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Social partner preferences of male and female fighting fish (Betta splendens).

While the social interactions of Betta splendens have been studied in the contexts of dominance hierarchies, mate choice and communication networks, the social partner preferences of Betta have been largely overlooked. In this study, we presented male and female Betta with a single male, a single female, and a group of three females in dichotomous choice tests in order to better understand basic social interactions in this largely nonsocial species. The highly territorial Betta preferred associating with conspecifics in nearly every configuration we tested, with exceptions noted when single females were given the choice between a lone male and an empty chamber, and when males were presented with a single female and an empty chamber. Also, in most tests, the fish chose to spend more time with the larger group of females. The motivation for this preference certainly varied from reproductive to anti-predator. While such behavior might not suggest true shoaling behavior, it does demonstrate a subtle degree of sociality.

Aggression↗

[Behavioral pharmacological action of Ca-4-(3,5-dihydroxy-3-methylpenthylamido) butyrate (mevalonic GABA, MV-GABA)].

The behavioral pharmacological effects of Ca-4-(3,5-dihydroxy-3-methylpenthylamido) butyrate (mevalonic-GABA, MV-GABA), a new GABA derivative were studied in comparison with those of Ca-hopantenate (HOPA) in mice. MV-GABA had no effect on the general behavior and electric shock-induced fighting behavior. The dosage of MV-GABA which caused locomotor hypoactivity produced an impairment of the rotarod performance. MV-GABA inhibited the hyperactivity induced by a dopamine (DA) agonist (methamphetamine) and acetylcholine (ACh) antagonists (scopolamine and atropine) at a dose which did not affect locomotor activity in normal mice. MV-GABA prolonged the pentobarbital-Na-induced sleeping time, and it prolonged the latencies until convulsion and death after administration of strychnine. MV-GABA and HOPA antagonized the electroconvulsive shock-induced amnesia in the passive avoidance response of mice. These results suggest that MV-GABA has effects on the central nervous systems, in particular, ACh and DA neural systems. The actions of MV-GABA were qualitatively similar to those of HOPA except for the effect on the DA neural system.

Agonistic Behavior↗

Serum NGF levels increase during lactation and following maternal aggression in mice.

In the present study, serum levels of nerve growth factor (NGF) were assessed in virgin and in lactating female CD-1 mice. In the case of the lactating females, NGF levels were assessed both under basal conditions and 60 and 180 min following a 10 min encounter with a male or a nonlactating female mouse. Basal serum NGF levels of lactating females were higher than those of virgin females but did not increase significantly above base after an aggressive encounter with a male or a female conspecific. Female intruders were attacked in a ritualized manner. In contrast, males received numerous bites to vulnerable regions of their body. A positive correlation was found between serum NGF levels and pattern of aggression in females confronting male conspecifics. Thus, in lactating mice, serum NGF levels following an aggressive encounter relate to the specific pattern of behavior the female uses to defend the offspring.

Aggression↗

Diterpene sclareol glycol inhibits clonidine-induced aggressive responses in mice.

The effects of a reversible activator of adenylate cyclase sclareol glycol (SG), a semisynthetic diterpene of the labdane family, on the aggressive behavior induced by a high dose of clonidine in mice were studied. SG was applied at doses well below the lethal dose. Aggressive behavior induced by clonidine at a dose of 30 mg/kg IP was decreased in a dose-dependent manner by SG (1, 5, 25 mg/kg IP). The aggressive responses were abolished by doses of 50 and 100 mg/kg. It is suggested that the inhibitory effects of SG on clonidine-induced aggressive behavior are realized mainly via its effect on adenylate cyclase and perhaps involving synaptic transmitter action.

Aggression↗

Dopaminergic alterations in cotreatments attenuating haloperidol-induced hypersensitivity.

Chronic treatment of the laboratory rat with haloperidol results in an increased stereotypic behavioral response to subsequent dopamine agonist challenge. This behavioral hypersensitivity (BH) is thought to reflect an increase in DA receptor number following chronic pharmacologic denervation. Using a cotreatment strategy, we demonstrate here that a variety of agents can attenuate or prevent the development of BH when administered chronically with haloperidol. Cotreatment with lithium and amantadine prevented the changes in DA biochemistry as well as the proliferation of DA receptors normally associated with chronic haloperidol treatment. Cotreatment with thioridazine or scopolamine did alter the changes in DA biochemistry normally associated with haloperidol treatment, but failed to attenuate the DA receptor proliferation. Taken together, these data suggest that mechanisms in addition to DA biochemical and receptor changes participate in the development and subsequent expression of BH. DA receptor proliferation must, therefore, be considered permissive to the development of BH.

