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Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases

Pathological neovascularization is a hallmark of late stage neovascular (wet) age-related macular degeneration (AMD) and the leading cause of blindness in people over the age of 50 in the western world. The treatments focus on suppression of choroidal neovascularization (CNV), while current approved...

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Autores principales: Benny, Ofra, Nakai, Kei, Yoshimura, Takeru, Bazinet, Lauren, Akula, James D., Nakao, Shintaro, Hafezi-Moghadam, Ali, Panigrahy, Dipak, Pakneshan, Pouya, D'Amato, Robert J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2931703/
https://www.ncbi.nlm.nih.gov/pubmed/20824139
http://dx.doi.org/10.1371/journal.pone.0012515
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author Benny, Ofra
Nakai, Kei
Yoshimura, Takeru
Bazinet, Lauren
Akula, James D.
Nakao, Shintaro
Hafezi-Moghadam, Ali
Panigrahy, Dipak
Pakneshan, Pouya
D'Amato, Robert J.
author_facet Benny, Ofra
Nakai, Kei
Yoshimura, Takeru
Bazinet, Lauren
Akula, James D.
Nakao, Shintaro
Hafezi-Moghadam, Ali
Panigrahy, Dipak
Pakneshan, Pouya
D'Amato, Robert J.
author_sort Benny, Ofra
collection PubMed
description Pathological neovascularization is a hallmark of late stage neovascular (wet) age-related macular degeneration (AMD) and the leading cause of blindness in people over the age of 50 in the western world. The treatments focus on suppression of choroidal neovascularization (CNV), while current approved therapies are limited to inhibiting vascular endothelial growth factor (VEGF) exclusively. However, this treatment does not address the underlying cause of AMD, and the loss of VEGF's neuroprotective can be a potential side effect. Therapy which targets the key processes in AMD, the pathological neovascularization, vessel leakage and inflammation could bring a major shift in the approach to disease treatment and prevention. In this study we have demonstrated the efficacy of such broad spectrum antiangiogenic therapy on mouse model of AMD. METHODS AND FINDINGS: Lodamin, a polymeric formulation of TNP-470, is a potent broad-spectrum antiangiogenic drug. Lodamin significantly reduced key processes involved in AMD progression as demonstrated in mice and rats. Its suppressive effects on angiogenesis, vascular leakage and inflammation were studied in a wide array of assays including; a Matrigel, delayed-type hypersensitivity (DTH), Miles assay, laser-induced CNV and corneal micropocket assay. Lodamin significantly suppressed the secretion of various pro-inflammatory cytokines in the CNV lesion including monocyte chemotactic protein-1 (MCP-1/Ccl2). Importantly, Lodamin was found to regress established CNV lesions, unlike soluble fms-like tyrosine kinase-1 (sFlk-1). The drug was found to be safe in mice and have little toxicity as demonstrated by electroretinography (ERG) assessing retinal and by histology. CONCLUSIONS: Lodamin, a polymer formulation of TNP-470, was identified as a first in its class, broad-spectrum antiangiogenic drug that can be administered orally or locally to treat corneal and retinal neovascularization. Several unique properties make Lodamin especially beneficial for ophthalmic use. Our results support the concept that broad spectrum antiangiogenic drugs are promising agents for AMD treatment and prevention.
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spelling pubmed-29317032010-09-03 Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases Benny, Ofra Nakai, Kei Yoshimura, Takeru Bazinet, Lauren Akula, James D. Nakao, Shintaro Hafezi-Moghadam, Ali Panigrahy, Dipak Pakneshan, Pouya D'Amato, Robert J. PLoS One Research Article Pathological neovascularization is a hallmark of late stage neovascular (wet) age-related macular degeneration (AMD) and the leading cause of blindness in people over the age of 50 in the western world. The treatments focus on suppression of choroidal neovascularization (CNV), while current approved therapies are limited to inhibiting vascular endothelial growth factor (VEGF) exclusively. However, this treatment does not address the underlying cause of AMD, and the loss of VEGF's neuroprotective can be a potential side effect. Therapy which targets the key processes in AMD, the pathological neovascularization, vessel leakage and inflammation could bring a major shift in the approach to disease treatment and prevention. In this study we have demonstrated the efficacy of such broad spectrum antiangiogenic therapy on mouse model of AMD. METHODS AND FINDINGS: Lodamin, a polymeric formulation of TNP-470, is a potent broad-spectrum antiangiogenic drug. Lodamin significantly reduced key processes involved in AMD progression as demonstrated in mice and rats. Its suppressive effects on angiogenesis, vascular leakage and inflammation were studied in a wide array of assays including; a Matrigel, delayed-type hypersensitivity (DTH), Miles assay, laser-induced CNV and corneal micropocket assay. Lodamin significantly suppressed the secretion of various pro-inflammatory cytokines in the CNV lesion including monocyte chemotactic protein-1 (MCP-1/Ccl2). Importantly, Lodamin was found to regress established CNV lesions, unlike soluble fms-like tyrosine kinase-1 (sFlk-1). The drug was found to be safe in mice and have little toxicity as demonstrated by electroretinography (ERG) assessing retinal and by histology. CONCLUSIONS: Lodamin, a polymer formulation of TNP-470, was identified as a first in its class, broad-spectrum antiangiogenic drug that can be administered orally or locally to treat corneal and retinal neovascularization. Several unique properties make Lodamin especially beneficial for ophthalmic use. Our results support the concept that broad spectrum antiangiogenic drugs are promising agents for AMD treatment and prevention. Public Library of Science 2010-09-01 /pmc/articles/PMC2931703/ /pubmed/20824139 http://dx.doi.org/10.1371/journal.pone.0012515 Text en Benny et al. http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Benny, Ofra
Nakai, Kei
Yoshimura, Takeru
Bazinet, Lauren
Akula, James D.
Nakao, Shintaro
Hafezi-Moghadam, Ali
Panigrahy, Dipak
Pakneshan, Pouya
D'Amato, Robert J.
Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases
title Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases
title_full Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases
title_fullStr Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases
title_full_unstemmed Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases
title_short Broad Spectrum Antiangiogenic Treatment for Ocular Neovascular Diseases
title_sort broad spectrum antiangiogenic treatment for ocular neovascular diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2931703/
https://www.ncbi.nlm.nih.gov/pubmed/20824139
http://dx.doi.org/10.1371/journal.pone.0012515
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