Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/S1678-91992011000200011 http://hdl.handle.net/11449/226358 |
Resumo: | In the present study, the effects of Polybia paulista venom (PPV) on renal and vascular tissues were investigated. Isolated kidneys perfused with PPV (1 and 3 μg/mL) had increased perfusion pressure, renal vascular resistance, urinary flow, and glomerular filtration rate; and reduced sodium tubular transport. Histological evaluation demonstrated deposits of proteins in Bowman's space and tubular lumen, and focal areas of necrosis. The venom promoted a cytotoxic effect on Madin-Darby canine kidney (MDCK) cells. A significant increase in lactic dehydrogenase levels was observed in response to venom exposure. In isolated mesenteric vascular beds, pressure and vascular resistance augmented in a dose-dependent manner. PPV increased the contractility of aortic rings maintained under basal tension. This contractile response was inhibited when preparations were maintained in Ca2+-free medium. Likewise, verapamil, a voltage-gated calcium channel blocker, also inhibited the contractile response. In this study, phentolamine, a blocker of α-adrenergic receptor blocker, significantly reduced the contractile effect of PPV in the aortic ring. In conclusion, PPV produced nephrotoxicity, which suggests a direct effect on necrotic cellular death in renal tubule cells. The vascular contractile effect of PPV appears to involve calcium influx through voltage-gated calcium channels via adrenergic regulation. © CEVAP 2011. |
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Renal- and calcium-dependent vascular effects of Polybia paulista wasp venomAortaKidneyMDCKPolybia paulistaVenomIn the present study, the effects of Polybia paulista venom (PPV) on renal and vascular tissues were investigated. Isolated kidneys perfused with PPV (1 and 3 μg/mL) had increased perfusion pressure, renal vascular resistance, urinary flow, and glomerular filtration rate; and reduced sodium tubular transport. Histological evaluation demonstrated deposits of proteins in Bowman's space and tubular lumen, and focal areas of necrosis. The venom promoted a cytotoxic effect on Madin-Darby canine kidney (MDCK) cells. A significant increase in lactic dehydrogenase levels was observed in response to venom exposure. In isolated mesenteric vascular beds, pressure and vascular resistance augmented in a dose-dependent manner. PPV increased the contractility of aortic rings maintained under basal tension. This contractile response was inhibited when preparations were maintained in Ca2+-free medium. Likewise, verapamil, a voltage-gated calcium channel blocker, also inhibited the contractile response. In this study, phentolamine, a blocker of α-adrenergic receptor blocker, significantly reduced the contractile effect of PPV in the aortic ring. In conclusion, PPV produced nephrotoxicity, which suggests a direct effect on necrotic cellular death in renal tubule cells. The vascular contractile effect of PPV appears to involve calcium influx through voltage-gated calcium channels via adrenergic regulation. © CEVAP 2011.Department of Physiology and Pharmacology Federal University of Ceará, FortalezaDepartment of Clinical and Toxicological Analyses Federal University of Ceará, Fortaleza, Ceará StateSão Paulo Experimental Coast Campus São Paulo State University (UNESP - Univ Estadual Paulista), São Vicente, São Paulo StateSão Paulo Experimental Coast Campus São Paulo State University (UNESP - Univ Estadual Paulista), São Vicente, São Paulo StateFederal University of CearáUniversidade Estadual Paulista (UNESP)Vinhote, J. F.C.Torres, A. F.C.Dantas, R. T.Praciano, T. P.Menezes, R. R.P.P.B.Sousa, D. F.Brito, T. S.Lima, F. J.B.Toyama, M. H. [UNESP]Magalhães, P. J.Monteiro, H. A.S.Martins-Nunes, A. M.C.2022-04-28T22:37:26Z2022-04-28T22:37:26Z2011-06-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article199-208http://dx.doi.org/10.1590/S1678-91992011000200011Journal of Venomous Animals and Toxins Including Tropical Diseases, v. 17, n. 2, p. 199-208, 2011.1678-9199http://hdl.handle.net/11449/22635810.1590/S1678-919920110002000112-s2.0-79958155374Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Venomous Animals and Toxins Including Tropical Diseasesinfo:eu-repo/semantics/openAccess2022-04-28T22:37:26Zoai:repositorio.unesp.br:11449/226358Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:31:47.698693Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