Amantadine↗

Effects of ACTH applications during pregnancy on the female offsprings' endocrine status and behavior in guinea pigs.

The present study was conducted to elucidate the effects of ACTH application during pregnancy on the female offsprings' endocrine status and behavior in a precocial animal, the guinea pig. We, therefore, studied daughters whose mothers were treated three times with either ACTH-depot or placebo during the sensitive phase of central nervous sexual differentiation of the foetus. From their 41st through their 80th day of age the spontaneous behavior of the daughters was recorded in their home cages, and concentrations of serum cortisol were determined from the 20th through the 90th day of age every 14 days. Daughters whose mothers had received ACTH displayed significantly lower amounts of a defensive aggressive behavior pattern, the urine spray, and they had higher cortisol concentrations than daughters whose mothers had received placebo. Thus, the number of species that shows consequences of an ACTH treatment during pregnancy for the offsprings' endocrine status and behavior is extended to include a precocial animal, the guinea pig.

Adrenocorticotropic Hormone↗

Gonadal hormones and aggression-maintaining effect of alcohol in male transgenic transforming growth factor-alpha mice.

We have characterized a new transgenic mouse model that offers the unique opportunity to study the biological mechanisms linking aggression to alcohol. In contrast to all other aggressive animal models, the male transgenic mice that overexpress transforming growth factor-alpha (TGF-alpha) maintain their highly elevated aggressive behavior following an alcohol administration. The transgenic mice also exhibit elevated plasma levels of 17 beta-estradiol (E2). Animal data support the role of E2 in aggression and alcohol intake in males. Further, type 2 alcoholism is male-limited, suggesting that gonadal hormones are important. We examined whether gonadal hormones play a role in the resistance to respond to alcohol in the resident-intruder test of aggression among the male transgenic TGF-alpha mice. As previously reported, alcohol had a biphasic effect on sham-operated, nontransgenic controls: 0.6 g/kg increased and 2.0 g/kg inhibited their aggressiveness. Alcohol did not significantly reduce the high levels of aggression in the sham-operated TGF-alpha mice. Castration abolished the difference in aggressive behavior between the transgenic and nontransgenic male mice by reducing aggression. Alcohol did not increase aggressive behavior in these mice. Treatment with pellets releasing 0.25 mg E2 over a 60-day period increased aggression in the castrated male TGF-alpha mice and nontransgenic controls to the levels seen in intact male transgenic mice. Alcohol did not significantly alter aggressive behavior in the E2-treated castrated mice.(ABSTRACT TRUNCATED AT 250 WORDS)

Aggression↗

Effects of methaqualone on social-sexual behavior in monkeys (M. mulatta) II. Simultaneously dosed subjects.

In a previous publication, we reported on the effects of 10 mg/kg i.m. injections of methaqualone on behavioral changes in treated animals and untreated members of a well-established colony of 10 rhesus monkeys (Macaca mulatta). The drug showed a biphasic effect, causing more passive behaviors in the first 80-100 min postinjection, followed by either aggression or increased sexual activity. After approximately 2 h, the social status and behavior of all animals returned to predrug levels. In general, affiliative activities increased under the influence of the drug, phenomena somewhat parallel tho those described among humans taking methaqualone in group settings. We also speculated that the drug may have an aphrodisiac potency. In the present experiments, 3 animals were caged together and injected simultaneously with the dose used earlier: an adult but naive male, who had been caged alone for infancy; an adult and subadult female, the 2 latter having had extensive social experience. After establishing baseline behaviors, five experiments with methaqualone were conducted, each lasting 2 h; and after the 2nd and 4th experiments, saline controls were carried out. There was a continuous increase from experiment to experiment in the affiliative behaviors of the animals; but during the saline trials, their behaviors returned nearly to those exhibited during baseline studies. Under the influence of methaqualone, the naive male attempted to copulate, which he achieved by the 4th drug trial; and at the same time he established his dominance. The conclusion was reached that methaqualone, indeed, has aphrodisiac potency, best measured by the time the male spent with erection under the influence of the drug, as compared with no erection during the baseline studies or the saline trials. The biphasic effect of methaqualone on behavior reported in the previous review [1] was also observed during the present experiments.

