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

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 a...

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Veröffentlicht in:Toxicology and applied pharmacology 2003-07, Vol.190 (1), p.65-71
Hauptverfasser: Lam, Chen-Fuh, Caterina, Paul, Filion, Pierre, Ilett, Kenneth F., van Heerden, Peter V.
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creator Lam, Chen-Fuh
Caterina, Paul
Filion, Pierre
Ilett, Kenneth F.
van Heerden, Peter V.
description 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.
doi_str_mv 10.1016/S0041-008X(03)00193-5
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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. 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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. 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Drug treatments</subject><subject>Polyamines - administration &amp; dosage</subject><subject>Polyamines - blood</subject><subject>Polyamines - toxicity</subject><subject>Pulmonary Surfactant-Associated Protein B - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Swine</subject><subject>Trachea - drug effects</subject><subject>Trachea - pathology</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcuKFTEQhoMozpnRR1CyUcZFa-XSfTqrQQZvMODCEdyFdFLxRLo7xyQtHp_JhzTngrMSVwmV7_-rUj8hTxi8ZMC6V58AJGsA-i-XIF4AMCWa9h5ZMVBdA0KI-2T1Fzkj5zl_AwAlJXtIzhjvBVv3ckV-326QZuOx7Gj01GCKOY7hFzrqApbNbsQZSwpmCjPSOdSrpfFncEiNc4st1PiCieYwfx2xcTHvHyocckmmhDjTEqmZMZcNloPvNlSy5Fp0dFrGErb_Fto4Zxvikmmt5UfkgTdjxsen84J8fvvm9vp9c_Px3Yfr1zeNlZyXxjnvwXvnHaie94PkTPJOKcm8RNYpHEzrmOFr1aIZsGWdU4YPXnG-dq3pxAV5fvTdpvh9qaPrKWSL41j_UWfRrF8rBT1UsD2Ctq4tJ_R6m8Jk0k4z0PuY9CEmvc9Ag9CHmHRbdU9PDZZhQnenOuVSgWcnwGRrRp_MbEO-46RqeSf2RldHDus6fgRMuq4LZ4suJLRFuxj-M8ofqm61fg</recordid><startdate>20030701</startdate><enddate>20030701</enddate><creator>Lam, Chen-Fuh</creator><creator>Caterina, Paul</creator><creator>Filion, Pierre</creator><creator>Ilett, Kenneth F.</creator><creator>van Heerden, Peter V.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20030701</creationdate><title>The safety of aerosolized diethylenetriamine nitric oxide adduct after single-dose administration to anesthetized piglets and multiple-dose administration to conscious rats</title><author>Lam, Chen-Fuh ; Caterina, Paul ; Filion, Pierre ; Ilett, Kenneth F. ; van Heerden, Peter V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-ddff0ffdfd09828b4214269941f4e169eba5d1a2795eabe516d9a2bf9227d5a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Administration, Inhalation</topic><topic>Aerosols</topic><topic>Anesthesia</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Guinea Pigs</topic><topic>Lung Diseases - chemically induced</topic><topic>Lung Diseases - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methemoglobin - metabolism</topic><topic>Microscopy, Electron, Scanning Transmission</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - metabolism</topic><topic>Nitric Oxide - chemistry</topic><topic>Nitric Oxide Donors - administration &amp; dosage</topic><topic>Nitric Oxide Donors - blood</topic><topic>Nitric Oxide Donors - toxicity</topic><topic>Nitrites - blood</topic><topic>Organ Size - drug effects</topic><topic>Pharmacology. 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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.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>12831784</pmid><doi>10.1016/S0041-008X(03)00193-5</doi><tpages>7</tpages></addata></record>
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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
title The safety of aerosolized diethylenetriamine nitric oxide adduct after single-dose administration to anesthetized piglets and multiple-dose administration to conscious rats
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