Faculty Advisor

Erica Holliday

Faculty Advisor

Kathryn A. Cunningham

Location

East and Center Ballrooms

Start Date

29-3-2017 12:00 PM

End Date

29-3-2017 2:00 PM

Session

Session 2

Session Topic

Poster

Abstract

Cocaine use disorder (CUD) affects 17 million people worldwide. The success in recovery from CUD is challenged by vulnerability to relapse driven in large part by cue reactivity (sensitivity to cues previously linked with drug-taking experience) and craving. Recently, the Cunningham group has demonstrated that the 5-HT2A receptor (5-HT2AR) and the 5-HT2C receptor (5-HT2CR) have oppositional effects on cue reactivity. Specifically, 5-HT2CR agonists and 5-HT2AR antagonists reduce cue reactivity in cocaine self-administration supporting the idea of that these two receptors act in opposition to control behaviors related to CUD. Previous work has demonstrated that higher expression of the 5-HT2AR coupled with lower expression of the 5-HT2CR in the medial prefrontal cortex (mPFC) is associated with heightened cue reactivity following a period of abstinence. In addition to the mPFC, the hippocampus is another key brain region that plays a critical role in the development of drug-cue associations. It is currently unknown if the expression patterns of the 5-HT2AR and the 5-HT2CR are different along the dorsal-ventral axis of the hippocampus. Given the functional differences between the dorsal (dHipp) and ventral hippocampus (vHipp), (i.e. the dHipp regulates cognitive functions and vHipp regulates mood and anxiety), we tested the hypothesis that there would be an increase in 5-HT2AR in the dHipp and an increase of the 5-HT2CR in the vHipp. We used immunohistochemistry methods to detect 5-HT2AR and 5-HT2CR expressions in the hippocampus in fixed rat brains. Our results indicate that vulnerability to relapse could be driven by altered interactions of the 5-HT2CR and the 5-HT2AR within the hippocampus formation.

Comments

**Abstract Only**

File Type

Poster

Included in

Psychology Commons

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Mar 29th, 12:00 PM Mar 29th, 2:00 PM

The Expression of 5- HT2aR And The 5-HT2cR In The Dorsal And Ventral Hippocampus

East and Center Ballrooms

Cocaine use disorder (CUD) affects 17 million people worldwide. The success in recovery from CUD is challenged by vulnerability to relapse driven in large part by cue reactivity (sensitivity to cues previously linked with drug-taking experience) and craving. Recently, the Cunningham group has demonstrated that the 5-HT2A receptor (5-HT2AR) and the 5-HT2C receptor (5-HT2CR) have oppositional effects on cue reactivity. Specifically, 5-HT2CR agonists and 5-HT2AR antagonists reduce cue reactivity in cocaine self-administration supporting the idea of that these two receptors act in opposition to control behaviors related to CUD. Previous work has demonstrated that higher expression of the 5-HT2AR coupled with lower expression of the 5-HT2CR in the medial prefrontal cortex (mPFC) is associated with heightened cue reactivity following a period of abstinence. In addition to the mPFC, the hippocampus is another key brain region that plays a critical role in the development of drug-cue associations. It is currently unknown if the expression patterns of the 5-HT2AR and the 5-HT2CR are different along the dorsal-ventral axis of the hippocampus. Given the functional differences between the dorsal (dHipp) and ventral hippocampus (vHipp), (i.e. the dHipp regulates cognitive functions and vHipp regulates mood and anxiety), we tested the hypothesis that there would be an increase in 5-HT2AR in the dHipp and an increase of the 5-HT2CR in the vHipp. We used immunohistochemistry methods to detect 5-HT2AR and 5-HT2CR expressions in the hippocampus in fixed rat brains. Our results indicate that vulnerability to relapse could be driven by altered interactions of the 5-HT2CR and the 5-HT2AR within the hippocampus formation.

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