The etiology of ischemic brain injury remains elusive. Studies of the mechanism(s) of injury during hypoxia and ischemia have faced three major limitations in the past. First, it has been difficult to measure some of the putative etiological factors with adequate sensitivity and temporal resolution. Either the sensors do not exist or they do not function well in the hypoxic environment in live tissue. Second, the experimental conditions have not mimicked brain ischemia effectively. Finally, studies of the effects of hypoxia in intact animals have often been limited to analyses of behavior and the anatomical extent of tissue damage after the injury rather than focusing on the activity of mediators of injury and repair as they evolve during the actual ischemic insult. As a result, the mediators of injury in reduced preparations (e.g., glutamate, lactate) have not been studied extensively in intact animals. To address these limitations, we have the following aims: 1: Develop and characterize novel electrochemical biosensors for glutamate and lactate based on metal oxide technology so that they work in a low oxygen environment. 2: Test the biosensors in the middle cerebral artery occlusion model of ischemic brain injury in intact animals to determine the temporal profile of changes in lactate and glutamate. The new enzyme sensor design will expand the arsenal of accessible electrochemical probes for in vivo measurement of glutamate and lactate, and provide new methods for studying the neurobiology of these neurotransmitters in hypoxic conditions. This research will facilitate study and further fundamental understanding of glutamate and lactate neurotransmission in a variety of neurological disorders in which oxygen is a restrictive factor.

Public Health Relevance

This project will develop, optimize and translate into clinical practice a novel sensing technology for in vivo monitoring of key analytes associated with neural signaling and function during hypoxia (glutamate and lactate). This technology will provide real-time assessment of the changes in these neurological factors in intact awake animals and provide mechanistic answers to fundamental questions related to the biochemical and cellular events involved in vivo in conditions of oxygen deprivation. These studies are important and have relevance for human health because tissue oxygen levels vary in many diseases, and the role of the mediators of injury like lactate and glutamate in hypoxic conditions is not well understood.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS078738-02
Application #
8413003
Study Section
Neurotechnology Study Section (NT)
Program Officer
Ludwig, Kip A
Project Start
2012-03-01
Project End
2015-02-28
Budget Start
2013-03-01
Budget End
2015-02-28
Support Year
2
Fiscal Year
2013
Total Cost
$187,200
Indirect Cost
$29,369
Name
Clarkson University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041590993
City
Potsdam
State
NY
Country
United States
Zip Code
13699
Ozel, Rýýfat Emrah; Ispas, Cristina; Ganesana, Mallikarjunarao et al. (2014) Glutamate oxidase biosensor based on mixed ceria and titania nanoparticles for the detection of glutamate in hypoxic environments. Biosens Bioelectron 52:397-402