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Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy
BACKGROUND: Caffeine or ketorolac decrease the risk of retinopathy of prematurity and may act synergistically to improve beneficial effect. Combination of caffeine (Caff) and ketorolac (Keto) to prevent oxygen-induced retinopathy was studied. METHODS: Newborn rats exposed to room air (RA) or intermi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030702/ https://www.ncbi.nlm.nih.gov/pubmed/27438224 http://dx.doi.org/10.1038/pr.2016.105 |
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author | Aranda, Jacob V. Cai, Charles L. Ahmad, Taimur Bronshtein, Vadim Sadeh, Jonathan Valencia, Gloria B. Lazzaro, Douglas R. Beharry, Kay D. |
author_facet | Aranda, Jacob V. Cai, Charles L. Ahmad, Taimur Bronshtein, Vadim Sadeh, Jonathan Valencia, Gloria B. Lazzaro, Douglas R. Beharry, Kay D. |
author_sort | Aranda, Jacob V. |
collection | PubMed |
description | BACKGROUND: Caffeine or ketorolac decrease the risk of retinopathy of prematurity and may act synergistically to improve beneficial effect. Combination of caffeine (Caff) and ketorolac (Keto) to prevent oxygen-induced retinopathy was studied. METHODS: Newborn rats exposed to room air (RA) or intermittent hypoxia (IH) consisting of 12% O(2) during hyperoxia (50% O(2)) from birth (P0) had single daily IP injections of Caff from P0-P13 or saline; and/or ocular Keto (Acuvail, 0.45% ophthalmic solution) administered subcutaneously over the eyes from P5-P7. Pups were studied at P14 or placed in RA for recovery from IH (IHR) until P21. Eyes were examined for neovascularization, histopathology, growth factors, and VEGF-signaling genes. RESULTS: Severe retinal damage noted during IHR in the untreated groups evidenced by hemorrhage, neovascularization, and oxygen-induced retinopathy (OIR) pathologies were prevented with Keto/Caff treatment. Keto and/or Caff treatment in IH also promoted retinal neural development evidenced by eye opening (92%, P < 0.001 vs. 31% in the placebo-treated IH group). No corneal pathologies were noted with Keto. CONCLUSION. Caff or Keto given individually reduced retinal neovascularization, but the two drugs given together prevented severe OIR. |
format | Online Article Text |
id | pubmed-5030702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50307022016-09-29 Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy Aranda, Jacob V. Cai, Charles L. Ahmad, Taimur Bronshtein, Vadim Sadeh, Jonathan Valencia, Gloria B. Lazzaro, Douglas R. Beharry, Kay D. Pediatr Res Translational Investigation BACKGROUND: Caffeine or ketorolac decrease the risk of retinopathy of prematurity and may act synergistically to improve beneficial effect. Combination of caffeine (Caff) and ketorolac (Keto) to prevent oxygen-induced retinopathy was studied. METHODS: Newborn rats exposed to room air (RA) or intermittent hypoxia (IH) consisting of 12% O(2) during hyperoxia (50% O(2)) from birth (P0) had single daily IP injections of Caff from P0-P13 or saline; and/or ocular Keto (Acuvail, 0.45% ophthalmic solution) administered subcutaneously over the eyes from P5-P7. Pups were studied at P14 or placed in RA for recovery from IH (IHR) until P21. Eyes were examined for neovascularization, histopathology, growth factors, and VEGF-signaling genes. RESULTS: Severe retinal damage noted during IHR in the untreated groups evidenced by hemorrhage, neovascularization, and oxygen-induced retinopathy (OIR) pathologies were prevented with Keto/Caff treatment. Keto and/or Caff treatment in IH also promoted retinal neural development evidenced by eye opening (92%, P < 0.001 vs. 31% in the placebo-treated IH group). No corneal pathologies were noted with Keto. CONCLUSION. Caff or Keto given individually reduced retinal neovascularization, but the two drugs given together prevented severe OIR. Nature Publishing Group 2016-10 2016-07-20 /pmc/articles/PMC5030702/ /pubmed/27438224 http://dx.doi.org/10.1038/pr.2016.105 Text en Copyright © 2016 Official journal of the International Pediatric Research Foundation, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Translational Investigation Aranda, Jacob V. Cai, Charles L. Ahmad, Taimur Bronshtein, Vadim Sadeh, Jonathan Valencia, Gloria B. Lazzaro, Douglas R. Beharry, Kay D. Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
title | Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
title_full | Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
title_fullStr | Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
title_full_unstemmed | Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
title_short | Pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
title_sort | pharmacologic synergism of ocular ketorolac and systemic caffeine citrate in rat oxygen-induced retinopathy |
topic | Translational Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030702/ https://www.ncbi.nlm.nih.gov/pubmed/27438224 http://dx.doi.org/10.1038/pr.2016.105 |
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