Neural circuitry mechanisms underlying maladaptive reward memories in drosophila

Active Project Grant Awarded

Award ID
R15AA031562
Recipient
Awarding agency
Obligated
$431,918

Award facts

Assistance listing
93.273 Alcohol Research Programs
Completion date 71% complete
Place of performance
Rhode Island, USA

Award details come from USAspending.gov.

About this award

This federal Project Grant award from the National Institute on Alcohol Abuse and Alcoholism (CFDA 93.273 - Alcohol Research Programs) provides $431,918 in funding to Bryant University for a research project focused on understanding the neural circuitry mechanisms underlying maladaptive reward memories related to alcohol addiction. The research aims to use the genetic tractability of the Drosophila melanogaster model organism to investigate how alcohol disrupts memory circuit activity and drives persistent, maladaptive reward-seeking behavior. Specific objectives include capturing changes in dopamine neuron dynamics during alcohol-odor associative learning, determining if activation of dopamine neurons alone can induce maladaptive memories, and examining the role of downstream brain regions in modulating alcohol reward memories. This 3-year project, with an award date of September 17, 2024, is expected to provide insights into the neural circuit principles underlying alcohol addiction in mammals that could inform the development of more effective treatment approaches.

Description

Abstract
Alcohol addiction constitutes one of the most serious public health problems worldwide. According to the CDC, the total economic cost of excessive alcohol use is estimated to be $249 billion. Despite its devastating impact, there are few effective treatments. Neural circuit based approaches to treat addiction provide a powerful opportunity to develop more specific and effective treatments. However, circuit complexity is a significant obstacle to a comprehensive understanding of the mechanisms by which memory circuits are altered to create enduring preferences for alcohol associated cues. The current proposal will take place at bryant university, a primarily undergraduate institution, and will capitalize on the genetic tractability of drosophila melanogaster and precise neurogenetic tools available to interrogate how identified memory circuits are altered by alcohol and why alcohol associated memories are so resistant to change. Although only 100,000 neurons comprise the central nervous system of drosophila, the neural circuitry underlying reward and addiction is remarkably complex and similar to mammals. Like mammals, drosophila show robust preference for cues associated with alcohol intoxication that persist in the face of aversive consequences. Studies proposed here will capitalize on established and newly developed neurogenetic tools that allow for the precise manipulation of individual neurons and visualization of circuit activity. Doing so will enable US to test the hypothesis that alcohol disrupts memory circuit activity and drives maladaptive reward seeking by engaging significantly more dopamine neurons during acquisition. Specifically, we will use a combination of optogenetics, thermogenetics, and two-photon microscopy to capture the precise changes in dopamine neural dynamics while drosophila learn to associate odor cues with alcohol intoxication. Additionally, we will determine if alcohol-independent activation of dopamine neurons is sufficient to induce maladaptive memories for natural rewards. Finally, we will investigate the role of recently identified downstream regions of the fan-shaped body in modulating alcohol reward memories to understand the stability and persistence of these memories. We expect that extracellular dopamine levels and number of recruited dopamine neurons will significantly increase across alcohol exposures and this increase is sufficient to drive maladaptive reward seeking behavior. Further, we predict that downstream convergent regions play a critical role in behavioral flexibility and disruption to these functional connections results in memories that lack flexibility and drive maladaptive reward seeking. Ultimately, understanding general circuitry principles described first in drosophila will provide insight to how alcohol CO-opts mammalian circuits to create enduring preference for alcohol and drive maladaptive choice. An area grant is essential to continue our efforts in exposing students to hands-on meritorious research, providing superior research experiences, and strengthening the research environment at bryant university, thereby enabling more students to participate.

Quick answers

Who received award R15AA031562?

R15AA031562 was awarded to Bryant University by National Institute on Alcohol Abuse and Alcoholism (National Institutes of Health) on September 17, 2024.

How much is award R15AA031562 worth?

$431,918 has been obligated on R15AA031562.

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