| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2005;36:2701.)
© 2005 American Heart Association, Inc.
Original Contributions |
From the Department of Neurology (Z.G.Z., L.Z., G.D., Q.J., R.L.Z., X.Z., M.C.), Henry Ford Health Sciences Center, Detroit, Mich; Department of Physics (M.C.), Oakland University, Rochester, Mich; Molecular Neurobiology Program (W.-B.G.), Skirball Institute, and Department of Neuroscience and Physiology, New York University School of Medicine, New York.
Correspondence to Zheng Gang Zhang, MD, PhD, Department of Neurology, Henry Ford Hospital, 2799 W Grand Blvd, Detroit, MI 48202. E-mail zhazh{at}neuro.hfh.edu
Background and Purpose To measure cerebral vascular and neuronal responses after stroke in the living mouse, we generated a mouse model of embolic stroke localized to the parietal cortex.
Methods Male C57/6J or male transgenic mice (2 to 3 months old) expressing yellow fluorescent protein (YFP) were used in the present study. A single fibrin-rich clot (8 mm in length) was injected into a branch of the right middle cerebral artery (MCA). MRI measurements were performed to measure ischemic lesion. Using confocal and 2-photon microscopy, changes in the embolus, dendrites, and dendritic spines were measured in the living mouse.
Results Eight of 11 mice (73%) had the embolus localized to a branch of the right MCA in the parietal cortex. Expansion of the embolus within the artery was observed 24 hours after stroke. The presence of ischemic lesion in the parietal cortex was verified by MRI measurements, and histopathological analysis revealed that these mice (n=8) had a cortical infarct volume of 4.9±3.6% of the contralateral hemisphere. In the living mouse, substantial loss of YFP-labeled axonal and dendritic structures as well as the formation of abnormal dendritic bulbs were detected in the ischemic boundary regions 24 hours after stroke compared with that 1 hour after stroke.
Conclusion This model offers a novel approach to study the neurovascular unit in cerebral cortex after stroke in the living mouse.
Key Words: cerebral ischemia image mice
This article has been cited by other articles:
![]() |
D. M. Hermann Review: Future perspectives for brain pharmacotherapies: implications of drug transport processes at the blood--brain barrier Therapeutic Advances in Neurological Disorders, November 1, 2008; 1(3): 167 - 179. [Abstract] [PDF] |
||||
![]() |
C. E. Brown and T. H. Murphy Livin' on the Edge: Imaging Dendritic Spine Turnover in the Peri-Infarct Zone during Ischemic Stroke and Recovery Neuroscientist, April 1, 2008; 14(2): 139 - 146. [Abstract] [PDF] |
||||
![]() |
C. Orset, R. Macrez, A. R. Young, D. Panthou, E. Angles-Cano, E. Maubert, V. Agin, and D. Vivien Mouse Model of In Situ Thromboembolic Stroke and Reperfusion Stroke, October 1, 2007; 38(10): 2771 - 2778. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2005 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |