Activation of the dynorphin-kappa opioid receptor (KOR) system produces a negative emotional state during drug withdrawal, thereby motivating continued cocaine-seeking behaviors. However, it is not clear whether dynorphin plays a functional role in the onset of compulsive cocaine-taking. Here, escalation of cocaine self-administration was significantly attenuated by pretreatment of a long-acting KOR antagonist, norbinaltorphimine (NBI), in long access (LgA; 6-hours) male rats, whereas there was no effect of NBI on short access (ShA; 1-hour) rats on a fixed or progressive ratio schedule of reinforcement. Additionally, optical density of prodynorphin was increased in the nucleus accumbens (NAc) core and shell, bed nucleus of the stria terminalis (BNST), central amygdala (CeA), and basolateral amygdala (BLA) of LgA rats compared to both ShA and drug-naïve rats. These results suggest dynorphin in the stress-sensitive extended amygdala (NAc shell, BNST, CeA), and BLA-NAc core circuitry mediating cue-controlled cocaine-taking may be associated with the onset of compulsive drug-taking.

Understanding how appetite is regulated, via exogenous or endogenous factors, is essential to animal agriculture in order to maximize production capabilities, as well as in human medicine to generate ways to treat conditions such as eating disorders or obesity. The aim of this thesis was to evaluate the effects of ferulic acid (FA), an exogenous factor found within plant cells, and oxyntomodulin (OXM), an endogenous hormone generated in the gastrointestinal tract, on food intake in avian models, as well as elucidate the hypothalamic mechanisms responsible. In broiler chicks (Gallus gallus), FA administered peripherally (IP) resulted in a transient yet potent reduction of food intake. A behavior analysis revealed that FA-treated chicks defecated fewer times than control birds. Within the arcuate nucleus (ARC) there was an increase in c-Fos immunoreactivity, indicating neuronal activation, in FA-treated chicks. Within the hypothalamus, there was a decrease in mRNA abundance of galanin, ghrelin, melanocortin receptor 3, and pro-opiomelanocortin (POMC), however within the ARC there was a decrease in POMC and an increase in c-Fos mRNA after FA treatment. OXM, a proglucagon-derived peptide produced in the gastrointestinal tract, administered intracerebroventricularly (ICV) or IP in Japanese quail (Coturnix japonica), resulted in a decrease in food intake for 3 hours post-injection. There was an increase in c-Fos immunoreactivity within the ARC as well as the dorsomedial nucleus (DMN) in quail ICV injected with OXM. In conclusion, these novel data provide insights on the similarities and differences between factors that can affect appetite regulation via anorexigenic effects. / Master of Science / Exogenous and endogenous factors affect appetite regulation. Exogenous factors originate in feed components, additives, and other environmental factors that can affect bodily functions but are derived from an external source. Endogenous factors are made within the body, such as hormones and neurotransmitters, usually in response to a stimulus, and serve to communicate signals both locally and distantly in the body. Ferulic acid (FA), a natural exogenous factor originating within plant cells, is found in commonly consumed plant-based foods. When administered peripherally into broiler chicks (meat-type birds), FA caused a direct and potent, yet quickly diminishing, decrease in food intake via activation of cells within the hypothalamus, the region of the brain that is responsible for appetite regulation. Oxyntomodulin (OXM), an endogenous peptide hormone generated within the gastrointestinal tract in response to the digestion of nutrients, is known to decrease food intake in humans, rodents, and the broiler chick. However, its effects in Japanese quail, a model closer to a "wild-type" bird, are unknown. Quail injected peripherally (outside the brain) or intracerebroventricularly (ICV; into lateral ventricle of brain) with OXM showed a reduction in food intake that was more persistent than FA's effects with the effects also mediated via activation within the hypothalamus, although through slightly different molecular mechanisms. Understanding different factors that can regulate appetite in animals is necessary for agricultural applications to maximize production and improve health and welfare, as well as in humans to elucidate methods to treat appetite-related conditions, such as eating disorders and obesity.

Thesis (Ph. D.)--University of Missouri--Columbia, 2000. / Typescript. Vita. Includes bibliographical references (leaves 189-210). Also available on the Internet.

Thesis (Ph. D.)--University of Washington, 2001. / Vita. Includes bibliographical references (leaves 98-112).

Alzheimer’s disease (AD) is a degenerative disorder where the distribution of pathology throughout the brain is not random but follows a predictive pattern used for pathological staging. While the involvement of defined functional systems is fairly well established for more advanced stages, the initial sites of degeneration are still ill defined. The prevailing concept suggests an origin within the transentorhinal and entorhinal cortex (EC) from where pathology spreads to other areas. Still, this concept has been challenged recently suggesting a potential origin of degeneration in nonthalamic subcortical nuclei giving rise to cortical innervation such as locus coeruleus (LC) and nucleus basalis of Meynert (NbM). To contribute to the identification of the early site of degeneration, here, we address the question whether cortical or subcortical degeneration occurs more early and develops more quickly during progression of AD. To this end, we stereologically assesses neurone counts in the NbM, LC and EC layer-II in the same AD patients ranging from preclinical stages to severe dementia. In all three areas, neurone loss becomes detectable already at preclinical stages and is clearly manifest at prodromal AD/MCI. At more advanced AD, cell loss is most pronounced in the NbM > LC > layer-II EC. During early AD, however, the extent of cell loss is fairly balanced between all three areas without clear indications for a preference of one area. We can thus not rule out that there is more than one way of spreading from its site of origin or that degeneration even occurs independently at several sites in parallel.

