Before starting my postdoctoral research at Princeton University, I worked primarily with whole-cell patch clamping in brain slices. Here is a summary of my most important research. Please see the Publications page for references.
Anticonvulsant effects of antidepressants
My PhD work showed that several antidepressants in the serotonin reuptake inhibitor (SSRI) class (such as Prozac) have properties that resemble those of some antiepileptic drugs (AEDs). I found that SSRIs blocked epileptic activity through modulation of sodium and potassium currents (common targets of AEDs) whereas their serotonergic actions were not involved. Through a detailed analysis of available preclinical data on the effects of SSRIs on seizures, I suggested that SSRIs may worsen some types of seizures and protect against others.
A treatment system for epilepsy
Together with Prof. John Reynolds and his team at the Department of Anatomy and Brain Health Research Centre at the University of Otago, New Zealand, I participated in the development of a new epilepsy treatment system. I designed, fabricated and tested a new brain slice chamber that allowed application of this technology during visualized patch clamp recording.
The neural basis of reward learning
As an undergraduate student in the Department of Physiology at the University of Otago, I worked with Prof. Brian Hyland and Prof. Allan Herbison, to investigate reward learning pathways in the brain using cFos immunohistochemistry and behavioral training. A few years later, I followed up on this interest in Prof. Ilana Witten's lab at Princeton, using optogenetics to study the role of thalamostriatal inputs in reward-related behaviors.