The safety of aerosolized diethylenetriamine nitric oxide adduct after single-dose administration to anesthetized piglets and multiple-dose administration to conscious rats

• Published in: Toxicology and applied pharmacology Vol. 190; no. 1; pp. 65 - 71
• Main Authors: Lam, Chen-Fuh, Caterina, Paul, Filion, Pierre, Ilett, Kenneth F., van Heerden, Peter V.
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 01.07.2003; Elsevier
• Subjects: Administration, Inhalation; Aerosols; Anesthesia; Animals; Biological and medical sciences; Drug toxicity and drugs side effects treatment; Guinea Pigs; Lung Diseases - chemically induced; Lung Diseases - pathology; Male; Medical sciences; Methemoglobin - metabolism; Microscopy, Electron, Scanning Transmission; Miscellaneous (drug allergy, mutagens, teratogens...); Neutrophils - drug effects; Neutrophils - metabolism; Nitric Oxide - chemistry; Nitric Oxide Donors - administration & dosage; Nitric Oxide Donors - blood; Nitric Oxide Donors - toxicity; Nitrites - blood; Organ Size - drug effects; Pharmacology. Drug treatments; Polyamines - administration & dosage; Polyamines - blood; Polyamines - toxicity; Pulmonary Surfactant-Associated Protein B - metabolism; Rats; Rats, Wistar; Swine; Trachea - drug effects; Trachea - pathology; Vasodilator agent; Rat; Respiratory disease; Toxicity; Lung; Rodentia; Single dose; Cardiovascular disease; Inducer; Pulmonary hypertension; Inhalation; Pig; Multiple dose; Vertebrata; Mammalia; Animal; Nitric oxide; Artiodactyla; Ungulata
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/S0041-008X(03)00193-5

Diethylenetriamine nitric oxide adduct (DETA/NO) is a slow-release NO donor. It has been shown to be a selective pulmonary vasodilator in acute pulmonary hypertension. However, its potential toxicity after inhalation is unknown. This study investigated the potential toxicity of aerosolized DETA/NO after single- and multiple-dose exposure in animals. In the first part of the study, a single dose of DETA/NO (60 μmol) or placebo was aerosolized into the lungs of anesthetized piglets. Arterial methemoglobin and serum nitrite (NO2−) concentrations were measured after exposure. In the second part of the study, rats were exposed to aerosolized DETA/NO (60 μmol) or placebo for 7 days, and animals were euthanized 1, 3, 7, and 14 days after the first exposure. Serum NO2− and plasma surfactant protein B (SP-B) concentrations were measured. In both studies, acute lung inflammation was evaluated histopathologically (polymorphonuclear leucocytes (PMN) infiltration) and by measuring lung wet to dry weight ratio (LWDR). The tracheas of rats, which had the highest exposure, were further examined for ultrastructural changes using electron microscopy. In both rats and pigs, serum NO2− concentrations were elevated in all the DETA/NO-treated animals, indicating significant exposure to DETA/NO. Arterial methemoglobin was not increased by DETA/NO treatment. In the rats, plasma SP-B was not elevated by DETA/NO treatment. In addition, DETA/NO had no effects on PMN infiltration or LWDR in either animal model nor on the ultrastructure of large airways in rats. This study shows no evidence of pulmonary or hematological toxicity following single or repeated doses of DETA/NO in animals.