Zeni Shabani

Picture of Zeni Shabani

Assistant Professor

Email 
shabanis@gvsu.edu

Office 
224 Henry Hall

Phone 
616-331-3229

Office Hours 

MWRF: 10-11a

COURSES TAUGHT

BMS 250 - Anatomy & Physiology I

EDUCATION

Ph.D. (Neurobiology & Behavior), Georgia State University, 2009
B.S. (Microbiology), Oklahoma State University, 2001

RESEARCH INTERESTS

My broad research interests are on genetic risks of drug use disorders and the associated neural substrates that influence specific aspects of drug use such as, drug taking, seeking and relapse.  Methamphetamine (MA) use like that of opioids is a widespread problem in US and is highly addictive drug with devastating consequences to the individual and society at large.  My research program explores binge MA use, MA withdrawal and relapse using a genetic mouse model for high and low MA intake.  The main aim of my research is to identify and explore drugable targets for future development of therapeutic interventions.  Extensive work by my collaborator at Oregon Healt & Science University, and her group, who developed this mouse model system have identified at least two quantitative trait loci (QTL) associated with MA intake, located in chromosome 10 and X. In particular, two gene candidates located in the chromosome 10 QTL, namely a u-opioid receptor and a g-protein coupled receptor, known as trace-amine associated receptor TAAR1, seem to play an important role in the MA intake, and other correlated traits.  Correlated behavioral traits of interest involve: sensitivity to rewarding and aversive effects through procedures such as, conditioned place preference, conditioned place aversion, conditioned taste aversion; drug reinforcement such as the operant self-administration paradigms; drug withdrawal in form of anxiety and depression-like symptoms tests, such as, zero or plus-maze, forced-swim, and tail-suspension. Recent pharmacological manipulations of TAAR1 receptor in a number of these experiments seem to support the hypothesis that TAAR1 receptor plays an important protective role in MA use and therefore is a prime drugable target to explore in the future.  In sum my lab pursues neuroscience related questions mostly at the behavioral genetics, physiological, neurochemical, and pharmacological level.