The goal of this proposal is to test whether reactivating dormant or depressed orexin circuits can reduce endoplasmic reticulum stress (ERS), improve neuroprotection and cognitive performance in mouse models of neurodegeneration. The long-term goal of this work is to identify a novel therapeutic strategy for improving cognition in neurodegenerative diseases such as narcolepsy, Parkinson's disease, Alzheimer's disease, and Huntington's disease. These diseases have differing causes and etiology, but loss of a specific subset of hypothalamic cells, the orexin-containing neurons, occurs in all. Hypothalamic orexin neurons project to the hippocampus, a brain area important to learning and memory. Orexin action in the hippocampus improves cognitive performance and was recently shown to protect against neurodegeneration. Neuroprotective signals are reduced and ERS is activated during neurodegenerative disease, suggestive of a common underlying mechanism. Together, these data suggest reduced orexin signaling in neurodegenerative disease may reduce neuroprotection and increase ERS, causing further neurodegeneration, and cognitive decline. A necessary step in determining whether therapeutic intervention can counter the effect of orexin loss in neurodegenerative disease is to test whether orexin-responsive pathways in the brain can be reactivated. The orexin/ataxin-3 mouse, first developed to study orexin loss in narcolepsy, is a transgenic model in which orexin neurons specifically and gradually decline during development, and cognitive processing deteriorates. Yet our preliminary data show that orexin receptor levels remain intact in young and old mice, and that stimulating these receptors with orexin restores cognition. These novel exciting data provide proof-of- concept that stimulation of orexin pathways, even when orexin neurons are lost, can be used as a strategy to improve cognition. We plan to determine the full potential of this strategy in the orexin ataxin (O/A3) mouse and in the alpha synucleinopathy mouse, a classic model of Parkinson disease. We will examine whether increasing hippocampal orexin tone rescues the cognitive deficit noted in these animals. We also have an established designer drug orexin activation model (DREADD), which is a transgenic mouse in which orexin neurons have been modified to be specifically activated by an otherwise metabolically inert drug. These mice will be crossed with the orexin ataxin and the Parkinson's disease (alpha synucleinopathy) mouse to determine whether stimulating remnant orexin neurons can also rescue dormant orexin-responsive pathways. To gain understanding of the underlying basis for observed cognitive changes resulting from manipulation of orexin pathways, we will measure markers of neuroprotection and ERS in hippocampus. Our overall hypothesis is that orexin promotes neuroprotection and reduces ERS, and that reactivating orexin-responsive pathways will ameliorate neurodegeneration-related cognitive disturbances. To test this, we will determine whether orexin replacement therapy and orexin neuron stimulation improves cognitive performance, markers of neuroprotection and ERS in 1) mice with mild, moderate, and severe orexin neuron loss; and 2) in a classic model of PD. We predict that enhancing orexin tone will improve cognitive performance by improving neuroprotection and decreasing ERS. The results of these studies will determine if orexin rescue is an important strategy in countering cognitive decline, and could ultimately provide a therapeutic pathway to target in neurodegenerative disease.

Public Health Relevance

Neurodegenerative diseases such as Alzheimer's (AD) and Parkinson's (PD) are major health concerns for Veterans. Obesity, increased age, and traumatic brain injury (TBI) are all risk factors contributing to neurodegeneration, placing Veterans at higher risk than general population. AD, PD, and TBI result in the loss of neurons producing the hormone orexin. Studies show this hormone protects against neurodegeneration, promotes healthy body weight, and may improve cognition. Orexin loss may thus result in reduced ability to defend against the biochemical processes driving neurodegeneration. The ability to 're-awaken' dormant orexin circuits by increasing orexin signaling represents a therapeutic intervention that could boost endogenous neuroprotective mechanisms and counteract some comorbidities of neurodegenerative disease. We propose a series of studies to test this theory, with a long-term goal of developing interventions aimed at slowing or preventing progression of neurodegenerative diseases.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
1I01BX003004-01A2
Application #
9143208
Study Section
Neurobiology A (NURA)
Project Start
2016-04-01
Project End
2020-03-31
Budget Start
2016-04-01
Budget End
2017-03-31
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Minneapolis VA Medical Center
Department
Type
DUNS #
071774624
City
Minneapolis
State
MN
Country
United States
Zip Code
55417
Mavanji, Vijayakumar; Butterick, Tammy A; Duffy, Cayla M et al. (2017) Orexin/hypocretin treatment restores hippocampal-dependent memory in orexin-deficient mice. Neurobiol Learn Mem 146:21-30