The production of reactive oxygen species (ROS) may be a contributor to the progression of sarcopenia. Sarcopenia is a generic term for the loss of skeletal muscle mass, quality and strength. ROS are usually produced by radiation, but are also the byproducts of aerobic metabolism. ROS have been found to mediate various pathological conditions in a variety of tissues, to cause oxidative damage to DNA, proteins, and lipids with advancing age, and is presumably a major factor contributing to changes associated with aging. The purpose of this investigation was to determine whether the sarcoplasmic reticulum (SR) of muscle from aged animals are more susceptible to the deleterious effects of ROS. Using isolated gastrocnemius SR vesicles extracted from adult (12m) and aged (27m) male Brown Norway-Fischer 344 hybrid rats, Ca2+ uptake and release measurements were obtained. The data showed that there was a 33% difference between aged and adult gastrocnemius mass. When gastrocnemius mass was corrected for body mass, the differences was ~20% between the two groups. A 20% decrease in SR Ca2+ uptake rate was noted in aged animals. HOCl also, decreased uptake by similar extents in both groups. This result suggest that the Ca2+ pump's response to ROS are similar in both groups. AgNO3 -induced and H2O2 -induced release in aged animals was 17.94 and 7.39 nmol/mg/min and in adult animals was 30.46 and 7.18 nmol/mg/min, respectively. H2O2-induced release, when expressed as a percent of AgNO3-induced release was increased in aged animals by 54%. The results suggest that the release channel of aged muscle appears to be more sensitive to ROS. In conclusion, the data support the theory that aged animal skeletal muscle is more susceptible to the adverse effects of ROS. / Master of Science

In this work a new technique for accelerating the aging of FPGA devices is proposed and demonstrated. The proposed technique uses harmful configurations (short circuits) to accelerate the aging process on targeted portions of an FPGA chip. A testbed is developed for the purpose of measuring FPGA degradation. Using this testbed it is shown that implementing thousands of short circuits in FPGA fabric generates enough heat to cause significant damage to the chip, reducing switching speeds by up to 8%. It is also demonstrated that different parts of the FPGA fabric can be aged at different rates, with some parts of the chip only slowing down 2% while other parts slowdown as much as 8%.

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Evidence from many recent studies has linked uncontrolled inflammatory processes to aging and aging-related diseases. Decreased a nuclear receptor subfamily of transcription factors, peroxisome proliferator-activated receptors (PPARs) activity is closely associated with increased levels of inflammatory mediators during the aging process. The anti-inflammatory action of PPARs is substantiated by both in vitro and in vivo studies that signify the importance of PPARs as major players in the pathogenesis of many inflammatory diseases. In this review, we highlight the molecular mechanisms and roles of PPARα, γ in regulation of age-related inflammation. By understanding these current findings of PPARs, we open up the possibility of developing new therapeutic agents that modulate these nuclear receptors to control various inflammatory diseases such as atherosclerosis, vascular diseases, Alzheimer's disease, and cancer.

The aim of this work is to characterize the effects of hygrothermal aging in the plain strain fracture toughness of the epoxy system composed by cycloaliphatic epoxy resin and diglycidyl ether of bisphenol-A (DGEBA). For this, after having been under hygrothermal aging in a climatic chamber, epoxy samples were studied using ASTM D5045 fracture toughness test, and micrography and roughness measurements of the fracture surface. It is reported a rapid decrease of GIc and KIc during the first 2 days. Moreover, a numerical model [13] was used to simulate and see with more detail the water absorption in the aged samples. From that, it was observed the heterogeneous distribution of water. Accordingly, it was proposed that the results should be correlated with the water content at the vicinity of the crack tip. Consequently, it was possible to obtain, by quasi-static simulations, the ideal load-displacement curves of crack propagation in the heterogeneous samples. Finally, another contribution of this work is the study of the fracture surface, that gives a clue of the relationship among the fracture energy, the appearance of microcracks in the fracture surface, and the roughness (Ra).

Emotional experiences are more likely to be remembered than more neutral, mundane ones. In young adults, negative information may be particularly memorable. Yet, an interesting change seems to happen in aging: As adults grow older, they may start remembering positive information more often than negative information. This positive memory bias in aging is commonly observed and is often explained in terms of changing time perspectives and motivation across the lifespan (i.e., Socioemotional Selectivity Theory; Carstensen, Isaacowitz, & Charles, 1999). However, few studies have considered the basic interactions between memory and emotion that could influence this positivity bias. In this thesis, I examine whether certain factors partially independent of aging (i.e., semantic relatedness and distinctiveness, Study 1; mood, Studies 2-4), might influence the presence and magnitude of the positivity bias in memory. In Study 1, I explore the cognitive mechanisms required to produce the positivity bias and apply what is learned in this paper to investigate, in Studies 2-4, whether differences in mood could explain why the positivity bias occurs. In all studies, memory is measured using immediate free recall of positive, negative, and neutral pictures. In Study 1, I manipulate item interrelatedness (i.e., the extent of relatedness among pictures of a same category) and relative distinctiveness (i.e., the processing of a picture category at the same time as or in isolation from the others) to show that older adults’ emotional memory can be entirely explained by these two factors. The distinctive processing of positive pictures relative to other pictures is necessary for producing a positivity bias in older adults, which completely disappears when the distinctive processing of positive pictures is removed. Therefore, in subsequent studies I encourage the distinctive processing of items to increase the likelihood of observing a positivity bias and its possible interaction with mood. In Study 2, I test whether differences in mood predict differences in emotional memory bias in young and older adults using a video mood induction technique validated in a separate pilot study. In Studies 3 and 4, I further test the effect of mood on the positivity bias beyond any age-specific factors, by examining young adults only. This serves to reduce the likelihood of confounds that might exist between age groups (i.e., related to neurocognitive changes or decline), in order to study the true effects of mood on the positivity bias. In Study 3, I use a written priming task to experimentally manipulate mood and time perspective in young adults. In Study 4, I compare differences in naturally occurring moods and emotional memory in two separate young adult samples: university students and non-students. The experimental mood manipulations have minimal influence on the presence of a negativity bias in young adults (Studies 2 and 3), and influence to a small extent the memory advantage of positive over neutral material in older adults (Study 2). Non-student young adults show a similar preferential memory for positive material that is different from what is observed in university students, but this is not easily attributed to differences in mood (Study 4). In light of these results, I argue that the positivity effect in aging memory reflects a temporary contextual advantage for positive information that is not permanent or irreversible. Rather, it seems to depend in varying degrees on the context of study (i.e., relatedness and distinctiveness), mood, and the young-adult reference group. This has implications for how future research defines and studies the positivity effect in aging.

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Accelerated aging of 15 kV Cross-linked Polyethylene (XLPE) and Ethylene Propylene Rubber (EPR) power cables was carried out in the experiments set for the study of this thesis. The degradation of cable insulation under different aging conditions was studied and compared. The study helped to understand the effects of different factors on the aging of XLPE and EPR cable insulation. In the study, degradation of XLPE cable insulation caused by switching impulses was investigated. The deterioration of EPR cable insulation initiated by elevated ac voltage and switching impulses were also studied. Measurements of partial discharge parameters, capacitance, and dissipation factor were analyzed to evaluate the condition of cable insulation during accelerated aging process. Measurement of ac breakdown voltage provided evidence of the cables’ remaining dielectric strength after accelerated aging.

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