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Current Neurovascular Research


ISSN (Print): 1567-2026
ISSN (Online): 1875-5739

Experimental Model Considerations for the Study of Protein-Energy Malnutrition Co-Existing with Ischemic Brain Injury

Author(s): Erin J. Prosser-Loose, Shari E. Smith and Phyllis G. Paterson

Volume 8, Issue 2, 2011

Page: [170 - 182] Pages: 13

DOI: 10.2174/156720211795495376

Price: $65


Protein-energy malnutrition (PEM) affects ∼16% of patients at admission for stroke. We previously modeled this in a gerbil global cerebral ischemia model and found that PEM impairs functional outcome and influences mechanisms of ischemic brain injury and recovery. Since this model is no longer reliable, we investigated the utility of the rat 2-vessel occlusion (2-VO) with hypotension model of global ischemia for further study of this clinical problem. Male, Sprague-Dawley rats were exposed to either control diet (18% protein) or PEM induced by feeding a low protein diet (2% protein) for 7d prior to either global ischemia or sham surgery. PEM did not significantly alter the hippocampal CA1 neuron death (p = 0.195 by 2-factor ANOVA) or the increase in dendritic injury caused by exposure to global ischemia. Unexpectedly, however, a strong trend was evident for PEM to decrease the consistency of hippocampal damage, as shown by an increased incidence of unilateral or no hippocampal damage (p = 0.069 by chi-square analysis). Although PEM caused significant changes to baseline arterial blood pH, pO2, pCO2, and fasting glucose (p < 0.05), none of these variables (nor hematocrit) correlated significantly with CA1 cell counts in the malnourished group exposed to 2-VO (p ≥ 0.269). Intra-ischemic tympanic temperature and blood pressure were strictly and equally controlled between ischemic groups. We conclude that co-existing PEM confounded the consistency of hippocampal injury in the 2-VO model. Although the mechanisms responsible were not identified, this model of brain ischemia should not be used for studying this co-morbidity factor.

Keywords: 2-vessel occlusion, global ischemia, protein-energy malnutrition, ischemic brain injury, rat, experimental stroke model, low protein, dendritic, ischemia, pCO2, hematocrit, Intra-ischemic, tympanic, hippocampal, PEM, 2-VO

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