| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2009;40:2836.)
© 2009 American Heart Association, Inc.
Original Contributions |
From the Departments of Neurology and Radiology (K.P., A.R., C.F., C.X., W.J.K., S.L., K.L.F., E.H.L.), Massachusetts General Hospital, Harvard Medical School, Charlestown, Mass; Department of Neurology (K.P.), Pusan National University Yangsan Hospital, Medical Research Institute, Pusan National University, Busan, Korea; Rega Institute for Medical Research (G.O.), Catholic University of Leuven, Leuven, Belgium.
Correspondence to Eng H. Lo, PhD, Neuroprotection Research Laboratory, MGH East 149-2401 Charlestown, MA 02129. E-mail Lo{at}helix.mgh.harvard.edu; or Kyung-Pil Park, MD, Department of Neurology, Pusan National University Yangsan Hospital, Busan, Korea. E-mail kppark@pusan.ac.kr
Background and Purpose— Plasma levels of matrix metalloproteinase-9 (MMP-9) have been proposed to be a useful biomarker for assessing pathological events in brain. Here, we examined the temporal profiles of MMP-9 in blood and brain using a rat model of acute focal cerebral ischemia.
Methods— Plasma and brain levels of MMP-2 and MMP-9 were quantified at 3, 6, 12, and 24 hours after permanent middle cerebral artery occlusion in male Sprague-Dawley rats. Infarct volumes at 24 hours were confirmed with 2,3,5-triphenyl-tetrazolium-chloride staining.
Results— In plasma, zymographic bands were detected between 70 and 95 kDa corresponding to pro-MMP-2, pro-MMP-9, and activated MMP-9. A higher 135-kDa band was also seen that is likely to be NGAL-conjugated MMP-9. After ischemia, there were no significant changes in pro-MMP-2, but plasma levels of pro-MMP-9 steadily increased over the course of 24 hours. Activated MMP-9 levels in plasma were significantly elevated only at 24 hours. Plasma NGAL-MMP-9 complexes showed a transient elevation between 3 to 6 hours, after which levels decreased back down to pre-ischemic baselines. In brain homogenates, pro-MMP-2, pro-MMP-9, and activated MMP-9 were seen but no NGAL-MMP-9 bands were detected. Compared to the contralateral hemisphere, MMP-2 and MMP-9 levels in ischemic brain progressively increased over the course of 24 hours. Overall levels of MMP-9 in plasma and brain were significantly correlated, especially at 24 hours. Plasma levels of pro-MMP-9 at 24 hours were correlated with final infarct volumes.
Conclusions— Elevated plasma levels of MMP-9 appear to be correlated with brain levels within 24 hours of acute cerebral ischemia in rats. Further investigation into clinical profiles of MMP-9 in acute stroke patients may be useful.
Key Words: cerebral ischemia matrix metalloproteinase stroke
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2009 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |