• A study on the interaction of Alzheimer's disease beta amyloid protein with cultured mouse neuroblastoma cell line NB41A3

      Zhao, Xiaohong (1994)
      The $\beta$ amyloid protein is the primary constituent of amyloid plaques in the brains of Alzheimer's disease patients. The generation of $\beta$ amyloid protein from $\beta$ amyloid precursor protein and its interaction with neuronal cells were studied in the mouse neuroblastoma cell line NB41A3. Immunoreactivity to the carboxyl terminal of the precursor protein was detected among the membrane proteins of these cells, indicating that $\beta$ amyloid precursor protein is produced by NB41A3 cells. Also amyloid precursor protein carboxyl terminal immunoreactivity was observed in the conditioned medium of the cells, demonstrating various cytosolic peptide fragments are secreted during the cellular processing of the $\beta$ amyloid precursor protein. Synthetic $\beta$ amyloid peptide was shown to negatively affect NB41A3 neuroblastoma cells as judged by decreasing cell numbers, decreasing amount of cell protein, and release of the cytosolic enzyme, lactic dehydrogenase, into the medium. At the ultrastructural level, internal damage to the nucleus could be observed. Synthetic $\beta$ peptide showed specific binding with neuroblastoma cells. The internalization of the $\beta$ peptide into the cells suggest a direct mechanism for $\beta$ amyloid protein toxicity in vivo. This research contributes to the knowledge of the processing of Alzheimer's disease $\beta$ amyloid precursor protein in NB41A3 cells and demonstrates that NB41A3 cell provides a practical in vitro model for studying the mechanism of Alzheimer's disease and amyloid toxicity.
    • Central Nervous System Regulation Of Metabolic Suppression In Arctic Ground Squirrels

      Jinka, Tulasi Ram; Drew, Kelly L. (2010)
      The main focus of this dissertation is central nervous system regulation of metabolic suppression in hibernating mammals in general, and the Arctic ground squirrel (Urocitellus parryii) as a model for seasonal hibernation. Hibernation is a unique physiological, morphological, and behavioral adaptation to overcome the periods of resource limitation. Metabolic suppression seen in torpor during hibernation has several biomedical applications. A multitude of studies have revealed the role of the central nervous system in regulating hibernation, including a role for neurotransmitters and neuromodulators. Previous studies have shown that the neuromodulator adenosine mediates altered thermoregulation during induction of torpor in facultative hibernators, but it is not clear how adenosine influences torpor in seasonal hibernators. The main focus of the current project was to test the hypothesis that a seasonal change in purinergic signaling is necessary for the onset of spontaneous torpor in the Arctic ground squirrel. My dissertation reports that adenosine meets all of the necessary requirements for an endogenous mediator of torpor in the hibernating Arctic ground squirrel. A progressive increase in sensitivity to adenosine A 1 receptors mediated signaling defines the seasonal transition into the hibernation phenotype. I show that adenosine A1 receptor activation is necessary and sufficient to induce torpor in the Arctic ground squirrel. Glutamate is an excitatory neurotransmitter which is widely studied in hibernation research. My dissertation demonstrates that N-methyl-D-aspartate type glutamate receptors, located in the periphery or circumventricular organs, are involved in inducing arousal from torpor in the hibernating Arctic ground squirrel. This dissertation also presents evidence that dietary restriction sensitizes adenosine A1receptors in rats through an increase in surface expression in thermoregulatory regions of the brain (hypothalamus). This contributes to the decline in body temperature and respiratory rate in animals subjected to a restricted diet, which mimics a torpor-like effect.
    • Ceramide Metabolism Regulates A Neuronal Nadph Oxidase Influencing Neuron Survival During Inflammation

      Barth, Brian M. (2009)
      Inflammation is a major component of acute and chronic pathologies of the central nervous system, including psychiatric disorders. Microglia respond to pathogens, injury, and toxins by secreting inflammatory mediators including pro-inflammatory cytokines in an event known as neuroinflammation. This thesis research investigated a link between neuroinflammation and oxidative stress, and ultimately neurodegeneration. The cytokine tumor necrosis factor alpha was shown to stimulate a neuronal NADPH oxidase (NOX), specifically by stimulating the production of ceramide and ceramide-1-phosphate via Mg 2+-neutral sphingomyelinase (Mg2+-nSMase) and ceramide kinase. Intriguingly, glucosylceramide blocked NOX activation, linking ceramide neutralization directly to a decline in oxidative stress. Most importantly, NOX activity interfered with actin and sphingosine kinase-1 via oxidation, demonstrating a positive and detrimental feedback mechanism that impedes neuronal survival pathways. Interestingly, crude extracts from wild Alaskan bog blueberries showed the ability to interfere with Mg2+-nSMase, demonstrating a specific neuroprotective property of the berry. Altogether, this thesis research defined a key neuronal pathway linking inflammation to oxidative stress via ceramide metabolism, potentially allowing for future therapeutic development to improve neuronal function and survival.
    • Circadian Rhythms, Neuroanatomy Of The Superchiasmatic Nucleus And Selective Breeding Of The Northern Red -Backed Vole (Clethrionomys Rutilus)