Thesis (Ph. D.)--University of Missouri-Columbia, 2008. / The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Vita. "June 2008" Includes bibliographical references.

La sociabilité de l’homme est un phénomène complexe. Les théories dominantes essayant d'expliquer les mécanismes neurobiologiques de cette sociabilité ont largement impliqué l'ocytocine (OXT), un neuropeptide qui facilite de nombreuses fonctions et comportements sociaux. L'hypothalamus, parmi ses nombreuses fonctions, synthétise et sécrète l’OXT via son noyau supraoptique (SON) et le noyau paraventriculaire (PVN), faisant de lui un candidat intéressant pour comprendre les bases neurales de cette sociabilité. Dans cette thèse, qui combine trois études en imagerie par résonance magnétique (IRM), nous avons examiné 1) les différences anatomiques au sein de l'hypothalamus entre des participants contrôles et des patients autistes; 2) l’activité de l'hypothalamus, et plus spécifiquement des sous-régions hypothalamiques incluant le SON et le PVN, en réponse à des visages portant différents niveaux de sociabilité; 3) les connections fonctionnelles que ces sous-régions hypothalamiques entretiennent avec d'autres réseaux cérébraux. Nos résultats révèlent une spécificité, tant dans leur activité fonctionnelle que dans leurs connections anatomiques, des deux sous-régions hypothalamiques (SON et PVN) en fonction du niveaux de sociabilité. Ce travail de thèse fournit donc non seulement de nouvelles méthodes pour explorer les petites sous-régions hypothalamiques mais confirme également le rôle de l’hypothalamus dans la sociabilité et ses anomalies, apportant ainsi un nouvel éclairage sur l’origine des dysfonctionnements sociaux dans l’autisme et d'autres pathologies. / Human sociality is a complex phenomenon. Prevailing theories attempting to explain the neurobiological mechanisms of human sociality have implicated neuropeptide oxytocin (OXT), which facilitates numerous social functions and behaviors. The hypothalamus, among its many functions, also synthesizes and secretes OXT via its supraoptic nucleus (SON) and the paraventricular nucleus (PVN), making them viable candidates to understand the underpinnings of various social processes. This thesis combines three magnetic resonance imaging (MRI) studies investigating 1) anatomical difference of the hypothalamus between neurotypics and patients with Autism Spectrum Disorders (ASD); 2) functional MRI of the hypothalamus, specifically in hypothalamic subregions containing SON and PVN in response to faces of individuals with varying social significance; 3) functional connectivity of these hypothalamic subregions to other brain networks. Results revealed differential activity of hypothalamic subregions in response to various faces and distinctive patterns of connectivity to other brain areas that are involved in social cognition, as well as anatomical abnormalities of the hypothalamus in ASD. Altogether, the work in this thesis provides novel methods of measuring small hypothalamic subregions and supporting evidence of hypothalamic involvement in social functions that may also shed some light on social dysfunctions in ASD and other pathologies.

