Administration of pilocarpine causes epilepsy in rats if status epilepticus (SE) is induced at an early age. To determine in detail the electrophysiological patterns of the epileptogenic activity in these animals, 46 Wistar rats, 7-17 days old, were subjected to SE induced by pilocarpine and electro-oscillograms from the cortex, hippocampus, amygdala, thalamus and hypothalamus, as well as head, rostrum and vibrissa, eye, ear and forelimb movements, were recorded 120 days later. Six control animals of the same age range did not show any signs of epilepsy. In all the rats subjected to SE, iterative spike-wave complexes (8.1 ± 0.5 Hz in frequency, 18.9 ± 9.1 s in duration) were recorded from the frontal cortex during absence fits. However, similar spike-wave discharges were always found also in the hippocampus and, less frequently, in the amygdala and in thalamic nuclei. Repetitive or single spikes were also detected in these same central structures. Clonic movements and single jerks were recorded from all the rats, either concomitantly with or independently of the spike-wave complexes and spikes. We conclude that rats made epileptic with pilocarpine develop absence seizures also occurring during paradoxical sleep, showing the characteristic spike-wave bursts in neocortical areas and also in the hippocampus. This is in contrast to the well-accepted statement that one of the main characteristics of absence-like fits in the rat is that spike-wave discharges are never recorded from the hippocampal fields.

This article is an edited transcription of a virtual symposium promoted by the Brazilian Society of Neuroscience and Behavior (SBNeC). Although the dynamics of sensory and motor representations have been one of the most studied features of the central nervous system, the actual mechanisms of brain plasticity that underlie the dynamic nature of sensory and motor maps are not entirely unraveled. Our discussion began with the notion that the processing of sensory information depends on many different cortical areas. Some of them are arranged topographically and others have non-topographic (analytical) properties. Besides a sensory component, every cortical area has an efferent output that can be mapped and can influence motor behavior. Although new behaviors might be related to modifications of the sensory or motor representations in a given cortical area, they can also be the result of the acquired ability to make new associations between specific sensory cues and certain movements, a type of learning known as conditioning motor learning. Many types of learning are directly related to the emotional or cognitive context in which a new behavior is acquired. This has been demonstrated by paradigms in which the receptive field properties of cortical neurons are modified when an animal is engaged in a given discrimination task or when a triggering feature is paired with an aversive stimulus. The role of the cholinergic input from the nucleus basalis to the neocortex was also highlighted as one important component of the circuits responsible for the context-dependent changes that can be induced in cortical maps.

This article is a transcription of an electronic symposium held on February 5, 2001 by the Brazilian Society of Neuroscience and Behavior (SBNeC) during which eight specialists involved in clinical and experimental research on sleep and dreaming exposed their personal experience and theoretical points of view concerning these highly polemic subjects. Unlike most other bodily functions, sleep and dreaming cannot, so far, be defined in terms of definitive functions that play an ascribable role in maintaining the organism as a whole. Such difficulties appear quite clearly all along the discussions. In this symposium, concepts on sleep function range from a protective behavior to an essential function for maturation of the nervous system. Kleitman's hypothesis [Journal of Nervous and Mental Disease (1974), 159: 293-294] was discussed, according to which the basal state is not the wakeful state but sleep, from which we awake to eat, to protect ourselves, to procreate, etc. Dreams, on the other hand, were widely discussed, being considered either as an important step in consolidation of learning or simply the conscious identification of functional patterns derived from the configuration of released or revoked memorized information.

Theta rhythm in many brain structures characterizes wakefulness and desynchronized sleep in most subprimate mammalian brains. In close relation to behaviors, theta frequency and voltage undergo a fine modulation which may involve mobilization of dorsal raphe nucleus efferent pathways. In the present study we analyzed frequency modulation (through instantaneous frequency variation) of theta waves occurring in three cortical areas, in hippocampal CA1 and in the dorsal raphe nucleus of Wistar rats during normal wakefulness and after injection of the 5-HT1a receptor agonist 8-OH-DPAT into the dorsal raphe. We demonstrated that in attentive states the variation of theta frequency among the above structures is highly congruent, whereas after 8-OH-DPAT injection, although regular signals are present, the variation is much more complex and shows no relation to behaviors. Such functional uncoupling after blockade demonstrates the influence of dorsal raphe nucleus efferent serotoninergic fibers on the organization of alertness, as evaluated by electro-oscillographic analysis.

