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Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers

BACKGROUND: Infusion of sodium nitrite could provide sustained therapeutic concentrations of nitric oxide (NO) for the treatment of a variety of vascular disorders. The study was developed to determine the safety and feasibility of prolonged sodium nitrite infusion. METHODOLOGY: Healthy volunteers,...

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Autores principales: Pluta, Ryszard M., Oldfield, Edward H., Bakhtian, Kamran D., Fathi, Ali Reza, Smith, René K., DeVroom, Hetty L., Nahavandi, Masoud, Woo, Sukyung, Figg, William D., Lonser, Russell R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018414/
https://www.ncbi.nlm.nih.gov/pubmed/21249218
http://dx.doi.org/10.1371/journal.pone.0014504
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author Pluta, Ryszard M.
Oldfield, Edward H.
Bakhtian, Kamran D.
Fathi, Ali Reza
Smith, René K.
DeVroom, Hetty L.
Nahavandi, Masoud
Woo, Sukyung
Figg, William D.
Lonser, Russell R.
author_facet Pluta, Ryszard M.
Oldfield, Edward H.
Bakhtian, Kamran D.
Fathi, Ali Reza
Smith, René K.
DeVroom, Hetty L.
Nahavandi, Masoud
Woo, Sukyung
Figg, William D.
Lonser, Russell R.
author_sort Pluta, Ryszard M.
collection PubMed
description BACKGROUND: Infusion of sodium nitrite could provide sustained therapeutic concentrations of nitric oxide (NO) for the treatment of a variety of vascular disorders. The study was developed to determine the safety and feasibility of prolonged sodium nitrite infusion. METHODOLOGY: Healthy volunteers, aged 21 to 60 years old, were candidates for the study performed at the National Institutes of Health (NIH; protocol 05-N-0075) between July 2007 and August 2008. All subjects provided written consent to participate. Twelve subjects (5 males, 7 females; mean age, 38.8±9.2 years (range, 21–56 years)) were intravenously infused with increasing doses of sodium nitrite for 48 hours (starting dose at 4.2 µg/kg/hr; maximal dose of 533.8 µg/kg/hr). Clinical, physiologic and laboratory data before, during and after infusion were analyzed. FINDINGS: The maximal tolerated dose for intravenous infusion of sodium nitrite was 267 µg/kg/hr. Dose limiting toxicity occurred at 446 µg/kg/hr. Toxicity included a transient asymptomatic decrease of mean arterial blood pressure (more than 15 mmHg) and/or an asymptomatic increase of methemoglobin level above 5%. Nitrite, nitrate, S-nitrosothiols concentrations in plasma and whole blood increased in all subjects and returned to preinfusion baseline values within 12 hours after cessation of the infusion. The mean half-life of nitrite estimated at maximal tolerated dose was 45.3 minutes for plasma and 51.4 minutes for whole blood. CONCLUSION: Sodium nitrite can be safely infused intravenously at defined concentrations for prolonged intervals. These results should be valuable for developing studies to investigate new NO treatment paradigms for a variety of clinical disorders, including cerebral vasospasm after subarachnoid hemorrhage, and ischemia of the heart, liver, kidney and brain, as well as organ transplants, blood-brain barrier modulation and pulmonary hypertension. CLINICAL TRIAL REGISTRATION INFORMATION: http://www.clinicaltrials.gov; NCT00103025
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spelling pubmed-30184142011-01-19 Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers Pluta, Ryszard M. Oldfield, Edward H. Bakhtian, Kamran D. Fathi, Ali Reza Smith, René K. DeVroom, Hetty L. Nahavandi, Masoud Woo, Sukyung Figg, William D. Lonser, Russell R. PLoS One Clinical Trial BACKGROUND: Infusion of sodium nitrite could provide sustained therapeutic concentrations of nitric oxide (NO) for the treatment of a variety of vascular disorders. The study was developed to determine the safety and feasibility of prolonged sodium nitrite infusion. METHODOLOGY: Healthy volunteers, aged 21 to 60 years old, were candidates for the study performed at the National Institutes of Health (NIH; protocol 05-N-0075) between July 2007 and August 2008. All subjects provided written consent to participate. Twelve subjects (5 males, 7 females; mean age, 38.8±9.2 years (range, 21–56 years)) were intravenously infused with increasing doses of sodium nitrite for 48 hours (starting dose at 4.2 µg/kg/hr; maximal dose of 533.8 µg/kg/hr). Clinical, physiologic and laboratory data before, during and after infusion were analyzed. FINDINGS: The maximal tolerated dose for intravenous infusion of sodium nitrite was 267 µg/kg/hr. Dose limiting toxicity occurred at 446 µg/kg/hr. Toxicity included a transient asymptomatic decrease of mean arterial blood pressure (more than 15 mmHg) and/or an asymptomatic increase of methemoglobin level above 5%. Nitrite, nitrate, S-nitrosothiols concentrations in plasma and whole blood increased in all subjects and returned to preinfusion baseline values within 12 hours after cessation of the infusion. The mean half-life of nitrite estimated at maximal tolerated dose was 45.3 minutes for plasma and 51.4 minutes for whole blood. CONCLUSION: Sodium nitrite can be safely infused intravenously at defined concentrations for prolonged intervals. These results should be valuable for developing studies to investigate new NO treatment paradigms for a variety of clinical disorders, including cerebral vasospasm after subarachnoid hemorrhage, and ischemia of the heart, liver, kidney and brain, as well as organ transplants, blood-brain barrier modulation and pulmonary hypertension. CLINICAL TRIAL REGISTRATION INFORMATION: http://www.clinicaltrials.gov; NCT00103025 Public Library of Science 2011-01-10 /pmc/articles/PMC3018414/ /pubmed/21249218 http://dx.doi.org/10.1371/journal.pone.0014504 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Clinical Trial
Pluta, Ryszard M.
Oldfield, Edward H.
Bakhtian, Kamran D.
Fathi, Ali Reza
Smith, René K.
DeVroom, Hetty L.
Nahavandi, Masoud
Woo, Sukyung
Figg, William D.
Lonser, Russell R.
Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers
title Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers
title_full Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers
title_fullStr Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers
title_full_unstemmed Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers
title_short Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers
title_sort safety and feasibility of long-term intravenous sodium nitrite infusion in healthy volunteers
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018414/
https://www.ncbi.nlm.nih.gov/pubmed/21249218
http://dx.doi.org/10.1371/journal.pone.0014504
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