This thesis focuses on how physical and biological factors influence the outcome of exposures to γ/X-rays. That the dose rate changes during real life exposure scenarios is well-known, but radiobiological data from exposures performed at increasing or decreasing dose rates is lacking. In paper I, it was found that an exposure where the dose rate decreases exponentially induces significantly higher levels of micronuclei in TK6 cells than exposures at an increasing or constant dose rate. Paper II describes the construction and validation of novel exposure equipment used to further study this “decreasing dose rate effect”, which is described in paper III. In paper I we also observed a radioprotective effect when cells were exposed on ice. This “temperature effect” (TE) has been known for decades but it is still not fully understood how hypothermia acts in a radioprotective manner. This was investigated in paper IV, where a multiparametric approach was used to investigate the underlying mechanisms. In paper V the aim was to investigate the role of biomarkers and clinical parameters as possible risk factors for late adverse effects to radiotherapy (RT). This was studied in a rare cohort of head-and-neck cancer patients that developed mandibular osteoradionecrosis (ORN) as a severe late adverse effect of RT. Biomarker measurements and clinical factors were then subjected to multivariate analysis in order to identify ORN risk factors. The results suggest that the patient’s oxidative stress response is an important factor in ORN pathogenesis, and support the current view that patient-related factors constitute the largest source of variation seen in the frequency of late adverse effects to RT. In summary, this thesis provides new and important insights into the roles of biological and physical factors in determining the consequences of γ/X-ray exposures. / <p>At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Submitted. Paper 5: Manuscript.</p>

Organic nitrates, such as glyceryl trinitrate (GTN), have been used clinically for more than a century. However optimal nitrate therapy is hindered by the development of tolerance, which is associated with a desensitized response to GTN, oxidative stress, and the inactivation of aldehyde dehydrogenase 2 (ALDH2). This thesis evaluated the ALDH2 inactivation hypothesis of GTN tolerance and investigated the role of oxidative stress in GTN tolerance mediated by the lipid peroxidation product, 4-hydroxynonenal (HNE). Evidence for a direct role of ALDH2 in nitrate action was sought using a stably transfected cell line that overexpressed ALDH2, or siRNA to deplete endogenous ALDH2. Neither manipulation altered GTN-induced cGMP formation, indicating that ALDH2 does not mediate GTN bioactivation and tolerance. In a second study using an in vivo GTN tolerance model and a cell culture model of nitrate action, a marked increase in HNE adduct formation was detected in GTN-tolerant tissues, and treatment with HNE reduced the cGMP and vasodilator responses to GTN, thus mimicking GTN-tolerance. Together, the results suggest a primary role for HNE in the development of GTN tolerance, and provide the framework for a unified hypothesis that accommodates the previous findings of sulfhydryl depletion, ALDH2 inactivation and oxidative stress that are associated with nitrate tolerance. Studies have implicated oxidative stress and increased HNE formation in the pathogenesis of Alzheimer’s disease (AD). It was hypothesized that the gene deletion of ALDH2 would result in increased HNE-adduct formation leading to impaired cognitive function, and AD-like pathological changes. We observed a marked increase in HNE-adduct formation in Aldh2-/- mouse hippocampi as well as hyperphosphorylated tau, activated caspases, age-related changes in hippocampal amyloid βeta1-42 (Aβ1-42), post-synaptic density protein 95 (PSD95) and phosphorylated cyclic adenosine monophosphate response element binding protein (pCREB) expression, endothelial dysfunction and other vascular pathologies. These data provide further evidence for the importance of HNE and oxidative stress in AD pathogenesis, and establish Aldh2-/- mice as a new, oxidative stress-based animal model of age-related cognitive impairment and AD. / Thesis (Ph.D, Pharmacology & Toxicology) -- Queen's University, 2013-05-31 11:10:58.145

Poly Brominated Diphenyl Ethers (PBDEs) are known flame retardants with highly persistent and lipophilic in nature. The continued usage of PBDE in various products amplifies the human burden of PBDEs. It is therefore, important to study the potential toxicological and/or biological effects of PBDE exposure in human. In this study we investigated the mode of action of PBDE induced toxicity in human liver by exposing human hepatocarcinoma cells in a time (24-72h) and dose (0-100μM) dependent manner. The highest test dose caused an inhibition in cell viability up to 50% after 72h, whereas lower doses (<50μM) showed slight increase in cell viability. Likewise, higher doses caused significant accumulation of intracellular ROS over time. Further, increase in caspase-3 enzyme levels and DNA fragmentation showed that, lower brominated PBDEs induce liver toxicity through accumulation of toxic metabolites and reactive oxygen species over time leading to caspase-mediated apoptotic cell death.

