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Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing
BACKGROUND: Better and safer antidotes against cyanide poisoning are needed. Prior study has shown a favorable effect of isosorbide dinitrate (ISDN) on the survival of cyanide-poisoned rabbits when administered as early as 1 min after poisoning. The aim of the current study was to further evaluate t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348846/ https://www.ncbi.nlm.nih.gov/pubmed/28288687 http://dx.doi.org/10.1186/s40360-017-0122-0 |
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author | Lavon, Ophir Avrahami, Amit Eisenkraft, Arik |
author_facet | Lavon, Ophir Avrahami, Amit Eisenkraft, Arik |
author_sort | Lavon, Ophir |
collection | PubMed |
description | BACKGROUND: Better and safer antidotes against cyanide poisoning are needed. Prior study has shown a favorable effect of isosorbide dinitrate (ISDN) on the survival of cyanide-poisoned rabbits when administered as early as 1 min after poisoning. The aim of the current study was to further evaluate the efficacy of intravenous ISDN administered in clinically relevant timing for first responders. METHODS: A comparative animal study using 24 rabbits in 4 randomized study groups was performed. Animals were poisoned with intravenous potassium cyanide (1 mg/kg). Animals in Group 1 served as controls and received no treatment. Groups 2–4 animals were treated intravenously with ISDN (50 μg/kg) after poisoning; one group after 3 min, another group after 5 min and the last after 7 min. Animals were observed for 30 min after poisoning. The study endpoints included survival rate, clinical status, blood pressure, pulse per minute, blood lactate and pH. RESULTS: Five of 6 animals (83.3%) from every treatment group survived the whole observation period while all control untreated animals died. All the rabbits collapsed immediately after exposure, showing rapidly deteriorated vital signs with lactic metabolic acidosis (peak blood lactate levels of 18.1 to 19.0 mmol/L on average at 10 min post exposure). Vital signs, clinical scores, and blood gases of treated rabbits gradually improved. CONCLUSION: Poisoned rabbits showed improved short-term survival following the administration of ISDN up to 7 min after lethal cyanide poisoning of. We see a potential for ISDN as an antidote against cyanide poisoning. |
format | Online Article Text |
id | pubmed-5348846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53488462017-03-14 Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing Lavon, Ophir Avrahami, Amit Eisenkraft, Arik BMC Pharmacol Toxicol Research Article BACKGROUND: Better and safer antidotes against cyanide poisoning are needed. Prior study has shown a favorable effect of isosorbide dinitrate (ISDN) on the survival of cyanide-poisoned rabbits when administered as early as 1 min after poisoning. The aim of the current study was to further evaluate the efficacy of intravenous ISDN administered in clinically relevant timing for first responders. METHODS: A comparative animal study using 24 rabbits in 4 randomized study groups was performed. Animals were poisoned with intravenous potassium cyanide (1 mg/kg). Animals in Group 1 served as controls and received no treatment. Groups 2–4 animals were treated intravenously with ISDN (50 μg/kg) after poisoning; one group after 3 min, another group after 5 min and the last after 7 min. Animals were observed for 30 min after poisoning. The study endpoints included survival rate, clinical status, blood pressure, pulse per minute, blood lactate and pH. RESULTS: Five of 6 animals (83.3%) from every treatment group survived the whole observation period while all control untreated animals died. All the rabbits collapsed immediately after exposure, showing rapidly deteriorated vital signs with lactic metabolic acidosis (peak blood lactate levels of 18.1 to 19.0 mmol/L on average at 10 min post exposure). Vital signs, clinical scores, and blood gases of treated rabbits gradually improved. CONCLUSION: Poisoned rabbits showed improved short-term survival following the administration of ISDN up to 7 min after lethal cyanide poisoning of. We see a potential for ISDN as an antidote against cyanide poisoning. BioMed Central 2017-03-14 /pmc/articles/PMC5348846/ /pubmed/28288687 http://dx.doi.org/10.1186/s40360-017-0122-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lavon, Ophir Avrahami, Amit Eisenkraft, Arik Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
title | Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
title_full | Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
title_fullStr | Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
title_full_unstemmed | Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
title_short | Effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
title_sort | effectiveness of isosorbide dinitrate in cyanide poisoning as a function of the administration timing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348846/ https://www.ncbi.nlm.nih.gov/pubmed/28288687 http://dx.doi.org/10.1186/s40360-017-0122-0 |
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