not depend on confrontation parameters. The results indicate that the decrement of aggression in mice in repeated confrontations may be the result of habituation but fatigue is an important cofactor.     

Some characteristics of the aggressive behavior of mice after prolonged Isolation: Intraspecific and interspecific aspects

Experiments on mice have demonstrated changes in the relationships, interdependence and sequence of behavioral items following prolonged isolation. It was found that aggression in isolates was stereotyped and hardly amenable to the control not only by intraspecific but also by interspecific factors. Isolated mice, in contrast to the group-reared animals, spontaneously attacked adult rats. This finding was interpreted as being due to a disruption of behavioral plasticity under circumstances of prolonged isolation from conspecifics.     

Differences between two strains of mice,selectively bred for high and low aggressiveness,in the capacity of male odors to affect aggressive behavior

The connection between a genetic disposition for aggressive behavior and the odor signal system in male mice was studied. The males belonged to two strains of mice which have been developed by selective breeding for high- (TA) and low aggressiveness (TNA). Urine from the high aggressive strain (TA), when applied to castrates, stimulated the aggressiveness of NMRI males while TA-soiled bedding suppressed their aggressiveness. In response to male odors from the low aggressive strain (TNA), the NMRI males showed quite contrasting reactions. The results provide evidences of a correlation between the hereditarily determined disposition for aggressive behavior and the odor signal system in TA- and TNA males.     

Differential sensitivity to the effects of nicotine and bupropion in adolescent and adult male OF1 mice during social interaction tests

Few studies have compared the action of both nicotine (NIC) and bupropion (BUP), an antidepressant used to treat NIC dependence, on social and aggressive behavior at different ages. This study aims to determine whether these drugs produce differential effects in adolescent (postnatal day: 36-37) and adult (postnatal day: 65-66) mice that have been housed individually for 2 weeks in order to induce aggressive behavior. Mice received BUP (40, 20, or 10 mg/kg), NIC (1, 0.5, and 0.25 mg/kg as base), or vehicle earlier to a social interaction test. BUP (40 mg/kg) decreased social investigation and increased nonsocial exploration in both adolescent and adult mice. The same effects were also observed in adult mice administered with a lower dose of the same drug (20 mg/kg). In adolescents, NIC (1 mg/kg) decreased social investigation, but this effect did not reach statistical significance in adults. In conclusion, a differential sensitivity to the effects of NIC or BUP emerged in some of the behavioral categories when the two age groups were compared.     

Community violence victimization and aggressive behavior: the moderating effects of coping and social support

Exposure to community violence (CV) as a victim is an established risk factor for exhibiting later aggressive behavior. It is unclear, however, what factors may mitigate this relationship. This study tested the relationship of CV victimization to aggressive behavior, and the roles of coping style and perceived social support in moderating that relationship. Five hundred and fifteen 18–22‐year‐old men and women completed self‐report inventories on CV exposure, aggressive behavior, perceived support from family and friends, and coping strategies. From a prior study, factor analysis of the coping scales yielded three factors of (1) disengagement (i.e., using primarily avoidant strategies), (2) interpersonal (i.e., using primarily emotion‐focused strategies) and (3) problem‐focused (i.e., using primarily active/approach strategies) coping styles. Results indicated that high CV victimization, high disengagement (i.e., avoidant) and interpersonal (i.e., emotion‐focused) coping styles, and low perceived support from friends significantly predicted increased aggression scores. Significant moderating effects indicated that, as CV victimization increased in frequency, aggression scores were highest for those with low perceived friend support and high use of disengagement coping. Findings suggest that avoidant and emotion‐focused coping styles are risk factors, and perceived support from friends is a protective factor, for a putative “cycle of violence.” Aggr. Behav. 32:502–515. 2006. © 2006 Wiley‐Liss, Inc.     