      Tavernier, Ronald J., Jr.; Bult-Ito, Abel (2007)
      The experiments performed in this thesis investigated the circadian rhythms and neuroanatomy of a subarctic rodent, the northern red-backed vole ( Clethrionomys rutilus). Arctic and subarctic light regimes are extreme, with long periods of light and dark and large daily changes in day-length, but very little is known about circadian rhythms of mammals at high latitudes. A colony of C. rutilus was established and proper husbandry techniques were developed to allow voles to reproduce in captivity. Wild-caught and laboratory reared animals were tested for circadian rhythms in a 16:8 hour light:dark (LD) cycle, constant dark (DD) and constant light (LL). Voles displayed predominantly nocturnal patterns of wheel-running in 16:8 LD. In LL and DD, animals displayed large phenotypic variation in circadian rhythms with many becoming non-circadian (60% in DD, 72% in LL), indicating highly labile circadian organization. The distributions of eight common neurotransmitters in the suprachiasmatic nucleus (SCN), the brain's master circadian clock, were characterized. The SCN of C. rutilus is similar to that found in other rodents. Larger quantities of cholecystokinin and neuropeptide Y are found in the SCN of C. rutilus pointing to the possible importance of non-photic cues in resetting the phase of the internal clock. An additional study also found a distinct distribution of Substance P fibers and neurokinin-1 receptors in the SCN of C. rutilus. Starting with the 5th generation, laboratory-bred voles were selectively bred to create two lines of voles that maintained a circadian rhythm in DD, two lines that lost their circadian rhythm in DD, and a randomly bred control line. After three additional generations no significant differences were found among the lines due to the variability in the response to selection over the first few generations. With a large phenotypic variation in circadian wheel-running rhythms and an SCN similar to other rodents studied, C. rutilus is an ideal candidate to study subarctic circadian adaptations. Continued selective breeding will develop a useful tool for elucidating natural genetic variation in circadian rhythm characteristics in a subarctic mammal.
    • Development of postsynaptic function in muscle membrane

      Owens, Jesse Lee; Kullberg, Richard W. (1987)
      The development of postsynaptic function in skeletal muscle of Xenopus laevis was studied in vivo in order to address the following questions: What changes take place in acetylcholine receptor (AChR) channel function during muscle development and when do they occur? Does muscle activity regulate the development of postsynaptic function? Do functionally different muscles have different programs of postsynaptic development? Single channel recordings from nonjunctional membrane revealed a class of low conductance (30 to 40 pS), long open time (2-3 ms) AChR channels which appeared on embryonic membrane within 21 h of fertilization. At 45 h of age, a second class of higher conductance (40 to 60 pS), brief open time ($<$1 ms) channels began to be expressed and over the course of 4 days became the most frequently observed channel type. Concurrently, the open time of the low conductance channel decreased by half during development. These data explain the developmental change in duration of synaptic currents previously observed in myotomal muscle, and they lay the foundation for further studies on the molecular mechanisms of AChR development. The effect of immobilization on the development of synaptic currents in myotomal muscle was investigated by allowing embryos to develop in a bath containing tetrodotoxin, which eliminated muscle activity during formation and maturation of the neuromuscular junction. In both control and tetrodotoxin-immobilized animals, synaptic current rise times and decays developed in an equivalent fashion, indicating that muscle activity is not required for normal development of AChR channel gating or acetylcholinesterase (AChE) deposition at the neuromuscular junction. The development of synaptic currents was compared in two functionally different muscles, the interhyoideus and the superior oblique. Each muscle has a characteristic program of synaptic current development during synaptogenesis and during metamorphosis. The contrasting development of synaptic currents from the two muscles can be explained by different programs of AChR and AChE development.
    • Effect of high latitude on the variability of human event-related brain potentials

