Evaluation of leukocyte dynamics in choroidal circulation with indocyanine green-stained leukocytes

I. Takasu, Fumio Shiraga, T. Okanouchi, Y. Tsuchida, H. Ohtsuki

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Purpose. To develop a new method with which to visualize leukocytes moving through the choroidal vessels of pigmented animals and enable the evaluation of leukocyte dynamics in the choroidal microcirculation. Methods. Pigmented rabbits and monkeys were used in this study. Leukocytes, collected by centrifugal separation of autologous blood, were stained with indocyanine green (ICG) dye. The ICG-stained leukocyte fluid was injected into the vein, and the fundus image was obtained with a scanning laser ophthalmoscope. The image was recorded on videotapes and analyzed with a personal computer-based image analysis system. Results. In pigmented rabbits, fluorescent leukocytes moving in the choroidal circulation were clearly visible for more than 1 hour. In monkeys, distinct fluorescent dots were seen moving approximately 50 to 200 μm in the foveal avascular zone for more than 30 minutes after the injection of the ICG-stained leukocyte fluid. Dim fluorescent dots were seen moving in the fundus. Although the movement of these dim dots was difficult to trace, they seemed to be moving in the choroidal vessels. In the rabbits, the mean flow velocity of leukocytes moving without plugging was 0.48 ± 0.14 mm/sec in the peripheral choriocapillaris. In the monkeys, the mean flow velocity of distinct fluorescent leukocytes without plugging was 2.45 ± 0.48 mm/sec in the posterior choroid. Conclusions. In pigmented rabbits and monkeys, this method allows visualization of leukocytes passing through the choroidal vessels and provides a new way to investigate, noninvasively and in vivo, leukocyte dynamics in the choroidal microcirculation.

Original languageEnglish
Pages (from-to)2844-2848
Number of pages5
JournalInvestigative Ophthalmology and Visual Science
Volume41
Issue number10
Publication statusPublished - 2000

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Indocyanine Green
Leukocytes
Haplorhini
Rabbits
Microcirculation
Ophthalmoscopes
Videotape Recording
Choroid
Microcomputers
Veins
Lasers
Coloring Agents
Injections

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Evaluation of leukocyte dynamics in choroidal circulation with indocyanine green-stained leukocytes. / Takasu, I.; Shiraga, Fumio; Okanouchi, T.; Tsuchida, Y.; Ohtsuki, H.

In: Investigative Ophthalmology and Visual Science, Vol. 41, No. 10, 2000, p. 2844-2848.

Research output: Contribution to journalArticle

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AU - Ohtsuki, H.

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N2 - Purpose. To develop a new method with which to visualize leukocytes moving through the choroidal vessels of pigmented animals and enable the evaluation of leukocyte dynamics in the choroidal microcirculation. Methods. Pigmented rabbits and monkeys were used in this study. Leukocytes, collected by centrifugal separation of autologous blood, were stained with indocyanine green (ICG) dye. The ICG-stained leukocyte fluid was injected into the vein, and the fundus image was obtained with a scanning laser ophthalmoscope. The image was recorded on videotapes and analyzed with a personal computer-based image analysis system. Results. In pigmented rabbits, fluorescent leukocytes moving in the choroidal circulation were clearly visible for more than 1 hour. In monkeys, distinct fluorescent dots were seen moving approximately 50 to 200 μm in the foveal avascular zone for more than 30 minutes after the injection of the ICG-stained leukocyte fluid. Dim fluorescent dots were seen moving in the fundus. Although the movement of these dim dots was difficult to trace, they seemed to be moving in the choroidal vessels. In the rabbits, the mean flow velocity of leukocytes moving without plugging was 0.48 ± 0.14 mm/sec in the peripheral choriocapillaris. In the monkeys, the mean flow velocity of distinct fluorescent leukocytes without plugging was 2.45 ± 0.48 mm/sec in the posterior choroid. Conclusions. In pigmented rabbits and monkeys, this method allows visualization of leukocytes passing through the choroidal vessels and provides a new way to investigate, noninvasively and in vivo, leukocyte dynamics in the choroidal microcirculation.

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