Safety and feasibility of long-term intravenous sodium nitrite infusion in healthy volunteers

Ryszard M. Pluta, Edward H. Oldfield, Kamran D. Bakhtian, Ali Reza Fathi, René K. Smith, Hetty L. DeVroom, Masoud Nahavandi, Sukyung Woo, William D. Figg, Russell R. Lonser

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94 Scopus citations

Abstract

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.

Original languageEnglish
Article numbere14504
JournalPLoS ONE
Volume6
Issue number1
DOIs
StatePublished - 2011
Externally publishedYes

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