      Bush, Anita Marie; Geist, Charles R.; Barnes, Brian M.; Connor, William; Ebbesson, Sven O.; Emery, Scott; Murphy, Edward C. (1993)
      European researchers (Anderson, Chambers, Myhre, Nicholson, & Stone, 1984) at 69 degrees north latitude, have reported seasonal changes in the human electroencephalogram, EEG. Other researchers from the North American mid-latitudes (Deldin, Duncan, & Miller, 1989a, 1989b), using event-related brain potentials, ERPs, have reported changes associated with ambient light. Similar changes in the event-related brain potentials of humans have not been reported from the high latitudes nor by longitudinal methods. This dissertation longitudinally investigated ERP variability in normal humans living at high latitude. One hundred and twelve residents of Fairbanks, Alaska participated in single-trial ERP testing, both auditory and visual, to evaluate criteria of validity and reliability. Subsequently, eight normal humans participated in auditory and visual ERP testing every month for twelve consecutive months. The longitudinally-studied subjects were residents of the Alaskan subarctic, where testing occurred, and each experienced naturally-occuring photoperiod variability of 3.31 hours in December to 21.98 hours in June. Dependent variables included P3 amplitude and latency in both sensory modalities. Independent variables included: age, estimated cranial volume, length of last sleep epoch, subjective wakefulness, ambient photoperiod, and ambient geomagnetic field. Distribution of the longitudinal ERP data satisfied Shapiro-Wilke criteria for normality. The GLM-ANOVA for ordered repeated measures was used and a month effect was observed in P3 amplitude and latency, as well as a month-by-sensory mode interaction. The principal components method of factor analysis evaluated the factor weights of the independent variables. Variables unique to each subject (e.g., age, cranial volume, length of last sleep) were more heavily weighted in the first factor. The environmental variables became heavily weighted in the second factor, and descriptors of the earth's natural geomagnetic activity were weighted more heavily than ambient photoperiod. Following PCA analysis, the environmental variables of geomagnetic field and photoperiod were separately investigated. No seasonal variability in the ERP characteristics was detected when using a photoperiod-based definition of season. However, variability in auditory P3 amplitude was observed when groupings were defined based on geomagnetic criteria.
    • Investigation Of The Allosteric Modulators Desformylflustrabromine And 4-(2-Hydroxyethyl)-1-Piperazineethanesulfonic Acid (Hepes) Interactions On Nicotinic Acetylcholine Receptors

      Daniello-Weltzen, Maegan M.; Schulte, Marvin K. (2011)
      Neuronal nicotinic acetylcholine receptors (nAChRs) are members of the Cys-loop super family of ligand gated ion channels. Dysregulation of nAChRs can lead to pathologies such as Alzheimer's disease, Parkinson's disease, Autism and nicotine addiction. Possible new therapeutic avenues are positive allosteric modulators (PAMs). The natural product desformylflustrabromine (dFBr), a tryptophan metabolite of the marine bryozoan Flustra foliacea, was found to be PAM of alpha4beta2 nAChR. Evaluation of our synthetic water soluble dFBr salt by two-electrode voltage clamp of Xenopus laevis oocytes expressing human nAChR confirmed that synthetic dFBr displayed similar properties as the natural product. Low concentrations of the synthetic dFBr enhanced ACh's efficacy on alpha4beta2 receptors. At higher dFBr concentrations, dFBr inhibited ACh potentiated responses. On alpha7 receptors, dFBr inhibited ACh induced currents. Further pharmacological characterization of dFBr revealed that dFBr was able to enhance partial agonist potencies and efficacies. Evaluation of dFBr on antagonists showed no effect on antagonist inhibition. The mechanisms of biphasic modulation (potentiation and inhibition) of dFBr on alpha4beta2 nAChR were also investigated. Enhanced efficacy of ACh induced currents by dFBr appeared to be accomplished by dFBr stabilization of the open receptor conformation by destabilization of the desensitized state. The inhibition of ACh potentiated currents by dFBr appeared to involve open-channel block. To better understand dFBr mechanisms, its putative binding site was examined. Alanine mutations were made in non-orthosteric clefts on the beta2+ and alpha4- faces. Results revealed residues located on these faces are involved in ACh induced conformational change of the receptor. In addition our data supports our hypothesis that allosteric modulation by dFBr interacts with residues located on the beta2+ and alpha4- faces. The new novel actions of (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) (HEPES) as a alpha4beta2 stoichiometric PAM was discovered and characterized. We showed that HEPES, a common buffering agent, potentiated the high ACh sensitivity alpha4beta2 receptor while only inhibiting the low ACh sensitivity alpha4beta2 receptor. Mutagenesis results suggested that residue beta2D217 is a critical residue in the HEPES binding site. Results from these studies will aid in the development of therapeutic ligands that will assist in the treatment of diseases where nAChRs are dysregulated.
    • Investigations into model systems of neurodegeneration: Organotypic brain slice culture and in vivo microdialysis

