Stroke or cerebral vascular accident (CVA) is the 4th leading cause of mortality and the principle cause of long-term disability in the United States. Unfortunately, current reperfusion-based treatments (e.g. thrombolysis, tPA) cannot be administered to the majority of patients presenting with ischemic stroke. Accordingly, new treatments for ischemic stroke are desperately needed. Reactive astrocytes perform key roles in tissue repair and remodeling following stroke such as preservation and repair of the blood-brain barrier, modulation of immune cell invasion, glutamate uptake and neuroprotection, and glial scar formation. The proliferative subpopulation of reactive astrocytes found immediately adjacent to the infarct core after stroke (known as the peri-infarct area) is particularly important for protecting the brain parenchyma from ischemic damage and inflammation. Defining the signaling network that controls reactive astrocyte formation and function has potential to provide new treatment strategies for patients ineligible for reperfusion therapy. Notch1 signaling is required for the proliferation of peri-infarct reactive astrocytes after stroke. To identify downstream targets and potential functional effectors of Notch1 signaling in reactive astrocytes, we developed an ex vivo forward signaling screen. To generate large quantities of adult reactive astrocytes, we employed adult Reactive astrocyte-derived Neural Stem Cells (Rad-NSCs) isolated from the peri-infarct area of mice after stroke. Astrocytes re-differentiated from Rad-NSCs (AstroRad-NSC) were then exposed to immobilized Jagged-1, a Notch1 ligand. In response to Jagged-1, many genes involved in reactive astrocyte-mediated tissue protection, metabolic regulation, angiogenesis and glial scar formation were up-regulated. Of special interest, several genes for proteins that regulate with glutamate uptake and metabolism were increased by Jagged-1/Notch signaling, including the glial-specific GLutamate-ASpartate Transporter (GLAST). With loss-of-function experiments, we determined that deletion of Notch1 decreased GLAST transcript and protein levels in cultured AstroRad-NSC. Furthermore, we isolated reactive astrocytes directly from cerebral cortex after stroke and confirmed the effects of Notch1 on GLAST in vivo. Our results suggest that treatments designed to stimulate Notch1 signaling after stroke may promote glutamate uptake, thereby decreasing excitotoxicity and neuronal cell death. Binding of Endothelin peptides to the type B Endothelin receptor (ETBR) has been shown to alter cell proliferation. Investigating a possible relationship between Jagged-1/Notch1 and Endothelin signaling in reactive astrocytes, we determined that Notch1 signaling regulated ETBR indirectly, by activating STAT3, an unidentified transcriptional activator of ETBR. Using inducible transgenic astrocyte-specific conditional knockout (cKO) mice (GFAP-ETBR-cKO), we found that specific deletion of ETBR in reactive astrocytes phenocopied the defect in reactive astrocyte proliferation observed in our previous work with GFAP-Notch1-cKO mice. Notably, the Notch1-STAT3-ETBR axis we identified is likely to control reactive astrocyte proliferation in most, if not all, forms of CNS injury. The experimental results presented in this doctoral dissertation provide novel insight into signaling mechanisms that may someday be exploited to improve care for patients with stroke and other forms of CNS injury or disease.

In the current study, we investigated the association between relational aggression and measures of delinquency and overt aggression in a sample of detained adolescent girls. We also tested the validity of the distinction between reactive and proactive subtypes of relational aggression by testing their independent associations with important emotional, behavioral, personality, social, and cognitive variables that have been studied in past research and found to be important for distinguishing between reactive and proactive overt aggression. Our sample consisted of 58 predominantly African-American (78%) adolescent girls recruited from three juvenile detention centers in the southeastern United States. Participants ranged in age from 12 to 18 (Mn = 14.98; SD = 1.30). Relational aggression was measured using both self-report and observation, while overt aggression, delinquency, and social-psychological variables were measured using self-report only. As predicted, both self-reported and observed relational aggression were associated with higher rates of self-reported delinquency. Self-reported relational aggression was also associated with self-reported overt aggression, while observed relational aggression was not. On a self-report rating scale, we found evidence for four subscales that were moderately correlated and had good internal consistency. These subscales corresponded to the four aggressive subtypes (i.e., reactive overt, reactive relational, proactive overt, proactive relational). Further, we found evidence for divergence between reactive and proactive relational aggression on emotional dysregulation, CU traits, and positive outcome expectations for aggression, supporting the hypothesis that these are important subtypes that could involve distinct developmental processes, similar to reactive and proactive subtypes of overt aggression. Finally, this study found that relational aggression accounted for unique variance in callous and unemotional (CU) traits among detained girls, even after controlling for levels of overt aggression. The current findings highlight the importance of assessing relational aggression in detained girls and could have implications for designing more successful interventions for girls in the juvenile justice system.

