Vicente M. Simón

Effects of competition and its outcome on serum testosterone, cortisol and prolactin

In various species, competitive encounters influence hormonal responses in a different way depending on their outcome, victory or defeat. This study aimed to investigate the effects of sports competition and its outcome on hormonal response, comparing it with those displayed in situations involving non-effort and non-competitive effort. To this end, serum testosterone (T), cortisol (C) and prolactin (PRL) were measured in 26 judoists who participated in three sessions (control, judo fight and ergometry). The relationship between hormonal changes and psychological variables before and after the fight were also analysed. Our results showed a hormonal response to competition, which was especially characterized by an anticipatory rise of T and C. Depending on outcome, significant higher C levels were found in winners in comparison to losers through all the competition but not in T or PRL, both groups expending a similar physical effort. Furthermore, similar hormonal responses to the fight and to a non-competitive effort with the same caloric cost were found, other than with PRL. Winners showed a higher appraisal of their performance and satisfaction with the outcome, and perceived themselves as having more ability to win than losers, although there were no significant differences in motivation to win. Finally, the relationships found between T changes in competition and motivation to win, as well as between C response and self-efficacy suggest that in humans hormonal response to competition is not a direct consequence of winning and losing but rather is mediated by complex psychological processes.

Attenuation of sucrose consumption in mice by chronic mild stress and its restoration by imipramine

Chronic exposure to mild unpredictable stressors (CMS) has previously been found to reduce the consumption of palatable, sweet solutions in rats. In the present study, the utility of this procedure was assessed in mice. Male AP mice subjected to CMS showed reduced consumption of a 2% or 4% sucrose solution. This effect was reversed by chronic (3 weeks) treatment with the tricyclic antidepressant imipramine (20 mg/kg per day). These results extend previous reports of a generalized decrease in sensitivity to reward (anhedonia) in rats caused by CMS and the efficacy of antidepressant treatment in this paradigm. Chronic unpredictable mild stress in mice appears to provide a realistic animal model of depression.

Correlating testosterone and fighting in male participants in judo contests

The role of hormones in human aggression is open to debate, but takes on a new urgency owing to the alarming abuse of androgenic anabolic steroids by some sports participants. In this study, video-taped behavior exhibited by 28 male competitors during a judo fight was assessed to analyze its relation to serum testosterone and cortisol levels measured before and after the bouts. A positive relation between testosterone and offensive behaviors was obtained in the sense that the greater the hormonal titer, the greater the number of threats, fights, and attacks. These findings coincide with the pattern of relationships found using observational scales. Conversely, cortisol also presented positive correlations with some of these behavioral categories but did not moderate the relationship between testosterone and competitive behavior. The present results corroborate and extend earlier findings on the role of these hormones in human behavior, giving support to the view that testosterone can be linked to the expression of competitive aggression.

Effects of risperidone and SCH 23390 on isolation-induced aggression in male mice

In this study, the antiaggressive effects of risperidone and SCH 23390 have been explored. Using the paradigm of isolation-induced aggression, 150 albino male mice of the OF1 strain were allocated to control and experimental groups which received three doses of risperidone (0.01, 0.05 and 0.1 mg/kg) or two doses of SCH 23390 (0.05 and 0.1 mg/kg). Only the highest doses of risperidone decreased threat and attack behaviours but all doses significantly impaired motor behaviour. SCH 23390 decreased attack with the two doses used and also produced significant increases in immobility. Although both antipsychotics are antiaggressive, this action seems to be more specific in the case of risperidone. Finally, both drugs failed to affect animals with short attack latency, being antiaggressive only in subjects with long attack latency, which suggests that these two types of animals are different in their dopamine and serotonin neurotransmission.

Testosterone and Cortisol Responses to Competitive Fighting in Human Males: A Pilot Study

Departamento de Psicologia Fisiologica (A.S., V.S., F.S.) and Laboratorio de MedicinaNuclear e Isotopos (L.L.), Hospital Clinico Universitario, Universitat de Valencia, Valencia,SpainSerum testosterone and cortisol levels were measured by radioimmunoassay in 14young male judo competitors, in samples taken 10 minutes before and 45 minutes aftertwo different pr(Redures. The first involved physical exercise and the second competi-tive fighting. Both procedures were of 5 minutes duration and sessions took plate atthe same time (between 10:00 \.M. and 12:00 P.M. liR-al lime) but on different days.Comparing the two situations over all subjects revealed that testosterone increasedafter exercise and decreased slightly after competition. Between subject comparisonssuggested that contrary to previous claims, winning or losing did not significantlychange the testosterone and cortisol levels. Comparisons of subjects who were membersof the Regional Team with individuals who were not part of thai gronp confirmed thatmemhers increased their testosterone levels after competition, whereas the nonniem-bers showed a significant decrease. Moreover, success of the individuals, in theirsporting record, correlated positively and significantly with the changes of testosteroneohserved during the competition. These preliminary results suggest that previouspersonal experience of success can infiuence the pattern of the psychoend(KTine re-sponse to a contest situation.Key words: physical exercise, judo competition, victory, defeatINTRODUCTIONPhysiological responses to the experiences oi victory and defeat include the modi-fication of circulating levels of some hormones. Clinically, sporting competitions havebeen seen as suitable situations to study hormonal responses to winning and losing.Mazur and Lamb 11980] found that the pattern in changes of testosterone was differentin winners and losers of a tennis match. Winners generally showed increases andlosers decreases in titers of this steroid and significant differences were evident I to2 hours after the match. Hlias [1981] found that subjects winning a wrestling matchshowed significantly greater increases than losers when he compared percentagechanges between testosterone levels seen 10 minutes before and 10 minutes after thematch. Winners also showed significantly greater increases in cortisol than losers.

