Research Director

Dr. W.T. O'Connor

Curriculum vitae

Name

Personal Details

Current Posts and Periods held

Institution

Positions Held

Educational Qualifications

Supervisory Role

Fellowship Awards

Research Awards

Professional

Invited Speaker

  • Sensors for Brain Mapping, Lund, Sweden. 2000.
  • 12th ECNP Congress, Brussels, Belgium, 2000.
  • 8th Int. Conference on In Vivo Methods, Stoney Brook, NY, USA.1999.
  • 21st CINP Congress, Glasgow, UK.1998.
  • Microdialysis user group meeting, BAS, Riverside, Cheshire, UK 1998.
  • 11th ECNP Congress, Paris. France. 1998.
  • Erasmus-Tempus Programme, University of East London, UK 1996
  • 6th Int. Conference on In Vivo Methods, Nordweokerout, The Netherlands, 1999.
  • Publications

    Research Interests


    Recent findings indicate that the neural mechanisms of neurological and psychiatric disorders can be understood as dysfunctions in specific nerve circuits and their functions and dysfunctions can be influenced or altered by a variety of cognitive and pharmacological factors. I use microdialysis (via a specially constructed and very small artificial blood capillary) to study the chemistry of intact conscious brain and to investigate those nerve pathways and circuits implicated in motor and psychiatric disorders. This is achieved by studying the effect of selective monoamine, neuropeptide and amino acid receptor activation and blockade on the release of dopamine, GABA, glutamate and aspartate.
    Main interests include the functional neuroanatomy of pathways and circuits implicated in the aetiology and treatment of neurological and psychiatric disorders. Working mechanisms of antipsychotic and antidepresant drugs including their actions on monoamines, acetlycholine, neuropeptides, glutamate and GABA release in the brain. Application of the microdialysis technique to study the chemistry of intact conscious brain of normal and transgenic animals.
    Published findings include a behavioural, physiological and neurochemical investigation of the olfactory bulbectomized rat model of depression. Working mechanisms of antipsychotic and antidepressant drugs including their actions on monoamines, acetlycholine, neuropeptides, glutamate and GABA release in the central nervous system (CNS). application of the microdialysis technique to study the chemistry of intact conscious brain of normal and transgenic animals. The contributions of the motor cortex, nigrostriatal dopamine and the caudate putamen to skilled forelimb use in the rat. The role of central cholinergic systems on striatal dopamine release, feeding, sensorimotor behaviour, locomotor activity and spatial navigation in the rat. The role of dopamine, glutamate, neurotensin and cholecystokinin in the modulation of GABA release in the brain. The relation between mRNA expression and blockade (i.e.,mRNA antisense technology) on changes in GABA release in the brain. The role of intracelluar Na+, K+, Ca2+ and Mg2+ on the release of dopamine, GABA and glutamate in the CNS.
    Current studies include the investigation of schizophrenia as a disorder of brain circuitry. The effect of acute and chronic antipsychotic administration on dopamine, GABA and glutamate and aspartate release in the CNS. The influence of endogenous peptides e.g. neurotensin and cholecystokinin on the release of these substances in this experimental situation. The application of microdialysis to study dopamine, GABA and glutamte transmission in brain and spinal cord. The effect of vigilance enhancing drugs such as caffeine, amphetamine and modafinil on these neurotransmitters in the CNS.



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