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Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels
PURPOSE: To assess the effects of retro-orbital (RO) injection of fluorescein isothiocyanate dextran (FITC-dextran) for observing mouse retinal vessels. METHODS: Oxygen-induced retinopathy (OIR) was induced in 7-day postnatal (P7) C57BL/6J mice by exposing them to a 75% oxygen atmosphere for 5 days...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250377/ https://www.ncbi.nlm.nih.gov/pubmed/22219652 |
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author | Li, Shiqing Li, Tao Luo, Yan Yu, Honghua Sun, Yuying Zhou, Huanjiao Liang, Xiaoling Huang, Juan Tang, Shibo |
author_facet | Li, Shiqing Li, Tao Luo, Yan Yu, Honghua Sun, Yuying Zhou, Huanjiao Liang, Xiaoling Huang, Juan Tang, Shibo |
author_sort | Li, Shiqing |
collection | PubMed |
description | PURPOSE: To assess the effects of retro-orbital (RO) injection of fluorescein isothiocyanate dextran (FITC-dextran) for observing mouse retinal vessels. METHODS: Oxygen-induced retinopathy (OIR) was induced in 7-day postnatal (P7) C57BL/6J mice by exposing them to a 75% oxygen atmosphere for 5 days and then returning them to room air at P12. At P17, 45 P17 OIR mice and 12 normal mice received an RO injection of FITC-dextran. Five P17 OIR mice were perfused with FITC-dextran via the left ventricle. Retinal flatmounts were viewed under a fluorescence microscope and a confocal microscope. Following RO injection or left ventricular (LV) perfusion, the areas of neovascularization, as well as the total retina areas, were measured and analyzed using Image Pro-Plus 5.1 software. RESULTS: The suitable volume of FITC-dextran for RO injection to observe the retinal vessels of a P17 OIR mouse was 0.05 ml, the 5% volume required to achieve similar results by administering FITC-dextran using LV perfusion. The total retinal vessels in P17 OIR mice could be fully observed under a fluorescence microscope 3 s after RO injection of FITC-dextran. Our study showed that RO injection of FITC-dextran was suitable for observing the retinal vessels of all postnatal mice. There was no significant difference in evaluating retinal neovascularization between RO injection and LV perfusion of FITC-dextran (p>0.05). CONCLUSIONS: Retro-orbital injection of FITC-dextran is an economical method for observing retinal vessels in mice, when compared with LV perfusion of FITC-dextran. |
format | Online Article Text |
id | pubmed-3250377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-32503772012-01-04 Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels Li, Shiqing Li, Tao Luo, Yan Yu, Honghua Sun, Yuying Zhou, Huanjiao Liang, Xiaoling Huang, Juan Tang, Shibo Mol Vis Research Article PURPOSE: To assess the effects of retro-orbital (RO) injection of fluorescein isothiocyanate dextran (FITC-dextran) for observing mouse retinal vessels. METHODS: Oxygen-induced retinopathy (OIR) was induced in 7-day postnatal (P7) C57BL/6J mice by exposing them to a 75% oxygen atmosphere for 5 days and then returning them to room air at P12. At P17, 45 P17 OIR mice and 12 normal mice received an RO injection of FITC-dextran. Five P17 OIR mice were perfused with FITC-dextran via the left ventricle. Retinal flatmounts were viewed under a fluorescence microscope and a confocal microscope. Following RO injection or left ventricular (LV) perfusion, the areas of neovascularization, as well as the total retina areas, were measured and analyzed using Image Pro-Plus 5.1 software. RESULTS: The suitable volume of FITC-dextran for RO injection to observe the retinal vessels of a P17 OIR mouse was 0.05 ml, the 5% volume required to achieve similar results by administering FITC-dextran using LV perfusion. The total retinal vessels in P17 OIR mice could be fully observed under a fluorescence microscope 3 s after RO injection of FITC-dextran. Our study showed that RO injection of FITC-dextran was suitable for observing the retinal vessels of all postnatal mice. There was no significant difference in evaluating retinal neovascularization between RO injection and LV perfusion of FITC-dextran (p>0.05). CONCLUSIONS: Retro-orbital injection of FITC-dextran is an economical method for observing retinal vessels in mice, when compared with LV perfusion of FITC-dextran. Molecular Vision 2011-12-31 /pmc/articles/PMC3250377/ /pubmed/22219652 Text en Copyright © 2012 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Shiqing Li, Tao Luo, Yan Yu, Honghua Sun, Yuying Zhou, Huanjiao Liang, Xiaoling Huang, Juan Tang, Shibo Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels |
title | Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels |
title_full | Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels |
title_fullStr | Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels |
title_full_unstemmed | Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels |
title_short | Retro-orbital injection of FITC-dextran is an effective and economical method for observing mouse retinal vessels |
title_sort | retro-orbital injection of fitc-dextran is an effective and economical method for observing mouse retinal vessels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250377/ https://www.ncbi.nlm.nih.gov/pubmed/22219652 |
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