Agonistic Behavior↗

Managing unmanageable physicians: leadership, stewardship and disruptive behavior.

Physician executives would undoubtedly prefer to spend the bulk of their time inspiring great employees and building productive teams instead of struggling with disruptive physician behavior. Explore ways to diminish the frequency and intensity of disruptive behavior in your organization and identify your role, rights, responsibilities and accountabilities as a physician leader.

Agonistic Behavior↗

Systematic comparison of apomorphine-induced behavioral changes in two mouse strains with inherited differences in brain dopamine receptors.

Dosage and time dependencies of apomorphine-induced changes in stereotyped behaviors (climbing, gnawing and sniffing), locomotor activity and rearing activity were compared in young adult male mice of two inbred strains, DBA/2 and C57BL/6. These two strains are known to differ in their genetically specified brain dopamine receptor number. Apomorphine administered intraperitoneally at dosages of 0.5-20 mg/kg failed to induced stereotyped climbing in DBA/2 at any of the doses tested but markedly increased climbing in C57BL/6 at higher dosages. Apomorphine-induced stereotyped gnawing occurred in both strains at higher dosages although the latency was shorter and maximal effect greater in C57BL/6. Stereotyped sniffing was induced in both strains to a comparable degree at doses greater than or equal to 2.0 mg/kg, and the duration of this stereotypy was indistinguishable between strains. Locomotor activity was inhibited maximally in DBA/2 at an apomorphine dosage of 2 mg/kg and was inhibited to a greater extent than was C57BL/6. Rearing was inhibited in both strains by doses of apomorphine greater than or equal to 0.5 mg/kg; however the duration of the effect was considerably greater in DBA/2 than in C57BL/6. These data suggest that genetically determined differences in central dopamine receptors may have profound and selective effects on behaviors mediated by dopamine pathways; that complex behavioral patterns, e.g., apomorphine-induced stereotypy, may be dissected in to individual components by identifying neuropharmaco genetic differences between strains; that marked strain-specific, inherited differences in dopamine agonist-induced behavioral changes do occur among inbred, non-mutant mouse strains and that their occurrence in other mammalian species including man should be considered.

Animals↗

Behavioral and neurophysiological responses of European sea bass groups reared under food constraint.

The individual food-demand behavior of juvenile European sea bass (Dicentrarchus labrax, L.) reared in groups under self-feeding conditions was investigated. The triggering activity on self-feeder, i.e. index of the food-demand activity, agonistic interactions and territorial behavior were monitored for periods of 42 to 68 days in six groups of 50 fish. The specific growth rate was calculated and the brain serotonergic activity was used as a stable index of social stress. Inter-individual differences appeared in triggering activity and three groups were distinguished: 3-5 high-triggering fish, 17-30 low-triggering fish and the remaining individuals were null-triggering fish. There were no significant differences in specific growth rates calculated at the end of the experiment (day 42 or day 68) between individuals with high, low, and null food-demand (ANOVA, p>0.05). No territorial or agonistic behaviors were observed, however, there were significant differences in brain serotonergic activity between the three triggering groups (ANOVA, p=0.050 in telencephalon and p=0.004 in cerebellum). Specifically, high-triggering fish had lower serotonergic turnover than low or null-triggering fish. We put forth the hypothesis that fish with low or null-triggering activity could be stressed by the high activity of high-triggering individuals.

Animals↗

Corticotropin-releasing hormone (CRH) antisense oligodeoxynucleotide treatment attenuates social defeat-induced anxiety in rats.

1. The neuropeptide corticotropin-releasing hormone (CRH) is the main mediator of the neuroendocrine and behavioral response to stress. End-capped phosphorothioate antisense and sense oligodeoxynucleotides (ODN) corresponding to the start coding region of rat CRH mRNA were infused intracerebroventricularly (30 micrograms/3 microliters per injection) three times at 12 hr intervals. Six hours after the last injection rats were subjected to social defeat stress and subsequently tested on the elevated plus maze. 2. Socially defeated CRH antisense-treated rats displayed markedly reduced anxiety-related behavior, as they spent significantly more time in the open arms of the plus maze compared to sense ODN- and vehicle-treated animals. 3. In controls, social defeat evoked a stress-induced elevation of CRH mRNA and CRH in the hypothalamus and a significant increase in plasma corticotropin (ACTH) levels. These parameters were attenuated in antisense-injected rats. 4. Our results suggest that CRH antisense treatment is effectively suppressing the neuroendocrine and behavioral effects of social defeat.