      Clapp, Kimberly Lara; Duffy, Lawrence K. (2000)
      The mechanisms behind neurodegeneration in disease and injury have yet to be fully defined. Many in vitro and in vivo model systems, have been developed to investigate the mechanisms of neurotoxicity and its relation to human disease and injury. There are a few resounding connections between most types of neurological disorder; namely oxidative stress and inflammation. The glutamate receptor agonist, N-methyl-D-aspartate, can be used to imitate excitotoxicity during stroke as it overstimulates the glutamate receptor, leading to rises in intracellular calcium levels, which in turn lead to oxidative stress within the cell. Amyloid-beta protein (Abeta) a useful in many of its isoforms in creating in vitro model systems of Alzheimer's disease (AD). Abeta can directly cause the production of potentially harmful free radicals. This study investigates the formation of model systems of neurodegeneration: in vivo microdialysis and organotypic brain slices culture in order to assess the role of oxidative stress and inflammation morphologically and biochemically. The effect of melatonin, an endogenous antioxident, on oxidative stress associated with NMDA and Abeta neurotoxicity was determined through morphological analysis and biochemical markers of oxidative stress. This study reports that both NMDA and Abeta(25--35) cause oxidative stress in an organotypic brain slice culture model system of stroke and Alzheimer's disease as established by: (1) morphological analysis of tissue and ultrastructure, (2) redox-active assay, (3) heme-oxygenase assay, (4) 8-hydroxyguanosine assay and (5) interleukin IL-1beta and IL-6 assay (Abeta only) These investigations also demonstrate that melatonin can attenuate the oxidative stress associated with NMDA and Abeta exposure. These findings expand upon previous evidence from cell culture analysis of oxidative stress induced by NMDA and Abeta. Therefore, this evidence supports the theory that oxidative stress is involved in neurodegeneration in both excitotoxicity in stroke and in Abeta-mediated damage in Alzheimer's disease, and that endogenous antioxidant treatment may be a useful therapeutic approach in such injury and disease.
    • Nest -Building Behavior In House Mice (Mus Musculus), A Potential Model Of Obsessive -Compulsive Disorder In Humans

      Greene-Schloesser, Dana M.; Bult-Ito, Abel (2007)
      OCD (obsessive-compulsive disorder) is a chronic and debilitating psychiatric condition characterized by intrusive and persistent thoughts (obsessions) and repetitive behaviors (compulsions) that become ritualistic in an attempt to escape the obsessions. Currently there is a paucity of animal models with robust and spontaneous (non-drug or non-behaviorally induced) compulsive-like behaviors. This study is aimed at validating a novel robust and spontaneous genetic mouse model of OCD. The compulsive-like nest-building behavior in mice selected for high levels of nest-building behavior (BIG) has good face validity, with a behavioral phenotype that resembles hoarding behavior characteristic of OCD. In addition, male and female BIG mice displayed compulsivelike digging behavior relative to mice selected for low levels of nest-building behavior (SMALL), as assessed by the marble-burying test. Both chronic oral fluoxetine and clomipramine treatment reduced compulsive-like nest-building behavior in male BIG mice. Furthermore, chronic oral fluoxetine administration decreased nest-building behavior of BIG mice in a dose-dependent manner, while desipramine, an antidepressant not effective for treating OCD, did not significantly alter this behavior. The administration of fluoxetine did not cause a decrease in general locomotor behavior. These findings suggest that the nest-building phenotype has predictive validity. In addition, chronic oral fluoxetine treatment reduced compulsive-like digging behavior in male and female BIG mice as compared to SMALL mice. Gender effects were also found in treatment response. Clomipramine did not reduce nest-building in female BIG mice in a dose-dependent manner, which is consistent with previous studies. These data are in contrast to previous studies using BIG male mice which had a significant decrease in nest-building behavior with oral clomipramine. These results are consistent with studies on humans, which have found gender differences in the treatment effects of antidepressants. Additional construct validity is implicated by the results of targeted serotonergic lesions of the raphe nuclei in male BIG mice, which reduced repetitive nest-building behavior. More research is necessary to confirm the appropriateness of this model for human OCD; however, this model is promising based on the data that support good face, predictive and construct validity.
    • Neural control of singing in the dark-eyed junco (Junco hyemalis)

      Gulledge, Cynthia Corbitt (1997)
      This dissertation includes several discrete projects addressing various aspects of the neural control of singing in the Dark-eyed Junco (Junco hyemalis), a migratory songbird. I collected the birds from a local wild population during the breeding season and migration. Chapter 2 addresses the role of testosterone in controlling volumes of the brain regions that control song learning and song production (vocal control regions, VCRs), which grow and shrink seasonally and are correlated with changes in singing behavior. I found that: the role testosterone plays may depend on the age of the bird and the brain region in question. Expanding on that study, I investigated the independent roles of testosterone and photoperiod in the control of VCR volumes in adolescent male juncos (Chapter 3). In seasonally breeding species, circulating androgens increase with increasing photoperiod, so increases in VCR volumes in the spring had been thought to be a result of photoperiod-induced increases in testosterone. Experimental separation of photoperiod and testosterone revealed that long photoperiod alone can have stimulatory effects on VCR growth, despite low testosterone levels. In fact, in adolescent male juncos, lengthening photoperiod may play a greater role in determining VCR volumes than testosterone does, again suggesting that the role of testosterone in the vocal control system may change with age. Other neurochemicals besides testosterone are present in the vocal control system; Chapter 4 describes the first description of opioid peptide receptor localization and density measurement in the vocal control system of adult male songbirds. I expanded that study to include nonsinging female and juvenile juncos (Chapter 5). The results of the expanded study indicate that opioids may modulate development of the vocal control system between adolescence and adulthood, as well as auditory processing throughout life.
    • Nmda Receptors In Hibernating Arctic Ground Squirrels

