Inter-male aggression in mice: Influence of gonadectomy and prior fighting experience

Groups of adult male mice of the Rockland-Swiss strain were paired 0, 2, 7, or 15 times with adult male stimulus animals rendered non-aggressive by extirpation of olfactory bulbs. All animals were castrated and tested until fighting ceased, following which each was given testosterone replacement and tested until fighting was reinstated. More than 50% of mice with no pre-castration fighting experience fought following gonadectomy. Castrated animals permitted 15 pre-castration pairings fought significantly longer than did animals of any of the other treatment groups. Finally, there was no difference among the groups with regard to the latency to resume fighting following the commencement of testosterone replacement. It is concluded that fighting experience enhances the persistence of the behavior following castration.     

Food deprivation: Effects on the predatory behavior of southern grasshopper mice (Onychomys torridus)

The southern grasshopper mouse (Onychomys torridus) is a predatory and aggressive rodent native to the semi-arid scrub deserts of the southwestern United States and northern Mexico. Its natural diet consists primarily of arthropods and small vertebrates. In this study, we have evaluated the effects of food deprivation on the predatory behavior of adult male and female grasshopper mice to crickets (Acheta domesticus) and laboratory mice (Mus musculus). Subjects that were food-deprived for 48 hours spent more time eating dead but not living crickets than did controls that were provided free access to laboratory chow. There were no sex differences in the predatory behavior of grasshopper mice to living or dead crickets. Food deprivation also influenced the predatory behavior of grasshopper mice toward laboratory mice. With laboratory chow available ad lib, 6 of 43 (14%) male and 22 of 45 (49%) female grasshopper mice killed and ate laboratory mice within 48 hours of pairing. When deprived of food for 48 hours, 16 of 36 (44%) males and 15 of 19 (79%) females that did not kill in the previous experiment killed and ate laboratory mice. We concluded that food deprivation and type of prey are two variables which influence the frequency and intensity of predatory behaviors of grasshopper mice.     

Factors influencing maternal attack on conspecific intruders by lactating female “TO” strain mice

Factors regulating maternal attack in “TO” strain mice were investigated to determine 1) optimal conditions for inducing this behaviour and 2) the likely utility of this activity. Lactating females were more likely to attack male intruders than female intruders. The mate's presence reduced maternal attack in this strain, or (putting it conversely) aggression was generated in the male's absence. Removal of the mothers from their litters for four to five hours also suppressed maternal attack. Investigation of the bite targets in the maternal attack suggested that it is a defensive, rather than an offensive, response.     

Analysis of the targets and tactics of conspecific attack and predatory attack in northern grasshopper mice onychomys leucogaster

Comparisons of tactics of fighting between species are often difficult to make since the body targets attacked may differ. Thus it becomes difficult to assess whether differences in fighting tactics are due to species-specific differences in the tactics themselves or due to the different targets attacked. A solution to this problem is to analyse the tactics of a species that attacks different targets under different circumstances. In this way, differences in tactics can be more readily attributed to differences in targets. In this study, resident male northern grasshopper mice (Onychomys leucogaster) were tested against intruding male conspecifics and against laboratory mice (Mus musculus domesticus). Conspecifics were mainly bitten on the lower dorsum, whereas prey were bitten and killed by bites to the nape of the neck. Therefore, it was possible to analyze the tactics of attack by grasshopper mice when attacking different body targets. For example, in order to defend the lower dorsum and the nape, both intruding conspecifics and prey adopted an upright defensive posture. Resident grasshopper mice used the lateral attack tactic to gain access to the lower flanks but not the nape. This illustrates that the lateral attack tactic is not merely a tactic suitable for overcoming the upright defense tactic, but is used in this context only when the target attacked is on the opponent's posterior dorsum. Such withinpecies comparison enables the identification of the contextual rules which govern the use of fighting tactics. © 1992 Wiley-Liss, Inc.     

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.     

Sleep deprivation impairs object recognition in mice

Many studies in animals and humans suggest that sleep facilitates learning, memory consolidation, and retrieval. Moreover, sleep deprivation (SD) incurred after learning, impaired memory in humans, mice, rats, and hamsters. We investigated the importance of sleep and its timing in an object recognition task in OF1 mice subjected to 6h SD either immediately after the acquisition phase (0-6 SD) or 6h later (7-12 SD), and in corresponding undisturbed controls. Motor activity was continuously recorded with infrared sensors. All groups explored two familiar, previously encountered objects to a similar extent, both at the end of the acquisition phase and 24h later during the test phase, indicating intact familiarity detection. During the test phase 0-6 SD mice failed to discriminate between the single novel and the two familiar objects. In contrast, the 7-12 SD group and the two control groups explored the novel object significantly longer than the two familiar objects. Plasma corticosterone levels determined after SD did not differ from time-matched undisturbed controls, but were significantly below the level measured after learning alone. ACTH did not differ between the groups. Therefore, it is unlikely that stress contributed to the memory impairment. We conclude that the loss of sleep and the activities the mice engaged in during the SD, impaired recognition memory retrieval, when they occurred immediately after acquisition. The delayed SD enabled memory consolidation during the 6h when the mice were allowed to sleep, and had no detrimental effect on memory. Neither SD schedule impaired object familiarity processing, suggesting that only specific cognitive abilities were sensitive to the intervention. Sleep may either actively promote memory formation, or alternatively, sleep may provide optimal conditions of non-interference for consolidation.     

