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This thesis examined post-stroke gait asymmetry: a prevalent issue and one that has a number of associated negative consequences (e.g. challenged balance control, gait inefficiencies, increased risk of musculoskeletal injury to the non-paretic limb and decreased overall activity levels). This thesis is comprised of three studies that focused on 1) how gait symmetry should be measured, 2) how gait asymmetry may change in the long term post-stroke and 3) whether gait asymmetry is responsive to a rehabilitation intervention. A comparison of the most common expressions of spatiotemporal gait symmetry revealed that the simple symmetry ratio calculation was most appropriate on the basis of ease of interpretation and clinical usefulness. Swing time, stance time and step length were found to be the most useful gait parameters to assess for symmetry. Although related, swing time, stance time and step length ratios exhibit variation in the discrimination of post-stroke individuals, in their inter-relationships and in their relationship velocity. When when used together, swing time, stance time and step length asymmetry ratios may provide a complementary picture of the gait pattern and the quality of gait control. It was also demonstrated that swing time and stance time asymmetry were worse in later stages post-stroke when assessed cross-sectionally. In contrast, gait velocity did not exhibit this pattern. These results indicate that the control of gait (symmetry) may decline over time post-stroke, independent from the capacity for gait which remains constant (velocity). This dissociation in characteristics supports the concept that these two variables (symmetry and velocity) may represent separate features of post-stroke gait. Finally, individuals with sub-acute stroke are capable of altering the temporal symmetry of their gait in response to visual biofeedback. Individuals with sub-acute stroke differ in terms of the strategy they employ in response to biofeedback and the observed improvements in gait symmetry were not always achieved in the desired manner: increased use of the paretic lower extremity. This thesis presents new information regarding the asymmetrical nature of post-stroke gait. Future work may extend these findings to develop a comprehensive approach to gait measurement as well as gait interventions that encourage increased paretic limb use instead of compensatory behaviour.

Pyramidal neurons (PyNs) in ‘higher’ brain are highly susceptible to acute stroke injury yet ‘lower’ brain regions better survive global ischemia, presumably because of better residual blood flow. Here we show that projection neurons in ‘lower’ brain regions of hypothalamus and brainstem intrinsically resist acute stroke-like injury independent of blood flow in the brain slice. In contrast `higher` projection neurons in neocortex, hippocampus, striatum and thalamus are highly susceptible. In live brain slices from rat deprived of oxygen and glucose (OGD), we imaged anoxic depolarization (AD) as it propagates through these regions. AD, the initial electrophysiological event of stroke, is a depolarizing front that drains residual energy in compromised gray matter. The extent of AD reliably determines ensuing damage in higher brain, but using whole-cell recordings we found that all CNS neurons do not generate a robust AD. Higher neurons generate strong AD and show no functional recovery in contrast to neurons in hypothalamus and brainstem that generate a weak and gradual AD. Most dramatically, lower neurons recover their membrane potential, input resistance and spike amplitude when oxygen and glucose is restored, while higher neurons do not. Following OGD, new recordings could be acquired in all lower (but not higher) brain regions, with some neurons even withstanding multiple OGD exposure. Two-photon laser scanning microscopy confirmed neuroprotection in lower, but not higher gray matter. Specifically pyramidal neurons swell and lose their dendritic spines post-OGD, whereas neurons in hypothalamus and brainstem display no such injury. Exposure to the Na+/K+ ATPase inhibitor ouabain (100 μM), induces depolarization similar to OGD in all cell types tested. Moreover, elevated [K+]o evokes spreading depression (SD), a milder version of AD, in higher brain but not hypothalamus or brainstem so weak AD correlates with the inability to generate SD. In summary, overriding the Na+/K+ pump using OGD, ouabain or elevated [K+]o evokes steep and robust depolarization of higher gray matter. We show that this important regional difference can be largely accounted for by the intrinsic properties of the resident neurons and that Na+/K+ ATPase pump efficiency is a major determining factor generating strong or weak spreading depolarizations. / Thesis (Ph.D, Anatomy & Cell Biology) -- Queen's University, 2012-10-02 17:59:20.589

Background: Prospective memory is the ability to remember to carry out previously planned actions at an appropriate point in the future. Impairments in prospective memory have been found in a range of neurological conditions. While it is assumed that stroke patients will have similar deficits, there is currently a dearth of evidence to support this. Methods: A between-subjects design was employed to compare 22 community-dwelling stroke patients to 22 healthy adult controls on a standardised objective measure of prospective memory. Subjective reports of everyday memory were measured using a validated questionnaire. Standardised tests were also administered to measure retrospective memory and executive functioning. Results: Stroke patient’s prospective memory performance was significantly poorer than controls. Depression had a significant influence on time-based prospective memory tasks. Executive functioning was shown to be a good predictor of overall prospective memory ability. Stroke patient’s insight into their everyday memory abilities was incomplete. Conclusion: Prospective memory abilities are reduced after stroke. In light of the potential impact of such difficulties on everyday functioning, this aspect of cognitive functioning should be routinely assessed in clinical practice.