| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on March 25, 2003
From the Department of Neurosurgery (S.Z., K.S., R.S.-E.) and Institute for Surgical Research (N.P.), Ludwig-Maximilians-Universität, Klinikum Grosshadern, Munich, Germany. * To whom correspondence should be addressed. E-mail: Stefan.Zausinger{at}nc.med.uni-muenchen.de.
Background and Purpose--We have recently demonstrated that pretreatment with magnesium (calcium and glutamate antagonist) and tirilazad (antioxidant) in combination with intraischemic mild hypothermia (33°C) (MTH) offers superior neuroprotective efficacy in a rat model of focal transient cerebral ischemia. In the present study, we investigated the time window of this treatment strategy with a posttreatment regimen to define its role for stroke patients. Methods--We subjected 48 Sprague-Dawley rats to 90 minutes of middle cerebral artery occlusion by an intraluminal filament. Bilateral regional cerebral blood flow was continuously recorded by laser Doppler flowmetry. Combination therapy with MTH was started at 0, 1, 3, and 5 hours after induction of ischemia. Drugs were given in 1-hour intervals, and hypothermia was maintained for 2 hours. Neurological deficits were assessed daily. Infarct size was planimetrically determined on postoperative day 7. Results--Combination therapy with MTH significantly reduced infarct volume compared with normothermic controls by -74%, -49%, and -45% when applied at 0, 1, and 3 hours after induction of ischemia. Furthermore, these treatment groups showed less neurological deficits on postischemic days 1 and 2 (P<0.05). Onset of treatment 5 hours after middle cerebral artery occlusion failed to significantly reduce infarct formation and neurological deficits. Conclusions--The therapeutic window of the new combination therapy is at least 3 hours after onset of ischemia, comparable to that of moderate hypothermia (30°C), a grade of hypothermia associated with higher risks of severe side effects.
Accepted on April 22, 2003
Combination Drug Therapy and Mild Hypothermia After Transient Focal Cerebral Ischemia in Rats
Stefan Zausinger MD*;
This article has been cited by other articles:
![]() |
T. M. Hemmen and P. D. Lyden Multimodal Neuroprotective Therapy With Induced Hypothermia After Ischemic Stroke Stroke, March 1, 2009; 40(3_suppl_1): S126 - S128. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. M. Hemmen and P. D. Lyden Induced Hypothermia for Acute Stroke Stroke, February 1, 2007; 38(2): 794 - 799. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Sena, P. Wheble, P. Sandercock, and M. Macleod Systematic Review and Meta-Analysis of the Efficacy of Tirilazad in Experimental Stroke Stroke, February 1, 2007; 38(2): 388 - 394. [Abstract] [Full Text] [PDF] |
||||
![]() |
NINDS ICH Workshop Participants Priorities for Clinical Research in Intracerebral Hemorrhage: Report From a National Institute of Neurological Disorders and Stroke Workshop Stroke, March 1, 2005; 36(3): e23 - e41. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Culmsee, V. Junker, W. Kremers, S. Thal, N. Plesnila, and J. Krieglstein Combination Therapy in Ischemic Stroke: Synergistic Neuroprotective Effects of Memantine and Clenbuterol Stroke, May 1, 2004; 35(5): 1197 - 1202. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2003 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |