A Comparison of Potential Azide Antidotes in a Mouse Model.


Journal

Chemical research in toxicology
ISSN: 1520-5010
Titre abrégé: Chem Res Toxicol
Pays: United States
ID NLM: 8807448

Informations de publication

Date de publication:
17 02 2020
Historique:
pubmed: 11 1 2020
medline: 3 7 2021
entrez: 11 1 2020
Statut: ppublish

Résumé

Three cobalt-containing macrocyclic compounds previously shown to antagonize cyanide toxicity have been comparatively evaluated for the amelioration of sublethal azide toxicity in juvenile (7-8 weeks) Swiss-Webster mice. The lowest effective doses were determined for hydroxocobalamin, a cobalt porphyrin, and a cobalt-Schiff base macrocycle by giving the antidotes 5 min prior to the toxicant, 27 mg (415 μmol) /kg sodium azide. Both male and female mice were evaluated for their response to the toxicant as well as the antidotes, and no significant differences were noted once weight differences were taken into account. Two of the three compounds significantly decreased the recovery time of azide-intoxicated mice at 10 min after the administration of sodium azide, as determined by a behavioral test (pole climbing). Additionally, azide was determined to cause a several degree drop (∼3 °C) in measured tail temperature, and warming the mice led to a more rapid recovery. The mice were also shown to recover more rapidly when given sodium nitrite, 24 mg (350 μmol)/kg, 5 min after the toxicant; this treatment also suppressed the azide-induced tail temperature decrease. Electron paramagnetic resonance (EPR) measurements of mouse blood treated with sodium azide demonstrated the presence of nitrosylhemoglobin at levels of 10-20 μM which persisted for ∼300 min. The presence of the methemoglobin azide adduct was also detected by EPR at a maximum level of ∼300 μM, but these signals disappeared around 200 min after the administration of azide. The treatment of mice with 

Identifiants

pubmed: 31922405
doi: 10.1021/acs.chemrestox.9b00422
doi:

Substances chimiques

Antidotes 0
Coordination Complexes 0
Hemoglobins 0
Macrocyclic Compounds 0
nitrosyl hemoglobin 0
Cobalt 3G0H8C9362
Sodium Azide 968JJ8C9DV
Electron Transport Complex IV EC 1.9.3.1

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

594-603

Subventions

Organisme : NINDS NIH HHS
ID : R21 NS098989
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS109793
Pays : United States

Auteurs

Kristin L Frawley (KL)

Department of Environmental and Occupational Health, Graduate School of Public Health , The University of Pittsburgh , 130 DeSoto Street , Pittsburgh , Pennsylvania 15219 , United States.

Samantha Carpenter Totoni (S)

Department of Environmental and Occupational Health, Graduate School of Public Health , The University of Pittsburgh , 130 DeSoto Street , Pittsburgh , Pennsylvania 15219 , United States.

Yookyung Bae (Y)

Department of Environmental and Occupational Health, Graduate School of Public Health , The University of Pittsburgh , 130 DeSoto Street , Pittsburgh , Pennsylvania 15219 , United States.

Linda L Pearce (LL)

Department of Environmental and Occupational Health, Graduate School of Public Health , The University of Pittsburgh , 130 DeSoto Street , Pittsburgh , Pennsylvania 15219 , United States.

Jim Peterson (J)

Department of Environmental and Occupational Health, Graduate School of Public Health , The University of Pittsburgh , 130 DeSoto Street , Pittsburgh , Pennsylvania 15219 , United States.

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Classifications MeSH