Differential sexual activity of isolated and grouped male mice despite testosterone administration

In Experiment 1, adult male C57 mice were castrated, housed individually or in groups of four, and repeatedly injected with either of two doses of testosterone. Control mice were sham-castrated, individually or group housed, and injected with oil vehicle. In repeated tests of sexual behavior with receptive females, isolated males in all surgery-dose combinations showed significantly more mounts and intromissions than did their group-housed counterparts. Ejaculations were fully restored by testosterone in castrated grouped males but not in castrated isolated males. In Experiment 2, administration of either of two doses of testosterone failed to elevate the sexual behavior of intact group-housed males. These experiments show that housing with other males depresses all major measures of sexual behavior, and suggest that this is probably independent of testicular hormones.     

Differential effect of handling on adult aggression in male mice bidirectionally selected for attack latency

Individual variation in intermale aggression is to a significant degree based upon genetic variation, but environmental factors can also exert their influence on the level of aggression. Moreover, genotype–environment interactions are a well‐known phenomenon. In the present experiment, I tested whether cage size or handling during development had an influence on adult attack latency scores. To be able to study a genotype–environment interaction, mice from two bidirectionally on attack latency selected lines were used. The size of the cage in which the mice grew up had no long‐term effect on aggression, neither in the high‐ nor in the low‐aggressive line. Handling, however, significantly increased the adult aggression of males from the low‐aggressive line. Despite the differential effect of handling on genetically high‐ and low‐aggressive mice, handling was not able to undo the marked differences in attack latencies between mice from both lines. Aggr. Behav. 25:365–368, 1999. © 1999 Wiley‐Liss, Inc.     

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.     

Selective antiaggressive effect of an alpha-2 adrenoceptor agonist naphthylmedetomidine in mice

Alpha-2 adrenoceptors (alpha(2)-ARs) are critically involved in regulating neurotransmitter release from sympathetic nerves and neurons and play an important role in the regulation of awareness, arousal and vigilance. In our recent study, dexmedetomidine, a full alpha(2)-AR agonist, produced antiaggressive effects in the social conflict test in mice at doses that were twice smaller than those producing sedation. The aim of this study was to ascertain antiaggressive effect of a novel drug naphthylmedetomidine, with a more selective alpha(2)-AR activity. Behavioral effects of naphthylmedetomidine (150-1200 microg/kg i.p.) were studied in the activity cage and in the social conflict tests in mice. Naphthylmedetomidine dose dependently decreased aggressive behavior during social conflict in aggressive mice with significant reduction already at the lowest doses tested (150 microg/kg), whereas locomotion and social investigation were significantly decreased only after four times bigger dose of naphthylmedetomidine (600 microg/kg) in aggressive mice. Naphthylmedetomidine had no effect on aggression in nonaggressive mice. Naphthylmedetomidine reduced locomotion in the activity cage significantly only at the highest doses tested (600 and 1200 microg/kg), and this effect was only partially reversed by administration of high doses of an alpha-2 antagonist atipamezole (3 and 10 mg/kg). In nonaggressive mice, the difference between the dose reducing dominant social behavior (social investigation) and locomotion (150 and 300 microg/kg, respectively) was smaller than in aggressive mice. In conclusion, naphthylmedetomidine showed a very strong and selective antiaggressive effect in aggressive mice, which was devoid of locomotion-inhibiting/sedative effect. This study suggests that naphthylmedetomidine may have clinical potential as antiaggressive drug.     

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.     

Mousekilling,intermale fighting,and conditioned emotional response in rats

Several possible relationships between two forms of aggression in rats were studied. First, mouse killing and spontaneous intermale fighting were found to be correlated. Rats which attacked other rats were those most likely to kill mice. To determine whether aggressive and nonaggressive rats were also differentially responsive to other situations involving emotional arousal, but not aggression, mouse-killers and nonkillers were compared in a conditioned emotional response (CER) situation. Mouse-killers showed greater suppression to the conditioned stimulus (CS) and to the situational cues of the apparatus. Therefore, a common arousal mechanism may underlie a number of diverse agonistic responses. Nevertheless, extensive mouse-killing experience did not increase the tendency of rats to fight with either adult males or juvenile males.     

