Emotional Geographies of Home: Place Identities Among Senior Women Residing in a Long-Term Care Facility

This research aimed to document the meanings and identities attached to the concept of ‘home’ among older women residing in long-term care. The study is based upon semi-structured, open-ended interviews with eleven senior women who reside in a long-term care home in The City of London, Ontario. This study contributes towards theoretical and methodological debates by combining critical humanism, feminism and the newly developing body of work called ‘emotional geographies’ in its approach. Along with the interview, the novel method of using the body as an ‘instrument of research’ is utilized (Longhurst, 2008). The methodology allows for ‘emotional spaces’ occupied by the participants to be revealed and documented. Findings problematize and provide nuance to previous studies about ‘home’. In particular, my findings demonstrate that spatialities, temporalities, boundaries, tension, and paradox need to be considered when theorizing, and more importantly, legislating ‘home’ into public policy. The landscape of the long-term care ‘home’ is identified to be located simultaneously and paradoxically ‘elsewhere’ – it is displaces from the ‘concrete’ wall of the long-term care institution – while being closely tied to the concept of a changing and fluid body and boundary zones that the body questions. The findings contribute to social theory about the experience of place, while having practical implications for policymakers, managers of long-term care facilities and senior citizens

The retrosplenial cortex and long-term spatial memory: from the cell to the network

In this review we briefly outline how lesion studies, temporary inactivation and neural activity assays have helped update functional models of the retrosplenial cortex, a region critical for episodic and spatial memory. We advocate for the continued importance of appropriately designed behavioural studies in the context of novel experimental methods, such as optogenetic and chemogenetic manipulations. At the same time, we caution against the overreliance on any given level of analysis or experimental technique. Complementary, multimodal strategies are required for understanding how the retrosplenial cortex contributes to the formation and storage of memories both at a structural and systems-level

Spatial memory engram in the mouse retrosplenial cortex

Memory relies on lasting adaptations of neuronal properties elicited by stimulus-driven plastic changes [1]. The strengthening (and weakening) of synapses results in the establishment of functional ensembles. It is presumed that such ensembles (or engrams) are activated during memory acquisition and re-activated upon memory retrieval. The retrosplenial cortex (RSC) has emerged as a key brain area supporting memory [2], including episodic and topographical memory in humans [3, 4, 5], as well as spatial memory in rodents [6, 7]. Dysgranular RSC is densely connected with dorsal stream visual areas [8] and contains place-like and head-direction cells, making it a prime candidate for integrating navigational information [9]. While previous reports [6, 10] describe the recruitment of RSC ensembles during navigational tasks, such ensembles have never been tracked long enough to provide evidence of stable engrams and have not been related to the retention of long-term memory. Here, we used in vivo 2-photon imaging to analyze patterns of activity of over 6,000 neurons within dysgranular RSC. Eight mice were trained on a spatial memory task. Learning was accompanied by the gradual emergence of a context-specific pattern of neuronal activity over a 3-week period, which was re-instated upon retrieval more than 3 weeks later. The stability of this memory engram was predictive of the degree of forgetting; more stable engrams were associated with better performance. This provides direct evidence for the interdependence of spatial memory consolidation and RSC engram formation. Our results demonstrate the participation of RSC in spatial memory storage at the level of neuronal ensembles

Mimicking of glutathione peroxidase deficiency by exposition of JAR cells to increased level of synthetic hydroperoxide

A short chain synthetic analogue of lipid hydroperoxides was used to overload glutathione peroxidase (GPx) in human choriocarcinoma cell line JAR cells. Cells exposed to 100 µM tBuOOH displayed a 40% reduction in ATP level and significantly increased in membrane permeability, visualised by the lactate dehydrogenase (LDH) release into the extracellular medium. The intracellular level of oxygen free radicals measured as an oxidation of the dichlorodihydro-fluorescein diacetate (H2DCF-DA) significantly increased after 2 hours of cell exposition to 100 µM tBuOOH. Concomitantly MDA, 4-HNE level increased to 2 nmol/mg of cell protein after 2 hours. Mitochondria stained with MitoTracker Red CMXRos displayed a filamentous appearance in control cells but changed into granular less energised organelles after exposition to tBuOOH. Collectively, the above results indicate the importance of the contribution of oxidative stress in the development of pre-eclampsia

Size exclusion chromatography for analyses of fibroin in silk : optimization of sampling and separation conditions

A direct goal of this paper was to improve the methods of sample preparation and separation for analyses of fibroin polypeptide with the use of size exclusion chromatography (SEC). The motivation for the study arises from our interest in natural polymers included in historic textile and paper artifacts, and is a logical response to the urgent need for developing rationale-based methods for materials conservation. The first step is to develop a reli- able analytical tool which would give insight into fibroin structure and its changes caused by both natural and arti- ficial ageing. To investigate the influence of preparation conditions, two sets of artificially aged samples were pre- pared (with and without NaCl in sample solution) and measured by the means of SEC with multi angle laser light scattering detector. It was shown that dialysis of fibroin dissolved in LiBr solution allows removal of the salt which destroys stacks chromatographic columns and prevents reproducible analyses. Salt rich (NaCl) water solutions of fibroin improved the quality of chromatograms

Properties of neutron doped multicrystalline silicon for solar cells

The technology of neutron transmutation doping of silicon wafers in MARIA nuclear research reactor is described. The studies of the radiation defects performed with positron annihilation confirmed that divacancies dominate in the irradiated material. Thermal treatment of irradiated silicon at 700-1000°C produces void - phosphorus complexes and void aggregates. The resistivity of the samples produced by neutron transmutation doping was found to be uniform within 2.5% limits. The severe reduction of the minority carrier lifetime in irradiated samples was confirmed

Lack of change in CA1 dendritic spine density or clustering in rats following training on a radial-arm maze task [version 2; peer review: 2 approved]

Background: Neuronal plasticity is thought to underlie learning and memory formation. The density of dendritic spines in the CA1 region of the hippocampus has been repeatedly linked to mnemonic processes. Both the number and spatial location of the spines, in terms of proximity to nearest neighbour, have been implicated in memory formation. To examine how spatial training impacts synaptic structure in the hippocampus, Lister-Hooded rats were trained on a hippocampal-dependent spatial task in the radial-arm maze. Methods: One group of rats were trained on a hippocampal-dependent spatial task in the radial arm maze. Two further control groups were included: a yoked group which received the same sensorimotor stimulation in the radial-maze but without a memory load, and home-cage controls. At the end of behavioural training, the brains underwent Golgi staining. Spines on CA1 pyramidal neuron dendrites were imaged and quantitatively assessed to provide measures of density and distance from nearest neighbour. Results: There was no difference across behavioural groups either in terms of spine density or in the clustering of dendritic spines. Conclusions: Spatial learning is not always accompanied by changes in either the density or clustering of dendritic spines on the basal arbour of CA1 pyramidal neurons when assessed using Golgi imaging