For the last twenty years, a large number of data has been provided in favor of the hypothesis of new neurons being generated throughout the entire lifespan of some groups of animals. This phenomenon is known as postnatal neurogenesis. However, the physiological relevance of the increase in the neuronal population of some brain areas is not yet clear. In this sense, reptiles seem to be useful models for the study of postnatal neurogenesis and neuronal regeneration. The tropical lizards Tropidurus hispidus were shown to be examples of that, since they form new neurons throughout their entire lifespan. However, data on neuroanatomy and neurogenesis of this species have not yet been fully provided. Therefore, the aims of this study were to characterize the neuroanatomy and neuromorphology, to study the distribution of zinc terminal areas, to verify the neuronal proliferation pattern of these lizards when under different temperatures and to describe proliferative areas and neuronal migration pathways of the T. hispidus telencephalon. We used the Nissl technique to characterize anatomy; Golgi impregnations to characterize neuronal morphology; Neo-Timm histochemistry to detect zinc terminals; Doublecortin (DCX) immunohistochemistry as a marker of neuronal proliferation; NeuN immunohistochemistry to detect mature neurons; Glial fibrillary acidic protein (GFAP) to detect glia; and 5-bromodioxiuridine (BrDU) to detect cellular divisions. Our results show that T. hispidus lizards have at least ten different neuronal types in their cortical areas: granular (uni-, bi- and multipolar), pyramidal (normal, inverted, open, bipyramidal and horizontal), spherical horizontal and fusiform. Furthermore, we verified that the zinc-positive regions were in cortical areas, septum, striatum and amygdaloid complex. BrDU immunohistochemistry showed that in lizards maintained in warm temperatures (28oC), new cells were evenly distributed in the ventricle walls and in the nervous parenchyma. In cold temperatures (16oC), new cells concentrated near ventricle walls. The number of new cells, however, was not different between groups. This suggested that temperature changes may impair migration but not formation of new cells. DCX immunohistochemistry showed that there are four main neurogenic foci in T. hispidus: lateral, septomedial, ventral and terminal sulci. We further observed the existence of four patterns of neuronal migration: radial, rostraltangential (similar to the mammalian rostral migratory stream), caudal-tangential and commissural. Therefore, these data seem to support the hypothesis that the Tropiduridae family is important to understanding mechanisms of postnatal neurogenesis, and is useful to future studies on comparative neurobiology. / Nos últimos vinte anos, um grande número de evidências vem se acumulando em favor da hipótese de que novos neurônios são gerados durante toda a vida de alguns grupos de animais vertebrados. Este fenômeno é conhecido como neurogênese pós-natal. Todavia, ainda não está claro o significado fisiológico do aumento da população neuronal em diferentes áreas cerebrais. Os répteis parecem constituir uma classe de animais favoráveis para o estudo de neurogênese pós-natal e regeneração neuronal. A espécie de lagarto tropical Tropidurus hispidus é um exemplo disso, uma vez que apresenta formação de novos neurônios durante toda sua vida, por outro lado, as informações a cerca dos padrões neuroanatômicos e de neurogênese dessa espécie ainda não estão totalmente elucidados. Dessa forma, objetivou-se inicialmente realizar a caracterização neuroanatômica e neuromorfológica do telencéfalo do lagarto T. hispidus como também estudar a distribuição das áreas ricas em terminais de zinco. Além disso, verificar o padrão de proliferação neuronal quando submetidos a alterações térmicas e também descrever as áreas proliferativas e as vias de migração neuronal no telencéfalo desses animais. Para o estudo foram utilizadas as técnicas histoquímica de coloração de Nissl com a finalidade de caracterizar as áreas anatômicas; coloração de Golgi para caracterização neuromorfológica dos neurônios presentes no córtex cerebral; histoquímica de Neo-Timm a fim de detectar os terminais de zinco; imunohistoquímica para Doublecortina (DCX), como marcador de proliferação neuronal; imunohistoquímica para neurônios maduros (NeuN); proteína presente em glia radial (GFAP) e o marcador de divisão celular 5-Bromodioxiuridina (5-BrDU). A partir da análise dos dados foi possível verificar que o lagarto T. hispidus apresenta dez diferentes tipos de neurônios distribuídos em suas três áreas corticais, são eles: o granular (unipolar, bipolar e multipolar), piramidal (normal, invertido, aberto, bipiramidal e horizontal), horizontal esférico e fusiforme, além disso, verificou-se que as regiões zinco positivas encontravam-se em áreas corticais, septum, estriado e no complexo amidaloide. Os resultados obtidos com a marcação de imunohistoquímica para BrdU permitiu concluir que animais mantidos a temperatura natural (média de 28 ºC) apresentavam núcleos positivamente marcados tanto na parede do ventrículo como também distribuídos pelo parênquima nervoso. No entanto, aqueles animais mantidos a uma temperatura média de 16 ºC, esses núcleos positivamente marcados encontravam-se próximo ao ventrículo. Analisando o número de células positivamente marcadas por BrdU, em ambas temperaturas, verificou-se que não havia diferença estatisticamente significante, sugerindo que mudanças de temperatura podem alterar a mig ração de novos neurônios, mas possivelmente não altera a formação dessas novas células. Testes imunohistoquímicos com DCX demonstraram a existência em T. hispidus de quatro principais regiões produtoras de novos neurônios, são elas: sulcos laterais, septomediais, ventrais e terminais. Observou-se também a existência de quatro tipos de migração neuronal, a radial, tangencial rostral (semelhante a migração rostral de mamíferos), a tangencial caudal e a comissural. Portanto, esses dados parecem sustentar a hipótese de que a família Tropiduridae parece ser importante para entender os mecanismos de neurogênese pós-natal e ser útil para estudos futuros de neurobiologia comparada.