The purpose of the current study is to examine the association between self-esteem and the forms and functions of aggression. Research supports the existence of four aggressive subtypes (i.e., reactive overt, reactive relational, proactive overt, and proactive relational), and past research has found associations between aggression and self-esteem. However, past studies have not examined the relationships between all four subtypes of aggression and self-esteem together. 141 adolescents were recruited from the community with a mean age of 13.55. The sampled group was composed of 51% females and 52% Caucasians. Participants completed self-report questionnaires on self-esteem and aggression. The results provide support for an association between proactive aggression and self-esteem. Additionally, overt aggression was more associated with self-esteem than relational aggression. These findings will help fill the gap in literature on the forms and functions of aggression and will further define the relationship between aggression and self-esteem.

Previous research has demonstrated an association between violence exposure and aggression; however, research exploring the association between violence exposure and the forms and functions of aggression is scarce. The aim of this study was to explore the associations between trauma exposure with both reactive and proactive functions of aggression by examining two potential mediators (e.g., psychopathic traits and emotional dysregulation). Participants included 132 male juvenile offenders mandated to treatment in a residential facility (M = 16.78 years old; SD = 1.25). Results indicate emotional dysregulation partially mediated the association between trauma exposure and reactive aggression while controlling for proactive aggression. However, no evidence was found to support the hypothesis that psychopathic traits mediated the association between trauma exposure and proactive aggression. Results suggest trauma exposure is important in the development of reactive aggression. Thus, treatment approaches for aggressive youth should address issues of trauma exposure.

Philosophiae Doctor - PhD / Magnesium hydride has long been regarded as a promising candidate for lightweight hydrogen storage applications, owing to reasonably high theoretical capacity (7.6 wt. %). It is burdened by slow absorption/desorption kinetics which has been the target for improvement of many research groups over the years. Nanostructured MgH2 prepared by high energy reactive ball milling (HRBM) of Mg under hydrogen atmosphere with the addition of V or Ti results in modified MgH2 that demonstrates superior hydrogenation/dehydrogenation kinetics without a crippling compromise in storage capacity. Mg – FeV nanocomposites prepared via ball milling of Mg and FeV raw materials demonstrated up to 96.4% of the theoretical storage capacity and comparable kinetics to Mg - V prepared via the same method using pure refined V (which is far costlier than FeV). In both cases, the hydrogenation/dehydrogenation kinetics was much improved than pure Mg alone, as evidenced by faster hydrogenation times. In terms of cyclic stability, Mg – 10FeV demonstrated improvement over pure Mg with final absorption and desorption capacities of 4.93 ± 0.02 wt. % and 4.82 ± 0.02 wt. % respectively over 30 cycles. When compared against Mg – V, Mg – FeV showed slightly inferior improvements, attributed to incomplete hydrogenation of V in the presence of Fe. However, they share similar crystalline BCC, BCT – V2H and FCC - VH phases with the size of less than 10 nm and demonstrated the same behaviour at high temperatures; at temperatures approaching 400 °C, particle sintering became an issue for both nanocomposites resulting in a drop in absorption capacity even in the first cycle. The further inclusion of carbonaceous species showed several effects, one of which was an improvement in hydrogen uptake speed as well as kinetics for the addition of 5 wt. % activated carbon. For the sample with 5 wt. % graphite, the appearance of an initial incubation period of up to 60 minutes was noted, presumably corresponding to the duration of time when the carbon was sheared and crushed before hydrogenation commences.