Foram obtidos potenciais evocados transcalosos por aplicação de pulsos quadrados de 1 ms, 5 c/s e intensidade variável e registro sobre a corticalidade de gatos anestesiados com quetamina. Os locais de estimulação e registro eram selecionados através de mapa cartesiano de grande parte do neocórtex. Além das bem conhecidas projeções calosas, foram discriminadas áreas posteriores cuja estimulação evocava potenciais de baixa amplitude em sua área homóloga e potenciais de grande amplitude em regiões mais anteriores, ipsi- e contralateralmente. Esta conexão transcalosa em forma de 'L' pode estar envolvida em processos corticais complexos e é compatível aos bons resultados obtidos por calosotomias parciais anteriores em pacientes com epilepsia multifocal e bissincronia frontal.

Transcallosal potentials evoked by electrical stimulation with rectangular pulses of 1 ms, 5 c/s and variable intensity were recorded from the cortical surface in cats anesthetized with ketamine hydrochloride. Sites of stimulation and recording were selected by means of a cartesian map of most of the neocortex. In addition to the well known transcallosal projection pattern it was found that stimulation of a restricted posterior area evokes low voltage potentials over the contralateral symmetric area while high voltage potentials are recorded from a few sites located at the ipsilateral anterior cortex and from the area symmetric as to the latter. This L-shaped transcallosal connection may be involved in complex cortical processes and is compatible with effective results of partial anterior callosotomies in patients with multifocal epilepsy and frontal bisynchronism.

Em dez gatos anestesiados com cetamina (Ketalar) o neocórtex foi exposto e pulsos retangulares (1 ms, 0,5Hz e intensidade variável) foram aplicados a pontos discretos de um lado enquanto se registravam os potenciais evocados no outro lado. As posições de estimulação e registro eram determinadas em mapa cartesiano que abrangia quase todo o neocórtex. Os potenciais foram analisados quanto aos seus componentes, voltagem e latência. A difusão passiva, potenciais eletrotônicos e os efeitos do incremento da frequência de estimulação sobre os vários componentes foram analisados. Os resultados mostram a presença de grandes potenciais evocados transcalosos em algumas regiões, com incremento de sua amplitude no sentido caudo-rostral, sendo máximos em áreas anteromediais do giro suprasilviano. Confirmando estudos anatômicos, em algumas regiões do córtex soma-tomotor e visual foram registrados potenciais bastante reduzidos ou ausentes. A estimulação de algumas áreas posteriores causava o aparecimento de pequenos potenciais em sua área homóloga contralateral ao mesmo tempo em que grandes potenciais eram registrados em áreas anteriores ipsi- e contralateralmente, constituindo uma conexão em L ainda não descrita. É possível que tal conexão esteja implicada em alguns tipos de epilepsia e possa explicar em parte a eficácia de calosotomias parciais para seu tratamento.

In ten adult cats anesthetized with ketamine hydrochloride the neocortex was exposed and rectangular pulses (1msec, 0.5 Hz and variable intensity) were applied to discrete points of one side and transcallosal evoked potentials were recorded from the other. The stimulation and recording positions were determined on a cartesian map of most of the exposable neocortical areas and the potentials were analysed as to their components, voltage and latency. Passive spread and electrotonic potentials and the effects of increasing frequency were also analysed. The results showed large transcallosal potentials in some areas and an increase of potentials in the caudorostral direction, attaining the highest values in anteromedial areas of the suprasylvian gyrus. Confirming anatomical studies, a few silent spots were found in the motor and somesthetic cortex and in restricted posterior regions of the visual cortex, where small or zero voltages occurred. While causing weak contralateral potentials, stimulation of some posterior sites provoked high voltage potentials in anterior regions of the side being stimulated and in the corresponding area of the opposite site. These posterior sites are. poorly interconnected by the corpus callosum. The L-shaped indirect connection described in this work may be involved in some types of epilepsy and may explain the effectiveness of partial callosotomy in their treatment.