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Theoretical review: a model of hormones and agonistic behavior.

A model of the interaction between endocrine function and agonistic responding was developed that incorporates three specific hypotheses about the relationship between hormones and agonistic behavior: (1) The baseline hormonal state of the organism contributes to the determination of whether, in what way, and how intensely the animal will react when it is exposed to appropriate environmental stimuli. (2) One function of the hormonal responses to environmental stimulation and behavioral experiences is to modify the continuing and future behavior of the individual in the same or similar situations. (3) Another function of these hormonal responses is to modify the individual's stimulus qualities so that other individuals' agonistic reactions to it will be modified. The data on hormones and agonistic behavior were reviewed in the context of this model, and some directions for future research were proposed.

Adrenal Glands

Agonistic behavior in the German cockroach, Blattella germanica.

Agonistic behavior in Blattella germanica is delineated with an emphasis on fighting techniques and population factors affecting aggressiveness. Male-male, male-female, and male-male encounters are not significantly different in either level of aggressiveness or frequency. Female-female carrying oothecae are, however, more aggressive than other female-female. The mean intensity of aggression increases as population density is increased, but number of contacts per individual per unit time remains constant. Defense of specific, territories does not occur and aggressive interactions are most common during the dark portion of the photocycle, when many of the cockroaches are observed to be foraging.

Aggression

[Classical conditioning of agonistic behavior in the Syrian golden hamster (Mesocricetus auratus Waterhouse)].

Nine different reactions of unconditioned agonistic behavior of golden hamsters (Mesocricetus auratus Waterhouse) which could be elicited by an air blow (UCS) were classically conditioned at a sound of a xylophone (tone g), a previously neutral stimulus. Tone g (CS) was paired with UCS for a different number of trials/day. In all animals exposed to over 20 pairings/day components of the agonistic behavior were brought under the control of CS, but it was not possible to predict which one of the agonistic reactions would appear. Most of the animals generalized and also showed conditioned reactions (CR) when presenting tone c' instead of tone g. When utilizing a differential conditioning procedure the animals learned to discriminate between the different tones. Extinction of CR at tone g was reached after an individually different number of trials.

Acoustic Stimulation

[Comparison of the effects of benzodiazepine and non-benzodiazepine anxiolytics on agonistic behavior in male mice].

The present study investigated whether there is any difference between the effects of benzodiazepine and non-benzodiazepine anxiolytics on agonistic behavior in male mice, using an ethopharmacological technique. Agonistic behavior was evoked using a resident-intruder paradigm. The effects of four doses of the following drugs were assessed in either resident or intruder mice: diazepam (vehicle, 1, 2.5 and 5 mg/kg, p.o.) and tandospirone (vehicle, 2.5, 5 and 10 mg/kg, p.o.). Residents and intruders were drugged on alternate test days, and all animals received different sequences of each of the drug conditions according to a random schedule. The injection-test interval was 30 min. When a resident mice were treated with either diazepam or tandospirone, the frequency of attack bite was suppressed significantly in a dose-dependent manner. When intruder mice were treated with diazepam, attack bites by untreated residents were significantly increased, whereas tandospirone was ineffective. Although diazepam caused a significant decrease in both locomotion and rearing, tandospirone did not cause motor dysfunction. These evidence indicate that tandospirone, a 5-HT1A receptor agonist, has different pharmacological properties from diazepam.

Agonistic Behavior

The effects of alcohol on agonistic behavior in the Telomian dog.

The study analyzed the effects of alcohol on agonistic behavior in three independent social systems, each compromised of two male and one female Telomian dog. Three dose levels were used: 0, 0.8, and 1.6 g/kg body weight of absolute alcohol diluted to 20%. Observations were made when none, one (top, middle or low ranking), or all dogs in a system received a given treatment. At the 0.8 g/kg level, low ranking dogs showed an increased frequency of attacks and bone possession time, while top and middle ranking dogs showed a decrease. At the 1.6 g/kg level, all subjects decreased their attacks and bone possession time. Alcohol decreased frequency of agonistic vocalizations under all conditions. There were differential social rank effects on frequency of retreats. Overall, the results were similar whether one or all dogs received the particular treatment.

Aggression

Long term reduction of male agonistic behavior in mice following early exposure to ethanol.