      Zhao, Huiwen; Drew, Kelly (2005)
      Hibernation is a unique physiological state characterized by suppressed metabolism and body temperature that is interrupted by multiple, brief periods of arousal throughout the hibernation season. Blood flow fluctuates during hibernation and arousal in a reperfusion-like manner without causing neurological damage. Previous studies show that hippocampal slices from hibernating animals tolerate experimental oxygen nutrient deprivation and N-methyl-D-aspartate (NMDA) toxicity better than slices from euthermic animals. However, the cellular mechanisms underlying these examples of tolerance remain unclear. Tolerance to NMDA toxicity suggests that modulation of NMDA receptors (NMDAR) contributes to intrinsic tissue tolerance in slices from hibernating Arctic ground squirrels (hAGS, Spermophilus parryii). NMDAR are one subtype of glutamate receptors. NMDAR play critical roles in excitatory synaptic transmission, synaptic plasticity, learning and memory, and excitotoxicity. NMDAR1 (NR1) is a fundamental subunit of NMDAR and required for receptor function. The main focus of the current project was to test the hypothesis that NMDAR are down-regulated in hAGS compared with interbout euthermic AGS (ibeAGS) and to explore the potential mechanisms of this down-regulation. NMDAR function can be modulated by protein phosphorylation, subunit composition, and internalization. Hence, the aim of chapter 2 was to determine the distribution of NRl in hAGS and ibeAGS using immunohistochemistry. The aim of chapter 3 was to examine NMDAR function in cultured hippocampal slices from hAGS, ibeAGS, and rats using calcium imaging, and to investigate potential modulation of NMDAR such as phosphorylation and internalization for altered function using western blot analysis. Given that synaptic remodeling and functional changes after arousal from hibernation, and NMDAR play an important role in learning and memory, the aim of chapter 4 was to address the effects of hibernation on learning and memory in AGS using an active avoidance task. Here, we report that NMDAR in hAGS are down-regulated via decreased phosphorylation of NR1. This down-regulation is not due to changes in NR1 distribution and internalization. In addition, the fraction of NR1 in the functional membrane pool in AGS is less than in rats. These findings provide evidence that modulation of NMDAR contributes to neuroprotection observed in hAGS.
    • Pharmacology Of A Novel Class Of Allosteric Modulators For The Alpha4 Beta2 Sub-Type Of Neuronal Nicotinic Acetylcholine Receptors

      Pandya, Anshul (2009)
      Neuronal nicotinic acetylcholine receptors (nAChRs) are members of a large family of ligand gated ion channels that mediate inhibitory and excitatory neural transmission in the central nervous system (CNS). The nicotinic subfamily has been implicated in a range of neurological disorders including autism, Alzheimer's disease and nicotine addiction; diseases that are currently both challenging and costly to treat. Despite the apparent importance of nAChRs in these disorders, only a limited number of drugs are currently available for altering nicotinic signalling in the CNS. No drug therapies are currently available that specifically target autism and only a limited number of drugs are available for the treatment of Alzheimer's disease. This thesis presents a novel class of nAChR ligands based on the natural product desformylflustrabromine (dFBr). Desformylflustrabromine (dFBr), a metabolite of the marine bryozoan Flustra Foliacea, was previously identified as an allosteric modulator of the alpha4beta2 subtype of nAChRs. In collaboration with Dr. Richard Glennon at the Virginia Commonwealth University, College of Pharmacy, we developed a synthetic dFBr and evaluated its interaction with two of the most common subtypes of nAChRS, alpha7 and alpha4beta2 (Chapter 2). We confirmed that dFBr is the active component of Flustra Foliacea and identified an additional inhibitory action that becomes evident as dFBr concentrations are increased beyond 10muM. This inhibition was not previously reported. Synthetic dFBr appears significantly more potent at potentiation of alpha4beta2 receptors then reported for the natural extract and shows only inhibitory action on alpha7 receptors. Multiple analogues of dFBr were designed and synthesized to determine the structure activity relation (SAR) for dFBr's action on alpha4beta2 receptors (Chapter 3). We identified three analogues capable of potentiating responses of acetylcholine. The majority of compounds inhibited responses on both alpha4beta2 and alpha7 receptors. The data presented here provide important information for determining a preliminary pharmacophore for dFBr and provide direction for the design of additional analogues on the path to development of more potent and potentially therapeutically useful analogues. To better understand the relationship of dFBr to other nAChR modulators, we also compared the action of dFBr to that of physostigmine, zinc and 17 beta-estradiol (Chapter 4). These compounds are thought to act at three different binding sites on nAChRs. All three compounds increase responses of alpha4beta2 receptors to acetylcholine. Our data show that dFBr is distinct from the clinically used modulator physostigmine but suggests similarities in mechanism with zinc and 17-beta-estradiol. These data provide important information regarding the mechanism of dFBr modulation and provide direction for future site directed mutagenesis studies that will identify the dFBr binding site. Identification of the binding site is critical for the development of receptor models that will facilitate computer assisted drug design.
    • Primary afferent projections in a diver, the muskrat

