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Stroke. 2001;32:2157-2163
doi: 10.1161/hs0901.095640
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(Stroke. 2001;32:2157.)
© 2001 American Heart Association, Inc.


Original Contributions

Combination of a Free Radical Scavenger and Heparin Reduces Cerebral Hemorrhage After Heparin Treatment in a Rabbit Middle Cerebral Artery Occlusion Model

Bing-Qiao Zhao, MD; Yasuhiro Suzuki, MS; Kazunao Kondo, MD, PhD; Yasuhiko Ikeda, MD, PhD Kazuo Umemura, MD, PhD

From the Department of Pharmacology, Hamamatsu University School of Medicine, Hamamatsu, 431-3192, Japan.

Correspondence to Dr Kazuo Umemura, Department of Pharmacology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, 431-3192, Japan. E-mail umemura{at}hama-med.ac.jp

Background and Purpose— We sought to investigate the effects of EPC-K1, a free radical scavenger, on reducing heparin-produced cerebral hemorrhage in a rabbit model of middle cerebral artery (MCA) photothrombosis and to investigate whether the combination of EPC-K1 and heparin enhances neuroprotection from cerebral ischemic damage.

Methods— In the heparin-alone group (n=8), heparin was administered intravenously for 24 hours, starting from 3 hours after MCA occlusion. In the EPC-K1-alone group (n=8), EPC-K1 was administered as a bolus injection (10 mg/kg) twice at 3 and 6 hours after MCA occlusion. In the combination group (n=8), EPC-K1 and heparin both were administered as in the single-drug procedures. In the vehicle group (n=10), saline were infused for 24 hours.

Results— Heparin prolonged activated partial thromboplastin time by {approx}3 times that of control animals. In the heparin-treated animals, the hemorrhage size was significantly increased (P<0.0001) and neurological symptoms were significantly worse (P<0.01) than in control animals at 48 hours. The combination of EPC-K1 and heparin dramatically reduced heparin-produced cerebral hemorrhage (P<0.0001), with a significant reduction in infarct volume (reduction by 63.2% and 57.2% of heparin-alone and control animals, respectively, P<0.0001) and a significant improvement in neurological symptoms (P<0.01 versus heparin-alone and control animals, respectively).

Conclusions— These data indicate that free radical formation may play a key role in intracerebral hemorrhage exacerbated by heparin treatment and that the combination of a free radical scavenger and heparin augmented neuroprotection from acute brain ischemia. The results of the present study may suggest a potential clinical approach for the treatment of acute stroke.


Key Words: cerebral ischemia • free radicals • heparin • intracerebral hemorrhage • middle cerebral artery occlusion • rabbits




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