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Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta
BACKGROUND: Apis mellifera stings are a problem for public health worldwide, particularly in Latin America due to the aggressiveness of its Africanized honeybees. Massive poisoning by A. mellifera venom (AmV) affects mainly the cardiovascular system, and several works have described its actions on h...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849866/ https://www.ncbi.nlm.nih.gov/pubmed/24066982 http://dx.doi.org/10.1186/1678-9199-19-24 |
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author | Sousa, Paulo César P Brito, Teresinha S Freire, Daniel S Ximenes, Rafael M Magalhães, Pedro Jorge C Monteiro, Helena SA Alves, Renata S Martins, Alice Maria C Toyama, Daniela O Toyama, Marcos H |
author_facet | Sousa, Paulo César P Brito, Teresinha S Freire, Daniel S Ximenes, Rafael M Magalhães, Pedro Jorge C Monteiro, Helena SA Alves, Renata S Martins, Alice Maria C Toyama, Daniela O Toyama, Marcos H |
author_sort | Sousa, Paulo César P |
collection | PubMed |
description | BACKGROUND: Apis mellifera stings are a problem for public health worldwide, particularly in Latin America due to the aggressiveness of its Africanized honeybees. Massive poisoning by A. mellifera venom (AmV) affects mainly the cardiovascular system, and several works have described its actions on heart muscle. Nevertheless, no work on the pharmacological action mechanisms of the AmV in isolated aorta has been reported. Thus, the present work aimed to investigate the actions of AmV and its main fractions, phospholipase A(2) (PLA(2)) and melittin, on isolated aorta rings and a probable action mechanism. RESULTS: AmV and the complex PLA(2) + melittin (0.1-50 μg/mL) caused contraction in endothelium-containing aorta rings, but neither isolated PLA(2) nor melittin were able to reproduce the effect. Endothelium removal did not change the maximum vasoconstrictor effect elicited by AmV. Ca(2+)-free medium, as well as treatment with phentolamine (5 μM), verapamil (10 μM), losartan (100 μM), and U-73122 (10 μM, a phospholipase C inhibitor), eliminated the AmV-induced contractile effects. CONCLUSIONS: In conclusion, AmV caused contractile effect in aorta rings probably through the involvement of voltage-operated calcium channels, AT1 and α-adrenergic receptors via the downstream activation of phospholipase C. The protein complex, PLA(2) + melittin, was also able to induce vasoconstriction, whereas the isolated proteins were not. |
format | Online Article Text |
id | pubmed-3849866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38498662013-12-05 Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta Sousa, Paulo César P Brito, Teresinha S Freire, Daniel S Ximenes, Rafael M Magalhães, Pedro Jorge C Monteiro, Helena SA Alves, Renata S Martins, Alice Maria C Toyama, Daniela O Toyama, Marcos H J Venom Anim Toxins Incl Trop Dis Research BACKGROUND: Apis mellifera stings are a problem for public health worldwide, particularly in Latin America due to the aggressiveness of its Africanized honeybees. Massive poisoning by A. mellifera venom (AmV) affects mainly the cardiovascular system, and several works have described its actions on heart muscle. Nevertheless, no work on the pharmacological action mechanisms of the AmV in isolated aorta has been reported. Thus, the present work aimed to investigate the actions of AmV and its main fractions, phospholipase A(2) (PLA(2)) and melittin, on isolated aorta rings and a probable action mechanism. RESULTS: AmV and the complex PLA(2) + melittin (0.1-50 μg/mL) caused contraction in endothelium-containing aorta rings, but neither isolated PLA(2) nor melittin were able to reproduce the effect. Endothelium removal did not change the maximum vasoconstrictor effect elicited by AmV. Ca(2+)-free medium, as well as treatment with phentolamine (5 μM), verapamil (10 μM), losartan (100 μM), and U-73122 (10 μM, a phospholipase C inhibitor), eliminated the AmV-induced contractile effects. CONCLUSIONS: In conclusion, AmV caused contractile effect in aorta rings probably through the involvement of voltage-operated calcium channels, AT1 and α-adrenergic receptors via the downstream activation of phospholipase C. The protein complex, PLA(2) + melittin, was also able to induce vasoconstriction, whereas the isolated proteins were not. BioMed Central 2013-09-25 /pmc/articles/PMC3849866/ /pubmed/24066982 http://dx.doi.org/10.1186/1678-9199-19-24 Text en Copyright © 2013 Sousa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Sousa, Paulo César P Brito, Teresinha S Freire, Daniel S Ximenes, Rafael M Magalhães, Pedro Jorge C Monteiro, Helena SA Alves, Renata S Martins, Alice Maria C Toyama, Daniela O Toyama, Marcos H Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta |
title | Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta |
title_full | Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta |
title_fullStr | Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta |
title_full_unstemmed | Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta |
title_short | Vasoconstrictor effect of Africanized honeybee (Apis mellifera L.) venom on rat aorta |
title_sort | vasoconstrictor effect of africanized honeybee (apis mellifera l.) venom on rat aorta |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849866/ https://www.ncbi.nlm.nih.gov/pubmed/24066982 http://dx.doi.org/10.1186/1678-9199-19-24 |
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