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CHRISTOPHER R. BISHOP
Assistant Professor of Psychology
Ph.D., Wayne State University
Post-doctoral training: Wayne State University School of Medicine
Area: Behavioral Neuroscience
E-mail: cbishop@binghamton.edu
Phone: 607-777-3410
Office: Science IV, Room 363 

Curriculum vita

Professional Activities: Member of the Society for Neuroscience, the Movement Disorders Society and the Center for Development and Behavioral Neuroscience

Research Interests: Parkinson's Disease, Neuroplasticity, Drug Development.

Research Description: Movement is an ancient and basic function that is integral to the survival of the individual and species. As such, disorders of movement have a profound impact upon all facets of life. One of the most common movement disorders is Parkinson's disease, a neurodegenerative disorder that compromises dopaminergic areas of the brain rendering the individual unable to initiate, coordinate and execute movement. By employing an animal model of Parkinson's disease and a combination of behavioral, neurochemical and neuroanatomical techniques our laboratory examines the role of various neurotransmitters and neurocircuits responsible for this debilitating disorder. As importantly, we explore pharmacological targets within the brain that may aid in the development of more efficacious treatment for the Parkinsonian patient. Current projects, funded by the National Institute of Neurological Disease and Stroke investigate neuroplasticity in the brain serotonin system that may provide a novel target for the reduction of parkinsonian symptoms and side effects that occur as a result of chronic drug therapy.

Philosophy of Graduate Training: My goal as a mentor is to provide students with the necessary tools, both theoretical and technical, to become productive independent researchers. Throughout the course of graduate curriculum and laboratory experience, students will have the opportunity to develop a unique scientific approach and master a number of behavioral, neurochemical and neuroanatomical techniques that will lead to the design, execution and communication of sound and innovative research questions.

Selected Publications:

Barnum, C.J., Eskow, K.L., Dupre, K.B., Blandino, P., Deak, T and Bishop C. (2008). Exogenous corticosterone reduces L-DOPA-induced dyskinesia in the hemiparkinsonian rat: role for interleukin- 1ß. Neuroscience (in press).

Dupre, K.B., Eskow, K.L., Steiniger, A., Klioueva, A., Negron, G.E., Lormand, L., Park, J.Y. and Bishop C. (2008). Coincident 5-HT1A receptor stimulation and NMDA receptor antagonism reduces L-DOPA-induced dyskinesia but enhances rotational behaviors in the hemiparkinsonian rat. Psychopharmacology (Epub ahead of print).

Dupre, K.B., Eskow, K.L., Negron, G. and Bishop, C. (2007). The differential effects of 5-HT1A receptor stimulation on dopamine receptor-mediated abnormal involuntary movements and rotations in the hemiparkinsonian rat. Brain Research 1158, 135-143.

Eskow, K.L., Gupta, V., Alam, S., Park, J. and Bishop, C. (2007). Acute and chronic Buspirone reduces L-DOPA-induced dyskinesia in the 6-hydroxydopamine-lesioned rat via 5-HT 1A receptor stimulation. Pharmacology Biochemistry and Behavior 87(3), 306-314.

Bishop, C., Taylor , J.L., Eskow, K., Park, J. and Walker , P.D. (2006). MDMA and Fenfluramine reduce L-DOPA-induced dyskinesia in the 6-hydroxydopamine-lesioned rat via 5-HT 1A receptor stimulation. European Journal of Neuroscience 23, 2669-2676.  

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