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Nitroxide pharmaceutical development for age-related degeneration and disease

Nitroxide small molecule agents are in development as preventative or therapeutic pharmaceutical drugs for age-related macular degeneration (AMD) and cardiovascular disease, which are two major diseases of aging. These aging diseases are associated with patient genetics, smoking, diet, oxidative str...

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Autores principales: Zarling, Jacob A., Brunt, Vienna E., Vallerga, Anne K., Li, Weixing, Tao, Albert, Zarling, David A., Minson, Christopher T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635221/
https://www.ncbi.nlm.nih.gov/pubmed/26594225
http://dx.doi.org/10.3389/fgene.2015.00325
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author Zarling, Jacob A.
Brunt, Vienna E.
Vallerga, Anne K.
Li, Weixing
Tao, Albert
Zarling, David A.
Minson, Christopher T.
author_facet Zarling, Jacob A.
Brunt, Vienna E.
Vallerga, Anne K.
Li, Weixing
Tao, Albert
Zarling, David A.
Minson, Christopher T.
author_sort Zarling, Jacob A.
collection PubMed
description Nitroxide small molecule agents are in development as preventative or therapeutic pharmaceutical drugs for age-related macular degeneration (AMD) and cardiovascular disease, which are two major diseases of aging. These aging diseases are associated with patient genetics, smoking, diet, oxidative stress, and chronic inflammation. Nitroxide drugs preventing aging-, smoking-, high sugar or high fat diet-, or radiation- and other environmental-induced pathophysiological conditions in aging disease are reviewed. Tempol (TP), Tempol Hydroxylamine (TP-H), and TP-H prodrug (OT-551) are evaluated in (1) non-smokers versus smokers with cutaneous microvascular dysfunction, rapidly reversed by cutaneous TP; (2) elderly cancer patients at risk for radiation-induced skin burns or hair loss, prevented by topical TP; and (3) elderly smoker or non-smoker AMD patients at risk for vision loss, prevented by daily eye drops of OT-551. The human data indicates safety and efficacy for these nitroxide drugs. Both TP and TP-H topically penetrate and function in skin or mucosa, protecting and treating radiation burns and hair loss or smoking-induced cutaneous vascular dysfunction. TP and TP-H do not penetrate the cornea, while OT-551 does effectively penetrate and travels to the back of the eye, preserving visual acuity and preserving normal and low light luminance in dry AMD smokers and non-smoker patients. Topical, oral, or injectable drug formulations are discussed.
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spelling pubmed-46352212015-11-20 Nitroxide pharmaceutical development for age-related degeneration and disease Zarling, Jacob A. Brunt, Vienna E. Vallerga, Anne K. Li, Weixing Tao, Albert Zarling, David A. Minson, Christopher T. Front Genet Genetics Nitroxide small molecule agents are in development as preventative or therapeutic pharmaceutical drugs for age-related macular degeneration (AMD) and cardiovascular disease, which are two major diseases of aging. These aging diseases are associated with patient genetics, smoking, diet, oxidative stress, and chronic inflammation. Nitroxide drugs preventing aging-, smoking-, high sugar or high fat diet-, or radiation- and other environmental-induced pathophysiological conditions in aging disease are reviewed. Tempol (TP), Tempol Hydroxylamine (TP-H), and TP-H prodrug (OT-551) are evaluated in (1) non-smokers versus smokers with cutaneous microvascular dysfunction, rapidly reversed by cutaneous TP; (2) elderly cancer patients at risk for radiation-induced skin burns or hair loss, prevented by topical TP; and (3) elderly smoker or non-smoker AMD patients at risk for vision loss, prevented by daily eye drops of OT-551. The human data indicates safety and efficacy for these nitroxide drugs. Both TP and TP-H topically penetrate and function in skin or mucosa, protecting and treating radiation burns and hair loss or smoking-induced cutaneous vascular dysfunction. TP and TP-H do not penetrate the cornea, while OT-551 does effectively penetrate and travels to the back of the eye, preserving visual acuity and preserving normal and low light luminance in dry AMD smokers and non-smoker patients. Topical, oral, or injectable drug formulations are discussed. Frontiers Media S.A. 2015-11-06 /pmc/articles/PMC4635221/ /pubmed/26594225 http://dx.doi.org/10.3389/fgene.2015.00325 Text en Copyright © 2015 Zarling, Brunt, Vallerga, Li, Tao, Zarling and Minson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Zarling, Jacob A.
Brunt, Vienna E.
Vallerga, Anne K.
Li, Weixing
Tao, Albert
Zarling, David A.
Minson, Christopher T.
Nitroxide pharmaceutical development for age-related degeneration and disease
title Nitroxide pharmaceutical development for age-related degeneration and disease
title_full Nitroxide pharmaceutical development for age-related degeneration and disease
title_fullStr Nitroxide pharmaceutical development for age-related degeneration and disease
title_full_unstemmed Nitroxide pharmaceutical development for age-related degeneration and disease
title_short Nitroxide pharmaceutical development for age-related degeneration and disease
title_sort nitroxide pharmaceutical development for age-related degeneration and disease
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635221/
https://www.ncbi.nlm.nih.gov/pubmed/26594225
http://dx.doi.org/10.3389/fgene.2015.00325
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