A atribuição da percepção da dor pelos peixes é um assunto controverso no meio científico. Alguns autores associam a percepção da dor a estruturas neocorticais que estão ausentes em peixes. Entretanto, estudos recentes têm demonstrado que os peixes são capazes de perceber e responder a estímulos nocivos de maneira semelhante ao que é observado em mamíferos, sendo estas respostas sensíveis à administração de morfina. Além disso, estudos pioneiros de nosso laboratório demonstraram a existência de um sistema analgésico endógeno em peixes. O objetivo deste estudo foi avaliar se este sistema analgésico endógeno pode ser ativado pelo estresse. A natureza neuroquímica deste sistema e a participação de uma região telencefálica, o telencéfalo dorsomedial (Dm), na modulação da antinocicepção também foram investigados. Nossos dados demonstram que o estresse de restrição de 3 e 5 minutos de duração inibe a resposta comportamental à injeção subcutânea de formalina a 3% na região da nadadeira adiposa no peixe Leporinus macrocephalus, sugerindo que este procedimento é capaz de ativar um sistema antinociceptivo endógeno. Além disso, a antinocicepção induzida pelo estresse de restrição de 3 e 5 min é de curta duração, sendo observada apenas por 5 min após o término da restrição. A análise da natureza neuroquímica da antinocicepção induzida pelo estresse de restrição revelou participação do sistema opióde e canabinoide na modulação desta resposta. O tratamento prévio com injeção intraperitoneal de naloxona (30 mg.kg-1), um antagonista opioide não seletivo, bloqueou a antinocicepção induzida pela restrição de 3 min de duração, mas não foi capaz de inibir a antinocicepção induzida pela restrição de 5 min de duração. Já o tratamento prévio com injeção intraperitoneal de AM251 (3 mg.kg-1), um antagonista de receptores canabinoides tipo 1, bloqueou a antinocicepção induzida pelo estresse de restrição de 3 e 5 min de duração, sugerindo que o sistema canabinoide desempenha um papel fundamental na antinocicepção induzida por esta modalidade de estresse na espécie estudada. Nosso estudo também demonstrou que a região do telencéfalo dorsomedial está envolvida na modulação da antinocicepção induzida pelo estresse de restrição no peixe L. macrocephalus. A microinjeção de midazolan (40 e 80 nmol), um agonista de receptores benzodiazepínicos, no telencéfalo Dm bloqueou a antinocicepção induzida pela restrição de 3 e 5 min de duração. Além disso, o tratamento prévio com flumazenil (80 e 160 nmol), um antagonista específico de receptores benzodiazepínicos, inibiu os efeitos do tratamento com midazolan, demonstrando que o bloqueio da antinocicepção promovido pelo midazolan ocorre pela ativação específica dos receptores benzodiazepínicos. Juntos estes resultados trazem novas perspectivas acerca do entendimento sobre a percepção nociceptiva em peixes. Este é o primeiro trabalho que traz evidências acerca da existência de um sistema de modulação da dor ativado pelo estresse e demonstra a participação de uma região encefálica específica na modulação desta antinocicepção. Estes resultados indicam que as vias analgésicas endógenas em peixes são ativadas de maneira semelhante aos mamíferos, sugerindo que estes animais possuem um processamento complexo da informação nociceptiva. / The assignment of pain perception by fish is controversial among scientists. Some authors associate the pain perception to neocortical structures that are absent in fish. However, recent studies have shown that fish are able to perceive and respond to noxious stimuli, similar to observed in mammals, and this responses are sensitive to morphine administration. Furthermore, pioneering studies from our laboratory have demonstrated the existence of an endogenous analgesic system in fish. This study aimed to evaluate if this endogenous analgesic system can be activated by stress, the neurochemical nature of this system and involvement of a telencephalic region, the dorsomedial (Dm) telencephalon, in the antinociception modulation. Our data demonstrate that 3 and 5 min of restraint stress inhibits the behavioral response to subcutaneous injection of formalin 3 % in the adipose fin in the fish Leporinus macrocephalus, suggesting that this procedure can activate an endogenous antinociceptive system. Furthermore, stress-induced antinociception induced by 3 and 5 min of restraint is short, with the antinociceptive effects being observed only for 5 min after the restriction. The analysis of the neurocheamical nature of antinociception induced by restraint stress revealed the involvement of opioid and cannabinoid systems in the modulation of this response. The pre-treatment with intraperitoneal injection of naloxone (30 mg.kg-1), a non-selective opioid receptors antagonist, blocked the antinociception induced by 3 min of restraint, but was not able to inhibit the antinociception induced by 5 min of restraint. The pre-treatment with intraperitoneal injection of AM251 ( 3 mg.kg-1), a type 1 cannabinoid receptors antagonist, blocked the stress-induced antinociception promoted by 3 and 5 min of restraint, suggesting that the cannabinoid system plays a critical role in this type of stress-induced antinociception in the studied species. Our study also showed that the dorsomedial telencephalon is involved in the modulation of stress-induced antinociception in fish L. macrocephalus. The microinjection of midazolan (40 and 80 nmol), a benzodiazepine receptors agonist, in the Dm blocked the stress-induced antinociception promoted by 3 and 5 min of restraint. Furthermore, pre-treatment with flumazenil (80 and 160 nmol), a benzodiazepine receptors selective antagonist, inhibited the effects of the midazolan treatment, demonstrating that the antinociception blockade by midazolan is promoted by specific activation of benzodiazepine receptors. Together these results provide new insights on the understanding of nociceptive perception in fish. This is the first study that demonstrates evidence for the existence of a pain modulation system activated by stress in fish and demonstrates the involvement of a specific brain region in the modulation of this antinociception. These results indicate that the endogenous analgesic pathways in fish are activated in a similar manner to mammals, suggesting that these animals have a complex processing of nociceptive information.