The effect of ethanol treatment on social behavior in male rats

The effect of 0.50 g/kg of EtOH in male rats interacting with a stimulus male juvenile in a newly developed test of social interaction was examined. The adult male rats were treated with EtOH (8.0 to 12.0 g/kg/day) or equicaloric dextrin maltose for 2 weeks (studies 1 and 2) or 8 weeks (study 3) and social interaction was assessed both before and after chronic drug treatment was ended in study 1 and after chronic drug treatment was ended in studies 2 and 3. It was found that prior to chronic drug treatment, in study 1, 0.50 g/kg of EtOH increased both aggressive behavior and time spent interacting with the stimulus juvenile male from the first presentation of the juvenile to the second presentation (20 min apart) while saline injection decreased it. After chronic drug treatment was ended, in study 1 animals treated chronically with EtOH were more aggressive when they were not intoxicated than when they had been treated with 0.50 g/kg of EtOH. In studies 2 and 3, after chronic drug treatment was ended, aggressive behavior and time spent interacting with the juvenile were greater in the animals treated chronically with EtOH, regardless of whether they were injected with saline or 0.50 g/kg of EtOH. The results of these studies showed that chronic EtOH treatment can produce long-lasting changes in social behavior after drug treatment is over and can alter the animal's normal response to EtOH in a social setting.     

Some consequences of aggressive behavior: A selective review of the literature on other animals

Animal experiments in which the opportunity to aggress was positively reinforcing are surveyed, with attention paid to field and laboratory reports on play and play fighting. A distinction is drawn between ways in which aggressive behavior may be elicited and factors which increase or decrease the probability that aggression will be emitted. Since aggression may be emitted and may also be reinforcing, the possibility that aggressive behavior may be self-reinforcing is mentioned. In addition to positive reinforcement, consequences of aggressive behavior are presented. These include punishment, removal of a noxious stimulus, feeding, arousal, and disinhibition.     

Exogenous testosterone and social experience each enhance the development of aggressive behavior in Cyprinodon variegatus

The combined effects of testosterone and social experience from the time of hatching on development of aggressive behaviors in Cyprinodon variegatus were investigated. Social experience was defined as a rearing condition allowing visual, tactile, chemosensory, and auditory contact with zero, three, or 15 additional conspecifics. Behaviors were videotaped once weekly from 3 weeks to 4 months post-hatching, using the focal animal method, and an ethogram was constructed. At 3 months post-hatching, half the fish were injected once with testosterone propionate (2 μg/g b. w., i. p., vehicle-Ringer's solution) and the other half were injected with Ringer's isotonic saline solution. Testosteronetreated subjects showed significantly greater frequencies and durations of behaviors that may be related to aggression than did saline controls. Two weeks after the treatments, a round-robin tournament was conducted between testosterone- and saline-treated fish from each rearing condition. Testosterone-treated fish won significantly more encounters than did saline-treated subjects over all rearing conditions. Furthermore, significantly more aggressive acts were displayed by fish raised in the groups of 16 and the groups of four than did the Isolates. Although the number of aggressive acts exhibited by the group of 16 was greater than the group of four, the difference was not statistically significant.     

The functions of freezing in the social interactions of juvenile high‐ and low‐aggressive mice

Selectively bred low‐aggressive mice are frequently observed to freeze on social contact, despite the fact that this behavior was never a direct target of selection. To elucidate this finding, the present research aimed to identify the possible functions freezing may serve in social interactions. It was hypothesized that freezing may modify social interactions through self‐regulatory mechanisms and/or via its modulating effects on the actions of social partners. These hypotheses were evaluated with respect to the sequential changes observed over the course of a 10‐min dyadic test in freezing, social reactivity, and approaches among juvenile (24–30‐day‐old) mice from the NC900 and NC100 high‐ and low‐aggressive lines. Analyses of the patterns of social interactions between subjects and partners revealed two primary results. First, freezing was more than an expression of fear; it also functioned as a regulator of emotional arousal, as suggested by the substantial reduction of reactive behaviors seen in animals that showed high levels of freezing. Second, freezing functioned to facilitate high levels of affiliative social interaction with social partners. The implications of these results for understanding how the differentiation of the NC900 and NC100 occurred within microevolution and development are discussed. Aggr. Behav. 27:463–475, 2001. © 2001 Wiley‐Liss, Inc.