The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice

Detalhes bibliográficos
Autor(a) principal: Santos, Flávia Almeida
Data de Publicação: 2017
Outros Autores: Batista-Lima, Francisco José, Nunes, Paulo Iury Gomes, Viana, Ana Flávia Seraine Custódio, Silva, Armenio André de Carvalho Almeida da, Fonseca, Said Gonçalves da Cruz, Chaves, Mariana Helena, Rao, Vietla Satyanarayana, Magalhães, Pedro Jorge Caldas, Brito, Teresinha Silva de, Carvalho, Karine Maria Martins Bezerra
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/26578
Resumo: To characterize the pro tective effects of the triterpenoid mixture alpha, beta-amyrin (AMY, 20 mg/kg, during 15 days) on the reactivity of isolated aorta of high- fat diet (HFD)-induced obese mice. Male Swiss mice were fed with HFD or normal diet (ND) for 15 weeks. Contractions of thoracic aorta in response to KCl or phen- ylephrine (PHE) and relaxation by acetylcholine (ACh) or sodium nitroprusside (SNP) were analyzed. HFD-fed mice developed hyperglycemia, hyperlipidemia, and significant body weight gain, parameters prevented by AMY treat- ment. Whereas aortic contractility did not differ in re- sponse to KCl, contractions induced by PHE (1 μ M) as well as relaxation induced by ACh (1 – 30 μ M) or SNP (1 nM – 0.1 mM) on PHE-contracted aorta were decreased ( p < 0.05) in tissues of HFD compared to ND mice, phenomenon significantly ( p < 0.05) diminished in HFD mice treated with AMY. The relaxant actions of ACh and SNP were inhibited ( p < 0.05) by tetraethylammonium (TEA, 5 mM), apamin (0.1 μ M), and 4-aminopyridine (4-AP; 3 mM) in aortae from ND group, but not from HFD. Treatment of HFD mice with AMY rescued the inhibitory effect of TEA ( p < 0.05) on vasorelaxant actions of ACh and SNP. 1H-[1,2,4]oxadiazolo[4,3- a]quinoxalin-1-one (ODQ) inhibited similarly the relaxant effects of SNP in all groups. 8-Br-cGMP relaxed with similar profile aortae of all groups. By preventing HFD- induced obesity in mice, AMY rescued the blunted con- tractile response to PHE, and the attenuated vasorelaxation and K + channel activation (opening) induced by ACh and SNP in isolated aorta.
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spelling The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese miceObesidadeDietaAorta TorácicaAorta, ThoracicTo characterize the pro tective effects of the triterpenoid mixture alpha, beta-amyrin (AMY, 20 mg/kg, during 15 days) on the reactivity of isolated aorta of high- fat diet (HFD)-induced obese mice. Male Swiss mice were fed with HFD or normal diet (ND) for 15 weeks. Contractions of thoracic aorta in response to KCl or phen- ylephrine (PHE) and relaxation by acetylcholine (ACh) or sodium nitroprusside (SNP) were analyzed. HFD-fed mice developed hyperglycemia, hyperlipidemia, and significant body weight gain, parameters prevented by AMY treat- ment. Whereas aortic contractility did not differ in re- sponse to KCl, contractions induced by PHE (1 μ M) as well as relaxation induced by ACh (1 – 30 μ M) or SNP (1 nM – 0.1 mM) on PHE-contracted aorta were decreased ( p < 0.05) in tissues of HFD compared to ND mice, phenomenon significantly ( p < 0.05) diminished in HFD mice treated with AMY. The relaxant actions of ACh and SNP were inhibited ( p < 0.05) by tetraethylammonium (TEA, 5 mM), apamin (0.1 μ M), and 4-aminopyridine (4-AP; 3 mM) in aortae from ND group, but not from HFD. Treatment of HFD mice with AMY rescued the inhibitory effect of TEA ( p < 0.05) on vasorelaxant actions of ACh and SNP. 1H-[1,2,4]oxadiazolo[4,3- a]quinoxalin-1-one (ODQ) inhibited similarly the relaxant effects of SNP in all groups. 8-Br-cGMP relaxed with similar profile aortae of all groups. By preventing HFD- induced obesity in mice, AMY rescued the blunted con- tractile response to PHE, and the attenuated vasorelaxation and K + channel activation (opening) induced by ACh and SNP in isolated aorta.Naunyn-Schmiedeberg's Archives of Pharmacology2017-10-11T13:17:49Z2017-10-11T13:17:49Z2017-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfSANTOS, F. A. et al. The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice. Naunyn-Schmiedeberg's Arch Pharmacol, v. 390, p. 1029-39, aug. 2017.0028-1298 Print1432-1912 On linehttp://www.repositorio.ufc.br/handle/riufc/26578Santos, Flávia AlmeidaBatista-Lima, Francisco JoséNunes, Paulo Iury GomesViana, Ana Flávia Seraine CustódioSilva, Armenio André de Carvalho Almeida daFonseca, Said Gonçalves da CruzChaves, Mariana HelenaRao, Vietla SatyanarayanaMagalhães, Pedro Jorge CaldasBrito, Teresinha Silva deCarvalho, Karine Maria Martins Bezerraengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2019-01-25T14:53:39Zoai:repositorio.ufc.br:riufc/26578Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2019-01-25T14:53:39Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
