6 results match your criteria: "The University of QueenslandSt. Lucia[Affiliation]"
Front Mol Neurosci
September 2017
IMB Centre for Pain Research, Institute for Molecular Bioscience, The University of QueenslandSt. Lucia, QLD, Australia.
Rodents are commonly used to study the pathophysiological mechanisms of pain as studies in humans may be difficult to perform and ethically limited. As pain cannot be directly measured in rodents, many methods that quantify "pain-like" behaviors or nociception have been developed. These behavioral methods can be divided into stimulus-evoked or non-stimulus evoked (spontaneous) nociception, based on whether or not application of an external stimulus is used to elicit a withdrawal response.
View Article and Find Full Text PDFFront Cell Neurosci
June 2017
Department of Molecular Genetics, Weizmann Institute of ScienceRehovot, Israel.
Current knowledge regarding regulation of radial neuronal migration is mainly focused on intracellular molecules. Our unbiased screen aimed at identification of non-cell autonomous mechanisms involved in this process detected differential expression of or C1 inhibitor, which is known to inhibit the initiation of the complement cascade. The complement cascade is composed of three pathways; the classical, lectin, and the alternative pathway; the first two are inhibited by C1 inhibitor, and all three converge at the level of C3.
View Article and Find Full Text PDFFront Behav Neurosci
January 2017
Queensland Brain Institute, The University of QueenslandSt Lucia, QLD, Australia; Queensland Centre for Mental Health Research, The Park Centre for Mental HealthRichlands, QLD, Australia.
Touchscreen technology is increasingly being used to characterize cognitive performance in rodent models of neuropsychiatric disorders. Researchers are attracted to the automated system and translational potential for touchscreen-based tasks. However, training time is extensive and some mouse strains have struggled to learn touchscreen tasks.
View Article and Find Full Text PDFFront Neurosci
July 2016
School of Psychology and Counselling, Faculty of Health, Queensland University of Technology Kelvin Grove, QLD, Australia.
Reliance on the hemodynamic response as a surrogate marker of neural activity imposes an intrinsic limit on the spatial specificity of functional MRI. An alternative approach based on diffusion-weighted functional MRI (DfMRI) has been reported as a contrast less reliant on hemodynamic effects, however current evidence suggests that both hemodynamic and unique neural sources contribute to the diffusion signal. Here we compare activation patterns obtained with the standard blood oxygenation level-dependent (BOLD) contrast to DfMRI in order to gain a deeper understanding of how the BOLD proportion contributes to the observable diffusion signal.
View Article and Find Full Text PDFFront Pharmacol
March 2016
Centre for Integrated Preclinical Drug Development, The University of Queensland St Lucia, QLD, Australia.
The direct peptide reactivity assay (DPRA) is a validated method for in vitro assessment of the skin sensitization potential of chemicals. In the present work, we describe a peptide reactivity assay using 96-well plate format and systematically identified the optimal assay conditions for accurate and reproducible classification of chemicals with known sensitizing capacity. The aim of the research is to ensure that the analytical component of the peptide reactivity assay is robust, accurate, and reproducible in accordance with criteria that are used for the validation of bioanalytical methods.
View Article and Find Full Text PDFFront Behav Neurosci
February 2016
Queensland Brain Institute, The University of QueenslandSt. Lucia, QLD, Australia; Queensland Centre for Mental Health Research, The Park Centre for Mental HealthRichlands, QLD, Australia.
Neuropsychiatric research has utilized cognitive testing in rodents to improve our understanding of cognitive deficits and for preclinical drug development. However, more sophisticated cognitive tasks have not been as widely exploited due to low throughput and the extensive training time required. We developed a modified signal detection task (SDT) based on the growing body of literature aimed at improving cognitive testing in rodents.
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