title |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
spellingShingle |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom Vinhote, J. F.C. Aorta Kidney MDCK Polybia paulista Venom |
title_short |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
title_full |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
title_fullStr |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
title_full_unstemmed |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
title_sort |
Renal- and calcium-dependent vascular effects of Polybia paulista wasp venom |
author |
Vinhote, J. F.C. |
author_facet |
Vinhote, J. F.C. Torres, A. F.C. Dantas, R. T. Praciano, T. P. Menezes, R. R.P.P.B. Sousa, D. F. Brito, T. S. Lima, F. J.B. Toyama, M. H. [UNESP] Magalhães, P. J. Monteiro, H. A.S. Martins-Nunes, A. M.C. |
author_role |
author |
author2 |
Torres, A. F.C. Dantas, R. T. Praciano, T. P. Menezes, R. R.P.P.B. Sousa, D. F. Brito, T. S. Lima, F. J.B. Toyama, M. H. [UNESP] Magalhães, P. J. Monteiro, H. A.S. Martins-Nunes, A. M.C. |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Federal University of Ceará Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Vinhote, J. F.C. Torres, A. F.C. Dantas, R. T. Praciano, T. P. Menezes, R. R.P.P.B. Sousa, D. F. Brito, T. S. Lima, F. J.B. Toyama, M. H. [UNESP] Magalhães, P. J. Monteiro, H. A.S. Martins-Nunes, A. M.C. |
dc.subject.por.fl_str_mv |
Aorta Kidney MDCK Polybia paulista Venom |
topic |
Aorta Kidney MDCK Polybia paulista Venom |
description |
In the present study, the effects of Polybia paulista venom (PPV) on renal and vascular tissues were investigated. Isolated kidneys perfused with PPV (1 and 3 μg/mL) had increased perfusion pressure, renal vascular resistance, urinary flow, and glomerular filtration rate; and reduced sodium tubular transport. Histological evaluation demonstrated deposits of proteins in Bowman's space and tubular lumen, and focal areas of necrosis. The venom promoted a cytotoxic effect on Madin-Darby canine kidney (MDCK) cells. A significant increase in lactic dehydrogenase levels was observed in response to venom exposure. In isolated mesenteric vascular beds, pressure and vascular resistance augmented in a dose-dependent manner. PPV increased the contractility of aortic rings maintained under basal tension. This contractile response was inhibited when preparations were maintained in Ca2+-free medium. Likewise, verapamil, a voltage-gated calcium channel blocker, also inhibited the contractile response. In this study, phentolamine, a blocker of α-adrenergic receptor blocker, significantly reduced the contractile effect of PPV in the aortic ring. In conclusion, PPV produced nephrotoxicity, which suggests a direct effect on necrotic cellular death in renal tubule cells. The vascular contractile effect of PPV appears to involve calcium influx through voltage-gated calcium channels via adrenergic regulation. © CEVAP 2011. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-06-13 2022-04-28T22:37:26Z 2022-04-28T22:37:26Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S1678-91992011000200011 Journal of Venomous Animals and Toxins Including Tropical Diseases, v. 17, n. 2, p. 199-208, 2011. 1678-9199 http://hdl.handle.net/11449/226358 10.1590/S1678-91992011000200011 2-s2.0-79958155374 |
url |
http://dx.doi.org/10.1590/S1678-91992011000200011 http://hdl.handle.net/11449/226358 |
identifier_str_mv |
Journal of Venomous Animals and Toxins Including Tropical Diseases, v. 17, n. 2, p. 199-208, 2011. 1678-9199 10.1590/S1678-91992011000200011 2-s2.0-79958155374 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Venomous Animals and Toxins Including Tropical Diseases |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
199-208 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128526832893952 |