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Assoc. Prof. Stephen Robinson
Professional ActivitiesEditorial boards
Research InterestsSteve's research is guided by the conviction that a better understanding of the involvement of astrocytes will lead to more effective treatments for many neurological disorders. His investigations on glia-neurone interactions, particularly the glutamate-glutamine cycle, have helped to focus international attention on the role of astrocytes in brain function. He has had an international profile as an outspoken critic of the rationale and efficacy of anti-amyloid-? approaches in the treatment of Alzheimer's disease. Steve directs two research teams: one undertakes laboratory research, the other clinical research. The laboratory team investigates the response of astrocytes to iron-mediated oxidative stress, and their involvement in age-related neurodegenerative disorders such as stroke and Alzheimer's disease. Insights contributed by this research include the discovery of a paradoxical interaction between amyloid-? and metal ions, key roles for astrocytes in accumulating iron and in reducing oxidative stress, and a novel quantitative assay for bio-iron. The clinical team uses the Subtle Cognitive Impairment Test (SCIT) and other neuropsychological tests to examine cognitive impairment in clinical and community populations including HIV-dementia, cardiac surgery, elderly, fatigue, post-traumatic stress disorder and drug intoxication. These studies are being undertaken from the viewpoint that impairments in cognition are often the consequence of impaired metabolic interactions between astrocytes and neurones, and that ultimately it might be possible to alleviate these impairments with treatments that are directed at astrocytes. Postgraduate Research ProjectsLaboratory-based research projects investigate glia-neuronal interactions with a view of understanding neurodegenerative disorders. Current PhD students are undertaking projects on oxidative stress, iron and hemin metabolism, cholesterol metabolism, amyloid-beta toxicity and glutamine synthetase. Clinically-based PhD students are investigating aspects of subtle cognitive impairment in a variety of populations including cardiac surgery patients, the elderly, alcohol-intoxicated subjects and children with developmental disorders. Potential Student ProjectsWe are interested in understanding the role of astrocytes in brain function and dysfunction. Our focus is on the role of iron and oxidative stress in age-related neurodegenerative disorders such as stroke and Alzheimer’s disease. The research conducted by the team uses cell culture, biochemical assays, in vivo paradigms, and behavioural experiments on animals and humans. We have a wide range of potential student projects and would be happy to discuss them with you. Teaching
CollaborationsWe enjoy fruitful collaborations with many research groups in Australia and overseas. Our current research collaborations include:
Grant Support
PublicationsRobinson, S.R., Hampson, E.C.G.M., Munro, M.N. and Vaney, D.I. (1993). Unidirectional coupling of gap junctions between neuroglia. Science, 262: 1072-1074. Pow, D.V. and Robinson, S.R. (1994). Glutamate in some retinal neurons is derived solely from glia. Neuroscience, 60: 355-366. Hertz, L., Dringen, R., Schousboe, A., and Robinson, S.R. (1999). Astrocytes: Glutamate producers for neurons. Journal of Neuroscience Research, 57: 417-428. Barnett, N.L., Pow, D.V. and Robinson, S.R. (2000) Inhibition of Muller cell glutamine synthetase rapidly impairs the retinal response to light. Glia 30, 64-73. Robinson, S.R. (2000) Neuronal expression of glutamine synthetase in Alzheimer's disease indicates a profound impairment of metabolic interactions with astrocytes. Neurochemistry Internatonal. 36, 471-482. Robinson, S.R. and Bishop, G.M. (2002) Amyloid beta as a bioflocculant: Implications for the amyloid hypothesis of Alzheimer's disease. Neurobiology of Aging 23, 1051-1072. Robinson, S.R., Bishop, G.M. and Münch, G. (2003) Amyloid-ß on trial. BioEssays 25, 283-288. Riemer, J., Hoepken, H.H., Czerwinska, H., Robinson, S.R. and Dringen, R. (2004) Colorimetric ferrozine-based assay for the quantitation of iron in cultured cells. Analytical Biochemistry, 331, 370-375. Fernandes, S.P., Edwards, T.M., Ng, K.T. and Robinson, S.R. (2006) HIV-1 protein GP120 rapidly impairs memory in chicks by interrupting the glutamate-glutamine cycle. Neurobiology of Learning and Memory, Epub. May 19, 2006. Liddell, J.R., Hoepken, H.H., Crack, P., Robinson, S.R. and Dringen, R. (2006) Glutathione peroxidase and GSH are required to protect mouse astrocytes from iron-mediated hydrogen peroxide toxicity. Journal of Neuroscience Research, Epub. May 23, 2006. PatentsYelland, Robinson, Hutchinson, Friedman. Detecting subtle cognitive impairment. National Phase of PCT (Patent Cooperation Treaty). International filing date: 7th January, 2004. There are three patents pending: Australia: AU2004203679 |