<p>Gonadotropin Releasing Hormone (GnRH) is a hypothalmic decapeptide, which regulates mammalian gonadotropin secretions by binding to specific, high affinity receptors in the pituitary. Two forms of GnRH (GnRH I and GnRH II) are expressed in the brain of human and some primates. Even though primates have been used extensively in a variety of investigations in relation to the role of GnRH in reproduction, there is no evidence of any research to investigate the direct effect of GnRH on primate sperm.</p>

<p>Gonadotropin Releasing Hormone (GnRH) is a hypothalmic decapeptide, which regulates mammalian gonadotropin secretions by binding to specific, high affinity receptors in the pituitary. Two forms of GnRH (GnRH I and GnRH II) are expressed in the brain of human and some primates. Even though primates have been used extensively in a variety of investigations in relation to the role of GnRH in reproduction, there is no evidence of any research to investigate the direct effect of GnRH on primate sperm.</p>

Masters of Science / Gonadotropin Releasing Hormone (GnRH) is a hypothalmic decapeptide, which regulates mammalian gonadotropin secretions by binding to specific, high affinity receptors in the pituitary. Two forms of GnRH (GnRH I and GnRH II) are expressed in the brain of human and some primates. Even though primates have been used extensively in a variety of investigations in relation to the role of GnRH in reproduction, there is no evidence of any research to investigate the direct effect of GnRH on primate sperm. / South Africa

No description available.

Thesis (Ph. D. (Dept. of Medical Biosciences)--University of the Western Cape, 2007. / Includes bibliographical references (leaves 215-239).

Computational methods in neuroscience have advanced our understanding of neuronal regulation of motor behavior and locomotion and have been applied to identify encoding of behavioral features in circuits. The cerebellum has an established role in sensorimotor processing during coordinated movements, referred to as the “head ganglion of the proprioceptive system” (Sherrington, 1906). Increasing evidence also highlights its role in the processing of behaviorally meaningful stimuli that have the potential of guiding adaptative movements relevant to the task and priming downstream targets for action. Yet the extent to which these diverse encodings of signals in complex motor tasks are present in the cerebellar nuclei and their influence on behavior remains unknown. To shed new light on the role of this subcortical region using computational approaches, this thesis begins with an introduction that reviews the circuity of the mammalian cerebellum, highlights its proposed functions in motor behavior, and explores our understanding of its role in locomotion. In the first chapter, I analyze electrophysiological recordings from cerebellar nuclei in a locomotor obstacle avoidance task in mice that involves a rich and diverse set of task relevant features. Given the complexity of and correlations between the behavioral features, statistical modeling is required to attribute the firing rates to the correct combinations. This model enables identifying the encoding of these signals and reporting on the prevalence and degree to which they are present across individual cells in the nuclei. Additionally, this model allows investigation into the encoding of groups of cells that are selective for specific features. Chapter 2 uses network modeling to generate hypotheses about population level activity in two cortical areas, the primary and supplementary motor areas, and differentiate their computations in monkeys performing a cycling task. Finally, in chapter 3 I concentrate on a specific class of recurrent network models in the balanced state and investigate the linkage between connectivity distribution and firing sparsity, which has the potential to further our understanding on the emergence of feature selectivity in excitatory/inhibitory circuits.

Understanding the host response immediately following mucosal HIV-1 infection will be pivotal in determining whether the immune response induced by a vaccine will successfully sense and control viral replication. In order for effective vaccine strategies and modalities to be developed, these earliest immunological events must be fully assessed in a non-biased manner. Nonhuman primates (NHP), specifically Rhesus macaques (RM), serve as a model to investigate the immunological landscape immediately post-challenge and to define the spatiotemporal path of simian immunodeficiency virus (SIV). SIV infection of RM serves as a model of human HIV infection as it recapitulates many of the virological, immunological, and pathological features of HIV infection in the human host. In this thesis I will test the hypothesis whether transcriptional analysis will allow a sensitive measure of the early innate immune responses that accompany detection of the SIV virus in the periphery. I have determined that an early inflammatory profile arises early in tissues proximal to the challenge site that precedes widespread immune activation and the systemic antiviral interferon response. This study defines in detail the spatiotemporal relationship between virus and host immune response and may be a valuable resource in guiding future vaccine design strategies. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2016. / FAU Electronic Theses and Dissertations Collection