A thesis submitted to the Faculty of Health Sciences, University of the Witwatersrand In fulfilment of the requirements for the degree of Doctor of Philosophy Johannesburg, 2003 / Dietary iron (Fe) overload, originally referred to as Bantu Visceral Siderosis, is an Reloading condition that is still prevalent in rural populations of sub-Saharan Africa. The better known Fe loading disease, hereditary haemochromatosis (HFI) is frequently complicated by hepatocellular carcinoma (HCC) and, in rare instances this occurs in the absence of cirrhosis. The latter, together with recent evidence that dietary Fe overload in the Black African carries an increased risk for HCC, suggests that excessive hepatic iron may itself be carcinogenic. The aim of the study was to determine if Fe alone could induce HCC in experimental rat models and, if so, to investigate possible mechanisms of hepatocarcinogenesis. 360 Wistar albino rats (Rattus norvegicus) were divided into 6 groups. The first group, the control animals, was designated C group. Groups 2-6 were Fe-fed alone or in combination with other chemicals: group 2 Fe alone (Fe group), group 3 (Fe + V) vitamins A & E supplementation [50 mg all trans-retinol (vitamin A) and 500 mg a-tocopherol (vitamin E) per kg diet], group 4 (Fe - V) received a diet totally devoid of vitamins A & E, group 5 (Fe + ASA) received 20 mg aspirin (ASA) per day, group 6 (Fe + Cu) received 300 mg/kg diet of copper sulphate (CuS04) supplementation for 12 months followed by 3% copper hydroxide carbonate [CuC03»Cu(0H)2] / IT2018

A thesis submitted to the Faculty of Health Sciences, University of the Witwatersrand In fulfilment of the requirements for the degree of Doctor of Philosophy Johannesburg, 2003 / Dietary iron (Fe) overload, originally referred to as Bantu Visceral Siderosis, is an Fe- loading condition that is still prevalent in rural populations of sub-Saharan Africa. The better known Fe loading disease, hereditary haemochromatosis (HH) is frequently complicated by hepatocellular carcinoma (HCC) and, in rare instances this occurs in the absence of cirrhosis. The latter, together with recent evidence that dietary Fe overload in the Black African carries an increased risk for HCC, suggests that excessive hepatic iron may itself be carcinogenic. The aim of the study was to determine if Fe alone could induce HCC in experimental rat models and, if so, to investigate possible mechanisms of hepatocarcinogenesis. 360 Wistar albino rats (Rattus norvegicus) were divided into 6 groups. The first group, the control animals, was designated C group. Groups 2 - 6 were Fe-fed alone or in combination with other chemicals: group 2 Fe alone (Fe group), group 3 (Fe + V) vitamins A & E supplementation [50 mg all trans-retinol (vitamin A) and 500 mg a-tocopherol (vitamin E) per kg diet], group 4 (Fe - V) received a diet totally devoid of vitamins A & E, group 5 (Fe + ASA) received 20 mg aspirin (ASA) per day, group 6 (Fe + Cu) received 300 mg/kg diet of copper sulphate (CuS04) supplementation for 12 months / IT2018

