Citation

Arrieta-Cruz I, Pfaff DW, Shelley DN. Exp. Neurol. 2007; 205(2): 449-460.

Affiliation

Laboratory of Neurobiology and Behavior, The Rockefeller University, Box 275, 1230 York Avenue, New York, NY 10021, USA. iarrieta@mail.rockefeller.edu

Copyright

(Copyright © 2007, Elsevier Publishing)

DOI

10.1016/j.expneurol.2007.03.005

PMID

17448465

PMCID

PMC2211732

Abstract

Diffuse brain damage following anoxia due to cardiac failure, drowning, carbon monoxide exposure or other accidents constitutes a major medical problem. We have created a novel mouse model using the breathing of pure nitrogen, followed by a recently developed assay that reflects an operational definition of generalized arousal. The operational definition is precise, complete, and leads to quantitative, physical measures in a genetically tractable animal. Exposure to pure nitrogen for controlled periods had a surprising bifurcate effect: about half the mice survived with neurological measures that were virtually normal while the other half died. The new assay detected behavioral deficits unrevealed by neurological screening. Two important features of the results were that (i) deficits were not equal across the circadian cycle, and (ii) deficits were not equal across all the measures within the operational definition of arousal. Specific voluntary motor measurements were decreased in a manner that depended on the phase of the circadian cycle. Sensory responses were also decreased, with an emphasis on vertical movement responses; but, interestingly, fear learning was not damaged. This study establishes the first useful approach to diffuse brain damage in a genetically tractable animal. The model and its outcome measurements will be useful during future attempts at amelioration of acquired neurological disabilities following hypoxic-ischemic injuries.

Language: en