The depression of immune cell function that is typically observed after prolonged exercise is thought to be largely mediated by increased plasma concentrations of stress hormones and cytokines and possibly oxidative stress. The aims of this thesis were to determine the effects of acute and longer term oral antioxidant supplementation on immunoendocrine responses following prolonged exercise. In study 1 (Chapter 3) it was shown that vitamin C ingested acutely before and during prolonged exercise has little or no effect on immunoendocrine responses. Furthermore, the combined ingestion of vitamin C with carbohydrate provides no additional effects compared with carbohydrate alone. However, when vitamin C was supplemented acutely, 2 h prior to, and during prolonged exercise in addition to on the night before (14 h prior) exercise this limited the fall in neutrophil oxidative burst activity (study 2, Chapter 4). This was probably a result of reduced direct oxidative damage to neutrophils with vitamin C supplementation since there were no effects on the cortisol, interleukin-6, leukocytosis or neutrophilia responses. Longer periods of antioxidant supplementation (2 - 4 weeks) may be effective at blunting the cortisol, leukocytosis and neutrophilia responses to prolonged exercise (Chapters 5 and 6) but this had no effect on in vitro measures of neutrophil function. In study 5 (Chapter 7) it was shown that acute pre-exercise dark chocolate (which contains polyphenols) ingestion has some effects on plasma oxidative stress markers and circulating insulin and glucose responses but not the immunoendocrine responses to prolonged exercise.

Humans are constantly exposed to different types of radiations. It has been suggested that low dose and low dose rate of γ-radiation as well as ultra violet A (UVA) induce oxidative stress in cells that may promote mutations. The mechanisms behind radiation-induced oxidative stress and its relation to genotoxicity and cancer induction are not well understood. In the majority of investigations, the DNA molecule has been studied as the target for mutations, however the results obtained in our group point out that DNA bases in the cytoplasm could also be a significant target. MTH1 and MYH are two of the key proteins of the repair pathway that prevent mutations arising from oxidized DNA bases. In this thesis, we studied the role of MTH1 and MYH in genotoxicity of UVA and γ-radiation. The adaptive response to low dose rates of γ-radiation was also investigated. MTH1 and/or MYH were knockdown in human lymphoblastoid TK6 cells. The clonogenic survival, mutant frequency and chromosomal aberration assays were performed following UVA or γ-radiation exposure. Our results indicated that acute exposure to UVA or γ-radiation affects cell survival and also increases the mutant frequency above the background. The mutant frequency in MTH1 deficient cells was higher than that in wild types after UVA exposure. Following γ-radiation exposure, a higher mutant frequency was observed in the MYH and MTH1 deficient cells, in comparison to either MYH or MTH1 deficient or wild type cells. No dose rate effect of γ-radiation for mutations was observed. An adaptive response to γ-radiation was observed at the mutation level in MCF-10A cells but not at the survival level. In summary, our results suggest that; a) MYH and MTH1 cooperatively protect cells against genotoxic effects of γ-radiation; b) MTH1 protects cells from UVA-induced mutations; c) low dose rates of γ-radiation may induce an adaptive response at the mutation level; d) there is no dose rate effect for γ-radiation at the mutation level. / <p>At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 2: Manuscript. Paper 3: Manuscript.</p>

