TY - JOUR
T1 - Hibernation, a model of neuroprotection
AU - Zhou, Fang
AU - Zhu, Xiongwei
AU - Castellani, Rudy J.
AU - Stimmelmayr, Raphaela
AU - Perry, George
AU - Smith, Mark A.
AU - Drew, Kelly L.
N1 - Funding Information:
Supported by the American Heart Association (grant 98-AK-301 ), a University of Alaska Fairbanks President’s Special Projects Fund grant (to K. L. D.), the National Institutes of Health (grant NS38648 to M. A. S.), and NS41069 funded in part by the National Institute of Neurological Disorders and Stroke, National Institute of Mental Health, and National Center for Research Resources.
PY - 2001
Y1 - 2001
N2 - Hibernation, a natural model of tolerance to cerebral ischemia, represents a state of pronounced fluctuation in cerebral blood flow where no brain damage occurs. Numerous neuroprotective aspects may contribute in concert to such tolerance. The purpose of this study was to determine whether hibernating brain tissue is tolerant to penetrating brain injury modeled by insertion of microdialysis probes. Guide cannulae were surgically implanted in striatum of Arctic ground squirrels before any of the animals began to hibernate. Microdialysis probes were then inserted in some animals after they entered hibernation and in others while they remained euthermic. The brain tissue from hibernating and euthermic animals was examined 3 days after implantation of microdialysis probes. Tissue response, indicated by examination of hematoxylin and eosin-stained tissue sections and immunocytochemical identification of activated microglia, astrocytes, and hemeoxygenase-1 immunoreactivity, was dramatically attenuated around probe tracks in hibernating animals compared to euthermic controls. No difference in tissue response around guide cannulae was observed between groups. Further study of the mechanisms underlying neuroprotective aspects of hibernation may lead to novel therapeutic strategies for stroke and traumatic brain injury.
AB - Hibernation, a natural model of tolerance to cerebral ischemia, represents a state of pronounced fluctuation in cerebral blood flow where no brain damage occurs. Numerous neuroprotective aspects may contribute in concert to such tolerance. The purpose of this study was to determine whether hibernating brain tissue is tolerant to penetrating brain injury modeled by insertion of microdialysis probes. Guide cannulae were surgically implanted in striatum of Arctic ground squirrels before any of the animals began to hibernate. Microdialysis probes were then inserted in some animals after they entered hibernation and in others while they remained euthermic. The brain tissue from hibernating and euthermic animals was examined 3 days after implantation of microdialysis probes. Tissue response, indicated by examination of hematoxylin and eosin-stained tissue sections and immunocytochemical identification of activated microglia, astrocytes, and hemeoxygenase-1 immunoreactivity, was dramatically attenuated around probe tracks in hibernating animals compared to euthermic controls. No difference in tissue response around guide cannulae was observed between groups. Further study of the mechanisms underlying neuroprotective aspects of hibernation may lead to novel therapeutic strategies for stroke and traumatic brain injury.
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U2 - 10.1016/S0002-9440(10)64686-X
DO - 10.1016/S0002-9440(10)64686-X
M3 - Article
C2 - 11395392
AN - SCOPUS:0034978320
VL - 158
SP - 2145
EP - 2151
JO - American Journal of Pathology
JF - American Journal of Pathology
SN - 0002-9440
IS - 6
ER -