Agonistic Behavior↗

Cocaine, social behavior, and alcohol-solution drinking in monkeys.

Eight group-living male monkeys received cocaine (0 to 3.0 mg/kg) individually or as a group. Cocaine suppressed social affiliative behaviors, eating, and drinking (of both alcohol and control solutions). It induced bizarre stereotypies, hypervigilance, panic-like fleeing, enhancement and then suppression of locomotion, and a seizure. Cocaine had little effect on aggressiveness or sexual behavior. Proportion of time spent lying or sitting changed significantly. Cocaine produced severe behavioral abnormality in this social setting.

Agonistic Behavior↗

Magnesium deficiency alters aggressive behavior and catecholamine function.

Magnesium is an abundant mineral in the brain and is important for monoamine neurotransmitter synthesis and receptor binding. It should, therefore, have behavior-altering effects. Three experiments were conducted to determine the influence of magnesium deficiencies on aggressive behavior and catecholamine function in mice. There were concentration- and time-dependent reductions in offensive aggressive behavior with magnesium deficiencies. Defensive behavior was affected in a manner opposite to that of offensive behavior. Upon administration of low doses of apomorphine and l-amphetamine, less dopamine- and norepinephrine-related behavior occurred with less magnesium in the diet. These reductions also showed a time dependency. These data demonstrate that magnesium has an influence on aggressive behavior in mice. Also, a magnesium deficiency is capable of altering the potency of catecholamine stimulating drugs.

Aggression↗

Functional relationships between genotypes and environments in behavior. Effects of different kinds of early social experience on interstrain fighting in male mice.

Comparisons are made of the interstrain fighting behavior of adult male mice from two inbred strains (ST-albino; CBA-black-agouti), raised in one of three postweaning social situations: 1) isolated from other males, 2) reared with males of the same strains, or 3) reared with males of the opposite strain. Using the fighting behavior of isolated males as a baseline, it is found that each type of early social experience affects the fighting behavior of the males from each of the two inbred strains differently, indicating that the functional relationships between genotype and environment studied in these experiments are nonadditive. The importance of these results in describing the norm of reaction of a behavioral phenotype and in extrapolating data from one experiment to another is discussed.

Aggression↗

Influence of estrogen-treated females on sexual behavior and male testosterone levels of a social group of rhesus monkeys during the nonbreeding season.

The effect of the sequential estradiol benzoate treatment of each of 6 ovariectomized (OVX) females on a social group of rhesus monkeys was examined during the period from May to August. The group was housed outdoors and was composed of 7 adult males and 5 intact females, in addition to the 6 OVX animals. Social behavior was observed and male testosterone levels were monitored before, during and after estrogen treatment of the OVX females. Behavior of an unmanipulated group was also examined, and no sexual behavior occurred in this control group from May through August. In contrast, the sexual behavior of both males and gonadally intact females of the experimental group increased when estrogen-treated females were present. Sexual behavior remained elevated after the estrogen-treated females had been removed and continued so into the breeding season. The sexual behavior of the untreated females was displayed in cycles about 26 days in length. Male testosterone levels increased to values typical of the breeding season. Aggressive and submissive behavior also increased during the treatment. These results confirm previous findings about the influence of estrogen-treated females on male sexual behavior, and present the first direct evidence of increased testosterone levels in this situation. In addition, the data suggest that the presence of estrogen-treated females can induce sexual behavior in the other females of the same social group.

Agonistic Behavior↗

Behavioral effect of 1A-serotonin receptor agonist ipsapirone in mice previously defeated in male-male encounters.

The effect of 1A-serotonin receptor agonist ipsapirone (3 mg/kg) on mouse behavior was studied in the "wall" and Porsolt tests. The effects of the test drug were compared in intact animals and mice previously defeated in 20 intermale encounters (victims). Ipsapirone was ineffective in victims and effective in intact mice in the wall test. In the Porsolt test the drug prolonged stupor in victims.

Animals↗