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An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom

BACKGROUND: Hemolyis of red blood cells is a serious toxic effect commonly found among patients envenomed by Hemiscorpius lepturus scorpion. OBJECTIVES: The aim of the present study was to evlaute the efficay of the avaible polyvalent antivneom in preventing this phenomena. MATERIALS AND METHODS: Us...

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Autores principales: Pipelzadeh, Mohammad Hassan, Pipelzadeh, Mahsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: DocS 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941864/
https://www.ncbi.nlm.nih.gov/pubmed/24624150
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author Pipelzadeh, Mohammad Hassan
Pipelzadeh, Mahsa
author_facet Pipelzadeh, Mohammad Hassan
Pipelzadeh, Mahsa
author_sort Pipelzadeh, Mohammad Hassan
collection PubMed
description BACKGROUND: Hemolyis of red blood cells is a serious toxic effect commonly found among patients envenomed by Hemiscorpius lepturus scorpion. OBJECTIVES: The aim of the present study was to evlaute the efficay of the avaible polyvalent antivneom in preventing this phenomena. MATERIALS AND METHODS: Using a red blood cell fragility test, the anti-hemolytic effectiveness of a new antivenom serum against Hemiscorpius lepturus venom was investigated. Hemolysis was measured using spectrophotometry. RESULTS: Addition of venom (2, 10, 20, and 40 µg/ml) to 0.5 ml of 5% washed red blood cell suspension produced concentration-dependent hemolysis. Both the pre-incubation of red blood cell suspensions with various concentrations of antivenom (4%, 10%, and 20% v/v) and the co-administration of antivenom with 20 µg/ml venom resulted in concentration-dependent protection against hemolysis. Both the methods resulted in protection against hemolysis at the antivenom concentration of 20% (v/v). However, the inhibition of hemolysis after 24 h was found to be greater for red blood cell suspensions preincubated with antivenom (75% inhibition) than for red blood cell suspensions that were co-administered with antivenom and venom (50% inhibition). CONCLUSIONS: The results suggest that the antivenom against H. lepturus venom is useful in inhibiting hemolysis produced by the venom, but the duration of protection is relatively short and appropriate measures need to be taken, depending on the patients’ clinical progress, to re-administer the antivenom at intervals less than 8 h. This proposed treatment method merits further clinical assessment.
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spelling pubmed-39418642014-03-12 An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom Pipelzadeh, Mohammad Hassan Pipelzadeh, Mahsa Jundishapur J Nat Pharm Prod Original Article BACKGROUND: Hemolyis of red blood cells is a serious toxic effect commonly found among patients envenomed by Hemiscorpius lepturus scorpion. OBJECTIVES: The aim of the present study was to evlaute the efficay of the avaible polyvalent antivneom in preventing this phenomena. MATERIALS AND METHODS: Using a red blood cell fragility test, the anti-hemolytic effectiveness of a new antivenom serum against Hemiscorpius lepturus venom was investigated. Hemolysis was measured using spectrophotometry. RESULTS: Addition of venom (2, 10, 20, and 40 µg/ml) to 0.5 ml of 5% washed red blood cell suspension produced concentration-dependent hemolysis. Both the pre-incubation of red blood cell suspensions with various concentrations of antivenom (4%, 10%, and 20% v/v) and the co-administration of antivenom with 20 µg/ml venom resulted in concentration-dependent protection against hemolysis. Both the methods resulted in protection against hemolysis at the antivenom concentration of 20% (v/v). However, the inhibition of hemolysis after 24 h was found to be greater for red blood cell suspensions preincubated with antivenom (75% inhibition) than for red blood cell suspensions that were co-administered with antivenom and venom (50% inhibition). CONCLUSIONS: The results suggest that the antivenom against H. lepturus venom is useful in inhibiting hemolysis produced by the venom, but the duration of protection is relatively short and appropriate measures need to be taken, depending on the patients’ clinical progress, to re-administer the antivenom at intervals less than 8 h. This proposed treatment method merits further clinical assessment. DocS 2012-01-04 2012 /pmc/articles/PMC3941864/ /pubmed/24624150 Text en Copyright © 2012 DocS. All rights reserved. http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Pipelzadeh, Mohammad Hassan
Pipelzadeh, Mahsa
An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom
title An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom
title_full An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom
title_fullStr An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom
title_full_unstemmed An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom
title_short An In Vitro Method for Assessing the Efficacy of Antivenom Against Hemiscorpius lepturus Venom
title_sort in vitro method for assessing the efficacy of antivenom against hemiscorpius lepturus venom
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941864/
https://www.ncbi.nlm.nih.gov/pubmed/24624150
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