A agressão maternal tem como função preservar a vida da prole. O desenvolvimento desse comportamento depende vastamente do reconhecimento do adversário como uma ameaça potencial e esse reconhecimento envolve a detecção de pistas feromonais. O núcleo pré-mamilar ventral (PMv) é um dos principais alvos do núcleo medial da amígdala, que representa o setor amigdalar crítico para o processamento de pistas feromonais. Desta forma, postulamos que possivelmente o PMv seja sensível às pistas feromonais do macho intruso, servindo como uma possível interface para os sistemas neurais envolvidos na agressão maternal. Neste sentido, inicialmente avaliamos o padrão de ativação do PMv, bem como alguns de seus alvos de projeção, durante o comportamento maternal e durante a agressão maternal. Notamos que tanto o PMv como a maioria de seus alvos principais (tais como, o núcleo posterior da amígdala, a parte posterodorsal do núcleo medial da amígdala, a área hipotalâmica lateral tuberal e a parte ventrolateral do núcleo ventromedial) apresentam um aumento significativo na expressão da proteína Fos durante a agressão maternal. Em seguida, avaliamos o papel do PMv na organização neural do comportamento de agressão maternal, em ratas lactantes portadoras de lesões citotóxicas com NMDA do PMv. Os resultados obtidos neste estudo demonstram que as fêmeas lactantes com lesão no PMv não apresentam qualquer alteração nos parâmetros comportamentais relacionados ao comportamento maternal, mas apresentam uma significante diminuição no comportamento agressivo maternal. Observamos ainda, que a lesão citotóxica do PMv resultou numa drástica diminuição da expressão da proteína Fos em alguns sítios de projeção do PMv que se apresentavam mobilizados durante a agressão maternal (tais como a parte ventrolateral do hipotálamo ventromedial, a área hipotalâmica lateral tuberal e o núcleo pré-óptico medial), sugerindo a participação destes sítios neurais como críticos na expressão do comportamento de agressão maternal. / Maternal aggression is critical to preserve the litters from male intruders, and the pheromonal cues from the males are important to drive such responses. The ventral premamillary nucleus (PMv) is one of the main targets of the medial amygdalar nucleus, and is critically involved in processing pheromonal information. In this regard, in the present study, we investigated whether the PMv would work as a putative interface between the pheromonal processing of the male intruder and the neural sites potentially involved in the expression of maternal aggression. First, we analyzed the pattern of Fos expression in dams expressing aggressive maternal behavior, and found a significant increase in Fos levels in the PMv, as well as, in most of its main targets, such as the posterior amygdalar nucleus, the posterodorsal part of the medial amygdalar nucleus, the tuberal nucleus of the lateral hypothalamic area, and the ventrolateral part of the ventromedial nucleus. Next, we examined how NMDA lesions bilaterally placed in the PMv would interfere in maternal aggression, and found that dams bearing those lesions presented a significant reduction in the expression of aggressive behavior, but showed no alterations on the maternal behavior responses. Moreover, we were able to see that PMv lesions resulted in significant drop in Fos expression in selected PMv targets, namely the tuberal nucleus of the lateral hypothalamic area and the ventrolateral part of the ventromedial nucleus, likely to be critically involved in the expression of the maternal aggression. Overall, the present results support the idea that the PMv is seemingly a key site in the network controlling maternal aggression; on one hand, the nucleus is likely to processes pheromonal cues from the intruder male, and, on the other, it conveys this information to sites critically related to the expression of maternal aggression.

Os comportamentos agonísticos sociais dispostos por animais dominantes e subordinados podem ser notados no paradigma residente intruso. No hipotálamo há o núcleo pré-mamilar ventral (PMv) ligado a um sistema sexualmente dimórfico e relacionado a reprodução e comportamentos agonísticos. A cópula é fundamental para a modulação do comportamento de dominância e aumenta os níveis de CART (Cocaine and Amphetamine Regulated Transcript) no PMv. Animais knockout de Sintase do Óxido Nítrico (NOS) apresentam agressão acentuada. Através da hibridização in situ estudamos a expressão de CART e de NOS nos animais com experiência sexual prévia ao encontro agonístico e sem experiência sexual (naive). No grupo que copulou foi visto aumento na expressão de CART e comportamento diferente do grupo naive visto que buscam a dominância e não apresentam posturas de submissão. Este aumento não foi observado nos níveis de NOS. Sugere-se que a experiência sexual esteja relacionada ao aumento de CART no PMv e possivelmente perda do comportamento subordinado e aumento da busca da dominância. / Aggressive behavior occurs when the interests of one or more individuals conflict. Territory is one of these interests, and the resident intruder paradigm is widely used to observe the expression of social agonistic behaviors. The dominance behavior has been studied under several views and it was shown that it can be raised by the presence of the female, its olfactory clues and by the sexual behavior. In the hypothalamus there is the premammillary ventralis nucleus (PMv) connected to a sexual dimorphic system and related to reproduction and agonistic behaviors. This nucleus was suggested as being involved in the modulation of aggressive behavior, and PMvs neuropeptides can have a direct relation with the expression of those agonistic behaviors. Males exposed to females olfactory clues show an increase in the expression of CART (C Cocaine and Amphetamine Regulated Transcript) in the PMv. Nitric oxide synthase (NOS) knockout animals show increased aggression. In the present investigation, using in situ hybridization we studied the expression of the mRNA of CART and NOS on intruders exposed to the resident-intruder paradigm. Two experimental groups were examined: one with sexual experience before the agonistic encounter and other naïve. It was observed increased expression of CART in the PMv in the sexual-experienced intruder. More, these animals behaved differently from naive intruders, and did not display submissive postures and start searching for dominance. Sexual experienced intruders presented increased expression of CART, but not NOS, mRNA. Thus, suggesting that the sexual experience is related to an increase in CART expression in the PMv and possibly with the lost of submissive behavior and increased search for dominance status.