Fighting in female mice in lines selected for laterality

Male and female mice from the Collins HI and LO laterality strains were isolated for 3–5 days. Thereafter on Day 1 each was given the Intruder Test followed by a Training Test; the latter was repeated 1 week later. All males of 36 days or older fought vigorously, but without line differences. Females of the HI strain showed higher numbers of fighters and greater intensity of fighting than those of the LO strain, and by the second Training Test these differences were significant at p < 0.01. The HI and LO laterality strains thus provide useful tools for investigating the functions of female agonistic behavior and the possible relationship between laterality and the expression of aggression.     

Maze-running and thigmotaxis in mice: Applicability of models across the sexes

Both male (n = 244) and female (n = 223) Swiss albino mice displayed a U-shaped pattern of thigmotaxis (wall-seeking) in a circular open-field (OF) before and after a daily maze-running. A significant increase of mice's tendency to occupy the inner partitions of the OF after the maze trial on the last three out of five days of training was observed. When factor analyzed, the variables indicating the wall-seeking behaviour of both sexes were divided into two factors interpreted as "spontaneous" in conjunction with the first three to four maze trials and as "learning-related thigmotactic behaviour" during the subsequent trials in the course of the learning process.     

Food choice in rats (Rattus norvegicus): the effect of exposure to a poisoned conspecific

Three experiments were conducted to examine the effects of exposure to a poisoned conspecific on subsequent food aversion in rats. In Experiment 1A, rats that had been aversively conditioned to a cocoa-flavored food were exposed to a poisoned conspecific that had eaten the same food. On the subsequent choice test, the animals increased their aversion to that food. These results were reconfirmed in Experiment 1B, in which a cinnamon-flavored food was used as the stimulus. In Experiment 2, subjects were first exposed to a poisoned conspecific and then conditioned to the food which the conspecific had eaten. On the test, they showed no sign of increased aversion to that food.     

Freedom deprivation in prisons of Serbia

The subject of this research is the deprivation of freedom at two time points. A total of 490 convicts from open, semi‐open, and closed prisons participated in the research. Freedom deprivation intensity was determined by using the freedom deprivation scale (α = .93). The results of the research indicate that almost all the participants reported freedom deprivation. The prison type had an impact on freedom deprivation intensity, whereas an influence of the ward type on deprivation was not demonstrated. Freedom deprivation intensity was consistent from the turn of the century to the present day.     

Prenatal testosterone treatment potentiates the aggression‐inhibiting effect of the neurosteroid dehydroepiandrosterone in female mice

The neurosteroid dehydroepiandrosterone (DHEA) is a powerful inhibitor of aggression in murine models when given for 15 days and potentially may be useful in the management of inappropriate human aggression. Although the biosynthesis and metabolism of DHEA have been described, little is known about the potential effect of the steroidal environment during sexual differentiation on the subsequent response to DHEA. Whether prenatal androgen exposure influences the subsequent response to DHEA was assessed by comparing the effect of DHEA (80 μg/d) on aggression in female offspring where dams were treated with 1, 10, or 100 μg of testosterone (T) on days 15 to 18 of gestation (Experiment I) or that developed in different uterine positions (Experiment II). The results showed that DHEA decreased attack behavior in general and that the 100‐μg prenatal T treatments enhanced the antiaggressive effect of this neurosteroid. Neither the lower doses of exogenously administered T nor the uterine position led to an enhanced response to DHEA. In addition, whether DHEA produced changes in social and nonsocial activities was examined. In the 100‐μg T females, DHEA increased the duration of the former and decreased the frequency and duration of the latter, indicating that it was not a general decrement in behavioral expression that mediated the enhanced response to the antiaggressive effect of DHEA. In the second experiment, DHEA treatment led to increased frequencies of social nonaggressive and nonsocial activities. However, the uterine positions × treatment interactions were not significant, demonstrating that contiguity to male fetuses did not differentially affect the response to DHEA. Aggr. Behav. 27:130–138, 2001. © 2001 Wiley‐Liss, Inc.     

Naloxone differentially alters parental aggression by female mice towards conspecific intruders of differing sex

Lactating mice respond differently to male and female conspecific intruders, displaying defensive attack towards the former and offensive attack towards the latter. Two studies are reported in which the effects of naloxone on this differential response pattern were assessed. In the first study, lactating residents were pretreated with saline or naloxone (0.5, 2.5 mg/kg) and consecutively confronted with intruders of differing sex. Results suggested that attack (offensive) against female conspecifics is more sensitive to the inhibitory effects of opiate-receptor blockade than attack (defensive) on males. This conclusion was strengthened in a follow-up study, in which independent groups of lactating residents were used to further examine the effects of naloxone (0.5 mg/kg) on response to male and female intrusion. Analysis indicated that this low dose of naloxone significantly inhibited attack on female, but not on male, intruders. Indeed, in response to male, but not to female, intrusion, naloxone-treated residents showed a significant increase in fear-related behaviour. Findings are discussed in relation to the motivational differences in the response of lactating mice to intruders of differing sex and to possible mechanisms underlying the reported differential effects of opiate-receptor blockade.     