As cores sempre exerceram fascínio sobre a humanidade e, por toda a história, os compostos coloridos sempre foram considerados ferramentas atrativas nas atividades comerciais. Os corantes sintéticos são amplamente utilizados na indústria têxtil, nas impressões de papel e fotografia, nas indústrias farmacêuticas, alimentícias e de cosméticos. Estes compostos são considerados importantes contaminantes ambientais, representando sérios riscos à flora, fauna e ao ser humano. Apesar da grande quantidade de corantes disponíveis, os estudos sobre a toxicidade desses compostos são escassos e pouco se sabe a respeito dos efeitos genotóxicos destas substâncias. Dentro deste contexto, o presente trabalho avaliou o potencial genotóxico dos corantes Sudan III, Vat Green 3, Reactive Orange 16 e Reactive Black 5, utilizando o Ensaio de Micronúcleos em células HepG2. Os corantes Sudan III e Reactive Orange 16 não induziram aumento, estatisticamente significativo, no número total de micronúcleos em relação aos controles, indicando assim que estes corantes não são capazes de induzir mutações cromossômicas no tipo celular e condições testadas. Entretanto, os corantes Vat Green 3 e Reactive Black 5 induziram mutagenicidade, concentrações de 10,0 e 25,0 ?g/mL, e 0,1; 0,25; 0,5 e 1,0 ?g/mL, respectivamente, demonstrada por um efeito concentraçãodependente, no qual há um aumento de MNs até a concentração de 25,0 ?g/mL para o Vat Green 3 e 0,5 ?g/mL para o Reactive Black 5 com p<0,05. Não foram observadas diferenças significativas entre os IDNs calculados para cada tratamento e controle dos corantes testados, indicando que esses corantes não interferem na proliferação celular das HepG2. Dessa forma, conclui-se que dos quatro compostos analisados, os corantes têxteis Vat Green 3 e Reactive Black 5 são capazes de induzir mutações cromossômicas em células HepG2 e, o potencial mutagênico do Reactive Black 5 é maior que o do Vat Green 3 no sistema celular avaliado, uma vez que foi capaz de induzir mutações, em concentrações menores. Os resultados obtidos neste trabalho permitem concluir que cada um desses importantes contaminantes ambientais deve ser avaliado individualmente a fim de proteger o meio ambiente, garantindo assim a proteção da saúde humana. / The colors have always caused fascination in mankind. Throughout history, colored compounds have always been considered attractive tools in industrial activities. The synthetic dyes are widely used in textile industry, paper and photography printing, in pharmaceutical, food, and cosmetic industries. These compounds are considered important environmental contaminants, and they can cause serious risks to wildlife and humans. Despite the large number of dyes available, studies on the toxicity of these compounds are scarce and little is known about the genotoxic effects of these substances. This study evaluated the genotoxic potential of the dyes Sudan III, Vat Green 3, Reactive Orange 16 and Reactive Black 5 using the micronucleus assay in HepG2 cells. The dyes Sudan III and, Reactive Orange 16, do not induce an increase statistically significant, in the total number of micronuclei when compared to controls. This result shows that these dyes are not able to induce chromosomal mutations in the cell type under the conditions tested. However, the dyes Vat Green 3 and Reactive Black 5 induced mutagenicity, following a dose-response effect, in which there is an increase of micronuclei until the concentration of 25.0 ?g/mL for Vat Green 3 and 0.5 ?g/mL for Reactive Black 5, with p <0.05. There were no significant differences between the NDI calculated for each treatment and control of the dyes studied, indicating that these dyes do not interfere in HepG2 cell proliferation. Thus, the textile dyes Vat Green 3 and Reactive Black 5 are able to induce chromosomal mutations in HepG2 cells, and the dye Reactive Black 5 is more mutagenic than the dye Vat Green 3, since it induced mutations in cellular system tested at lower concentrations. The results of this study indicate that each one of these important environmental contaminants should be assessed individually in order to protect the environment, thus ensuring the protection of human health.