      Delisa, Susan Manette; Ebbesson, S. O. E. (1989)
      In a preliminary search for primary afferent connections involved in the diving response, cutaneous afferents from the nose were traced in muskrats and compared with those in rats, and with projections from the soft palate, posterior pharynx and larynx. Horseradish peroxidase (HRP) was injected into the skin or mucosa, under anesthesia. After 48 h survival, the deeply anesthetized animal was transcardially perfused and the brain was frozen and sectioned transversely in a cryostat. The sections were reacted for HRP according to standard techniques, using tetramethylbenzidine; alternate sections were Nissl stained. HRP-labeled structures were mapped using darkfield photomicrographs and camera lucida drawings. Cutaneous afferents from the nose in the muskrat project densely to layers I-II of the ventral and dorsolateral parts of the caudal subnucleus of the spinal trigeminal nucleus (Sp5C) and sparsely to layers V-VI of Sp5C, sparsely to the ventromedial part of the interpolar subnucleus of the spinal trigeminal nucleus (Sp5I), moderately to the oral subnucleus of the spinal trigeminal nucleus (Sp5O)--particularly the dorsomedial part, possibly overlapping with the nucleus of the solitary tract, and with processes of labeled cells of other lateral facial nucleus extending into ventromedial Sp5O,--moderately to the principal trigeminal nucleus (Pr5); and to the paratrigeminal nucleus (Pa5). Projections in the rat were the same, except that little or no labeling of layers V-VI of Sp5C, dorsomedial Sp5O, or Pa5 was present. Projections from the soft palate to layers I-II of rostral Sp5C, Sp5O, Sp5I, and Pr5 were similar to those from the nose in the muskrat. Heavy projections from the soft palate, and less dense projections from the posterior pharynx and larynx, to Pa5 also were found. Those regions receiving dense projections from the nose, overlapping projections from the various sites, and more highly developed projections from the nose in the muskrat than in the rat, are of particular interest for further investigation of the neural substrate underlying the diving response. The projections traced from the nose correspond particularly with nociceptive and thermoreceptive projections, which suggests that thermoafferent function may be involved in the elicitation of the diving response.
    • Raphe Chemosensory Amplifier: A Carbon Dioxide-Sensitive Brain Network

      Iceman, Kimberly Erin; Harris, Michael; Edmonds, Brian; O'Brien, Kristin; Taylor, Barbara (2013)
      Central chemosensitivity is the vital ability of the brain to detect and respond to changes in tissue CO<sub>2 /pH. Changing CO<sub> 2 /pH causes brainstem central chemoreceptors to modulate ventilation, but the cellular basis of this chemosensitivity is not well understood. When studied in vitro, neurons within the rat medullary raphe are intrinsically sensitive to changes in pH. Serotonin/ substance P (5-HT) synthesizing raphe neurons are stimulated, and gamma-aminobutyric acid (GABA) synthesizing neurons are inhibited by CO<sub>2 /acidosis. The contribution of these neurons to central chemosensitivity in vivo, however, is controversial. Also unknown is whether there are other types of chemosensitive cells in the raphe. Here I tested the hypothesis that rat medullary raphe neurons are responsive to CO<sub>2 in a relatively intact preparation, that raphe 5-I-IT neurons are CO<sub> 2-stimulated, and that CO<sub>2inhibited raphe neurons are GABAergic. I used extracellular recording of individual raphe neurons in the unanesthetized juvenile rat in situ perfused decerebrate brainstem preparation to assess chemosensitivity of raphe neurons. I subsequently used juxtacellular labeling, and immunohistochemistry for markers of 5-HT and GABA synthesis to identify neurotransmitter phenotype of individually recorded cells. Results demonstrate that the medullary raphe is heterogeneous and clearly contains at least three distinct classes of CO<sub>2-sensitive neurons: modestly CO<sub>2-stimulated 5-I-IT neurons, CO<sub>2-inhibited GABAergic neurons that possess this sensitivity independent of major fast synaptic inputs, and robustly CO<sub>2-stimulated non-5-HT neurons. The CO<sub>2-stimulated non-5-HT neurons constitute a previously unrecognized class of chemosensitive raphe neuron that express receptors for substance P and are dependent on network inputs from 5-HT and GABA raphe cells for chemoresponsiveness. Based on my identification of these three distinct types of chemosensitive raphe cells, I propose a new raphe chemosensory amplifier (RCA) network model to explain raphe contributions to central chemosensitivity. In this model the three cell types interact as a CO<sub> 2-sensing network that potentially amplifies the chemosensory responses to CO<sub>2 and may limit toxic over excitation of 5-HT neurons. In this way, the RCA network could integrate inputs and respond to changes in tissue CO<sub>2 with an appropriate modulation of sympathetic and/or parasympathetic outflow, consistent with the broad role that brainstem raphe nuclei play in maintaining homeostasis.
    • Reconstruction of the damaged central nervous system and spine

