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While single neurons in inferior temporal (IT) cortex show differential responses to distinct complex stimuli, little is known about the responses of populations of neurons in IT. We recorded single electrode data, including multi-unit activity (MUA) and local field potentials (LFP), from 618 sites in the inferior temporal cortex of macaque monkeys while the animals passively viewed 78 different pictures of complex stimuli. The LFPs were obtained by low-pass filtering the extracellular electrophysiological signal with a corner frequency of 300 Hz. As reported previously, we observed that spike counts from MUA showed selectivity for some of the pictures. Strikingly, the LFP data, which is thought to constitute an average over large numbers of neurons, also showed significantly selective responses. The LFP responses were less selective than the MUA responses both in terms of the proportion of selective sites as well as in the selectivity of each site. We observed that there was only little overlap between the selectivity of MUA and LFP recordings from the same electrode. To assess the spatial organization of selective responses, we compared the selectivity of nearby sites recorded along the same penetration and sites recorded from different penetrations. We observed that MUA selectivity was correlated on spatial scales up to 800 m while the LFP selectivity was correlated over a larger spatial extent, with significant correlations between sites separated by several mm. Our data support the idea that there is some topographical arrangement to the organization of selectivity in inferior temporal cortex and that this organization may be relevant for the representation of object identity in IT.

Understanding the complex brain computations leading to object recognition requires quantitatively characterizing the information represented in inferior temporal cortex (IT), the highest stage of the primate visual stream. A read-out technique based on a trainable classifier is used to characterize the neural coding of selectivity and invariance at the population level. The activity of very small populations of independently recorded IT neurons (~100 randomly selected cells) over very short time intervals (as small as 12.5 ms) contains surprisingly accurate and robust information about both object ‘identity’ and ‘category’, which is furthermore highly invariant to object position and scale. Significantly, selectivity and invariance are present even for novel objects, indicating that these properties arise from the intrinsic circuitry and do not require object-specific learning. Within the limits of the technique, there is no detectable difference in the latency or temporal resolution of the IT information supporting so-called ‘categorization’ (a.k. basic level) and ‘identification’ (a.k. subordinate level) tasks. Furthermore, where information, in particular information about stimulus location and scale, can also be read-out from the same small population of IT neurons. These results show how it is possible to decode invariant object information rapidly, accurately and robustly from a small population in IT and provide insights into the nature of the neural code for different kinds of object-related information.

<p>This project advocates an urgent role for neurobiological evidence and models in the study of altruism. I argue for two claims: that neurobiological evidence should be used to constrain candidate scientific accounts of altruistic behavior, and that neurobiological techniques can be used to elucidate component mechanisms of altruistic behavior. </p><p>Chapter 1 reviews the historical progression of theories of altruism, and the empirical observations that motivated their development. A distinction is drawn between evolutionary altruism -- any self-sacrificial, fitness-reducing behavior, and psychological altruism -- self-sacrificial behaviors that are caused by psychological states like desire and motivation. Three theories of psychological altruism are described, and it is argued that the crucial difference between these theories is their conceptions of the role of affect in motivation, and how the processes of affect and motivation contribute to psychological altruism.</p><p>Chapter 2 describes dominant theories of motivation and the neurobiological and psychological mechanisms that support motivated behavior. Although the evidence is not conclusive, I argue that our best scientific models and neurobiological evidence support affective models of psychological altruism, and that other models are at best incomplete and possibly implausible in light of neurobiological considerations.</p><p>Chapter 3 introduces mind reading approaches to altruism, which argue that the capacity for altruistic motivations depends upon the capacity to represent the psychological states or circumstances of others. I conclude that altruism requires at a minimum the ability to attribute affective experiences to others. Further, I argue that the representations produced by mind reading processes provide a means for distinguishing between self-regarding and altruistic motivations. In contrast with the dominant philosophical theory of psychological altruism, the mind reading model I propose is compatible with the affective theory of motivation depicted in Chapter 2. My own empirical work is described as an example of how neurobiological techniques can reveal the differential role of neural systems in producing self-regarding and altruistic behavior.</p><p>Chapter 4 departs from the mechanistic approach to altruism discussed in the previous chapters, and presents an overview of how the fields of philosophy, psychology, psychobiology and genetics, have investigated altruism as a stable characteristic or personality trait. Recent technological advances make this a promising approach for investigating the psychological and neurobiological systems supporting altruistic behavior.</p> / Dissertation

