4.5 Article

Long-term, repeated measurements of mouse cortical microflow at the same region of interest with high spatial resolution

Journal

BRAIN RESEARCH
Volume 1372, Issue -, Pages 59-69

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2010.11.014

Keywords

2-D flow map; Confocal microscopy; Focal cerebral ischemia; Mouse; Cerebral blood flow; Optical imaging

Categories

Funding

  1. INSERM
  2. CNRS
  3. University Paris 7

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A method for long-term, repeated, semi-quantitative measurements of cerebral microflow at the same region of interest (ROI) with high spatial resolution was developed and applied to mice subjected to focal arterial occlusion. A closed cranial window was chronically implanted over the left parieto-occipital cortex. The anesthetized mouse was placed several times, e.g., weekly, under a dynamic confocal microscope, and Rhodamine B-isothiocyanate-dextran was each time intravenously injected as a bolus, while microflow images were video recorded. Left and right tail veins were sequentially catheterized in a mouse three times at maximum over a 1.5 months' observation period. Smearing of the input function resulting from the use of intravenous injection was shown to be sufficiently small. The distal middle cerebral artery (MCA) was therrnocoagulated through the cranial window in six mice, and five sham-operated mice were studied in parallel. Dye injection and video recording were conducted four times in this series, i.e., before and at 10 mm, 7 and 30 days after sham operation or MCA occlusion. Pixelar microflow values (1/MTT) in a matrix of approximately 50 x 50 pixels were displayed on a two-dimensional (2-D) map, and the frequency distribution of the flow values was also calculated. No significant changes in microflow values over time were detected in sham-operated mice, while the time course of flow changes in the ischemic penumbral area in operated mice was similar to those reported in the literature. This method provides a powerful tool to investigate long-term changes in mouse cortical microflow under physiological and pathological conditions. (C) 2010 Elsevier B.V. All rights reserved.

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