Sexually-selected communication signals can be used by competing males to settle contests without incurring the costs of fighting. The ability to dynamically regulate the signal in a context-dependent manner can further minimize the costs of male aggressive interactions. Such is the case in the gymnotiform fish Brachyhypopomus gauderio, which, by coupling its electric organ discharge (EOD) waveform to endocrine systems with circadian, seasonal, and behavioral drivers, can regulate its signal to derive the greatest reproductive benefit. My dissertation research examined the functional role of the EOD plasticity observed in male B. gauderio and the physiological mechanisms that regulate the enhanced male EOD. To evaluate whether social competition drives the EOD changes observed during male-male interactions, I manipulated the number of males in breeding groups to create conditions that exemplified low and high competition and measured their EOD and steroid hormone levels. My results showed that social competition drives the enhancement of the EOD amplitude of male B. gauderio. In addition, changes in the EOD of males due to changes in their social environment were paralleled by changes in the levels of androgens and cortisol. I also examined the relationship between body size asymmetry, EOD waveform parameters, and aggressive physical behaviors during male-male interactions in B. gauderio, in order to understand more fully the role of EOD waveforms as reliable signals. While body size was the best determinant of dominance in male B. gauderio, EOD amplitude reliably predicted body condition, a composite of length and weight, for fish in good body condition. To further characterize the mechanisms underlying the relationship between male-male interactions and EOD plasticity, I identified the expression of the serotonin receptor 1A, a key player in the regulation of aggressive behavior, in the brains of B. gauderio. I also identified putative regulatory regions in this receptor in B. gauderio and other teleost fish, highlighting the presence of additional plasticity. In conclusion, male-male competition seems to be a strong selective driver in the evolution of the male EOD plasticity in B. gauderio via the regulatory control of steroid hormones and the serotonergic system.

Between 15 March and 29 July 1998 we quantified aggressive movements (AMs) in a breeding colony of 44 adult magellanic penguins (MPs) during their nesting season at San Francisco Zoo (SFZ). We sampled their behavior for a total of 149.5 hrs in 46 sessions of 195 min each, all starting at 0945 hrs and stopping at 1300 hrs. We recognized 4 types of AMs, of which 2 (eye-pointing and charging) were threat signals, I (bill-fencing) was a ritualized contest of strength and agility, and I (biting) was physical attack. MPs only performed AMs within 2-3 m of nest entrances. Males performed 83% of all AMs, females 17%. The eye-pointing threat signal accounted for 92% of all AMs, and the 3 non-attack AMs combined accounted for 99% of all AMs; only I% involved physical assault. Both sexes performed eye-pointing and bill-fencing, but only males charged or bit their adversaries.

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Play fighting is common in juvenile mammals as a peri-pubertal form of agonistic behavior preceding adult aggressive behavior. In golden hamsters, play fighting peaks in early puberty around postnatal day 35 (P-35), and gradually matures into adult aggression in late puberty. Though extensively studied, the neural mechanisms underlying play fighting remains poorly understood. My dissertation focuses on identifying the neural circuitry and neural transmitter systems that mediate this behavior in juvenile golden hamsters. Based on behavioral similarities between the offensive components of play fighting and adult aggression, I predicted that the neural circuitries mediating both behaviors shared common components. This possibility was tested by quantifying the immunolabeling of c-Fos expression in juvenile hamsters after the consummation of play fighting. In support of my hypothesis, I found that areas previously associated with offensive aggression in adult hamsters, including the ventrolateral hypothalamus (VLH), the posterior dorsal part of the medial amygdala (MePD), and the bed nucleus of the stria terminalis (BST), also showed enhanced c-Fos expression after play fighting, which supported my hypothesis. Vasopressin (AVP) facilitates aggression in adult hamsters. Therefore, I hypothesized that AVP also activates play fighting. To test my hypothesis, juvenile male golden hamsters were tested for play fighting after they received central microinjections of an AVP V1A-receptor antagonist into the anterior hypothalamus (AH). Also, immunocytochemistry was performed to identify possible AVP neurons associated with this behavior. I found that the AVP antagonist selectively inhibited the attack components of play fighting in experimental animals. In addition, AVP cells in the nucleus circularis (NC) and the medial division of the supraoptic nucleus (mSON), which were associated with offensive aggression, also showed increased c-Fos activity after play fighting. Together, these results show that AVP facilitates offensive behaviors throughout hamster development, from play fighting in juveniles to aggression in adults. A recent study shows that oral administration of a CRH receptor antagonist inhibits aggression in adult hamsters. Therefore, I predicted that CRH plays a similar role in play fighting. To test my prediction, juvenile hamsters were tested for play fighting after central microinjections of a CRH receptor antagonist. I found that microinjections of the CRH receptor antagonist within the lateral septum (LS) resulted in an inhibition of several aspects of play fighting. The possible source of CRH affecting the behavior was tested through combined immunocytochemistry to CRH and c-Fos. I found CRH neurons in the diagonal band of Broca (DBB), an area with extensive connections with the LS, were particularly activated in association with play fighting. In conclusion, I find that shared neural elements participating in the “vertebrate social behavior neural network” are associated with both aggression and play fighting in hamsters. This circuitry is activated before the onset of puberty and is affected by rising levels of steroid hormones during the developmental period leading to adult behaviors. Within the circuitry, vasopressin release in the AH appears to control the activation of play fighting attacks. In contrast, CRH release in the LS affects a broader range of aspects of play fighting, including not just consummatory aspects of the behavior, but apparently also appetitive components in the form of contact duration. / text