Predicting how equipotent doses of chlorpromazine, haloperidol, sulpiride, raclopride and clozapine reduce locomotor activity in mice

Distinguishing the specific effects of neuroleptics on one particular behaviour from its non-specific effects on motility is not easy. In this study, the effects of five neuroleptics on spontaneous motor activity were compared and the ED(50) values of these drugs to impair activity were calculated. Male and female mice were evaluated in an actimeter or in a shuttle-box used as an open field after the administration of chlorpromazine (0.4, 1.2, 3.6 mg/kg), haloperidol (0.1, 0.3, 0.9 mg/kg), raclopride (0.1, 0.3, 0.9 mg/kg), sulpiride (10, 30, 90 mg/kg) and clozapine (0.4, 1.2, 3.6 mg/kg), and two automatic and two observational activity measures were obtained. A very high correlation between automatic and observational measures, absence of sex differences, and a dose-dependent decrease of activity were observed with every compound. The results allow us to make accurate comparisons between these drugs in their potency in reducing spontaneous motor activity.

Behavioral profile of raclopride in agonistic encounters between male mice

Raclopride is a substituted benzamide with high selectivity as an antagonist of central dopaminergic D2 receptors and potential antipsychotic effects. In comparison with a classic DA receptor blocking agent like haloperidol, raclopride displays an atypical profile in preclinical tests for extrapyramidal side effects. Antiaggressive properties of raclopride on agonistic behavior have not yet been fully explored. In this work the effects of raclopride (0.1, 0.3, or 0.6 mg/kg) on aggressive and motor behaviors in male mice were studied. Aggression tests were performed 30 min after injections. Encounters were videotaped and behavior was evaluated, measuring the time spent in 11 broad categories of behavior. The results show a clear antiaggressive effect of raclopride, with very little motor impairment and some increase in exploratory behavior. This behavioral profile is very similar to the one observed with other atypical neuroleptics and differs somewhat from that found in the classic compounds.

DOSE–DEPENDENT IMPAIRING EFFECTS OF MORPHINE ON AVOIDANCE ACQUISITION AND PERFORMANCE IN MALE MICE

The effects of morphine (6.3, 12.6, and 25.2 mg/kg) on active avoidance behavior of BALB/C mice are explored in three acquisition sessions and in two subsequent performance sessions. Morphine-treated animals showed an increase in avoidance acquisition with respect to control group without differences in performance. However, a dramatical, concomitant rise in the locomotor activity of the animals (increase in the number of crossings during the intertrial intervals) prompted us to transform the data employing a formula with which a measure of actual learning was obtained. Applying this formula, we have observed that morphine administration impairs, dose-dependently, acquisition and performance of avoidance. Thus, the impairing effects of morphine on avoidance could be masked by their stimulant effects on locomotor activity.

Long-Term Chronic Treatment with Stanozolol Lacks Significant Effects on Aggression and Activity in Young and Adult Male Laboratory Mice

1. Repeated doses of the anabolic-androgenic steroid stanozolol were assessed for their effects on agonistic behavior, motor activity, and body weight in both young and adult male laboratory mice. 2. Stanozolol significantly increased weight gain in young, but not older subjects, especially at the highest doses. 3. There were, however, no significant differences in motor activity or in ethologically assessed social behavior (including aggression) in young or adult mice.

Antiaggressive and motor effects of haloperidol show different temporal patterns in the development of tolerance

The study of the temporal course of tolerance development was used as a means to separate different aspects of the action of haloperidol on social behavior. Agonistic behavior was studied in isolated male mice that confronted standard opponents (anosmic and grouped conspecifics) in a neutral area. The aggressive and motor behaviors of the experimental animals were evaluated 30 min or 24 h either after a single injection of haloperidol (0.4 mg/kg) or following the last of a series of 15 or 30 injections. When animals were evaluated 30 min after the haloperidol injection, no tolerance to the antiaggressive effects was evident. The action on immobility, on the contrary, showed a clear tolerance development with repeated drug administration, both with 15 and 30 injections. When evaluated 24 h after the last injection, tolerance to the antiaggressive effects developed with repeated injections. Increased immobility was never found in the tests carried out after 24 h, not even in the single injection group. The clear divergence found in the temporal courses of tolerance to haloperidol in its antiaggressive and motor effects suggests that these actions are mediated through different neurophysiological mechanisms. A parallel with extrapyramidal and therapeutic effects is discussed.