title The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
spellingShingle The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
Santos, Flávia Almeida
Obesidade
Dieta
Aorta Torácica
Aorta, Thoracic
title_short The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
title_full The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
title_fullStr The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
title_full_unstemmed The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
title_sort The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
author Santos, Flávia Almeida
author_facet Santos, Flávia Almeida
Batista-Lima, Francisco José
Nunes, Paulo Iury Gomes
Viana, Ana Flávia Seraine Custódio
Silva, Armenio André de Carvalho Almeida da
Fonseca, Said Gonçalves da Cruz
Chaves, Mariana Helena
Rao, Vietla Satyanarayana
Magalhães, Pedro Jorge Caldas
Brito, Teresinha Silva de
Carvalho, Karine Maria Martins Bezerra
author_role author
author2 Batista-Lima, Francisco José
Nunes, Paulo Iury Gomes
Viana, Ana Flávia Seraine Custódio
Silva, Armenio André de Carvalho Almeida da
Fonseca, Said Gonçalves da Cruz
Chaves, Mariana Helena
Rao, Vietla Satyanarayana
Magalhães, Pedro Jorge Caldas
Brito, Teresinha Silva de
Carvalho, Karine Maria Martins Bezerra
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santos, Flávia Almeida
Batista-Lima, Francisco José
Nunes, Paulo Iury Gomes
Viana, Ana Flávia Seraine Custódio
Silva, Armenio André de Carvalho Almeida da
Fonseca, Said Gonçalves da Cruz
Chaves, Mariana Helena
Rao, Vietla Satyanarayana
Magalhães, Pedro Jorge Caldas
Brito, Teresinha Silva de
Carvalho, Karine Maria Martins Bezerra
dc.subject.por.fl_str_mv Obesidade
Dieta
Aorta Torácica
Aorta, Thoracic
topic Obesidade
Dieta
Aorta Torácica
Aorta, Thoracic
description To characterize the pro tective effects of the triterpenoid mixture alpha, beta-amyrin (AMY, 20 mg/kg, during 15 days) on the reactivity of isolated aorta of high- fat diet (HFD)-induced obese mice. Male Swiss mice were fed with HFD or normal diet (ND) for 15 weeks. Contractions of thoracic aorta in response to KCl or phen- ylephrine (PHE) and relaxation by acetylcholine (ACh) or sodium nitroprusside (SNP) were analyzed. HFD-fed mice developed hyperglycemia, hyperlipidemia, and significant body weight gain, parameters prevented by AMY treat- ment. Whereas aortic contractility did not differ in re- sponse to KCl, contractions induced by PHE (1 μ M) as well as relaxation induced by ACh (1 – 30 μ M) or SNP (1 nM – 0.1 mM) on PHE-contracted aorta were decreased ( p < 0.05) in tissues of HFD compared to ND mice, phenomenon significantly ( p < 0.05) diminished in HFD mice treated with AMY. The relaxant actions of ACh and SNP were inhibited ( p < 0.05) by tetraethylammonium (TEA, 5 mM), apamin (0.1 μ M), and 4-aminopyridine (4-AP; 3 mM) in aortae from ND group, but not from HFD. Treatment of HFD mice with AMY rescued the inhibitory effect of TEA ( p < 0.05) on vasorelaxant actions of ACh and SNP. 1H-[1,2,4]oxadiazolo[4,3- a]quinoxalin-1-one (ODQ) inhibited similarly the relaxant effects of SNP in all groups. 8-Br-cGMP relaxed with similar profile aortae of all groups. By preventing HFD- induced obesity in mice, AMY rescued the blunted con- tractile response to PHE, and the attenuated vasorelaxation and K + channel activation (opening) induced by ACh and SNP in isolated aorta.
publishDate 2017
dc.date.none.fl_str_mv 2017-10-11T13:17:49Z
2017-10-11T13:17:49Z
2017-10
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 SANTOS, F. A. et al. The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice. Naunyn-Schmiedeberg's Arch Pharmacol, v. 390, p. 1029-39, aug. 2017.
0028-1298 Print
1432-1912 On line
http://www.repositorio.ufc.br/handle/riufc/26578
identifier_str_mv SANTOS, F. A. et al. The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice. Naunyn-Schmiedeberg's Arch Pharmacol, v. 390, p. 1029-39, aug. 2017.
0028-1298 Print
1432-1912 On line
url http://www.repositorio.ufc.br/handle/riufc/26578
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Naunyn-Schmiedeberg's Archives of Pharmacology
publisher.none.fl_str_mv Naunyn-Schmiedeberg's Archives of Pharmacology
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
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