Investigating the Effects of Antide Treatment on the Preventative and Restorative Effects of Hippocampal Damage in Alzheimer’s Disease Rats
Location
King Building 343
Document Type
Presentation
Start Date
4-28-2017 4:30 PM
End Date
4-28-2017 5:50 PM
Abstract
After menopause women are more likely to develop Alzheimer’s disease (AD) than men. This predisposition is due to the drop in estrogens (E) that occurs following menopause. This drop in neuroprotective estrogens is accompanied by a rise in luteinizing hormone (LH). Elevated LH has been associated with decreased performance on cognitive tasks as well as loss of memory, and the development of AD. Prior work in the Thornton Lab has utilized Antide, a GnRH antagonist, to decrease the production of LH in an AD rat model. By infusing small doses of neurotoxins Beta-Amyloid and ibotenic acid into the dorsal hippocampus, a brain region critical for learning and memory, we are able to produce a rat model, displaying early stages of AD. We are presently testing whether lowering LH with Antide can decrease cognitive defects and/or damage to neurons when administered either prior to or following neurotoxin infusion. We will use immunocytochemistry for NeuN, a marker for neurons, to examine the number of neurons in animals that received Antide treatment just before or following neurotoxin infusion to investigate the potential for preventative as well as restorative effects of Antide treatment on memory and cell death associated with AD. Although E has neuroprotective effects, E replacement therapies heighten the risks of ovarian, breast, and other forms of cancer. If targeting LH effectively reduces the neuronal damage associated with AD, this could introduce a safer way to treat post-menopausal women in either a preventative or restorative manner to combat early signs of AD.
Keywords:
Alzheimer's disease, estrogens, spatial memory, hippocampus, luteinizing hormone
Recommended Citation
Curley, Emily, "Investigating the Effects of Antide Treatment on the Preventative and Restorative Effects of Hippocampal Damage in Alzheimer’s Disease Rats" (04/28/17). Senior Symposium. 16.
https://digitalcommons.oberlin.edu/seniorsymp/2017/presentations/16
Major
Neuroscience
Award
Robert Rich Student Research Grant
Advisor(s)
Jan Thornton, Neuroscience
Project Mentor(s)
Janice Thornton, Neuroscience
April 2017
Investigating the Effects of Antide Treatment on the Preventative and Restorative Effects of Hippocampal Damage in Alzheimer’s Disease Rats
King Building 343
After menopause women are more likely to develop Alzheimer’s disease (AD) than men. This predisposition is due to the drop in estrogens (E) that occurs following menopause. This drop in neuroprotective estrogens is accompanied by a rise in luteinizing hormone (LH). Elevated LH has been associated with decreased performance on cognitive tasks as well as loss of memory, and the development of AD. Prior work in the Thornton Lab has utilized Antide, a GnRH antagonist, to decrease the production of LH in an AD rat model. By infusing small doses of neurotoxins Beta-Amyloid and ibotenic acid into the dorsal hippocampus, a brain region critical for learning and memory, we are able to produce a rat model, displaying early stages of AD. We are presently testing whether lowering LH with Antide can decrease cognitive defects and/or damage to neurons when administered either prior to or following neurotoxin infusion. We will use immunocytochemistry for NeuN, a marker for neurons, to examine the number of neurons in animals that received Antide treatment just before or following neurotoxin infusion to investigate the potential for preventative as well as restorative effects of Antide treatment on memory and cell death associated with AD. Although E has neuroprotective effects, E replacement therapies heighten the risks of ovarian, breast, and other forms of cancer. If targeting LH effectively reduces the neuronal damage associated with AD, this could introduce a safer way to treat post-menopausal women in either a preventative or restorative manner to combat early signs of AD.
Notes
Session III, Panel 20 - Water | Health
Moderator: Marcelo Vinces, Director, Center for Learning, Education, and Research (CLEAR) in the Sciences; Associate Director, Center for Teaching Innovation and Excellence (CTIE)