A system was developed to study the ability of early (pre- and neonatal) ethanol input to induce long lasting neural and behavioral changes. Ethanol was administered to E7b1/10bg and DBA/1Bg offspring through their parents who received 10% ethanol as their only liquid supply either before and during pregnancy, or from delivery until 14 days post partum, or during both periods. Thus, the offspring received ethanol transplacentally and/or through the mother's milk. The present paper is concerned with the male agonistic behavior at age 50 days of the treated offspring as compared with their pair fed controls. Early ethanol input resulted in a 23% increase in latency to attack in C57 mice and 58% in DBA, as well as a 49% (C57) and 38% (DBA) decrease in time spent fighting. The sensitive period to ethanol effect was apparently postnatal. Prenatal administration had no effect on agonistic behavior. DBA offspring were more aggressive than C57 and the scores of C57 offspring were more variable, thus indicating a lower phenotypic buffering in this strain.

Aggression

Agonistic behavior elicited by electrical stimulation of the brain in western collared lizards, Crotaphytus collaris.

Western collared lizards, Crotaphytus collaris, were tested in three experiments using electrical stimulation of the brain. In experiment 1, agonistic behavior (defensive, aggressive and escape) responses were elicited in free-moving unanesthetized lizards. In experiment 2, areas were localized from which gular extension, a common component of defensive and aggressive behavior, could be evoked in anesthetized animals. Experiment 3 was carried out to demonstrate that defensive and aggressive behavior could be elicited from the same stimulation sites both in anesthetized and unanesthetized lizards. Initially, gular extension was evoked while the animal was anesthetized and later the animal was tested while freely moving and unanesthetized. Based on a combined plot of the sites from which defensive and aggressive behavior was evoked in experiments 1--3, the higher threshold sites (51--750 muA) were in the dorsal ventricular ridge anterior, amygdaloid complex, septal and preoptic areas, hypothalamus, thalamus and adjacent to the nucleus profundus mesencephali (NPM) and reticular formation. Lower threshold sites (up to 50 muA) are found in the NPM and the reticular formation. Escape behavior can be evoked from stimulation sites within or adjacent to areas from which defensive and aggressive behavior can be elicited.

Aggression

5,7-Dihydroxytryptamine lesions of the ascending 5-hydroxytryptamine pathways: habituation, motor activity and agonistic behavior.

Rats were injected stereotactically in mesencephalon with 5,7-dihydroxytryptamine (5,7-DHT) in the medial 5-hydroxytryptamine (5-HT) pathway (n = 8) and in the medial plus the lateral 5-HT pathways (n = 7) or injected with vehicle (n = 8), or sham-operated (n = 8). The 5,7-DHT lesions reduced the in vitro 3H-5-HT uptake in the hypothalamus and the cortex cerebri to 27-51% of control values, 3H-noradrenaline uptake was not significantly changed. 5,7-DHT lesions of the medial, and of the medial plus the lateral, 5-HT induced mouse killing behavior and increased number of boxing positions in the shock elicited fighting test. Both lesions also reduced the rate of habituation to touch, but only the lesion of the medial plus the lateral 5-HT pathway significantly reduced the rate of habituation to acoustic stimulation. Activity in the home cage was not significantly changed by the lesions. It was concluded that selective chemical lesions of the ascending 5-HT pathways result in prolonged habituation of the orienting response and increase in particular components of agonistic behavior. The increase in locomotor activity observed after electrolytic lesions of nucleus raphe medianus seems not to be due only to lesion of the 5-HT neurons ascending from this nucleus.

5,7-Dihydroxytryptamine

Platelet monoamine oxidase activity correlates with social affiliative and agonistic behaviors in normal rhesus monkeys.

After a 4-mo study period, quantitative measures of stable behavioral traits in individual rhesus monkeys correlated significantly with platelet monoamine oxidase (MAO) activity. In particular, behavioral items reflecting social activity and social contact, both agonistic and affiliative, were inversely correlated with enzyme activity. Time spent alone was positively correlated. Since platelet MAO activity is generally stable and predominantly controlled by genetic factors, it might serve as a "genetic marker" for individual differences in "normal" behaviors possibly related to differences in MAO activity in the brain and other tissues.

Age Factors