Heavy alcohol consumption is associated with a decline in cognitive ability with age and may contribute to neurodegenerative disease such as Alzheimer's disease (AD). However, the causal mechanisms underlying this association are essentially unknown. One of the major readouts of AD is a buildup of neurotoxic amyloid beta-peptide (A?) in the brain. The integral membrane enzyme ?-secretase cleaves amyloid precursor protein (APP), which in some conditions is converted to A? after proteolysis. ?-secretase also cleaves Notch, a highly conserved cell-signaling receptor. Several recent studies suggest that enhanced Notch signaling is instrumental in AD-associated neurodegeneration. Data derived from the parent R01 for this supplement suggests that alcohol directly activates Notch signaling in memory circuits in the Drosophila brain. Using a Drosophila model of AD, we will determine whether alcohol causally exacerbates AD pathology through the highly-conserved Notch signaling pathway. We hypothesize that alcohol increases Notch activity, which leads to enhanced AD pathology. Thus, genetically decreasing Notch activity will nullify the effects of alcohol on AD pathology. Together, this data may provide new pharmacological targets for developing more effective treatments for AD.

Public Health Relevance

Heavy alcohol consumption is associated with a decline in cognitive ability with age and may contribute to neurodegenerative disease such as Alzheimer?s disease (AD); however, the causal mechanisms underlying this association are essentially unknown. Using a Drosophila model of AD, we will determine whether alcohol causally exacerbates AD pathology through the highly-conserved Notch signaling pathway. This may provide new targets for developing more effective treatments for AD.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
3R01AA024434-03S1
Application #
9716929
Study Section
Neurotoxicology and Alcohol Study Section (NAL)
Program Officer
Cui, Changhai
Project Start
2016-08-01
Project End
2021-07-31
Budget Start
2018-09-15
Budget End
2019-07-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Brown University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
001785542
City
Providence
State
RI
Country
United States
Zip Code
Petruccelli, Emily; Kaun, Karla R (2018) Insights from intoxicated Drosophila. Alcohol :
Nunez, Kavin M; Azanchi, Reza; Kaun, Karla R (2018) Cue-Induced Ethanol Seeking in Drosophila melanogaster Is Dose-Dependent. Front Physiol 9:438
Petruccelli, Emily; Feyder, Michael; Ledru, Nicolas et al. (2018) Alcohol Activates Scabrous-Notch to Influence Associated Memories. Neuron 100:1209-1223.e4