Die transkranielle Gleichstromstimulation (tDCS) erwies sich in der bisherigen Grundlagenforschung als bewährte Methode zur Aufschlüsselung von komplexen kognitiven Funktionen. Bisher deuten bildgebende Verfahren auf ein Zusammenwirken parietaler und temporaler Kortizes beim Rekognitionsprozess deklarativer Gedächtnisinhalte hin. In der vorliegenden Arbeit sollten nun die Auswirkungen einer bilateral temporal und parietal applizierten tDCS auf die deklarative Gedächtnisleistung während der Rekognition untersucht werden. Unter Verwendung eines einfach-blinden, kontrollierten und randomisierten Studiendesigns wurden junge, gesunde Probanden drei voneinander unabhängigen, hinsichtlich der individuellen Gedächtniskapazität ausgeglichenen Studiengruppen für Placebo-, parietale und temporale Stimulation zugeordnet. Während der Bearbeitung eines computergestützten Alt-Neu-Rekognitions-Paradigmas erhielten zwei Gruppen bilaterale tDCS mit linkshemisphärischer a-tDCS über dem parietalen bzw. temporalen Kortex und eine Gruppe Placebo-Stimulation. Zielsetzend wurde die Einflussnahme der tDCS auf die deklarative Rekognitionsleistung bezüglich verbaler Gedächtnisinformationen gemessen. Eine Verbesserung der deklarativen Rekognitionsleistung äußerte sich in höheren Trennschärfeindex- und Treffgenauigkeitswerten der beiden verumstimulierten Gruppen im Vergleich zur Placebo-stimulierten Gruppe. Ein konträres Dissoziationsmuster zeigte sich insofern, als die temporale Stimulationsgruppe eine signifikant höhere Treffgenauigkeit bei der Rekognition alter Items im Vergleich zu neuen aufwies und die parietale Stimulationsgruppe mit einer signifikant höheren Treffgenauigkeit neue Items im Vergleich zu alten wiedererkannte. Diese Ergebnisse unterstreichen die Involvierung der temporalen und parietalen Hirnareale in möglicherweise unterschiedliche Stadien des Rekognitionsprozesses deklarativer Gedächtnisinhalte.

No condicionamento clássico de medo, os animais são treinados associando-se um estímulo neutro, por exemplo, som, contexto ou luz a um estímulo aversivo incondicionado, como um choque elétrico nas patas. Apos repetidos pareamentos, a presença do estímulo que inicialmente era neutro passa a eliciar uma resposta condicionada de medo no animal. O congelamento é a resposta mais proeminente dos animais expostos aos estímulos condicionados previamente pareados com choques nas patas, sendo freqüentemente utilizado como medida de medo condicionado (MC). Circuitos cerebrais independentes subjacentes a diferentes formas de memória, e, dentro de um determinado domínio de memória, o envolvimento de estruturas específicas pode depender do tipo de condicionamento se utilizando contexto ou explícito tais sinais leves ou som. Diversos relatos clínicos têm implicado o prejuízo do lobo temporal medial (LTM) com amnésia retrógrada. Embora muito tenha sido feito para desvendar os circuitos neurais subjacentes ao medo condicionado, utilizando contexto, som ou luz como estímulo condicionado (EC) o envolvimento do LTM nessas formas de condicionamento ainda não está claro. Para abordar esta questão foi avaliada a distribuição de Fos no LTM de ratos após a exposição a um contexto, um som ou luz, previamente emparelhado com choques nas patas. Vinte e quatro horas após as sessões de condicionamento, os animais foram colocados na mesma caixa experimental ou a um contexto distinto ou foram expostos ao som e luz sem receber choques nas patas. Diferença significativa na expressão de Fos foi determinada por análise de regiões do lobo temporal medial (córtex ectorrinal, perirrinal e entorrinal) e do hipocampo ventral. Os resultados comportamentais mostraram que houve congelamento nos três tipos de medo condicionado, mas o padrão de distribuição Fos foi diferente em ratos expostos a estímulos específicos ou contexto previamente emparelhado com choques nas patas. Apesar da saliente aquisição da resposta do medo se simular nas três condições, o achado mais saliente foi uma distribuição selectiva de Fos no córtex ectorrinal, perirrinal e entorrinal do grupo. Surpreendentemente, esses animais não mostraram significativa expressão Fos no hipocampo ventral. Isto sugere que o contexto e estímulos aversivos explícitos apresentam propriedades distintas de mapeamento ao de distribuição de Fos no circuito cortico-hipocampal cerebral. Estes resultados indicam que regiões corticais no LTM parecem ser críticas no armazenamento de informações contextuais, mas não de informações associadas a estímulos explícitos previamente pareados a choques nas patas. / Conditioned fear (CF) is one of the most frequently used animal models of associative memory to background or foreground stimuli. Independent brain circuits underlie different forms of memory, and, within a particular memory domain, the involvement of specific structures may depend upon the type of conditioning whether using context or explicit cues such light or tone. Several clinical reports have implicated the damage to the medial temporal lobe (MTL) with retrograde amnesia. Although much has been done to disclose the neural circuits underlying CF using context, tone or light as conditioned stimuli (CS) the involvemet of the MTL in these forms of conditioning is still unclear. To address this issue we assessed the Fos distribution in the MTL of rats following exposure to a context, a tone or a light previously paired with footshocks. Twenty-four hours later the conditioning sessions they were placed to the same chamber or to a distinct context and presented with tone or light only without any footshocks. Significant group differences in regional Fos expression were determined by analysis in regions of the medial temporal lobe (ectorhinal, perirhinal and entorhinal cortices) and the ventral hippocampus. The behavioral results showed comparable freezing in the three types of CF but the pattern of Fos distribution was distinct in rats exposed to specific cues or context previously paired with footshocks. Despite comparable acquisition of the conditioned fear response, the most remarkable finding was a selective distribution of Fos in the entorhinal, perirhinal and ectorhinal cortices of the MTL for context-CS groups. Remarkably, these animals did not show significant Fos expression in the ventral hippocampus. It is suggested that context and explicit stimuli endowed with aversive properties through conditioning cause distinct Fos brain mapping in the corticohippocampal circuitry. These results indicate that tasks requiring the association between context and an aversive stimulus depend on subregions of the MTL. Such findings suggested that cortical regions of the MTL appears to be critical for storing context but not explicit cue footshock associations.

