Drew University Library : University Archives : Theses and Dissertations
    
author Alexandra Greulich
title Bed Nucleus of the Stria Terminalis: Potential Odor Responsivity and Cannabidiol Modulation
abstract Anxiety disorders exist at a high prevalence in the United States. Current research examining anxiety-related brain regions, as well as studies on drugs that alter the activity in these regions, contribute to improvements of therapies for the disorder. Recently, studies looking characterizing the activity of the bed nucleus of the stria terminalis (BNST) have determined that this region plays a key role in sustained anxiety and contextual fear, as opposed to the well defined amygdala, which is primarily involved in phasic fear. Further, presentation of predator odors have induced anxiety behaviors in animal models, likely because of the non-volatile processing projections from the vomeronasal organ (VNO) to accessory olfactory bulb (AOB), medial amygdala (MeA), and finally, the BNST. In the present study, electrophysiological methods were used to search for baseline and odor-elicited activity in the BNST to further confirm this region's role in anxiety, as well as test the potential for this methodology to be an efficient tool in studying anxiety. It was hypothesized that the BNST would present with baseline activity in the anesthetized rat and have non-volatile odor (2-heptanone) elicited activity, but not volatile odor-elicited activity. Ultimately, there was sufficient baseline activity but no odor-elicited activity to either odor types. Previously obtained data recorded in the olfactory tubercle (OT) were also analyzed to provide a comparison for baseline and odor-elicited activity. The OT had a similar baseline frequency but, in contrast, were responsive to isoamyl acetate, 2-heptanone, propyl butyrate, and 1,7-octadiene. Additionally, intracerebroventricular doses of cannabidiol (CBD; 1, 2, and 3 µL) were presented to the rats while being presented with odors to test the if drug's potential therapeutic effects may be enacted through altering the activity in the BNST. It was hypothesized that CBD would change the activity of both baseline and odor-elicited activity; however, since there was no odor-elicited activity, only the effect on baseline activity could be observed. CBD did not consistently change baseline activity. One of three cells presented with 1 µL of CBD demonstrated a change in activity that occurred at an appropriate time relative to drug administration. Overall, the potential for using this model and drug likely remains in question due to the potential areas of improvement including altering the mechanism of odor or drug introduction as well as fine tuning existing methods.
school The College of Liberal Arts, Drew University
degree B.A. (2019)
advisor Graham Cousens
committee Christopher Medvecky
Sandra Keyser
full textAGreulich.pdf