      Helm, Gregory Anthony (1996)
      The field of neuronal transplantation has received a great deal of interest since the 1970's and is currently considered a possible treatment option for both neurodegenerative diseases and spinal cord injury. In this dissertation, fetal neostriatal transplants grafted into the lesioned striatum were studied in both the rat and rhesus monkey. Golgi-impregnation and immunohistochemical techniques were extended to the light and electron microscopic levels to determine the detailed anatomy of the developing striatal implants. Choline acetyltransferase immunoreactive and substance P-like immunoreactive neurons within the rat striatal transplants were morphologically and ultrastructurally similar to normal striatal neurons. When the striatal grafting studies were extended into the rhesus monkey, normal neuronal maturation was demonstrated three months postoperative, both at the light and electron microscopic levels, using various neuroanatomical techniques. From these studies it can be concluded that fetal striatal grafts may be a useful treatment option for Huntington's disease, although numerous difficulties including neuronal degeneration and transplant rejection need to be addressed before this approach is applied in the clinical setting. In a second group of experiments, various approaches to improve autologous bone spinal fusions were studied. Specifically, the utilization of demineralized bone matrix, Type I collagen gel, and recombinant human bone morphogenetic proteins were evaluated for their effects on autologous bone spinal fusions in canines. The study demonstrated that recombinant human bone morphogenetic protein has a strong effect on the amount of bone deposition at the fusion site and, in addition, increases the number of vertebral levels which solidly fuse. The Type I collagen gel appeared to improve the interface between the autologous bone grafts and the host bone, while the demineralized bone matrix had a strong negative effect on the autologous bone graft fusions. Spinal fusion operations in the future will be much more successful if these various methods to improve spinal arthrodesis are utilized to their full potential. It is now clear that reconstruction of the central nervous system and its bony coverings is a real possibility in the very near future, although extensive clinical studies need to be performed before they are widely used in the neurosurgery community.
    • Serotonergic And Hypocretinergic Systems Modulate Ventilation And Hypercapnic Ventilatory Responses

      Corcoran, Andrea E. (2009)
      Serotonergic (5-HT) cells of the medullary raphe are putative central chemoreceptors, one of multiple chemoreceptive sites in the brainstem that interact to produce the respiratory chemoreflex. This role is debated, and the importance of 5-HT neurons as chemoreceptors in relatively intact systems is unclear. The main focus of this dissertation is to provide further physiological evidence for the involvement and modulation of 5-HT neurons in CO2 chemosensitivity. This is of interest as a large number of Sudden Infant Death Syndrome (SIDS) cases report dysfunction in the 5-HT system, and CO2 may be an exogenous stressor leading to SIDS when in combination with this underlying vulnerability. Also, since SIDS occurs primarily during sleep, I also focus on the potential functional interaction between the 5-HT and hypocretinergic systems, as hypocretins play a role in arousal and also potentially in chemosensitivity. I confirm the hypothesis that the serotonergic and hypocretinergic systems modulate ventilation and hypercapnic ventilatory responses. Using the in situ preparation derived from juvenile rats and the in vitro medullary slice preparation from mice, I verify that 5-HT neurons are critical in generating a response to CO2, primarily via facilitation of the respiratory rhythm through 5-HT2 receptors. I also find evidence to support the hypothesis that hypocretins play a significant role in the neuroventilatory response to CO2 through activation of hypocretin receptors type 1. By comparing results from rhythmic medullary slice preparations from wildtype (normal 5-HT function) and Lmx1bf/f/p (lack central 5-HT neurons) neonatal mice, I attempt to identify whether changes in hypoglossal nerve output in response to acidosis are affected by hypocretin receptors, and whether this is dependent on the presence of 5-HT neurons. Frequency results from such studies are inconclusive; however, hypocretins do appear to mediate the burst duration response via serotonergic mechanisms. I also find that hypocretins facilitate baseline neural ventilatory output in part through 5-HT neurons. Thus, both the 5-HT and hypocretinergic systems are involved in modulating ventilation and hypercapnic ventilatory responses.
    • Stabilization of secondary structure of synthetic Alzheimer beta-amyloid protein analogs in the presence of aluminum (III) ions