Made available in DSpace on 2014-12-17T15:37:05Z (GMT). No. of bitstreams: 1 RayaneBSN_DISSERT.pdf: 693632 bytes, checksum: a22430e8639b4b9e576ca8573f8e7d9d (MD5) Previous issue date: 2011-08-03 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior / The suprachiasmatic nucleus (SCN) of the anterior hypothalamus, together with the intergeniculate leaflet (IGL) of the thalamus are considered the central components of the circadian timing system (CTS) of mammals. This system is responsible for the generation and regulation of circadian rhythms by establishing a temporal organization of physiological processes and behaviors. The neuronal specific nuclear protein (NeuN) has been widely used as a neuronal marker in several studies. Since glial fibrillary acidic protein (GFAP) is a component of intermediate filaments found in the cytoplasm of astrocytes and is commonly used as a specific marker for these cells. This study aims to identify, in the marmoset, the NeuN immunoreactive neurons and glial cells immunoreactive to GFAP, as well as map the major route of photic synchronization of the STC, retinohypothalamic tract (RHT), and identify the indirect pathway to the SCN and pregeniculate nucleus (PGN) - structure homologous to IGL rodents, using immunohistochemical and cytoarchitectonic techniques. Observed in SCN the presence of neurons immunoreactive to NeuN and terminals immunoreactive subunit b of cholera toxin (CTb), neuropeptide Y (NPY) and serotonin (5- HT). In the PGN noted the presence of the NeuN and NPY immunoreactive neurons and the immunoreactive terminals CTb and 5-HT. Astrocytes are present throughout the extent of the SCN and the PGN this New World primate / O n?cleo supraquiasm?tico (NSQ) do hipot?lamo anterior, juntamente com o folheto intergeniculado (FIG) do t?lamo s?o considerados os componentes centrais do sistema de temporiza??o circadiana (STC) de mam?feros. Tal sistema ? respons?vel pela gera??o e regula??o dos ritmos circadianos estabelecendo uma organiza??o temporal dos processos fisiol?gicos e comportamentos. A prote?na nuclear neuronal espec?fica (NeuN) tem sido amplamente utilizada como um marcador neuronal em diversos estudos. J? a prote?na ac?dica fibrilar glial (GFAP) ? um componente dos filamentos intermedi?rios encontrada no citoplasma dos astr?citos e ? comumente usada como um marcador espec?fico para essas c?lulas. Este trabalho tem como objetivo identificar, no sagui, neur?nios imunorreativos a NeuN e c?lulas gliais imunorreativas a GFAP, bem como mapear a principal via de sincroniza??o f?tica do STC, o trato retinohipotal?mico (TRH), e identificar as vias indiretas para o NSQ e n?cleo pr?-geniculado (NPG) estrutura hom?loga ao FIG dos roedores, utilizando t?cnicas citoarquitet?nica e imunoistoqu?mica. Observamos no NSQ a presen?a de neur?nios imunorreativos a NeuN, bem como terminais imunorreativos a subunidade b da toxina col?rica (CTb), a neuropept?do Y (NPY) e a serotonina (5-HT). J? no NPG notamos a presen?a de neur?nios imunorreativos a NeuN e a NPY e terminais imunorreativos a CTb e a 5-HT. Os astr?citos est?o presentes em toda a extens?o do NSQ e do NPG deste primata do Novo Mundo

Background: The neuropeptide S receptor (NPSR1) and its ligand neuropeptide S (NPS) have received increased attention in the last few years, as both establish a previously unknown system of neuromodulation. Animal research studies have suggested that NPS may be involved in arousal/wakefulness and may also have a crucial role in sleep regulation. The single nucleotide polymorphism (SNP) rs324981 in NPSR1 has begun to shed light on a function of the NPS-system in human sleep regulation. Due to an amino acid exchange, the T-allele leads to an increased sensitivity of the NPSR1. In the only genomewide association study to date on circadian sleep parameters in humans, an association was found between rs324981 and regular bedtime. However, the sleep parameters in this study were only measured by self-rating. Therefore, our study aimed to replicate these findings using an objective measure of sleep. Methods: The study included n = 393 white subjects (62–79 years) who participated in an actigraphic assessment for determining sleep duration, rest duration, sleep onset, rest onset and sleep onset latency. Genotyping of the SNP rs324981 was performed using the TaqMan OpenArray System. Results: The genotype at rs324981 was not significantly associated with rest onset (bedtime) or sleep onset (p = .146 and p = .199, respectively). However, the SNP showed a significant effect on sleep- and rest duration (p = .007 and p = .003, respectively). Subjects that were homozygous for the minor T-allele had a significantly decreased sleep- and rest duration compared to A-allele carriers. Conclusion: The results of this study indicate that the sleep pattern in humans is influenced by the NPS-system. However, the previously reported association between bedtime and rs324981 could not be confirmed. The current finding of decreased sleep duration in T/T allele carriers is in accordance with studies in rodents reporting similar results after NPS application.:Background; Methods; Results; Conclusions

The origin of cardiac preganglionic neurons in the rat was investigated using the retrograde transport of horseradish peroxidase (HRP). A single injection of HRP was made into the right myocardium in either a sinoatrial or mid-ventricular location. Labeled cells were found in the mid- and lower medulla primarily in and around the nucleus ambiguus (NA) 600-1800 μm above the obex. The dorsal motor nucleus of X (DMN) was sparsely labeled and a few cells were found in an intermediate zone near the level of the obex. Labeling was bilateral with slightly heavier labeling found ipsilateral to the injection site than contralateral to it. Following a unilateral vagotomy, labeled cells were only found ipsilateral to the intact vagus. Atrial and midventricular injections yielded similar results. Occasionally only 1- cells in the NA were labeled per section. Inspection of serial sections revealed that in these sparsely labeled rats, the HRP was often in the same location within the NA forming a column of cells within the nucleus. The columns sometimes extended at least 240 μm in the rostral-caudal direction. The columnar organization was most apparent in rats with few labeled cells presumably because it was obscured in nuclei that were heavily labeled. In a second group of rats, the right vagus was cut at the cervical level and dipped in HRP to determine the extent of the NA and DMN in rats. In these animals, heavier labeling was found in the DMN than in the NA. Cells in the DMN were filled from the upper spinal cord to its most rostral extent 1200 μm above the obex. Thus, although the DMN and NA send projections in the vagus nerve, those axons terminating in the myocardium primarily originate in the NA.