The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of Health & Biological Sciences |
DOI: | 10.12662/2317-3076jhbs.v5i4.1351.p306-310.2017 |
Texto Completo: | https://periodicos.unichristus.edu.br/jhbs/article/view/1351 |
Resumo: | Background: The vasorelaxant effect of lectins from leguminous plants (Diocleinae subtribe) is well described. However, this effect has been little explored for lectins isolated from Dalbergieae tribe, except for that of Vatairea guianensis, that induces vasorelaxation involving nitric oxide and the lectin domain. Objective: To evaluate the vasorelaxant effect of a lectin isolated from Lonchocarpus araripensis (LAL), Dalbergieae tribe, and the involvement of the lectin domain and endothelium derived relaxing factors. Methods: Aortic rings of Wistar rats (250 - 300 g) were mounted in organ bath and mantained in physiological conditions (CEUA No. 10130208-8/40). LAL (0.1–100 µg/ml) was added to phenylephrine (0.1 µM)-contracted tissues with either endothelium intact or denuded. In order to investigate the mechanisms of LAL relaxation, inhibitors of NOS (L-NAME: 100 µM), cyclooxygenase (indomethacin: 10 µM), or potassium channels (TEA: 5 mM) were added to endothelized tissues 30 min before contraction. The involvement of lectin domain was assessed by previous incubation of LAL (30 µg/ml) with GlcNAc (0.1 M). Results: LAL (0.1-100 µg/ml) induced relaxation only in endothelized aorta, being maximal at 100 µg/ml (62.57 ± 7.8%). The relaxant effect induced by LAL at 30 µg/ml (52.49 ± 10.32%) was abolished by previous incubation with GlcNAc. LAL relaxant effect (IC50 9.75 ± 7.1) was partially reversed by indomethacin (IC50 LAL + indomethacin: 30.47 ± 10.93) and was abolished by L-NAME or TEA. Conclusion: LAL exhibits vasorelaxant activity in contracted endothelized aorta of rats, involving the lectin domain, muscarinic receptor of acetylcholine and endothelial derived relaxing factors. |
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Journal of Health & Biological Sciences |
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The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxationCiências da Saúde; Ciências BiológicasLonchocarpus araripensis; Lectin; Vasorelaxant effect; Endothelium-derived relaxing factors; Lectin domainBackground: The vasorelaxant effect of lectins from leguminous plants (Diocleinae subtribe) is well described. However, this effect has been little explored for lectins isolated from Dalbergieae tribe, except for that of Vatairea guianensis, that induces vasorelaxation involving nitric oxide and the lectin domain. Objective: To evaluate the vasorelaxant effect of a lectin isolated from Lonchocarpus araripensis (LAL), Dalbergieae tribe, and the involvement of the lectin domain and endothelium derived relaxing factors. Methods: Aortic rings of Wistar rats (250 - 300 g) were mounted in organ bath and mantained in physiological conditions (CEUA No. 10130208-8/40). LAL (0.1–100 µg/ml) was added to phenylephrine (0.1 µM)-contracted tissues with either endothelium intact or denuded. In order to investigate the mechanisms of LAL relaxation, inhibitors of NOS (L-NAME: 100 µM), cyclooxygenase (indomethacin: 10 µM), or potassium channels (TEA: 5 mM) were added to endothelized tissues 30 min before contraction. The involvement of lectin domain was assessed by previous incubation of LAL (30 µg/ml) with GlcNAc (0.1 M). Results: LAL (0.1-100 µg/ml) induced relaxation only in endothelized aorta, being maximal at 100 µg/ml (62.57 ± 7.8%). The relaxant effect induced by LAL at 30 µg/ml (52.49 ± 10.32%) was abolished by previous incubation with GlcNAc. LAL relaxant effect (IC50 9.75 ± 7.1) was partially reversed by indomethacin (IC50 LAL + indomethacin: 30.47 ± 10.93) and was abolished by L-NAME or TEA. Conclusion: LAL exhibits vasorelaxant activity in contracted endothelized aorta of rats, involving the lectin domain, muscarinic receptor of acetylcholine and endothelial derived relaxing factors.Instituto para o Desenvolvimento da EducacaoConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico (FUNCAP).Pires, Alana de FreitasAlmeida, Lívia Mendes deSilva, Débora Helen Marques daMarques, Gabriela Fernandes OliveiraCajazeiras, João BatistaNeto, Cornevile CorreiaNascimento, Kyria SantiagoCavada, Benildo SousaAssreuy, Ana Maria Sampaio2017-10-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAvaliado por ParesPeer ReviewRevisado por paresapplication/pdfhttps://periodicos.unichristus.edu.br/jhbs/article/view/135110.12662/2317-3076jhbs.v5i4.1351.p306-310.2017Journal of Health & Biological Sciences; v. 5, n. 4 (2017): Journal of Health and Biological Sciences; 306-310Journal of Health & Biological Sciences; v. 5, n. 4 (2017): Journal of Health and Biological Sciences; 306-310Journal of Health and Biological Sciences; v. 5, n. 4 (2017): Journal of Health and Biological Sciences; 306-3102317-30762317-308410.12662/2317-3076jhbs.v5i4.2017reponame:Journal of Health & Biological Sciencesinstname:Centro Universitário Christus (Unichristus)instacron:CHRISTUSenghttps://periodicos.unichristus.edu.br/jhbs/article/view/1351/489https://periodicos.unichristus.edu.br/jhbs/article/downloadSuppFile/1351/255https://periodicos.unichristus.edu.br/jhbs/article/downloadSuppFile/1351/256Direitos autorais 2017 Journal of Health & Biological Scienceshttp://creativecommons.org/licenses/by-nc-sa/4.0info:eu-repo/semantics/openAccess2017-10-03T20:52:18Zoai:ojs.unichristus.emnuvens.com.br:article/1351Revistahttps://periodicos.unichristus.edu.br/jhbs/indexPRIhttps://periodicos.unichristus.edu.br/jhbs/oaisecretaria.jhbs@unichristus.edu.br || editor.jhbs@fchristus.edu.br2317-30762317-3084opendoar:2023-01-13T09:47:24.886571Journal of Health & Biological Sciences - Centro Universitário Christus (Unichristus)true |
dc.title.none.fl_str_mv |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
title |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
spellingShingle |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation Pires, Alana de Freitas Ciências da Saúde; Ciências Biológicas Lonchocarpus araripensis; Lectin; Vasorelaxant effect; Endothelium-derived relaxing factors; Lectin domain Pires, Alana de Freitas Ciências da Saúde; Ciências Biológicas Lonchocarpus araripensis; Lectin; Vasorelaxant effect; Endothelium-derived relaxing factors; Lectin domain |
title_short |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
title_full |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
title_fullStr |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
title_full_unstemmed |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
title_sort |
The lectin isolated from Lonchocarpus araripensis seed elicits endothelium-dependent vasorelaxation |
author |
Pires, Alana de Freitas |
author_facet |
Pires, Alana de Freitas Pires, Alana de Freitas Almeida, Lívia Mendes de Silva, Débora Helen Marques da Marques, Gabriela Fernandes Oliveira Cajazeiras, João Batista Neto, Cornevile Correia Nascimento, Kyria Santiago Cavada, Benildo Sousa Assreuy, Ana Maria Sampaio Almeida, Lívia Mendes de Silva, Débora Helen Marques da Marques, Gabriela Fernandes Oliveira Cajazeiras, João Batista Neto, Cornevile Correia Nascimento, Kyria Santiago Cavada, Benildo Sousa Assreuy, Ana Maria Sampaio |
author_role |
author |
author2 |
Almeida, Lívia Mendes de Silva, Débora Helen Marques da Marques, Gabriela Fernandes Oliveira Cajazeiras, João Batista Neto, Cornevile Correia Nascimento, Kyria Santiago Cavada, Benildo Sousa Assreuy, Ana Maria Sampaio |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico (FUNCAP). |
dc.contributor.author.fl_str_mv |
Pires, Alana de Freitas Almeida, Lívia Mendes de Silva, Débora Helen Marques da Marques, Gabriela Fernandes Oliveira Cajazeiras, João Batista Neto, Cornevile Correia Nascimento, Kyria Santiago Cavada, Benildo Sousa Assreuy, Ana Maria Sampaio |
dc.subject.none.fl_str_mv |
|
dc.subject.por.fl_str_mv |
Ciências da Saúde; Ciências Biológicas Lonchocarpus araripensis; Lectin; Vasorelaxant effect; Endothelium-derived relaxing factors; Lectin domain |
topic |
