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PMID: 11546914 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Collateral growth and angiogenesis around cortical stroke.

Stroke ·Vol. 32 ·No. 9 ·2001-09-00 ·Pages 2179-84

Wei L, Erinjeri JP, Rovainen CM, Woolsey TA

Abstract

We tested the hypothesis that there are significant long-term local vascular changes after ministroke that could form a basis for functional recovery. A 6- to 8-mm cranial window was opened over the barrel cortex, which was identified by an intrinsic optical signal during mechanical stimulation of the whiskers in anesthetized female Wistar rats. Branches of the middle cerebral artery (MCA) to this region were ligated. Fluorescein isothiocyanate (FITC) transits were recorded by videomicroscopy in each rat just before, immediately after, and 30 days after ligation. Changes in surface vessels and parenchymal perfusion were measured. In similarly prepared rats, angiogenesis was identified by 5-bromo-2-deoxyuridine labeling and immunohistochemistry for the integrin family member alpha(v)beta(3). The intrinsic optical signal disappeared immediately after MCA ligations. FITC injection just after ligation demonstrated 3 concentric regions: 1 region of unchanged perfusion, surrounding 1 region of reduced perfusion (the ischemic border) surrounding a central core with little observable perfusion. At 30 days, the following had taken place: (1) diameters and lengths of surface collaterals in the ischemic border had grown significantly, but no new surface vessels were detected, (2) FITC entered occluded MCA segments, (3) arteriocapillary latencies in the ischemic border were shortened compared with latencies just after ligation, and (4) small infarcts were virtually identical to the poorly perfused core. Angiogenesis was confined to the ischemic border. Arteriolar collateral growth and new capillaries support restored perfusion in the ischemic border after ministroke and could support long-term functional recovery.

MeSH Terms
Animals Arterioles/diagnostic imaging,pathology Brain Ischemia/pathology Bromodeoxyuridine Cerebral Angiography Cerebrovascular Circulation Collateral Circulation Endothelium, Vascular/metabolism Female Fluorescent Dyes Ligation Microcirculation/diagnostic imaging,metabolism,pathology Microscopy, Video/methods Middle Cerebral Artery Neovascularization, Physiologic Rats Rats, Wistar Receptors, Vitronectin/metabolism Somatosensory Cortex/blood supply,metabolism,pathology Stroke/pathology
Chemicals
Fluorescent Dyes Receptors, Vitronectin Bromodeoxyuridine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wei L
Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA. weil@neuro.wustl.edu
Erinjeri J P
Rovainen C M
Woolsey T A
Article Info
Journal
Stroke
Abbr.
Stroke
ISSN
1524-4628
Published
2001-09-00
Pages
2179-84
Language
English
Region
United States
NLM ID
0235266
Subset
IM
Grants
NHLBI NIH HHS · HL-41075 · United States
NINDS NIH HHS · NS-07057 · United States
NINDS NIH HHS · NS-26004 · United States
NINDS NIH HHS · NS-28781 · United States
NINDS NIH HHS · NS-37372 · United States
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