Effects of Early Maternal Separation on Subsequent Reproductive and Behavioral Outcomes in Male Rats

To investigate effects of maternal separation on reproductive and behavioral outcomes, male Wistar rats were separated from their mothers daily for 3 hr (maternal separation; MS) or 0 hr (control) from postnatal day (PND) 1 to 14. Timing of puberty, reproductive parameters, hormone levels, and aggressive behaviors in juvenile and adult rats were examined. Contrary to expectations, there was no effect of maternal separation on any measure of aggression. However, maternal separation altered peripubertal testosterone secretion and increased mean day of preputial separation. In addition, adult MS males demonstrated less total sexual behavior. There was no difference in sperm counts or testosterone levels at necropsy on PND 56 or in adulthood, but seminal vesicle weights were increased in adult MS rats. These results suggest that early life stress may influence hypothalamic-pituitary-gonadal axis development in males, at least during peripuberty.     

Effects of pairing aggressive and nonaggressive children in strategic peer affiliation

Examined the behavior of 118 second graders who participated in a 6-week summer school program that incorporated strategic peer affiliation (a buddy system). Moderately aggressive children (the targets of the intervention) were paired with nonaggressive peers throughout the program. All participants were observed playing foosball with their buddies and with aggressive and nonaggressive nonbuddies as teammates. Aggressive children had lower levels of disruptive behavior when their teammate was nonaggressive, regardless of whether the teammate was a buddy. Nonaggressive children showed elevated disruptive behavior when playing with an aggressive nonbuddy, but not when playing with an aggressive buddy. The highest level of aggressive behavior was seen in pairs of aggressive teammates who were friends. One year later, no increase in peer-rated aggressive behavior was found in either group. Results suggest that unidirectional peer influence is possible and that strategic peer affiliation can be an effective intervention that does not put nonaggressive children at risk for acquiring undesired behaviors.     

Studies on wild house mice iv: On the heredity of testosterone and readiness to attack

An attempt was made to determine the role of the Y chromosome in the development of aggression in wild house mice. The aggression-eliciting property of testosterone depends not only on circulating adult testosterone, but also on perinatal sensitization of the central nervous system to this steroid. Results of crosses between aggressive (SAL) and non-aggressive (LAL) mice indicate that adult plasma testosterone in these mice is determined by the autosomes, high testosterone levels being dominant over low levels. Conversely, the Y-chromosomal effect seems related to perinatal processes that sensitize the brain for testosterone.     

睾酮与人类攻击行为

睾酮是一种可以在男性的睾丸间质细胞、女性卵巢和胎盘的皮层细胞中合成并分泌的雄性激素, 它可以调节个体的各种生理、形态和行为过程, 对个体生存和繁殖至关重要。大量研究表明, 睾酮与社会行为的关联存在双向性, 睾酮可以调节社会行为, 社会行为可以反馈并进一步影响睾酮水平。我们将关注点聚焦于睾酮与人类攻击行为之间的关联。早期研究发现, 高睾酮水平个体表现出更高的攻击性; 近期的研究根据挑战假设理论模型和生物社会地位模型得出, 人体内的睾酮水平对竞争性相互作用具有高度反应性。此外, 通过对大量研究的回顾与分析, 我们总结出睾酮水平的变化可以通过增强杏仁核的反应性或减少前额叶皮质-杏仁核功能耦合来影响攻击行为。未来的研究者应考虑其他激素(如皮质醇)和人格特征调节睾酮和人类攻击行为之间关系的潜在作用, 以及相关的生物学机制。     

Sex differences in behavioral consequences of defeat in the rat are not organized by testosterone during early development

Male and female rats react differently to losing an aggressive encounter, the presence of testosterone (at the time of confrontation) being a critical factor in the manifestation of this sex difference. Female rats were androgenized by 250 μg testosterone propionate sc on days 1 and 5 after birth. When adult they received a sc testosterone proprionate (TP) implant and were subjected to repeated defeats by being placed in the cage of an aggressive resident female. In contrast to males, which freeze and become permanently submissive, androgenized females showed no freezing or other signs of submission. The sex difference in response to defeat is therefore not dependent on the presence of testosterone during the period of post-natal sexual differentiation.     

Effects of neonatal treatment with cyproterone acetate on aggressive behavior induced by footshock in adult male rats

High levels of androgens are required to organize aggressive behavior in adult male rats. Footshock-induced aggression was tested in Wistar rats allocated to one of three experimental groups: control (oil-injected) males (M), males neonatally injected with the antiandrogen cyproterone acetate (CA), and males treated as in the CA group but gonadectomized just before puberty (CAG). An antiaggressive effect of CA in those adult male rats neonatally treated with this compound was found. Neonatal exposure to cyproterone acetate exerts an antiandrogenic effect over the expression of shock-induced aggressive behavior. The behavioral effects of CA were not countered by adult treatment with testosterone propionate.     