Ciências da Saúde; Ciências Biológicas Lonchocarpus araripensis; Lectin; Vasorelaxant effect; Endothelium-derived relaxing factors; Lectin domain |
description |
Background: The vasorelaxant effect of lectins from leguminous plants (Diocleinae subtribe) is well described. However, this effect has been little explored for lectins isolated from Dalbergieae tribe, except for that of Vatairea guianensis, that induces vasorelaxation involving nitric oxide and the lectin domain. Objective: To evaluate the vasorelaxant effect of a lectin isolated from Lonchocarpus araripensis (LAL), Dalbergieae tribe, and the involvement of the lectin domain and endothelium derived relaxing factors. Methods: Aortic rings of Wistar rats (250 - 300 g) were mounted in organ bath and mantained in physiological conditions (CEUA No. 10130208-8/40). LAL (0.1–100 µg/ml) was added to phenylephrine (0.1 µM)-contracted tissues with either endothelium intact or denuded. In order to investigate the mechanisms of LAL relaxation, inhibitors of NOS (L-NAME: 100 µM), cyclooxygenase (indomethacin: 10 µM), or potassium channels (TEA: 5 mM) were added to endothelized tissues 30 min before contraction. The involvement of lectin domain was assessed by previous incubation of LAL (30 µg/ml) with GlcNAc (0.1 M). Results: LAL (0.1-100 µg/ml) induced relaxation only in endothelized aorta, being maximal at 100 µg/ml (62.57 ± 7.8%). The relaxant effect induced by LAL at 30 µg/ml (52.49 ± 10.32%) was abolished by previous incubation with GlcNAc. LAL relaxant effect (IC50 9.75 ± 7.1) was partially reversed by indomethacin (IC50 LAL + indomethacin: 30.47 ± 10.93) and was abolished by L-NAME or TEA. Conclusion: LAL exhibits vasorelaxant activity in contracted endothelized aorta of rats, involving the lectin domain, muscarinic receptor of acetylcholine and endothelial derived relaxing factors. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-10-03 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Avaliado por Pares Peer Review Revisado por pares |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://periodicos.unichristus.edu.br/jhbs/article/view/1351 10.12662/2317-3076jhbs.v5i4.1351.p306-310.2017 |
url |
https://periodicos.unichristus.edu.br/jhbs/article/view/1351 |
identifier_str_mv |
10.12662/2317-3076jhbs.v5i4.1351.p306-310.2017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://periodicos.unichristus.edu.br/jhbs/article/view/1351/489 https://periodicos.unichristus.edu.br/jhbs/article/downloadSuppFile/1351/255 https://periodicos.unichristus.edu.br/jhbs/article/downloadSuppFile/1351/256 |
dc.rights.driver.fl_str_mv |
Direitos autorais 2017 Journal of Health & Biological Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Direitos autorais 2017 Journal of Health & Biological Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.coverage.none.fl_str_mv |
|
dc.publisher.none.fl_str_mv |
Instituto para o Desenvolvimento da Educacao |
publisher.none.fl_str_mv |
Instituto para o Desenvolvimento da Educacao |
dc.source.none.fl_str_mv |
Journal of Health & Biological Sciences; v. 5, n. 4 (2017): Journal of Health and Biological Sciences; 306-310 Journal of Health & Biological Sciences; v. 5, n. 4 (2017): Journal of Health and Biological Sciences; 306-310 Journal of Health and Biological Sciences; v. 5, n. 4 (2017): Journal of Health and Biological Sciences; 306-310 2317-3076 2317-3084 10.12662/2317-3076jhbs.v5i4.2017 reponame:Journal of Health & Biological Sciences instname:Centro Universitário Christus (Unichristus) instacron:CHRISTUS |
instname_str |
Centro Universitário Christus (Unichristus) |
instacron_str |
CHRISTUS |
institution |
CHRISTUS |
reponame_str |
Journal of Health & Biological Sciences |
collection |
Journal of Health & Biological Sciences |
repository.name.fl_str_mv |
Journal of Health & Biological Sciences - Centro Universitário Christus (Unichristus) |
repository.mail.fl_str_mv |
secretaria.jhbs@unichristus.edu.br || editor.jhbs@fchristus.edu.br |
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1822178658188525568 |
dc.identifier.doi.none.fl_str_mv |
10.12662/2317-3076jhbs.v5i4.1351.p306-310.2017 |