Non-invasive transcutaneous auricular vagus nerve stimulation (taVNS) is a neuromodulatory technique used to activate vagal afferent fibers located in the concha of the outer ear. Vagal afferents project to the nucleus of the solitary tract (NTS) where information is processed and propagated to higher brain regions. Widespread NTS connections provide a mechanism through which taVNS can be used to influence multiple systems and be a potential treatment for many disorders including heart failure, gastric motility disorders, and migraines. Recent studies are now investigating taVNS as an alternative treatment option to invasive cervical vagus nerve stimulation (cVNS) which is FDA approved to treat drug-resistant epilepsy and depression but has limited patient availability due to the invasiveness of the procedure. Migraine and epilepsy clinical studies have shown therapeutic taVNS benefits and human fMRI studies have demonstrated comparable brain activation between cVNS and taVNS. However, questions remain regarding optimal taVNS parameters, and no study has compared the direct mechanisms responsible for cVNS and taVNS effects. In this study, a high-impedance tungsten electrode was stereotaxically placed into NTS in 10 chloralose-anesthetized rats, and 40-70 neurons were interrogated using electrophysiological methods. Firing rate changes during stimulation on-times were compared to activity levels during stimulation off-times. Neurons were classified as positive responders if they displayed consistent firing rate increases during stimulation, negative responders if they displayed consistent decreases, and non-responders if there was no consistency using a mathematical cosine similarity score. Six taVNS stimulation parameters were investigated using three frequencies (20, 100, 250Hz) at two intensities (0.5, 1.0mA) to identify parameter-specific effects on NTS neurons. Additionally, neuronal activity was evaluated following cVNS at 20 and 250Hz at the bradycardic intensity (lowest intensity to generate a transient 5% decrease in heart rate, BI) and compared to taVNS effects at the corresponding frequencies. Our data shows that taVNS at 20Hz, 1.0mA yields the greatest number of positive responders and 100Hz, 1.0mA yields the greatest number of negative responders (p<0.05) suggesting different taVNS parameters can differentially influence NTS activity. Comparisons between the number of responders generated with cVNS and taVNS revealed significantly fewer negative responders with cVNS at 20Hz compared to taVNS at 20Hz regardless of intensity (p<0.01) but yielded comparable positive responders between cVNS at 20Hz, BI and taVNS at 20Hz, 1.0mA. No significant differences were observed between the number of cVNS and taVNS responders at 250Hz. Interestingly, individual neuronal responses were different between both methods of stimulation, suggesting that they could work through different neuronal pathways.

Alcohol use disorder (AUD) is a chronic, relapsing condition with a complex etiology and heritable susceptibility factors interact with environmental factors to produce and maintain the disease. One goal of current neuroscience research is to identify the neuroadaptations mediating the propensity to consume high amounts of alcohol, of either innate or environmental origin. Dysfunctional neuronal communication between prefrontal cortical regions and the nucleus accumbens (NAcc) have been implicated in excessive alcohol drinking and proposed to play a critical role in AUD. However, the exact mechanism by which altered prefrontostriatal transmission may perpetuate excessive drinking is poorly understood. In addition, the exact role of dopamine receptor 1 (D1R) or dopamine receptor 2 (D2R)-expressing medium spiny neurons in the NAcc is unclear and adds another layer of complexity to this framework. This thesis concerns pituitary adenylate cyclase-activating polypeptide (PACAP), a highly conserved 38 amino acid neuropeptide, and its receptor PAC1R. Studies in rodents and humans have implicated PACAP and PAC1R in the actions of drugs of abuse, including more recently, alcohol. Notably, the PACAP/PAC1R system has also been shown to increase glutamatergic neurotransmission in several circuits. The overall hypothesis of this project was that the PACAP/PAC1 system in the prefrontal cortex-NAcc pathway regulates excessive drinking and the long-lasting neuroplastic changes observed in alcohol addiction, via the modulation of the glutamatergic system. Using alcohol-preferring rats, a hereditary model of AUD, we found that intracerebroventricular administration of a PAC1R antagonist blocked excessive alcohol drinking, motivation to drink, and alcohol seeking behavior selectively in this line and not in outbred rats. Alcohol-preferring rats displayed a higher number of PAC1R positive cells in the NAcc Core. Blockade of PAC1R in the NAcc Core, via pharmacology or gene knockdown, resulted in reduced alcohol drinking. Conversely, we found that knockdown of the PAC1R in the NAcc Shell led to increased alcohol drinking and motivation to drink in alcohol-preferring rats, suggesting that the PACAP/PAC1R system may play an opposite role in these two NAcc subregions. Using a mouse exposure model of excessive drinking, a glutamatergic projection from PACAP-expressing cells in the prelimbic portion of the prefrontal cortex (PrL) to the NAcc Core circuit was found to be recruited by alcohol exposure. Inhibition of these neurons, as well as PACAP neuron ablation or PACAP deletion, led to decreased alcohol intake that was specific to male mice. Systemic PAC1R antagonism, and specific knockdown of PAC1R in the NAcc Core, also decreased alcohol intake in male mice. Using slice electrophysiology and channelrhodopsin assisted circuit mapping, we found that this pathway is biased to D1R-expressing neurons in the NAcc Core following alcohol exposure in males, and that PACAP application increases post-synaptic measures of glutamatergic transmission in this circuit. Overall, these data describe a key role for the corticostriatal PACAP/PAC1R system in aberrant alcohol drinking in both hereditary- and exposure-based models of AUD and give novel insights into the underlying mechanisms of alcohol addiction. / 2025-01-23T00:00:00Z