No description available.

The hypothalamus is a subcortical brain region whose limits and constituent nuclei lack consensus. The hypothalamus has been linked to emotion and different states of stress, providing critical feedback about the internal environment to the prefrontal cortex, a region known for executive function within the cortex of humans. An understanding of the developmental origin of the hypothalamus can provide a basis for defining which limits and nuclei are ontologically hypothalamic, and which are not, as well as a framework for understanding its connectional relationship with other brain regions. The Prosomeric Model (Rubenstein et al. 1994; Puelles and Rubenstein 2003; Nieuwenhuys and Puelles 2016; Puelles 2018) explains the embryological development of the central nervous system (CNS) shared by all vertebrates as a Bauplan. As a primary event, the early neural plate is patterned by intersecting longitudinal plates and transverse segments, forming a mosaic of progenitor units. The hypothalamus is specified by three prosomeres [hp1, hp2, and the acroterminal domain (At)] of the secondary prosencephalon with corresponding alar and basal plate parts, which develop apart from the diencephalon. Mounting evidence suggests that progenitor units within alar plate and basal plate parts of hp1 and hp2 give rise to distinct hypothalamic nuclei, which preserve their relative invariant positioning (topology) in the adult brain. Nonetheless, the principles of the Prosomeric Model have not been applied to the hypothalamus of adult primates. The Structural Model (Barbas 1986; Barbas and Rempel-Clower 1997) highlights the variation of laminar structure in the grey matter of the prefrontal cortex as a basis for predicting specific cortico-cortical connections. The areas of the prefrontal cortex vary along a spectrum by number of layers, laminar definition, and cellularity of those layers. The systematic laminar patterns of different areas of the prefrontal cortex seem to be associated with differential rates of development or maturation. A topographical analysis of bidirectional projections between the prefrontal cortex and the hypothalamus was previously applied using the Structural Model (Rempel-Clower and Barbas 1998). The authors found the prefrontal cortex has highly specific projections to the hypothalamus, originating mostly from limbic orbital and medial prefrontal areas, which have lower laminar definition than other prefrontal areas. In addition, the hypothalamus has relatively specific patterns of projection to the prefrontal cortex. We previously lacked an organizing principle to examine the specific pattern of connections between the hypothalamus and prefrontal cortex in adult rhesus monkey. In the present study, hypothalamic nuclei in the rhesus monkey (Macaca mulatta) were parcellated using classic architectonic boundaries and stains. The topological relations of hypothalamic nuclei and adjacent hypothalamic landmarks were then analyzed with homology across rodent and primate species to trace the origin of adult hypothalamic nuclei to the alar or basal plate components of hp1 and hp2. A novel atlas of the hypothalamus of the adult rhesus monkey was generated with developmental ontologies for each hypothalamic nucleus. This atlas was then applied to a topological analysis of the strength and pattern of connections between the hypothalamus and prefrontal cortex in the adult rhesus monkey. The result is a systematic reinterpretation of the adult hypothalamus of the rhesus monkey whose prosomeric ontology was used to study connections and neuraxial pathways linking the hypothalamus and prefrontal cortex. The convergence of the Prosomeric and Structural Models provides a framework through development to explain the structural patterns found in the adult primate cortex and hypothalamus, and the likely consequences of their disruption.

京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第19568号 / 医博第4075号 / 新制||医||1013(附属図書館) / 32604 / 京都大学大学院医学研究科医学専攻 / (主査)教授 伊佐 正, 教授 渡邉 大, 教授 影山 龍一郎 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM

No description available.

No description available.

No description available.