Using Articulated Thoughts in Simulated Situations to Assess Cognitive Activity in Aggressive and Nonaggressive Adolescents

Articulated Thoughts in Simulated Situations (ATSS) is a think aloud method for examining a person's thought content as it unfolds in the situation. We used the ATSS to investigate the cognitive activity of aggressive and nonaggressive male and female adolescents as they listened to an audiotaped depiction of an ambiguous but provocative interaction with another student. Eighty-one adolescents participated in a 2 × 2 factorial experiment. The two factors were gender and aggressive vs. nonaggressive background. Students in the aggressive group had a history of aggressive behavior in the past year that was severe enough to warrant their arrest or suspension from school. Students in the nonaggressive group had no such history. As a secondary measure of anger and aggressiveness, we administered the State-Trait Anger Expression Inventory-2 (STAXI-2). As predicted, males, compared to females, expressed more aggressive intent on the ATSS. Likewise, aggressive, compared to nonaggressive, adolescents expressed more anger and aggressive intent on the ATSS, as well as more intense feelings of anger, less control over their anger, and a greater tendency to externalize angry feelings on the STAXI-2. As expected, scores on the ATSS were related to scores on the STAXI-2. We concluded that the ATSS is a useful method for assessing cognitive activity that may mediate aggressive behavior in adolescents.     

Stress induces glucocorticoid-mediated apoptosis of rat Leydig cells in vivo

Stress can disrupt endocrine signalling in the male reproductive axis through high concentrations of glucocorticoids, the hallmark of stress. Our previous work revealed that a stress level of exogenous glucocorticoids could induce apoptosis of rat Leydig cells, which are the primary source of testosterone. The aim of this study was to investigate whether stress can induce apoptosis in rat Leydig cells in vivo and, if so, whether the process is the result of a direct effect of glucocorticoids. In a chronically stressed rat model, serum corticosterone concentration was increased significantly whereas serum testosterone was decreased. The frequency of apoptotic Leydig cells in stressed rats was also increased. Adrenalectomised rats subjected to chronic stress showed an elevated serum testosterone, while the apoptotic frequency of Leydig cells was not increased. It was established that glucocorticoid-induced Leydig cell apoptosis is mediated by glucocorticoid receptors (GRs), which translocate from cytoplasm to nucleus. Adenovirus microRNA-induced downregulation of GR expression in vitro alleviated the corticosterone-induced increase in apoptosis of Leydig cells. These results indicate that the stress-induced increase in corticosterone secretion resulted in apoptosis in rat Leydig cells in vivo, and thereby decreased testosterone synthesis.     

The decline of aggressiveness in male mice during group caging as determined by punishment delivered by the cage mates

Group-housed rodents are generally less aggressive than isolated counterparts. The present study examined the role of defeat by cage mates as a reason for this decline in aggressiveness. In Experiment I, highly aggressive isolated male mice were introduced into aggressive or nonaggressive resident groups. The intruder's level of aggressiveness directed toward a group-housed standard opponent declined more rapidly after daily exposure to the aggressive than to the nonaggressive groups. Intruders in the aggressive groups received more attacks from their cage mates, and delivered fewer attacks to them than did the intruders in the nonaggressive groups. In Experiment II, the intruders lived for seven days in small wire net cages in the middle of the group cages. Their level of aggressiveness toward standard opponents decreased little during the preexposure but after being put freely into the groups, their aggressiveness declined to a minimal level within a day. Experiment III showed that when the wire net protection in the middle of the cage was installed after the group caging experience, the aggressiveness of the intruders did not return to the isolation level as effectively as it did in isolation. This is explained by the aggression-inhibiting content that the cues from the cage mates have acquired during group caging. The decline of aggressiveness in male mice during group caging is determined by punishment delivered by the cage mates.     