      Vyas, Sandip Bipin (1995)
      The gradual accretion of fibrillar protein deposits in a tissue or organ is a hallmark of all amyloidogenic diseases. These deposits accumulate as senile plaques and cerebrovascular deposits in the brain and are characteristics of Alzheimer's disease. A majority of the brain amyloid deposits consist of a 40 amino acid protein, the Alzheimer $\beta$-protein, A$\beta$P, which in a soluble form is ubiquitous in biological tissues. In order to provide a more detailed understanding of the structural transformations of soluble A$\beta$P, sequence analogs derived from $\beta$1-40, and having His $\to$ Arg, and scL-Asp- $\to$ scD-Asp substitutions were synthesized. The kinetic variations of $\beta$1-40 and $\beta$6-25 were studied using amide circular dichroism spectroscopy by monitoring ellipticity changes of the peptide backbone. In both peptides, the gradual loss of secondary structure was a multiphasic process which was also dependent on concentration. The circular dichroism titrations with metal ions revealed the involvement of at least two ions in the conformational transitions of $\beta$1-40 and $\beta$6-25. The association of Al(III) with scL-Asp $\to$ scD-Asp derived analogs caused surprising conformational changes in $\beta$6-25, which were distinct from $\beta$1-40. Microheterogeneous products corresponding to Al(III)-bound peptide species were resolvable on the reversed-phase surface. The association of aluminum was investigated by low field $\sp{27}$Al nuclear magnetic resonance spectroscopy. The signal corresponding to Al(III)-bound peptide species revealed that at least four Al(III) ions were bound to $\beta$1-40 and $\beta$6-25 between pH 5 and 6. Moreover, $\beta$1-40 effectively competed with EDTA to bind with Al(III). This study also describes a strategy which resolved the band broadening in reversed-phase high-performance liquid chromatography of $\beta$1-40 and derived analogs. Chromatographic parameters related to interactive contact area of $\beta$1-40 and derived analogs were determined on reversed-phase matrix. The peptides were bound to the reversed-phase surface in their monomeric form. Slow partition kinetics appear to contribute to significant band broadening, which suggests a secondary retention effect--indicating a conformational change due to unfolding on the stationary phase surface.
    • Structure-Function Relationship Of The Developing Acetylcholine Receptor In Amphibians

      Sullivan, Michael Patrick; Duffy, Larry (2001)
      The nicotinic acetylcholine receptor is responsible for the transfer of signals from the peripheral nervous system to skeletal muscle, resulting in movement. Despite the importance of the acetylcholine receptor, many questions remain unanswered about the relationship between the structure and function of the receptor. The purpose of our research was to explain certain features of the relationship between the amino acid sequence and the function of the amphibian nicotinic acetylcholine receptor. We focused on describing the structural elements underlying the physiologic changes that occur during development and re-innervation of damaged mature muscle. We used molecular biological techniques to alter the amino acid sequence of the receptor and then studied the effects of these alterations using the electrophysiological technique of single channel recording. Our research resulted in the discovery of critical residues involved in two important characteristics of receptor function, the conductance and open time of the ion channel. These results offer new molecular insights into the classic observation that synaptic currents become briefer in duration during the course of muscle development in vertebrates.
    • Structure-Function Studies Of The Serotonin Type -3 Receptor Ligand -Binding Domain

      Joshi, Prasad Ramesh; Schulte, M. K. (2005)
      The serotonin type-3 receptor (5-HT3R) is widely distributed in peripheral and central nervous systems. This pentameric protein is a member of the Cys-loop superfamily of ligand gated ion channels and plays a role in mediating physiological processes in nervous, cardiovascular, and digestive systems. The ligand-binding domain of this receptor is extracellularly located and is composed of multiple putative loop structures. Based on structural and sequence homology with other members of the superfamily, it has been proposed that at least six such loops (loops A to F) contribute to the ligand-binding domain. Binding of agonist initiates a conformational change which is transduced to the channel, leading to channel opening (gating). The aim of this study was to elucidate the contribution of residues in loops B and E to the mechanism of channel gating in the 5-HT3R. To this end, the three critical tyrosine residues in the loop E region were characterized employing site-directed mutagenesis, electrophysiological studies as well as radio-ligand binding assays involving two structural classes of 5-HT3R agonists. In addition, structure/function analysis of the loop B region was carried out alanine-scanning mutagenesis. Experimental data were correlated with molecular modeling studies. These studies show that the hydroxytryptamine and phenylbiguanide class of compounds utilize different mechanisms of ligand binding and gating in the 5-HT3R. Studies involving the loop B reveal that this region plays a critical role in ligand binding and channel gating. Data obtained from comparison of ground state and agonist-bound models of the 5-HT 3R was correlated with biochemical data. Taken together, these data suggest that agonist interaction with loop B region probably initiates a conformational wave that results in intra- and inter- subunit hydrogen bonding interactions. Our data suggest that these interactions play a critical role in agonist-induced channel opening.