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Intracerebral Hemorrhage Models in Rat: Comparing Collagenase to Blood Infusion
Author(s) -
Crystal L. MacLellan,
Gergely Silasi,
Candice C. Poon,
Carmen Lynne Edmundson,
Richard Buist,
James Peeling,
Frederick Colbourne
Publication year - 2007
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/sj.jcbfm.9600548
Subject(s) - striatum , collagenase , intracerebral hemorrhage , magnetic resonance imaging , medicine , hematoma , white matter , stroke (engine) , neuroscience , rat model , blood–brain barrier , pathophysiology , pathology , anesthesia , surgery , psychology , radiology , central nervous system , chemistry , mechanical engineering , biochemistry , dopamine , subarachnoid hemorrhage , engineering , enzyme
Many therapies have shown promise in preclinical stroke studies, but few benefit patients. A greater understanding of stroke pathophysiology is needed to successfully develop therapies, and this depends on appropriate animal models. The collagenase and blood infusion models of intracerebral hemorrhage (ICH) are widely used; yet, investigators often prefer using one model for a variety of reasons. Thus, we directly compared these to highlight advantages and limitations of each as well as the assessment approach. An ICH was created by infusing blood or bacterial collagenase into the rats' striatum. We matched initial hematoma volume in each model (Experiment 1) and assessed the time course of bleeding (Experiment 2). Functional deficits and the progression of injury were tracked over 6 weeks using behavior, magnetic resonance imaging, and histology (Experiment 3). Despite similar initial hematoma volumes, collagenase-induced ICH resulted in a greater blood-brain barrier breakdown and more damage to the striatum, substantia nigra, white matter, and cortex. Magnetic resonance imaging revealed faster hematoma resolution in the blood model, and little increase in the volume of tissue lost from 1 to 6 weeks. In contrast, tissue loss continued over 4 weeks in the collagenase model. Finally, functional deficits recovered more quickly and completely in the blood model. This study highlights key differences between these models and that neither closely replicates the human condition. Thus, both should be used whenever possible taking into account the significant differences between these models and their limitations. Furthermore, this work illustrates significant weaknesses with several outcome measures.

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