Made available in DSpace on 2016-06-02T20:19:28Z (GMT). No. of bitstreams: 1 887.pdf: 469528 bytes, checksum: fc5bcdbae3a402aaac1aae4dbf59bcd1 (MD5) Previous issue date: 2006-03-03 / Universidade Federal de Sao Carlos / This work intended to investigate in forebrain ablated Carassius auratus the effect of the H1 receptor blockade in a spatial choice task using a T-maze test with positive reinforcement. Sixty-nine goldfish were submitted to surgery for removal of both telencephalic lobes five days before the beginning of the experiment. A T-shaped glass aquarium, which had two feeders located at the extremities of the long arm, was employed. One of the two feeders was blocked. The experimental trials were performed in nine consecutive days. Each fish was individually placed in the short arm and confined there for thirty seconds, then it was allowed to swim through the aquarium to search for the food for ten minutes (maximum period). Time to find food was analysed in seconds. Animals were injected intraperitoneally with chlorpheniramine (CPA) at 16 mg/kg of body weight or saline after every trial, ten minutes after it had been replaced at house aquarium. Data were analyzed via a three-way analysis of variance (ANOVA) with repeated measures, and post hoc comparisons were analyzed using the Student Newman-Keuls test (p<0.05). All the training latencies of A-SAL group were significantly higher than latencies of S-SAL group (p<0.05). S-SAL group showed a significative decrease in latencies at the second trial and maintained that reduction until the end of the experiment (p<0.05), S-CPA group demonstrated a decrease only after the fourth trial (p<0.01), A-SAL group showed reduced latencies after the fifth trial (p<0.05), and ACPA group did not showed any difference between training latencies. Thus, our results showed that CPA seems to impair the consolidation of memory either on telencephalon ablated animals and in sham-operated ones. Furthermore, this work supports evidence that histamine plays a facilitatory role in learning and memory processes of a spatial task through its action in primitive structures of the brain in teleost fish. / O objetivo deste trabalho foi investigar, em peixes da espécie Carassius auratus submetidos à ablação telencefálica, o efeito do bloqueio do receptor H1 em uma tarefa de escolha espacial utilizando um teste de labirinto em T com reforço positivo. Sessenta e nove peixes foram submetidos à cirurgia para a remoção de ambos os lobos telencefálicos cinco dias antes do início do experimento. Foi empregado um aquário de vidro transparente em forma de T, o qual teve dois comedouros fixados nas extremidades do braço longo, sendo que um dos comedouros foi bloqueado durante as sessões de treino. O experimento foi realizado em nove sessões consecutivas realizadas com intervalos de 24 horas. Individualmente, cada peixe foi confinado no compartimento de saída do aquário experimental durante trinta segundos, e então foi permitido a ele explorar todo o aquário para procurar o alimento durante dez minutos (período máximo). O tempo utilizado para encontrar o alimento foi cronometrado em segundos. Os animais foram injetados intraperitonealmente com clorfeniramina (CPA), na dose de 16 mg/kg de peso corporal, ou salina após cada treino, dez minutos após o peixe ter sido recolocado no aquário de manutenção. Os dados foram analisados através de ANOVA de três vias seguida pelo teste de comparações múltiplas de Student Newman-Keuls. Todas as latências de treino do grupo A-SAL foram significativamente maiores do que as do grupo LFSAL (p<0,05). O grupo LF-SAL demonstrou diminuição significativa das latências apartir do segundo dia de treino (p<0,05), o LF-CPA apresentou esta diminuição após o quarto dia de treino (p<0,01), o A-SAL apresentou redução após o quinto dia de treino (p<0,05), e não foram encontradas diferenças entre as latências no grupo A-CPA. Assim, nossos resultados mostraram que a CPA parece prejudicar a consolidação da memória tanto nos animais que tiveram o telencéfalo removido quanto nos que foram submetidos à lesão fictícia. Além disto, este trabalho dá suporte às evidências de que a histamina desempenha um papel facilitatório nos processos de aprendizagem e memória em uma tarefa de escolha espacial, atuando em estruturas primitivas do cérebro de teleósteos.