No condicionamento clássico de medo, os animais são treinados associando-se um estímulo neutro, por exemplo, som, contexto ou luz a um estímulo aversivo incondicionado, como um choque elétrico nas patas. Apos repetidos pareamentos, a presença do estímulo que inicialmente era neutro passa a eliciar uma resposta condicionada de medo no animal. O congelamento é a resposta mais proeminente dos animais expostos aos estímulos condicionados previamente pareados com choques nas patas, sendo freqüentemente utilizado como medida de medo condicionado (MC). Circuitos cerebrais independentes subjacentes a diferentes formas de memória, e, dentro de um determinado domínio de memória, o envolvimento de estruturas específicas pode depender do tipo de condicionamento se utilizando contexto ou explícito tais sinais leves ou som. Diversos relatos clínicos têm implicado o prejuízo do lobo temporal medial (LTM) com amnésia retrógrada. Embora muito tenha sido feito para desvendar os circuitos neurais subjacentes ao medo condicionado, utilizando contexto, som ou luz como estímulo condicionado (EC) o envolvimento do LTM nessas formas de condicionamento ainda não está claro. Para abordar esta questão foi avaliada a distribuição de Fos no LTM de ratos após a exposição a um contexto, um som ou luz, previamente emparelhado com choques nas patas. Vinte e quatro horas após as sessões de condicionamento, os animais foram colocados na mesma caixa experimental ou a um contexto distinto ou foram expostos ao som e luz sem receber choques nas patas. Diferença significativa na expressão de Fos foi determinada por análise de regiões do lobo temporal medial (córtex ectorrinal, perirrinal e entorrinal) e do hipocampo ventral. Os resultados comportamentais mostraram que houve congelamento nos três tipos de medo condicionado, mas o padrão de distribuição Fos foi diferente em ratos expostos a estímulos específicos ou contexto previamente emparelhado com choques nas patas. Apesar da saliente aquisição da resposta do medo se simular nas três condições, o achado mais saliente foi uma distribuição selectiva de Fos no córtex ectorrinal, perirrinal e entorrinal do grupo. Surpreendentemente, esses animais não mostraram significativa expressão Fos no hipocampo ventral. Isto sugere que o contexto e estímulos aversivos explícitos apresentam propriedades distintas de mapeamento ao de distribuição de Fos no circuito cortico-hipocampal cerebral. Estes resultados indicam que regiões corticais no LTM parecem ser críticas no armazenamento de informações contextuais, mas não de informações associadas a estímulos explícitos previamente pareados a choques nas patas. / Conditioned fear (CF) is one of the most frequently used animal models of associative memory to background or foreground stimuli. Independent brain circuits underlie different forms of memory, and, within a particular memory domain, the involvement of specific structures may depend upon the type of conditioning whether using context or explicit cues such light or tone. Several clinical reports have implicated the damage to the medial temporal lobe (MTL) with retrograde amnesia. Although much has been done to disclose the neural circuits underlying CF using context, tone or light as conditioned stimuli (CS) the involvemet of the MTL in these forms of conditioning is still unclear. To address this issue we assessed the Fos distribution in the MTL of rats following exposure to a context, a tone or a light previously paired with footshocks. Twenty-four hours later the conditioning sessions they were placed to the same chamber or to a distinct context and presented with tone or light only without any footshocks. Significant group differences in regional Fos expression were determined by analysis in regions of the medial temporal lobe (ectorhinal, perirhinal and entorhinal cortices) and the ventral hippocampus. The behavioral results showed comparable freezing in the three types of CF but the pattern of Fos distribution was distinct in rats exposed to specific cues or context previously paired with footshocks. Despite comparable acquisition of the conditioned fear response, the most remarkable finding was a selective distribution of Fos in the entorhinal, perirhinal and ectorhinal cortices of the MTL for context-CS groups. Remarkably, these animals did not show significant Fos expression in the ventral hippocampus. It is suggested that context and explicit stimuli endowed with aversive properties through conditioning cause distinct Fos brain mapping in the corticohippocampal circuitry. These results indicate that tasks requiring the association between context and an aversive stimulus depend on subregions of the MTL. Such findings suggested that cortical regions of the MTL appears to be critical for storing context but not explicit cue footshock associations.

