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A caminhada e a corrida são formas de exercício físico que promovem mudanças no estilo de vida, mas, existem muitas controvérsias dos possíveis benefícios e riscos a respeito da caminhada ou corrida quando realizada em diferentes inclinações. O presente estudo teve como objetivo determinar o limiar anaeróbio bem como avaliar e comparar as respostas fisiológicas durante exercícios contínuos (45 minutos) com intensidade correspondente ao limiar anaeróbio executados na esteira rolante nas condições de inclinação positiva (+10%), plano (0%) e inclinação negativa (-10%). Participaram deste estudo 9 mulheres com idades entre 21 e 31 anos, fisicamente ativas. Primeiramente elas realizaram testes crescentes para determinação da intensidade correspondente ao limiar anaeróbio em cada inclinação. Após essa determinação foram realizados os protocolos contínuos na intensidade correspondente ao limiar anaeróbio por 45 minutos. Os resultados encontrados mostraram que o valor médio (\'+ OU -\' desviopadrão) da velocidade correspondente ao limiar anaeróbio no plano foi de 6,56 \'+ OU -\' 0,53 Km/h, na inclinação positiva foi de 5,44 \'+ OU -\' 0,53 Km/h (com redução percentual de 17,07% em relação ao plano) e na inclinação negativa foi de 7,22 \'+ OU -\' 0,67 Km/h (com elevação percentual de 9,14% em relação ao plano). Nos protocolos contínuos foi observado que os valores das variáveis ventilatórias apresentaram-se mais elevados para o protocolo com inclinação positiva, já a freqüência cardíaca apenas apresentou diferença até o 15º minuto do exercício entre os protocolos com inclinação positiva e o protocolo com inclinação negativa. Mas apesar disso, as voluntárias não relataram dificuldade do gesto motor na realização dos exercícios. Conclui-se que mesmo com a tentativa de se trabalhar na velocidade ideal para cada condição imposta, as respostas cardiovasculares e metabólicas são diferentes, ) principalmente entre o protocolo com inclinação positiva e o protocolo com inclinação negativa. O presente trabalho mostrou pontos importantes que devem ser levados em consideração, quanto à escolha do protocolo aplicado nos treinamentos físicos em indivíduos com diferentes condições físicas quando se propõem diferentes velocidades de corrida e inclinações da esteira. / Walking and running are forms of exercise that promote changes in lifestyle, but there are many controversies about the possible benefits and risks regarding the walking or running when performed at different slopes. This study aimed to determine the anaerobic threshold and to evaluate and compare the physiological responses during continuous exercise (45 minutes) with intensity corresponding to anaerobic threshold run on the treadmill in terms of positive slope (+10%), level (0%) and negative slope (-10%). The study included 9 women aged between 21 and 31 years old, physically active. First they performed increasing intensity tests to determine the intensity corresponding to anaerobic threshold on each slope. After determining these parameters the continuous protocols were performed in intensity corresponding to anaerobic threshold for 45 minutes. The results showed that the speed average (\'+ OU -\' standard deviation) at level the anaerobic threshold was 6.56 \'+ OU -\' 0.53 km/h, atthe positive slope was 5.44 \'+ OU -\' 0.53 km/h (with a percentage reduction of 17.07% over the level) and the negative slope was 7.22 \'+ OU -\' 0.67 km/h (with high percentage of 9.14% over the level). In continuous protocols was observed that the values of ventilatory variables were more elevated for the protocol with positive slope and the heart rate showed only significant difference until the 15th minute of exercise between protocols with positive slope and with negative slope. But despite this, the volunteers reported no difficulty in motor gesture in exercises. It was conclude that even with the attempt to run at ideal speed for each condition the cardiovascular and metabolic responses are different, especially between the protocol with positive slope and with negative slope. This study showed important points that should be taken into account in the choice of protocol used in physical training in individuals with different physical conditions when they propose different running speeds and inclinations of the treadmill.

My thesis has accomplished 3 significant contributions to neuroscience. Firstly, I have discovered a novel example of vertebrate deep-brain photoreception. Spontaneously generated fictive locomotion from the isolated nervous system of pro-metamorphic Xenopus tadpoles is sensitive to the ambient light conditions, despite input from the classical photoreceptive tissues of the retina and pineal complex being absent. The photosensitivity is found to be tuned to short wavelength UV light and is localised to a small region of the caudal diencephalon. Within this region, I have discovered a population of neurons immuno-positive for a UV-specific opsin protein, suggesting they are the means of phototransduction. This may be a hitherto overlooked mechanism linking environmental luminance to motor behaviour. Secondly, I have advanced the collective knowledge of how both nitric oxide and dopamine contribute to neuromodulation within motor control systems. Nitric oxide is shown to have an excitatory effect on the occurrence of spontaneous locomotor activity, representing a switch in its role from earlier in Xenopus development. Moreover, this excitatory effect is found to be mediated in the brainstem despite nitric oxide being shown to depolarise spinal neurons. Thirdly, I have developed a new preparation for patch-clamp recording in pro-metamorphic Xenopus tadpoles. My data suggest there are several changes to the cellular properties of neurons in the older animals compared with the embryonic tadpole; there appears to be an addition of Ih and K[sub](Ca) channels and the presence of tonically active and intrinsically rhythmogenic neurons. In addition, I have shown that at low doses dopamine acts via D2-like to hyperpolarise the membrane potential of spinal neurons, while at higher doses dopamine depolarises spinal neurons. These initial data corroborate previously reported evidence that dopamine has opposing effects on motor output via differential activation of dopamine receptor subtypes in Xenopus tadpoles.

It has long been established that the spinal cord is able to produce locomotor activity on its own. Despite extensive research identifying and describing the involvement of multiple spinal neuron populations that are part of the spinal locomotor circuit, the manner in which these different components act together to precisely control the rhythm and the pattern of activation of muscles during locomotion remains largely undetermined. We sought to shed light on how the components of spinal locomotor circuits interact to produce robust locomotion using a developmental approach in zebrafish larvae. We used electrophysiological techniques to observe how the rhythm generation mechanism developed while the fish was transitioning from an early form of swimming to a more mature swimming behaviour. In the process we were able to highlight fundamental changes in the organization of spinal locomotor circuits as its operation moves from a pacemaker-based architecture relying on intrinsic properties of neurons to a network oscillator-based architecture relying on synaptic connectivity to generate proper rhythm driving the fish tail beats. Additionally, we revealed that this transition occurred at different times along the spinal cord progressing in a caudorostral direction. By combining these experimental observations with already published insights we were able to propose models of spinal locomotor circuits reproducing the successive locomotor behaviours encountered through development. By incrementing supplementing the circuit model in a manner that reflected biological processes by which the nervous system maturates (neurogenesis, synaptic connectivity refinement and maturation of intrinsic properties) we mirrored the natural development of the spinal locomotor circuit. This series of successively constructed models permitted us to pinpoint possible roles of specific neural populations for swimming behaviour as well as eventual targets and mechanism of actions of neuromodulators (serotonin and dopamine). In the process, I further provided testable hypotheses for future inquiries. Overall, the experimental findings in combination with the modeling work are an important step forward in fully understanding how the spinal cord generates swimming movements in zebrafish.