The hippocampus is a brain structure critical for learning, memory, and emotional regulation, whose function is disrupted in neurological and psychiatric disorders including Alzheimer disease (AD) and posttraumatic stress disorder (PTSD). To function properly, the hippocampus requires neurogenesis, the continual division of new neurons and the integration of these neurons into the existing circuitry. The survival and differentiation of these new neurons is highly dependent on experience. Exposure to enriched environments (EEs), consisting of large arenas with objects to explore and opportunities for learning and exercise, leads to increased hippocampal neurogenesis, and concomitant decreases in anxiety- and depression-like behaviors and improved performance on memory tests. However, disentangling the effects of exercise versus enrichment on hippocampal neurogenesis has proven challenging. In the modern age of technology, it is natural to wonder how computer-based virtual reality (VR) may influence the structure and function of the hippocampus, and in particular, how it may be used to improve memory and emotional control in healthy and pathological states. VR training has demonstrated clinical benefit in slowing age-related cognitive decline and in the diagnosis and treatment AD and PTSD. Yet, little remains known about how immersive VR experiences influence the physiology and network activity of the hippocampus. We developed a novel, programmable, and interactive VR system for experimental mice that allows us to investigate the effects of VR exposure on the brain and behavior. Using this system, I found in my preliminary study that mice exposed to an enriched virtual environment (EVE) exhibited increased hippocampal activation and neurogenesis, as compared to mice exposed to an impoverished virtual environment (IVE). One advantage of my system is the capability to build complex virtual worlds in which mice can explore in a tightly exercise- controlled fashion. In this proposal, I seek to determine 1) whether virtual spatial navigation requires hippocampal neurogenesis; 2) whether the complexity of, and exploration time within a VR environment impact hippocampal neurogenesis, memory function and anxiety-like behavior; and 3) how activity of mature dentate granule cells of the hippocampal circuit modulates neurogenesis in an EVE context. Understanding how experience shapes the neural pathways underlying learning and memory is crucial to the eventual development of non-pharmacological interventions for diseases that affect the hippocampus, and normal age-related cognitive decline. Results from this study will provide insight into the future development of computer programs and web-based applications that can prevent and treat age-related cognitive decline, and hold promise for the treatment of a variety of neuropsychiatric disorders.

Public Health Relevance

Environmental enrichment has demonstrated many beneficial effects in terms of memory improvement and anxiety reduction, functions that rely importantly upon the hippocampus. In addition, exposure to enriched environments (EEs) increases hippocampal neurogenesis, the continuous division and integration of new neurons into its existing circuitry that is important for the hippocampus to function. Teasing apart the aspects of EEs that contribute to their effects on hippocampal neurogenesis and behavior has been complicated due to the many factors that comprise EEs, including learning, exercise, and different sensory experiences. Using a novel virtual reality (VR) system for experimental mice that we have developed, I will study the effects of virtual EE exposure in a more controlled setting, examining changes in hippocampal physiology and function at the cellular, network, and behavioral levels.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
1F30MH110103-01A1
Application #
9251453
Study Section
Special Emphasis Panel (ZRG1-F01B-N (20)L)
Program Officer
Driscoll, Jamie
Project Start
2016-09-01
Project End
2020-08-31
Budget Start
2016-09-01
Budget End
2017-08-31
Support Year
1
Fiscal Year
2016
Total Cost
$35,116
Indirect Cost
Name
State University New York Stony Brook
Department
Pharmacology
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Kirschen, Gregory W; Ge, Shaoyu; Park, Il Memming (2018) Probability of viral labeling of neural stem cells in vivo. Neurosci Lett 681:17-18
Kirschen, Gregory W; Kéry, Rachel; Ge, Shaoyu (2018) The Hippocampal Neuro-Glio-Vascular Network: Metabolic Vulnerability and Potential Neurogenic Regeneration in Disease. Brain Plast 3:129-144
Rao, Sneha; Kirschen, Gregory W; Szczurkowska, Joanna et al. (2018) Repositioning of Somatic Golgi Apparatus Is Essential for the Dendritic Establishment of Adult-Born Hippocampal Neurons. J Neurosci 38:631-647
Kirschen, Gregory W; Kéry, Rachel; Liu, Hanxiao et al. (2018) Genetic dissection of the neuro-glio-vascular machinery in the adult brain. Mol Brain 11:2
Kirschen, Gregory W; Xiong, Qiaojie (2017) Primary cilia as a novel horizon between neuron and environment. Neural Regen Res 12:1225-1230
Kirschen, Gregory W; Shen, Jia; Tian, Mu et al. (2017) Active Dentate Granule Cells Encode Experience to Promote the Addition of Adult-Born Hippocampal Neurons. J Neurosci 37:4661-4678
Kirschen, Gregory W; Liu, Hanxiao; Lang, Tracy et al. (2017) The radial organization of neuronal primary cilia is acutely disrupted by seizure and ischemic brain injury. Front Biol (Beijing) 12:124-138