Alterações morfológicas e funcionais ocorrem durante o envelhecimento, período da vida com maior incidência de doenças neurodegenerativas. No presente trabalho acompanhou-se a evolução dos grânulos de lipofucsina durante o envelhecimento para investigar alterações sinápticas, assim como proteínas associadas com doenças neurodegenerativas (alfa-sinucleína) e com o sistema ubiquitina-proteossoma em indivíduos de diferentes idades. No córtex temporal humano e de ratos determinou-se, nos diferentes grupos etários, seguindo a área, o número e as características dos grânulos de lipofucsina, o número de sinapses excitatórias, inibitórias e elétricas, os locais de contatos pós-sinápticos, o número de vesículas sinápticas por terminal e a expressão das proteínas alfa-sinucleína e ubiquitina. Amostras de córtex temporal humano de indivíduos com diferentes idades (20 - 28, 37 - 41 e 50 - 55 anos) foram coletadas de pacientes com epilepsia submetidos à lobectomia do lobo temporal. Amostras de ratos de 2, 6, 10 e 12 meses também foram coletadas. Foram utilizadas técnicas de microscopia de luz, eletrônica, confocal e western blots. Os dados obtidos de grânulos de lipofucsina são consistentes com outros estudos que observaram aumento dessa estrutura em mamíferos de maior idade. No entanto, os grânulos parecem crescer em volume, mas não em número, com aumento considerável da fração elétron lúcida (lipídica). Não houve diferença na expressão das proteínas alfa-sinucleína e ubiquitina entre os grupos das idades estudadas. A densidade sináptica foi similar entre os grupos experimentais, assim como o local de contato pós-sináptico. O aumento de vesículas elétron densas em sinapses inibitórias deve estar associado à demanda de neurotransmissores catecolaminérgicos. Estes resultados não expressam totalmente o processo de envelhecimento, pois as faixas etárias de humanos e ratos correspondem a uma idade ainda jovem. A coleta de material humano mais idoso foi impossibilitada pela faixa etária dos doentes submetidos à lobectomia. Os ratos do biotério da FMRP, não sobrevivem mais do que 12 meses em no nosso ambiente, incluindo manutenção dos animais isolados em racks. / Morphological and functional changes occur during the aging, period of life with increased incidence of neurodegenerative diseases. Following the evolution of the lipofuscin granules along three periods of life in humans and rats, the present work investigated synaptic changes, as well as proteins associated with neurodegenerative diseases (alpha-synuclein) and the ubiquitin-proteossoma system in individuals of different ages. The objectives of the study were to analyze the temporal cortex of humans and rats: the number of excitatory, inhibitory, and electric synapses, the site of postsynaptic contacts, the number of synaptic vesicles per terminal, and the expression of the proteins alpha-synuclein and ubiquitin following the size and features of the lipofuscin granules. Samples of temporal cortex of human subjects with different ages (20-28, 37-41 and 50-55 years) were collected from patients with epilepsy who underwent temporal lobectomy. Samples from rats of 2, 6, 10 and 12 months were also collected. Light, confocal, and electron microscopy, and western blots techniques were used as procedures. The data obtained on lipofuscin granules were coincident with other studies that observed a higher area occupied by this structure in older mammals. However, the granules seem to grow in volume, but not in number, with considerable increase of the electron lucid fraction (lipidic). There was no difference in the alpha-synuclein and ubiquitin expressions between the experimental groups. The synaptic densities were similar between the groups, as well as the postsynaptic contacts. Increase of the electron dense vesicles in inhibitory synapses, appeared to be associated with the demand of catecholamines. These results do not express totally the aging process, because the range of age used in humans, and rats belong to a young age. The human samples from older ages was difficult because, in general, of the age of the patients submitted to lobotomy. The rats of the FMRP bioterium do not survived more that 12 months in our environment, even in controlled conditions.