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Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation

BACKGROUND: Nowadays use of specific antivenin for latrodectism is considered as the most effective treatment in the world. This study was undertaken to investigate the efficacy of specific antivenom against histopathological complications caused by Latrodectus dahli venom on liver, heart and kidney...

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Autores principales: Valikhanfard-Zanjani, Elham, Zare-Mirakabadi, Abbas, Zayerzadeh, Ehsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629305/
https://www.ncbi.nlm.nih.gov/pubmed/29018830
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author Valikhanfard-Zanjani, Elham
Zare-Mirakabadi, Abbas
Zayerzadeh, Ehsan
author_facet Valikhanfard-Zanjani, Elham
Zare-Mirakabadi, Abbas
Zayerzadeh, Ehsan
author_sort Valikhanfard-Zanjani, Elham
collection PubMed
description BACKGROUND: Nowadays use of specific antivenin for latrodectism is considered as the most effective treatment in the world. This study was undertaken to investigate the efficacy of specific antivenom against histopathological complications caused by Latrodectus dahli venom on liver, heart and kidneys tissues within 72h. METHODS: Two groups were selected, each one contained 6 male New Zealand rabbits weighing 2±0.5kg. The animals were anesthetized with 0.5ml ketamine and 0.5ml xylazine by intramuscular route. The L. dahli venom (0.5mg/kg) was injected subcutaneously to both the groups. The second group of rabbits 24h after the venom injection received specific antivenom by intravenous route. Seventy-two hours after the venom and antivenom injections, the rabbits were dissected to obtain heart, liver and kidney tissues. The tissues were stained by hematoxylin and eosin stains and histopathological studies were examined by optical microscope. RESULTS: In group one, the venom induced myocytolysis, myocarditis, coagulation necrosis in the heart tissue and the liver tissue showed central vein congestion, congested vessels, dilated sinusoids and inflammation. However, no significant histopathological complications were observed in kidney tissues. In the second group, antivenom injection greatly prevented escalation of the complications on foresaid tissues. CONCLUSION: Latrodectus dahli venom induces histopathological complications on vital organs. Specific antivenom injection, 24h after the venom injection, could protect the tissues from incidence and intensification of histopathological complications. Future studies in human beings should be conducted to assess the protection against the specific-Latrodectus antivenin.
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spelling pubmed-56293052017-10-10 Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation Valikhanfard-Zanjani, Elham Zare-Mirakabadi, Abbas Zayerzadeh, Ehsan J Arthropod Borne Dis Original Article BACKGROUND: Nowadays use of specific antivenin for latrodectism is considered as the most effective treatment in the world. This study was undertaken to investigate the efficacy of specific antivenom against histopathological complications caused by Latrodectus dahli venom on liver, heart and kidneys tissues within 72h. METHODS: Two groups were selected, each one contained 6 male New Zealand rabbits weighing 2±0.5kg. The animals were anesthetized with 0.5ml ketamine and 0.5ml xylazine by intramuscular route. The L. dahli venom (0.5mg/kg) was injected subcutaneously to both the groups. The second group of rabbits 24h after the venom injection received specific antivenom by intravenous route. Seventy-two hours after the venom and antivenom injections, the rabbits were dissected to obtain heart, liver and kidney tissues. The tissues were stained by hematoxylin and eosin stains and histopathological studies were examined by optical microscope. RESULTS: In group one, the venom induced myocytolysis, myocarditis, coagulation necrosis in the heart tissue and the liver tissue showed central vein congestion, congested vessels, dilated sinusoids and inflammation. However, no significant histopathological complications were observed in kidney tissues. In the second group, antivenom injection greatly prevented escalation of the complications on foresaid tissues. CONCLUSION: Latrodectus dahli venom induces histopathological complications on vital organs. Specific antivenom injection, 24h after the venom injection, could protect the tissues from incidence and intensification of histopathological complications. Future studies in human beings should be conducted to assess the protection against the specific-Latrodectus antivenin. Tehran University of Medical Sciences 2017-03-14 /pmc/articles/PMC5629305/ /pubmed/29018830 Text en Copyright© Iranian Society of Medical Entomology & Tehran University of Medical Sciences http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Valikhanfard-Zanjani, Elham
Zare-Mirakabadi, Abbas
Zayerzadeh, Ehsan
Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation
title Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation
title_full Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation
title_fullStr Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation
title_full_unstemmed Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation
title_short Antivenom Efficacy in Neutralizing Histopathological Complications Following Latrodectus dahli Envenomation
title_sort antivenom efficacy in neutralizing histopathological complications following latrodectus dahli envenomation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629305/
https://www.ncbi.nlm.nih.gov/pubmed/29018830
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