On a daily basis, sensory stimuli acquire learned values that inform our essential behaviors. Understanding the neural substrates for the emotional associations of stimuli, sometimes referred to as valence, will yield important insights into a wide range of human conditions. This is especially the case for neurodegenerative disorders, including Alzheimer's disease (AD), wherein aberrant assignments of odor valence may impact ingestive behaviors and thus entail malnutrition and subsequent bodily wasting disorders ? further worsening progression of the disease. In the mammalian olfactory system, second order neurons in the olfactory bulb (OB) distribute odor information into several secondary structures, including the olfactory tubercle (OT) and piriform cortex (PCX). Odor information at this stage is shaped and later transmitted into tertiary structures involved in reward, emotion, and learning. The present proposal seeks to assess the impact of AD pathogenesis on the representation of odor valence within the olfactory system and the display of valence-based behaviors. Experiments will be performed taking advantage of a well-established accelerated mouse model of AD, in the context of odor-guided behaviors, and in some cases with simultaneous neural recordings. Using this approach, we will determine whether odor valence is aberrantly reflected across olfactory cortex neural ensembles in the context of AD (Aim 1). Next, we will utilize unbiased, quantitative behavioral and neuroanatomical methods to provide evidence for a relationship between the magnitude of specific components of AD pathology within the OB, OT, and PCX, and the display of odor hedonic behaviors (Aim 2). Together, these investigations will provide much needed information regarding mechanisms underlying reports for diminished odor hedonics in persons with AD.

Public Health Relevance

The results of this project will yield insights into fundamental aspects of sensory information processing in the brain, how sensory information can acquire meaning, and mechanisms which impact these critical features in the context of Alzheimer's disease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
3R01DC014443-04S2
Application #
9706194
Study Section
Somatosensory and Chemosensory Systems Study Section (SCS)
Program Officer
Sullivan, Susan L
Project Start
2015-07-01
Project End
2020-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Florida
Department
Pharmacology
Type
Schools of Medicine
DUNS #
969663814
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Rey, Nolwen L; Wesson, Daniel W; Brundin, Patrik (2018) The olfactory bulb as the entry site for prion-like propagation in neurodegenerative diseases. Neurobiol Dis 109:226-248
Carlson, Kaitlin S; Whitney, Meredith S; Gadziola, Marie A et al. (2016) Preservation of Essential Odor-Guided Behaviors and Odor-Based Reversal Learning after Targeting Adult Brain Serotonin Synthesis. eNeuro 3:
Xiong, Angeline; Wesson, Daniel W (2016) Illustrated Review of the Ventral Striatum's Olfactory Tubercle. Chem Senses 41:549-55
Gadziola, Marie A; Wesson, Daniel W (2016) The Neural Representation of Goal-Directed Actions and Outcomes in the Ventral Striatum's Olfactory Tubercle. J Neurosci 36:548-60
Xia, Christina Z; Adjei, Stacey; Wesson, Daniel W (2015) Coding of odor stimulus features among secondary olfactory structures. J Neurophysiol 114:736-45
Gadziola, Marie A; Tylicki, Kate A; Christian, Diana L et al. (2015) The olfactory tubercle encodes odor valence in behaving mice. J Neurosci 35:4515-27