Oxidative stress has recently been highlighted as a potential physiological mechanism underpinning life-history trade-offs in animals. While the role of oxidative stress in mediating such trade-offs is receiving increasing attention, its importance in wild populations remains poorly understood. In this thesis, I use a wild population of cooperatively breeding white-browed sparrow weavers (Plocepasser mahali) to investigate the role that oxidative stress plays in mediating the costs of reproduction and immune defence. Cooperative animal societies offer a unique opportunity to investigate the costs of reproduction, because dominants frequently monopolise breeding opportunities (exhibiting higher reproductive effort than subordinates), and subordinate cooperative contributions frequently lighten reproductive workloads. My findings reveal, first, that dominants’ reproductive monopolies do not arise because they exhibit superior oxidative balance, as no such rank-related differences in oxidative state exist prior to breeding (Chapter 2). However, the higher reproductive effort of dominant females may underpin their differential declines in antioxidant protection after the breeding season (Chapter 2). Second, experimental manipulation of reproductive effort reveals marked oxidative damage and body mass costs incurred during reproduction. However, these costs are entirely mitigated in large social groups, suggesting that the cooperative contributions of helpers may offset the costs of reproduction for all group members (Chapter 3). While this represents rare evidence of an oxidative stress cost of reproduction in the wild, longitudinal data suggests that these costs do not endure after the breeding season (Chapter 4), highlighting that circulating markers of oxidative balance are unlikely to mediate long-term costs of reproduction. Finally, an immune activation experiment reveals that, while mounting an immune response causes no net change in oxidative balance, the scale of the response can be adjusted according to baseline antioxidant protection in an oxidative-condition-dependent manner (Chapter 5). Together my results provide support for the role of oxidative stress in shaping life histories in the wild. Furthermore, evidence of rank-related disparities in oxidative balance and the avoidance of reproductive costs in large social groups may have important implications for our understanding of both the evolution of cooperative breeding and the patterns of health and ageing in societies.

Nicotinamide delivered in drinking water at about 2 g/kg/day significantly prolonged survival and showed a suggestive improvement on memory in the Npc1 (nih) / Npc1 (nih) mouse model of infantile NPC1 disease. It is likely that this role is due to its function as a histone deacetylase (HDAC) inhibitor although another HDAC inhibitor, valproic acid, was without effect. Nicotinamide could also work by preventing/reversing oxidative stress.

This literature review posits that the transcription factor Nuclear factor (erythroid-derived 2)-like 2 (Nrf2) is an attractive candidate therapeutic target in the setting of acute myocardial infarction (AMI). This transcription factor binds to antioxidant response elements (ARE) in the promoter region of a battery of genes that collectively encode an array of antioxidant, phase II drug metabolism, metabolically stabilizing, and overall cytoprotective enzymes, facilitating their transcription at basal levels and increasing transcription in response to various cellular stressors. Following a brief background tutorial on normal cardiac myocyte cellular physiology, key events that occur early in ischemia and reperfusion are outlined and integrated. These include ionic and metabolic dysregulation, electron transport chain uncoupling, mitochondrial depolarization, and the generation of reactive oxygen species (ROS). Abrupt changes in response to ischemia prime opening of the mitochondrial permeability transition pore (MPTP) and cardiac myocytes to generate a burst of ROS upon reperfusion–two key events that contribute to the umbrella term ischemia-reperfusion injury (IRI). How ROS damage cells is then outlined, and through a ROS-centric viewpoint, a case will be made as to how exogenous upregulation of Nrf2 could protect and/or salvage at-risk tissue immediately subjected to infarction and neighboring tissue in the peri-infarct zone (PIZ). The history of how Nrf2 came to be known as the "master regulator of oxidative stress" is reviewed, as well as the discovery of the canonical mechanism of Nrf2 regulation via Kelch-like ECH-associated protein 1 (Keap1) and other alternative mechanisms of endogenous Nrf2 regulation. Finally, compiling interdisciplinary evidence from research publications around the world, the benefits of therapeutically targeting Nrf2 are considered given the timescale and context of acute MI. Drug delivery methods, potential challenges, and limitations are then considered. Cardiac tissue is a dynamic substrate that exhibits changes for up to 90 days after AMI and patient outcomes are directly related to the extent of tissue lost following infarction/reperfusion. Targeting Nrf2 addresses an unmet need, as current clinical therapies focus on precluding occlusions and prompt reperfusion of infarcted tissue, but do not explicitly target at-risk tissue following infarcts and/or present-day reperfusion methodologies.