Olfactory stimuli and intermale aggression in androgen-treated castrated sheep

The ability of olfactory stimuli to elicit aggression in male sheep was assessed in testosterone-treated castrates. Ablation of the olfactory bulbs (Exp. 1) did not reduce the capacity of sheep to participate in aggressive behaviour after testosterone treatment. Topical application of urine from castrates treated with propionated testosterone, 5α-dihydrotestosterone, 17β-oestradiol, or an oil vehicle to the fleeces of untreated castrates (Exp. 2) did not result in different levels of aggressive responsiveness in testosterone-treated castrates.     

Adrenal mediation of intermale aggression maintained by aromatized and reduced metabolites of testosterone

Individually housed CD-1 mice were either sham castrated or castrated and treated with testosterone (T), estradiol benzoate (EB), dihydrotestosterone (DHT), a combination of EB and DHT (EB+DHT), or the injection vehicle. Following 16 days of isolation and subcutaneous injections, animals were tested repeatedly for fighting behavior in paired encounters with nonaggressive stimulus males. Results indicated that the T and EB+DHT groups fought to the same extent as the gonadally intact group. Both the EB and DHT groups fought more than the vehicle-treated group but less than the T, EB+DHT and sham castrated groups. A similar study was subsequently performed with adrenalectomized animsls. Adrenalectomy eliminated agonistic responses in animals receiving metabolites of testosterone (EB, DHT, EB+DHT) but had only slight effects in gonadally intact and T-treated, castrated mice. The results suggested that a) EB and DHT, either singly or in combination, maintain aggression through a synergism with adrenal steroids; b) the combined effects of EB and DHT reflect an additive action rather than synergistic interaction, notwithstanding the synergism with adrenal steroids; c) metabolism of testosterone to estrogen and dihydrotestosterone does not sufficiently account for the action of testosterone.     

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.     

Agonistic rank,aggression, social context,and testosterone in male pigtail monkeys

Two groups of pigtail monkeys were merged, a third was formed, and individual males were introduced into a group in a series of experiments examining the effects of social context upon agonistic rank, aggressive expression, and testosterone levels. In the first experiment, two heterosexual groups, containing adult males unfamiliar to the other group, were merged. The two groups fought, and the smaller group was defeated. The alpha and beta males of the defeated group were singled out for repeated attack and both showed significant drops in circulating levels of testosterone. Both males were removed from the group during the first day, but testosterone levels did not recover to baseline levels for several days. The alpha male of the victorious group, on the other hand, showed a significant rise in testosterone, which was apparent only on the day following the merger. In order to study the influence of previous social familiarity on male reception into a group, another group was formed by removing males from the victorious group and placing them in a separate enclosure. The males in the new group established a dominance hierarchy unrelated to their previous social ranks with one another. Three months later, each of the six adult males remaining in the parent group was individually introduced into the new group for one day or less. Each of the males introduced into the new group accepted a social position at the lower end of the dominance hierarchy without regard to his previous rank relationships with the host males when they were all in the parent group. Even the alpha and beta males of the parent group were relegated to low rank positions in the new group, despite having ranked over each of the host males since birth. In contrast to the aggression directed at the unfamiliar males in the first experiment, a minimum of aggression was directed to the familiar males introduced into the new group in the second experiment. Although the males introduced accepted low social ranks, it appeared that each was readily integrated into the group with a minimum of aggressive interaction during the time he was scheduled to remain in the group. There were no significant changes in circulating levels of testosterone in any of the males during the introductions of familiar males to one another.     

The Role of Relational Aggression in Identifying Aggressive Boys and Girls

Peer perceptions of relational and overt aggression and peer evaluations of social competencies were obtained for 461 boys and 443 girls in second and third grades. In contrast to Crick and Grotpeter (1995), boys obtained higher relational and overt aggression scores than girls, and the relation between both types of aggression and peer evaluations were similar for boys and girls. When controlling for levels of overt aggression, relational aggression made a statistically significant but small contribution to the prediction of both peer-evaluated competencies and teacher ratings of aggression in boys and girls. Analyses treating relational and overt aggression as categorical variables revealed gender differences in the prevalence and corresponding sociometric status of aggressive subtypes. When peer-rated relational aggression status is not considered, 60% of aggressive girls, compared to 7% of aggressive boys, are not identified as aggressive. High levels of overt aggression were more likely to result in peer rejection for girls than for boys. In a subsample of 112 children, peer-rated relational aggression contributed more to the discrimination of teacher-identified aggressive and nonaggressive girls, whereas peer-rated overt aggression contributed more to the discrimination of teacher-identified aggressive and nonaggressive boys.