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Original

Automated Method for Tracking Vast Numbers of FITC-Labeled RBCs in Microvessels of Rat Brain In Vivo Using a High-Speed Confocal Microscope System

, , , , , , & show all
Pages 163-174 | Received 15 Feb 2007, Accepted 11 Jul 2007, Published online: 10 Jul 2009
 

Abstract

High-speed camera investigation of rapidly moving red blood cells (RBCs) in the microvasculature has been limited by an inability to handle the vast volume of data. We have developed a novel method to analyze large numbers of RBC images captured by a high-resolution, high-speed camera fitted on a confocal fluorescence microscope, to determine the velocities of individual RBCs in capillaries in vivo. Fluorescein isothiocyanate (FITC)-labeled RBCs flowing in the microvasculature of the cerebral cortex of urethane-anesthetized Wistar rats were recorded through the skull window on video clips during specified periods at high frame rates (500 fps). Sequential frames of moving RBCs in the video clips for a specified period were analyzed offline with in-house software (KEIO-IS2). Images of RBCs acquired were numbered automatically in order of appearance and displayed in a two-dimensional (2-D) RBC tracking map. The velocities of individual RBCs were automatically computed based on the RBC displacement per frame multiplied by the frame rate (fps), and the results were displayed in a 2-D velocity map and a 2-D RBC number map. Single capillaries were identified by staining with FITC-dextran. The mean capillary velocity of RBCs was evaluated as 2.05 ± 1.59 mm/second in video clips obtained at 500 fps. This method is considered to have wide potential applicability.

ACKNOWLEDGMENTS

The present address of Dr. Istvan Schiszler is Petofi utca 4, Torokbalint 2045, Hungary. We thank Professors Jacque Seylaz and Elizabeth Pinard for training Dr. Yutaka Tomita in small animal experimental techniques. We also thank Dr. Hidetaka Takeda, Saitama Hospital, Otsuka Pharmaceutical Co., Ltd., and Mr. Harukuni Tsumura, Sankei, Co., Ltd., for their various assistance and valuable suggestions.

The KEIO-IS1 and KEIO-IS2 programs are freely available to researchers in nonprofit organizations; for details, please contact Minoru Tomita at [email protected].

This work was supported by JSPS Grant-in-Aid #17390255. The authors have no conflicts of interest.

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