Effects of Delayed Intraischemic and Postischemic Hypothermia on a Focal Model of Transient Cerebral Ischemia in Rats
- 1 August 2000
- journal article
- research article
- Published by Wolters Kluwer Health in Stroke
- Vol. 31 (8) , 1982-1989
- https://doi.org/10.1161/01.str.31.8.1982
Abstract
Intraischemic mild hypothermia has been shown to be neuroprotective in reducing cerebral infarction in transient focal ischemia. As a more clinical relevant issue, we investigated the effect of delayed intraischemic and postischemic hypothermia on cerebral infarction in a rat model of reversible focal ischemia. We also examined the effect of hypothermia on the inflammatory response after ischemia-reperfusion to assess the neuroprotective mechanism of brain hypothermia. Rats were subjected to 2 hours of middle cerebral artery occlusion followed by 22 hours of reperfusion under the following protocols: (1) rats were treated with normothermia (37.0 degrees C, 4 hours) and then housed in room temperature (25 degrees C, 18 hours) and (2) rats were treated with hypothermia (33.0 degrees C, 4 hours, brain temperature modulation was started 30 minutes before the reperfusion) and then housed in cold temperature (5 degrees C, 18 hours). Animals were killed 24 hours after the onset of ischemia. The infarct volume was examined with 2,3,5-triphenyl-tetrazolium chloride staining. The accumulation of polymorphonuclear leukocytes (PMNLs) and the expression of intercellular adhesion molecule-1 mRNA were evaluated in both groups. A significant reduction (P<0.05) in infarct volume was found in the hypothermia group compared with the normothermia group. Compared with the normothermia group, hypothermic treatment also significantly reduced the accumulation of PMNLs (P<0.01) and inhibited the overexpression of intercellular adhesion molecule-1 mRNA at 22 hours of reperfusion after 2 hours of ischemia. Ischemic brain damage can be reduced with delayed intraischemic and prolonged postischemic hypothermia in a focal model of transient cerebral ischemia in rats. The neuroprotective mechanism of hypothermia may be mediated by suppression of PMNL-mediated inflammatory response after ischemia-reperfusion in this model.Keywords
This publication has 29 references indexed in Scilit:
- Reperfusion Injury: Demonstration of Brain Damage Produced by Reperfusion after Transient Focal Ischemia in RatsJournal of Cerebral Blood Flow & Metabolism, 1997
- The Effect of Brain Temperature on Acute Inflammation after Traumatic Brain Injury in RatsJournal of Neurotrauma, 1997
- Delayed induction of mild hypothermia to reduce infarct volume after temporary middle cerebral artery occlusion in ratsJournal of Neurosurgery, 1994
- Intraischemic but Not Postischemic Brain Hypothermia Protects Chronically following Global Forebrain Ischemia in RatsJournal of Cerebral Blood Flow & Metabolism, 1993
- Recombinant tissue plasminogen activator in acute thrombotic and embolic strokeAnnals of Neurology, 1992
- Mild Hypothermia Prevents Ischemic Injury in Gerbil HippocampusJournal of Cerebral Blood Flow & Metabolism, 1990
- Recognition of an endothelial determinant for CD 18-dependent human neutrophil adherence and transendothelial migration.Journal of Clinical Investigation, 1988
- Neutrophil adherence to human endothelium in vitro occurs by CDw18 (Mo1, MAC-1/LFA-1/GP 150,95) glycoprotein-dependent and -independent mechanisms.Journal of Clinical Investigation, 1988
- Small Differences in Intraischemic Brain Temperature Critically Determine the Extent of Ischemic Neuronal InjuryJournal of Cerebral Blood Flow & Metabolism, 1987
- Measurement of Cutaneous Inflammation: Estimation of Neutrophil Content with an Enzyme MarkerJournal of Investigative Dermatology, 1982