Life Sciences Commons^™

Contribution Of Trpm2 To Memory Loss In An Alzheimer's Mouse Model, Megan M. Chen

Electronic Thesis and Dissertation Repository

Alzheimer’s disease (AD) is a neurodegenerative disease characterized by the progressive deterioration of memory and other intellectual abilities. Accumulation of amyloid-β (Aβ) peptide, the major contributor to the senile plaques central to AD, is thought to mediate neurotoxicity by inducing oxidative stress and calcium dysregulation. Transient Receptor Potential Melastatin type 2 (TRPM2) is a calcium permeable, non-selective cation channel activated under oxidative stress and ultimately induces cell death. The APPSWE/PSEN1ΔE9 double transgenic mouse model carries the human APPswe (Swedish mutations K594N/M595L) and PS1 mutations with a deletion in exon 9 (PS1-dE9), and is one of the most commonly used AD …

The Plastic And Evolutionary Responses Of Fish To Anthropogenic Stressors, Ross D. Breckels

Electronic Thesis and Dissertation Repository

Ecosystems are being altered at unprecedented rates with little knowledge of the potential impacts on biodiversity. Two of the most pressing contemporary anthropogenic stressors are pollution and global warming. Species can respond to these stressors via dispersal, phenotypic plasticity, or evolutionary adaptation. Many species, especially aquatic organisms, experience ecological or physical barriers to dispersal and will therefore have to respond via phenotypic plasticity or evolutionary responses. I examined the responses of multiple traits associated with fitness in fish to pollution and increased temperature using a 2 × 2 common garden experimental design. I examined the effects of pollution on behaviour …

Neurodevelopmental Consequences Of Prenatal Alcohol Exposure: Behavioural And Transcriptomic Alterations In A Mouse Model, Katarzyna Mantha

Electronic Thesis and Dissertation Repository

Fetal Alcohol Spectrum Disorder (FASD) is an umbrella term referring to a range of physical, behavioural, and cognitive deficits resulting from prenatal alcohol exposure. The resulting abnormalities are heterogeneous and often attributed to timing and dosage of alcohol exposure. However, the specific effects of developmental timing are not well-known.

This research used C57BL/6J (B6) as an animal model for early (human trimester one) and mid-gestation (human trimester two) alcohol exposure. Pregnant B6 mice were injected with 2.5 g/kg ethanol on gestational day (GD) 8 and 11 (trimester one equivalent), or on GD 14 and 16 (trimester two equivalent). Resulting pups …