The telencephalon is the most highly evolved region of the vertebrate central nervous system (CNS). The major structures of the telencephalon - the cortex and basal ganglia – derive from the dorsally positioned pallium and the ventrally positioned subpallium, respectively. Differences in morphology, gene expression, and connectivity permit a subdivision of the developing telencephalon into domains that give rise to discrete regions of the adult brain. In mammals, the ventral region of the developing telencephalon can be subdivided into the medial (MGE) and lateral (LGE) ganglionic eminences. The dorsal midline cells give rise to the choroid plexus, and cells in the more lateral domain, the dorsal pallium, give rise to the cerebral cortex. Genetic studies have provided evidence that crossregulatory interactions between transcription factors contribute to the regionalization of the telencephalon. Less is known, however, about the secreted signals that induce the initial dorsoventral character of telencephalic cells. Sonic hedgehog (SHH) is required for the specification of ventral character along the entire anteroposterior (AP) extent of the developing CNS, including the telencephalon. We show that WNT activity imposes an early generic dorsal telencephalic character and that Fibroblast Growth Factor (FGF) act sequentially, and in concert with WNT, to specify cells of definitive dorsal telencephalic character. We also show that retinoic acid (RA)-mediated signaling induces intermediate character in telencephalic cells, and that FGFs maintain cells of ventral character by opposing RA activity. The following model emerges from these findings. At gastrula stages, most or all prospective telencephalic cells become specified as ventral cells in response to node-derived SHH signals. At neural fold- and early neural plate stages, cells in the prospective dorsal and intermediate regions of the telencephalon cells are exposed to WNT signaling that induce a generic dorsal character. The head ectoderm adjacent to the telencephalon then starts to express the retinoic acid producing enzyme, Raldh3, thus exposing telencephalic cells to RA signals. At the same time prospective dorsal cells start to express WNT signals. RA signaling appears to promote the generation of intermediate/prestriatal cells, whereas WNT signal suppress the actions of RA on dorsal cells, which therefore maintain their dorsal character. From the neural plate stage, prospective ventral 6 telencephalic cells are exposed to FGF8 derived from the anterior neural ridge, and FGF8 maintains ventral telencephalic character by opposing the influence of RA signals in ventral cells. At early neural tube stages, the domain of Fgf8 expression expands dorsally and FGF signals derived from the dorsal midline region induce definitive dorsal/precortical cells. In the intermediate region of the telencephalon cells evade high levels of WNT and FGF signals, resulting in an environment in which RA signaling is able to induce prestriatal character.