The triterpenoid alpha, beta-amyrin prevents the impaired aortic vascular reactivity in high-fat diet-induced obese mice
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , |
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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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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1823806750156914688 |