A produção de mantas de tecido não tecido (TNT) por processo de extrusão a partir do poli(tereftalato de etileno) (PET) reciclado é uma forma interessante de reciclagem de polímeros adotada pela indústria que consegue conciliar viabilidade econômica com benefícios ambientais. Entretanto, durante a etapa de extrusão, muito material é perdido devido a entupimentos do equipamento ou outros motivos que acarretam na geração de uma quantidade considerável de rejeitos que não podem ser reaproveitados no sistema, devido à depreciação de propriedades ocorridas no material durante o processamento, levando ao descarte deste material geralmente em aterros sanitários. Neste trabalho foi feito um estudo sobre a reciclagem de rejeitos de PET das linhas de produção de mantas de tecido não tecido (TNT), adotando aditivos do tipo extensores de cadeia, para recuperar as propriedades que haviam sofrido grande depreciação. A incorporação de extensores de cadeia do tipo anidridos, isocianatos e fosforados, por meio de extrusão reativa, proporcionou melhorias consideráveis nas propriedades químicas, mecânicas e reológicas do rejeito de PET como aumento de massa molar, aumento de iscosidade no fundido e resistência à tração, facilitando o processamento e favorecendo a utilização do rejeito em novas etapas de reciclagem mecânica. Para as indústrias, a possibilidade de converter custos relacionados às operações de descarte de rejeitos em lucros com a agregação de valor a estes rejeitos poliméricos é extremamente interessante. Da mesma forma, a diminuição do volume de materiais poliméricos depositados no meio ambiente significa menos poluição e menos contaminação a diversos ecossistemas, apoiando os esforços que estão sendo feitos para a preservação e redução de poluentes na natureza. / The production of nonwoven fabrics (NWF) by extrusion process from recycled poly(ethylene terephthalate) (PET) is an interesting way for polymer recycling used by industry which to allow conciliate economic viability with environmental benefits. However, during extrusion step, a fraction of material is lost due to equipment clogging or others factors, leading to production of considerable amount of wastes which can not reinserted in system, due to the depreciation of material properties that occurs during thermal-mechanical processing. These rejects are generally deposited in land wastes. In this work was carried out a study about recycling of PET wastes from NWF production lines, using additives of chain extender kind to recoup properties that had been highly depreciated. The incorporation of chain extenders of kind anhydride, isocyanate and phosphorous compounds by reactive extrusion improved considerably some chemical, mechanical and rheological properties of PET waste such as increase in molecular weight, melt viscosity and strain strength, easing the thermal-mechanical processing and making possible the use of PET waste in news steps of mechanical recycling. The possibility to convert expenditures with wastes discarding operations into profits due to the values aggregation on these polymeric wastes is very interesting for the industries. Then, the decrease of amount of polymeric materials deposited in natural environment signifies less contamination to several ecosystems, supporting the works that have been realized to decrease pollutants and to preserve the nature.

Thesis advisor: Clare O'Connor / Within cells, reactive oxygen species (ROS) are synthesized naturally and in response to environmental stimuli. However, ROS have deleterious effects on a wide range of cellular molecules. Oxidative stress, caused by the ROS generated by the partial reduction of oxygen, is a major cause of cell damage linked to the initiation and progression of numerous diseases. Thioredoxin peroxidase (Tpx1) plays important roles in cellular defense against ROS. Although homologous genes and their functions have been identified in other eukaryotes, the level of activity as well as the necessity of this protective enzyme in S. pombe exposed to oxidative stress has yet to be fully elucidated. To explore the role of the Tpx1 protein in oxidative stress resistance, novel strains were constructed in which the tpx1 gene was overexpressed. The polymerase chain reaction was used to amplify txp1, and the amplified sequence was cloned into the yeast overexpression plasmid, pNMT41, which allows overexpression under the control of the powerful promoter. DNA sequencing was used to determine that the sequences had been properly inserted into the vector. The plasmids were transformed into two leu- yeast strains: FWP6 and TP108-3C. Production of the Tpx1 protein was ensured using Western Blot techniques. Experimentation to test the responses of the tpx1 strain to oxidative stress will employ a variety of reactive oxygen generators, including hydrogen n peroxide, menadione, tert-butyl hydroperoxide, and paraquat. The results generally supported the proposed role of Tpx1 to confer additional resistance against the oxidative stress. In a complementary line of investigation, knockout strains are being constructed to reduce the levels of the Tpx1 in S. pombe. Gene deletion cassettes were constructed for tpx1. Currently, the strains are being analyzed for the successful replacement of the endogenous tpx1 gene by homologous recombination. If the absence of the protein results in decreased cell viability, the role of Tpx1 indicated by the overexpression experiments could be supported. / Thesis (BS) — Boston College, 2006. / Submitted to: Boston College. College of Arts and Sciences. / Discipline: Biology. / Discipline: College Honors Program.