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.     

Effects of ritanserin on offense and defense in male mice

Effects of ritanserin on agonistic behavior of isolated mice exhibiting aggressive or nonaggressive behavioral strategies were studied in pair-wise encounters with group-housed opponents. An ethological approach to behavioral scoring is adopted, which allows for examination of the profiles of individual subjects. Although the data generally support the view that ritanser in has little effect on offense or defense in male mice, the stimulation of pre-aggressive behavior (threats, alerts, tail rattles) was detected in some nonaggressive mice. © 1995 Wiley-Liss, Inc.     

Relationships between testosterone metabolism in the brain,other endocrine variables and intermale aggression in mice

Relationships between some endocrine variables (plasma testosterone and estradiol; in vitro gonadal biosynthesis from pregnenolone precursor and adrenocortical biosynthesis from progesterone precursor; in vitro activity of 17β-hydroxysteroid de-hydrogenase (17β-HSDH) and of aromatizing enzymes in the subcellular fractions of the brain) and isolation-induced inter-male aggressiveness were studied. A significant positive correlation was found between fighting behavior, measured by the number of wins in a series of paired encounters, and the activity of brain 17β-HSDH. A significant inverse correlation was found between fighting behavior and the activity of aromatizing enzymes in the nuclear fraction of the brain. No significant correlations were found between fighting and the other endocrine variables investigated. These results may suggest that the conversions testosterone → androstenedione and testosterone → estradiol in the brain play a role in the control of inter-male fighting in the mouse. These results may also account for the effect of repeated wins and defeats on brain steroidogenesis.     

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.     

Some adrenal correlates of aggression in isolated female mice

Forty-six female mice (CFW) were isolated for a period of 23 weeks. The effect of isolation on fighting behavior was tested weekly by introducing a naive brown female mouse into the subject's home cage. Total leucocyte counts were obtained at 8 and 14 weeks of isolation. The appearance of leucopenia was used as an index of elevated adrenocortical activity. After 23 weeks of isolation all animals were sacrificed by decapitation. Plasma was collected for corticosterone assay, and paired adrenals were used to assay catecholamine levels. On the basis of the frequency and/or the absence of fighting, the mice were segregated into fighters (n = 22) and non-fighters (n = 17). Analysis of the data by Pearson's product moment correlation and Student's t-test showed that elevated sympathetic-adrenal activity was positively correlated with aggression and that elevated adrenocortical activity was negatively correlated with aggression.     

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.     

Leaving patches: effects of economy, deprivation, and session duration

Three pigeons pecked keys for food reinforcers in a laboratory analogue of foraging in patches. Half the patches contained food (were prey patches). In prey patches, pecks to one key occasionally produced a reinforcer, followed by a fixed travel time and then the start of a new patch. Pecks to another key were exit responses, and immediately produced travel time and then a new patch. Travel time was varied from 0.25 to 16 s at each of three session durations: 1, 4, and 23.5 hr. This part of the experiment arranged a closed economy, in that the only source of food was reinforcers obtained in prey patches. In another part, food deprivation was manipulated by varying postsession feeding so as to maintain the subjects' body weights at percentages ranging from 85% to 95% of their ad lib weights, in 1-hr sessions with a travel time of 12 s. This was an open economy. Patch residence time, defined as the time between the start of a patch and an exit response, increased with increasing travel time, and consistently exceeded times predicted by an optimal foraging model, supporting previously published results. However, residence times also increased with increasing session duration and, in longer sessions, consistently exceeded previously reported residence times in comparable open-economy conditions. Residence times were not systematically affected by deprivation levels. In sum, the results show that the long residence times obtained in long closed-economy sessions should probably be attributed to session duration rather than to economy or deprivation. This conclusion is hard to reconcile with previous interpretations of longer-than-optimal residence times but is consistent with, in economic terms, a predicted shift in consumption towards a preferred commodity when income is increased.     

A sensory contact model for the study of aggressive and submissive behavior in male mice

The technique for simultaneous development of aggressive and submissive behaviors as a result of successive experiences of defeats or victories in daily intermale confrontations in male mice permanently living under sensory contact conditions is offered for behavioral, pharmacological, and neurophysiological studies of mechanisms of agonistic social relations. Distant sensory contact is achieved by placing a pair of males into a common cage separated by a transparent partition with holes permitting visual contact and the individuals perceiving each other's odors but preventing any physical at contact all times except for 10-min daily tests. These conditions essentially elicit aggression in winner males and quickly result in submission by losers of the same strain of mice. The meaning of consecutive stages of the technique, the problem of controls, and applications of this model are discussed.