(Stroke. 2001;32:232.)
© 2001 American Heart Association, Inc.
Original Contributions |
From the Laboratory for Cerebrovascular Disorders (H.Y., Y.N., Z.Z., J.-H.X.), Research Institute of National Cardio-Vascular Center (H.K.), and the Department of Cerebrovascular Surgery (H.Y., I.N., N.S.), Hospital of National Cardio-Vascular Center (H.K.), Osaka, Japan.
Correspondence to Hiroji Yanamoto, MD, DMSci, Laboratory for Cerebrovascular Disorders, Research Institute of National Cardio-Vascular Center, 5-7-1 Fujishiro-dai, Suita, 565-8565 Japan. E-mail yanamoto{at}ri.ncvc.go.jp
Background and PurposeThe efficacy of hypothermic intervention for permanent focal ischemia has yet to be clarified. This study investigated the effect of a prolonged moderate or mild hypothermia on permanent focal ischemia in rats.
MethodsTwo permanent focal ischemia models in male Sprague-Dawley rats were used. Moderate (30°C, in experiment 1) or mild (33°C, in experiment 2) hypothermia was achieved at the time of the induction of focal ischemia and was maintained for 2 hours under general anesthesia. Thereafter, the hypothermic condition was maintained by means of a cold room for a total of 24 hours. The infarct volume and neurological function were analyzed for a maximum of 21 days and compared with that of the normothermia group. Regional cerebral blood flow was monitored for 6 hours in the ischemic core and penumbra region.
ResultsIn experiment 1, the total infarct volume in the normothermic group was 368±59 mm3; in contrast, it was significantly smaller in the hypothermia group: 169±33 mm3 at 48 hours (mean±SEM, P<0.05). In experiment 2, the infarct volume was 211±19 mm3 in the normothermia group and 88±15 mm3 in the hypothermia group at 21 days (P<0.05). There were significant differences in neurological function from days 2 through 21 between the two groups. Mean regional cerebral blood flow in the penumbra region increased to a level >50% of baseline.
ConclusionsProlonged mild hypothermia suppressed the development of cerebral infarct and neurological deficit chronically after the induction of permanent focal ischemia.
Center for Clinical and Molecular Neurobiology, Departments of Neurology and Neuroscience, University of Minnesota, Minneapolis, Minnesota
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