British Association for Pyschopharmacology. To advance education and research in the science of psychopharmacology
Co-Opted Council Member: Dr Hugh Marston, PhD, BScSchering-Plough Corporation. hugh.marston@spcorp.com
Co-opted in January 2008
Hugh Marston currently leads the Psychopharmacology Section at Schering-Plough Corporation’s research site at Newhouse in Scotland. Hugh gained a BSc jointly in physiology, pharmacology and statistics before studying with Trevor Robbins for a PhD in experimental psychology at Cambridge University. During his period in Cambridge he began to develop his interest in animal models of human CNS disorders initially focussing on manipulations to the cholinergic system on learning, memory and attention. Following completion of a visiting fellowship at NIDA in Baltimore working with Jon Katz on the substrates of cocaine addiction he joined the Fujisawa Institute of Neuroscience, University of Edinburgh directed by John Kelly. Here he developed a behavioural laboratory supporting a number of drug development projects ranging from neuroprotection in stroke, through adenosinergic pharmacology to the development of animal models of cognition relating to schizophrenia. In parallel, academic collaborations included; a foray into chronobiology in association with Tony Harmar and Mick Hastings exploring the role of the VPAC2 receptor and the development of a battery of mouse cognitive tasks to complement those available for rats.
Hugh moved to Organon, latterly Schering-Plough seven years ago and now heads a team providing in vivo expertise in support of the Company’s psychiatry and neuroscience pipe lines from early Lead Finding to Registration. These include late phase projects such as; Bridion – a neuromuscular blocking reversal agent, Asenapine – a novel psychotherapeutic, and AMPA and Glycine modulatory approaches. Earlier in development work is focused on manipulations to the HPA axis, cannabinoids and glutamate as well as a number of highly novel approaches. In particular, he has a keen interest in improving our animal models of psychiatric disease. As such he has established a network of academic collaborations in the UK and Europe to help stimulate innovative approaches. The goals being three fold; to develop pre-clinical approaches that are truly related to the processes perturbed in psychiatric illness, to improve our ability to validate novel targets and find molecules of real value, and finally to allow a better translation of projects from the pre-clinical to clinical phase.
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