Paul Slesinger, PhD
- PROFESSOR | Neuroscience
Research Topics:Addiction, Biophysics, Electrophysiology, Neurophysiology, Neuroscience, Protein Trafficking & Sorting, Signal Transduction, Synaptic Plasticity
Paul Slesinger PhD is Lillian and Henry M. Stratton Professor of Neuroscience and Director of the Center for Neurotechnology and Behavior. Our long-term objective is to discover new drugs for treating addiction to drugs of abuse and alcohol. We focus on changes in neuronal excitability with drugs, and take a broad approach of combining structural biology, biochemistry, electrophysiology and behavior. Visit Paul Slesinger's Laboratory of Membrane Excitability & Disease for more details.
Multi-Disciplinary Training AreasNeuroscience [NEU], Pharmacology and Therapeutics Discovery [PTD]
BA, Reed College
PhD, University of California, San Francisco
Postdoctoral Fellow, University of California, San Francisco
NARSAD Independent Investigator Award
McKnight Technological Innovations in Neuroscience Award
Human Frontiers Science Program Young Investigator Grant
McKnight Scholars Award in Neuroscience
Alfred P. Sloan Research Fellow
II) Advancing novel techniques for elucidating neuropeptide signaling in the brain
Project: We are developing tools for measuring the real-time release of neuropeptides in freely behaving animals using new biosensors (i.e., CNiFERs) and custom-made Miniscopes. Project: We are developing nanovesicles engineered for photorelease of drugs in vivo in real-time.
I) Neural circuits underlying addiction – role of potassium channels.
Project: Investigating the structural and molecular determinants of GIRK channel gating and modulation. Project: Investigating the neuronal activity and neurotransmitter release in the reward circuitry during alcohol intake, using fiber photometry to measure fluorescence in freely moving animals that express genetically encoded calcium and neurotransmitter indicators. Project: Investigating the physiological roles of the GIRK channels in the brain disorders, and developing pharmacological tools to modulate GIRK channels in these disorders.
III) Human neuronal models of schizophrenia and alcohol use disorder
Project: Investigating the role of GIRK2 function in excitatory neurons in the context of alcohol use disorder, using hiPSC-derived neurons and a combination of electrophysiology, calcium imaging, and transcriptomic analysis. Project: Investigating the impact of the effects of polygenic alterations related to alcohol use disorder (AUD) on the human neuronal function using iPSC-derived excitatory neurons from control individuals and AUD patients.