<p> This thesis examines the rotation-vibration spectra of systems of two and three particles (spin zero). The results in the two-particle case agree with many of the gross features of the spectra of deformed axially symmetric even-even nuclei. In the three-particle case, the set of basis functions used i n the expansions of the wavefunctions was too small to give accurate eigenvalues and eigenvectors, but nevertheless the spectrum clearly corresponds to that of an asymmetric even-even nucleus. </p> / Thesis / Master of Science (MSc)

<p> The level structure of the Odd-A nucleus 163Lu has been studied by the 148Sm (19F,4n) 163Lu reaction through gamma-ray singles and gamma-gamma coincidence methods.</p> <p> A number of rotational band structures have been observed up to a spin of 43/2. The backbending behaviour of the two signatures of the h11/2 band, α = -1/2 and α = 1/2, has been observed. The critical frequencies for the backbends are wc = 0.264 and 0.284 respectively.</p> / Thesis / Master of Science (MSc)

Immune-brain-endocrine communication influences behaviour and contributes to the development of the central nervous system (CNS) in a sexually dimorphic manner. The bed nucleus of the stria terminalis (BST) is a highly sexually dimorphic brain region; in most mammalian species the male BST is larger than the female BST. Previously, our lab has shown that male and female mice lacking T cells due to knock out of the beta (b) and delta (d) chains of the T cell receptor (TCRb-/-d-/-) have reduced anxiety-like behaviour. This was shown with increased time spent in the open arms of the elevated plus maze by TCRb-/-d-/- mice compared to wild type (WT) mice of both sexes. T cell deficient mice also show differences in brain volume compared to WT, including a lack of sexual dimorphism in volume of the BST. The present study explored the impact of T cell deficiency on immune and endocrine factors implicated in sex differences of the CNS. The first analysis was of serum Anti-Müllerian hormone (AMH). AMH is a key determinant of the male phenotype during fetal development. It has also been shown by others to contribute to sexual dimorphic development of the BST. Our postnatal analysis of serum AMH using ELISA demonstrated an age and genotype effect, where a peak in serum AMH levels in WT mice of both sexes was absent in both male and female TCRb-/-d-/- mice at postnatal day (P) 7. These results suggest that T cells have an impact on the endocrine system in early life but the process does not appear to be sexually dimorphic. The present study also explored the impact of TCR knockout on microglia, the resident immune cells of the brain. Other have shown microglia contribute to sexual dimorphic brain development. This contribution occurs through interaction with endocrine factors, making them a key player in the immune-brain-endocrine crosstalk. Using immunohistochemistry and the microglial marker, anti-Iba1, microglia were examined in adult and P7 WT and TCRb-/-d-/ mice. To quantify microglia, soma were traced using AxioVision microscope software, and microglia cell number, perimeter, radius, feret ratio, and area in dorsal and ventral BST were assessed. Our results show sex differences in microglia number in dorsal BST in adult WT mice, where female WT mice had a lower number of microglia compared to WT males, however this difference was absent in TCRb-/-d-/- adult mice. There were no effects on microglia number in the ventral BST and morphology analysis did not reveal any effects in the dorsal or ventral BST. Furthermore, the difference in microglia number was absent in all groups of P7 mice and analysis of soma morphology did not reveal any significant effects. This study explored the impact of TCR knockout on the BST by exploring the immune and endocrine factors shown to contribute to its sexual dimorphic development. The results suggest a non-dimorphic impact on the endocrine system in the postnatal period and a dimorphic impact on microglia that is age and region-specific. The findings reveal a complex network emphasizing the importance of a systems-wide approach to the study of sex differences in the CNS. / Thesis / Master of Science (MSc)

京都大学 / 新制・論文博士 / 博士(医学) / 乙第13570号 / 論医博第2296号 / 新制||医||1069(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 花川 隆, 教授 渡邉 大, 教授 高橋 淳 / 学位規則第4条第2項該当 / Doctor of Medical Science / Kyoto University / DFAM

京都大学 / 新制・課程博士 / 博士(理学) / 甲第24413号 / 理博第4912号 / 新制||理||1702(附属図書館) / 京都大学大学院理学研究科物理学・宇宙物理学専攻 / (主査)准教授 上田 佳宏, 教授 嶺重 慎, 教授 太田 耕司 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DFAM

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