| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2002;33:2999.)
© 2002 American Heart Association, Inc.
Original Contributions |
From the Department of Experimental Neurology, Max-Planck Institute for Neurological Research, Cologne, Germany.
Correspondence to Dr K-A. Hossmann, Department of Experimental Neurology, Max-Planck Institute for Neurological Research, Gleueler Strasse 50, D-50931 Cologne, Germany. E-mail hossmann{at}mpin-koeln.mpg.de
Background and Purpose We sought to test the hypothesis that intra-arterial recombinant tissue plasminogen activator (rtPA) treatment of thromboembolic stroke is more efficient than intravenous application.
Methods Rats were embolized by intracarotid injection of autologous fibrin-rich blood clots. One hour later rtPA (10 mg/kg) was infused either intravenously (n=8) or intra-arterially (n=8). Control rats (n=8) received intra-arterial infusion of saline. Treatment was monitored by MR perfusion-weighted imaging and apparent diffusion coefficient (ADC) imaging, and outcome was evaluated by comparing incidence of hemorrhages and lesion volumes of ATP and pH.
Results Clot embolism led to a decline of perfusion-weighted imaging signal intensity in the middle cerebral artery territory to <40% of control. Both intra-arterial and intravenous treatment significantly improved blood flow in cerebral cortex but not in caudate putamen. In untreated animals, ATP and pH lesion volumes were 510.3±94.5 and 438.6±39.2 mm3 at 7 hours after clot embolism, respectively. Both intravenous and intra-arterial rtPA treatment produced hemorrhagic complications but reduced ATP lesion size to 296.2±136.1 and 370.3±103.7 mm3 and reduced pH lesion size to 263.3±114.6 and 303.3±103.0 mm3, respectively (P<0.05 for untreated versus treated rats; no difference between intravenous and intra-arterial treatment). ADC imaging revealed that lesion reduction was due to inhibition of infarct growth but not to reversal of primary injury.
Conclusions This study documents reduction of injury by rtPA treatment but does not reveal a difference between intra-arterial and intravenous application. Our data do not support an advantage of intra-arterial thrombolysis.
Key Words: embolism magnetic resonance imaging thrombolytic therapy rats
This article has been cited by other articles:
![]() |
F. Chen, Y. Suzuki, N. Nagai, X. Sun, H. Wang, J. Yu, G. Marchal, and Y. Ni Microplasmin and Tissue Plasminogen Activator: Comparison of Therapeutic Effects in Rat Stroke Model at Multiparametric MR Imaging Radiology, August 1, 2007; 244(2): 429 - 438. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Henninger, K. M. Sicard, K. F. Schmidt, J. Bardutzky, and M. Fisher Comparison of Ischemic Lesion Evolution in Embolic Versus Mechanical Middle Cerebral Artery Occlusion in Sprague Dawley Rats Using Diffusion and Perfusion Imaging Stroke, May 1, 2006; 37(5): 1283 - 1287. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Rottger, K. Madlener, M. Heil, T. Gerriets, M. Walberer, T. Wessels, G. Bachmann, M. Kaps, and E. Stolz Is Heparin Treatment the Optimal Management for Cerebral Venous Thrombosis?: Effect of Abciximab, Recombinant Tissue Plasminogen Activator, and Enoxaparin in Experimentally Induced Superior Sagittal Sinus Thrombosis Stroke, April 1, 2005; 36(4): 841 - 846. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Niessen, T. Hilger, M. Hoehn, and K.-A. Hossmann Differences in Clot Preparation Determine Outcome of Recombinant Tissue Plasminogen Activator Treatment in Experimental Thromboembolic Stroke Stroke, August 1, 2003; 34(8): 2019 - 2024. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2002 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |