Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by CROWELL, R. M.
Right arrow Articles by OMMAYA, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by CROWELL, R. M.
Right arrow Articles by OMMAYA, A.

(Stroke. 1970;1:439.)
© 1970 American Heart Association, Inc.


Temporary Occlusion of the Middle Cerebral Artery in the Monkey: Clinical and Pathological Observations

ROBERT M. CROWELL M.D.1; YNGVE OLSSON M.D.2; IGOR KLATZO M.D.2; AYUB OMMAYA F.R.C.S.2

1 Branch of Surgical Neurology, and the Laboratory of Neuropathology and Neuroanatomical Sciences, National Institute of Neurological Diseases and Stroke, National Institutes of Health, Public Health Service, U. S. Department of Health, Education and Welfare, Bethesda, Maryland, 20014; Neurosurgical Service, Massachusetts General Hospital, Boston, Massachusetts
2 Branch of Surgical Neurology, and the Laboratory of Neuropathology and Neuroanatomical Sciences, National Institute of Neurological Diseases and Stroke, National Institutes of Health, Public Health Service, U. S. Department of Health, Education and Welfare, Bethesda, Maryland, 20014

The right middle cerebral artery (MCA) was exposed in monkeys via a retro-orbital microsurgical approach. In 43 animals a temporary occlusive clip was placed on the MCA origin for one to 24 hours. In 20 animals, the origin of the MCA was permanently occluded.

Clinical evaluation of the monkeys one to three days postoperatively showed that one to two-hour clipping caused no or mild neurological deficits, four-hour clipping caused mild to moderate deficits, six to eight-hour clipping caused moderate to severe deficits, and 24-hour clipping produced severe deficits or death, a result equivalent to that produced by permanent occlusion. Gross and microscopical evaluation of the brains showed that one to two-hour clipping usually caused no or mild damage, four-hour clipping caused mild to moderate damage (often with capsular sparing), and six to eight-hour clipping and 24-hour clipping produced severe extensive infarction not different from that caused by permanent occlusion. Six to eight-hour clipping and 24-hour clipping were associated with a high incidence of hemorrhagic infarction, but other clipping times were not. The results suggest that reestablishment of flow by surgical means within a few hours after MCA occlusion in selected patients might result in significant restoration of neurological function. If flow renewal were done within about four hours, an increased incidence of hemorrhagic infarction might be avoided.


Key Words: focal cerebral ischemia • stroke surgery • microsurgical approach to MCA • collateral blood supply




This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Rink, G. Christoforidis, A. Abduljalil, M. Kontzialis, V. Bergdall, S. Roy, S. Khanna, A. Slivka, M. Knopp, and C. K. Sen
Minimally invasive neuroradiologic model of preclinical transient middle cerebral artery occlusion in canines
PNAS, September 16, 2008; 105(37): 14100 - 14105.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
P. Enblad, P. Frykholm, J. Valtysson, H. C:s. Silander, J. Andersson, K.-J. Fasth, Y. Watanabe, B. Langstrom, L. Hillered, and L. Persson
Middle Cerebral Artery Occlusion and Reperfusion in Primates Monitored by Microdialysis and Sequential Positron Emission Tomography
Stroke, July 1, 2001; 32(7): 1574 - 1580.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
J. Huang, J. Mocco, T. F. Choudhri, A. Poisik, S. J. Popilskis, R. Emerson, R. L. DelaPaz, A. G. Khandji, D. J. Pinsky, E. S. Connolly Jr, et al.
A Modified Transorbital Baboon Model of Reperfused Stroke Editorial Comment
Stroke, December 1, 2000; 31(12): 3054 - 3063.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
F. C. Tortella, P. Britton, A. Williams, X. C. M. Lu, and A. H. Newman
Neuroprotection (Focal Ischemia) and Neurotoxicity (Electroencephalographic) Studies in Rats with AHN649, a 3-Amino Analog of Dextromethorphan and Low-Affinity N-Methyl-D-Aspartate Antagonist
J. Pharmacol. Exp. Ther., October 1, 1999; 291(1): 399 - 408.
[Abstract] [Full Text]


Home page
StrokeHome page
A. M. Kaufmann, A. D. Firlik, M. B. Fukui, L. R. Wechsler, C. A. Jungries, and H. Yonas
Ischemic Core and Penumbra in Human Stroke
Stroke, January 1, 1999; 30(1): 93 - 99.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
K. Yanaka, P. J. Camarata, S. R. Spellman, D. E. McDonald, and R. C. Heros
Optimal Timing of Hemodilution for Brain Protection in a Canine Model of Focal Cerebral Ischemia
Stroke, May 1, 1996; 27(5): 906 - 912.
[Abstract] [Full Text]