Approximately 1 in 11 births in the United States are preterm (gestation). Within the United States, there are huge racial disparities for risk of preterm birth, an issue understudied and rarely addressed by research in the field. There is a wealth of biological knowledge surrounding pregnancy and labor, but causes for preterm birth are poorly understood. A genetic factor that has been shown to play a key role in many biological processes crucial to a healthy pregnancy and timely labor is microRNA (miRNA). MiRNA have an active role in the regulation of various tissues, especially developing tissues like those found in the placenta and uterus. Additionally, oxidative stress has been shown essential to placental development and the initiation of labor. Here, a study is proposed that aims to address the effect of oxidative stress on myometrial miRNA expression, specifically the miR-200 family and miR-199/214 cluster. This work also underscores the importance of addressing racial disparities with regards to preterm labor during research, while bringing up ethical considerations for conducting such research. The thesis will conclude with an outline of the many considerations vital for discussing the research and analysis of preterm birth disparities using a feminist, antiracist, queer self-reflexive analysis.

On étudie les potentialités d'action de la consommation de jus de fruits et de vins riches en polyphénols sur modèle pathologique de stress oxydant, l'athérosclérose précoce, d'origine nutritionnelle, ainsi que leur effet protecteur spécifique vis à vis de cette pathologie. Dans une première partie expérimentale, nous avons analysé les polyphénols de trois variétés de jus de framboises (Cardinal, Glen Ample et Tulameen) et deux vins (Kaki et Merlot) par HPLC. Nous avons identifié et quantifié les composants phénoliques de la famille des anthocyanes et des ellagitanins, les deux constituants majeurs des polyphénols de framboise. Leurs compositions diffèrent significativement, en particulier entre Glen Ample et Tulameen. Concernant les vins, les flavan-3-ols (monomères et oligomères) ont été analysés. Les concentrations de chaque composant étaient fondamentalement différents entre les deux vins, sauf pour les dimères. Ceci nous a conduit à aborder l'étude in vivo sur hamster syrien doré recevant un régime riche en lipides et cholestérol, et carencé en antioxydants alimentaires. L'ingestion de Glen Ample (équivalent à 250 mL de jus de framboise par jour pour une homme de 70 kg) inhibe les facteurs pro-oxydants et améliore le statut antioxydant alors que le jus Tulameen a un effet protecteur contre la dyslipidémie. Ces effets peuvent être liés aux ellagitanins et anthocyanes respectivement. Nous avons montré que la consommation de vin à dose nutritionnelle (équivalent à 2 verres par repas pour un homme de 70 kg) améliorait la réactivité vasculaire, la dyslipidémie et le statut antioxydant. Parmi ces effets bénéfiques, aucune différence n'apparaît entre le vin de kaki et le Merlot, ce qui suggère que les dimères de procyanidines sont impliqués dans les effets biologiques des polyphénols. / The purpose of this study is to explore the potential of fruit juices and wines consumption rich in polyphenol on pathological models of oxidative stress, diet-induced early atherosclerosis, and to research their specific protective effect against the pathology.In the first part of this work we analyzed the polyphenols in three varieties of raspberry juices (Cardinal, Glen Ample and Tulameen) and two wines (Persimmon and Merlot) by HPLC. We identified and quantified phenolic components of anthocyanins and ellagitannins family, the two major constituents in raspberries polyphenols. Their compositions differed significantly especially between Glen Ample and Tulameen. For wines, flavan-3-ols (monomers and oligomers) were analyzed. Concentrations of each component were fundamentally different in two wines except for procyanidin dimers.These results led us to address in vivo studies on Syrian Golden hamsters fed a high-fat, high-cholesterol diet deprived in dietary antioxidants. Consumption of Glen Ample (equivalent to 250 mL of raspberry juice per day for a 70 kg human) inhibits pro-oxidant factors and improves antioxidant status whereas Tulameen shows a protective effect against dyslipidemia which may be due to its ellagitannins and anthocyanins respectively.Nutritional dose of wines (equivalent to 2 glasses of wine per meal for a 70 kg human) improves vascular reactivity, dyslipidemia and antioxidant status. No difference appeared between persimmon and merlot wine antioxidant properties suggesting that procyanidin dimers are implicated in the biological effects of polyphenols.