https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Slowing and stopping in schizophrenia https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:16476 Wed 11 Apr 2018 12:54:46 AEST ]]> Assessing social cognition in adults https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:43073 Tue 13 Sep 2022 11:37:32 AEST ]]> Functional MRI BOLD response to Tower of London performance of first-episode schizophrenia patients using cortical pattern matching https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:561 Thu 25 Jul 2013 09:10:39 AEST ]]> Brief neuropsychological profiles in psychosis: a pilot study using the Audio Recorded Cognitive Screen (ARCS) https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:10315 Sat 24 Mar 2018 08:07:00 AEDT ]]> Decision processes and the slowing of simple choices in schizophrenia https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:26194 Sat 24 Mar 2018 07:24:09 AEDT ]]> The effects of phenylethanoid glycosides, derived from Herba cistanche, on cognitive deficits and antioxidant activities in male SAMP8 mice https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:34031 Herba cistanche, are known to exert protective effects on cognitive deficits in Alzheimer's disease (AD); however, the underlying mechanisms of this herbal extract on cognitive performance remain unclear. The aim of this study was thus to examine the protective mechanism attributed to PhG on cognitive deficits in an AD senescence accelerated mouse prone 8 (SAMP8) model. Cognitive deficit parameters examined included (1) Morris water maze (MWM) assessing cognitive performance and (2) quantification of dendritic spine density in hippocampal CA1 region by Golgi staining, a molecular biomarker of synaptic function. In addition, levels of malondialdehyde (MDA) and activities of superoxide dismutase (SOD) and gluthathione peroxidase (GSH-Px) were determined to examine the potential role of oxidant processes in cognitive dysfunction. Data showed that PhG significantly decreased escape latency and path length, associated with a rise in the percentage of time spent in the target quadrant and number of platform crossings. In addition, PhG significantly increased dendritic spine density in the hippocampal CA1 region accompanied by elevated expression levels of synaptophysin (SYN) and post synaptic density 95 (PSD-95), reduced MDA content, and elevated the activities of SOD and GSH-Px. Data suggest that the ability of PhG to ameliorate cognitive deficits in SAMP8 mice may be related to promotion in synaptic plasticity involving antioxidant processes.]]> Mon 04 Feb 2019 11:38:53 AEDT ]]>