High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses

Detalhes bibliográficos
Autor(a) principal: Toque, Haroldo A.
Data de Publicação: 2011
Outros Autores: da Silva, Fabio H., Calixto, Marina C., Lintomen, Leticia, Schenka, Andre A., Saad, Mario J., Zanesco, Angelina [UNESP], Antunes, Edson
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1111/j.1464-410X.2010.09704.x
http://hdl.handle.net/11449/20884
Resumo: What's known on the subject? and What does the study add?Erectile dysfunction (ED) is defined as the persistent inability to achieve and/or maintain an erection sufficient for satisfactory sexual performance. ED has been found in patients with cardiovascular and endocrine-metabolic diseases. Overweight, obesity and weight gain have been shown to be independent risk factors for the development of ED. Clinical studies show that ED should be considered an early clinical manifestation of risk factors for cardiovascular events, including acute myocardial infarction. However, the mechanisms that explains ED associated with obesity are yet to be fully elucidated.Using a mice model of high-fat diet associated with obesity, we have demonstrated that ED is the result of impaired endothelial and nitrergic cavernosal relaxations along with increased contractile responses, favouring penile detumescence.OBJECTIVEObesity induced by high-fat diet (HFD) is one of the most important risk factor for the development of erectile dysfunction (ED) in man. This study aimed to characterize the ED resulting from obesity associated with HFD in mice.MATERIALS and METHODSC57BL/6 mice fed for 10 weeks with either HFD to induce obesity or a standard-chow diet (SD) were used. Corpus cavernosum was surgically dissected free, and strips were mounted in 10-mL organ baths containing Krebs solution.Functional responses to endothelium-dependent and -independent agents, as well as to electrical-field stimulation were measured in the cavernosal tissue. Levels of cGMP in erectile tissue were detected by enzyme immunoassay assay.RESULTSThe potency (pEC(50)) and maximal response (E(max)) to acetylcholine were significantly lower in the HFD group compared with the SD group. A marked decrease in the non-adrenergic non-cholinergic (nitrergic) cavernosal relaxations in the HFD group was also detected. There were no significant differences between the SD and HFD groups for the cavernosal relaxations in response to sodium nitroprusside.The contractile responses elicited by the alpha(1)-adrenoceptor agonist phenylephrine were significantly greater in the HFD group compared with the SD group.Similarly, the electrical-field stimulation (2-8 Hz)-induced adrenergic contractions were markedly greater in HFD mice. The pEC(50) for endothelin-1 was about 6.9-fold higher in the HFD compared with SD group.The basal cGMP content was 47% lower in HFD strips compared with SD group. There were no morphological alterations in erectile tissue of HFD group compared with SD mice.CONCLUSIONObesity associated with HFD favours ED as result of impaired endothelial and nitrergic cavernosal relaxations along with increased contractile responses to adrenergic stimulation and endothelin-1 receptor activation.
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spelling High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responsesobesitymale impotencenitric oxideendothelin-1noradrenalinecyclic GMPWhat's known on the subject? and What does the study add?Erectile dysfunction (ED) is defined as the persistent inability to achieve and/or maintain an erection sufficient for satisfactory sexual performance. ED has been found in patients with cardiovascular and endocrine-metabolic diseases. Overweight, obesity and weight gain have been shown to be independent risk factors for the development of ED. Clinical studies show that ED should be considered an early clinical manifestation of risk factors for cardiovascular events, including acute myocardial infarction. However, the mechanisms that explains ED associated with obesity are yet to be fully elucidated.Using a mice model of high-fat diet associated with obesity, we have demonstrated that ED is the result of impaired endothelial and nitrergic cavernosal relaxations along with increased contractile responses, favouring penile detumescence.OBJECTIVEObesity induced by high-fat diet (HFD) is one of the most important risk factor for the development of erectile dysfunction (ED) in man. This study aimed to characterize the ED resulting from obesity associated with HFD in mice.MATERIALS and METHODSC57BL/6 mice fed for 10 weeks with either HFD to induce obesity or a standard-chow diet (SD) were used. Corpus cavernosum was surgically dissected free, and strips were mounted in 10-mL organ baths containing Krebs solution.Functional responses to endothelium-dependent and -independent agents, as well as to electrical-field stimulation were measured in the cavernosal tissue. Levels of cGMP in erectile tissue were detected by enzyme immunoassay assay.RESULTSThe potency (pEC(50)) and maximal response (E(max)) to acetylcholine were significantly lower in the HFD group compared with the SD group. A marked decrease in the non-adrenergic non-cholinergic (nitrergic) cavernosal relaxations in the HFD group was also detected. There were no significant differences between the SD and HFD groups for the cavernosal relaxations in response to sodium nitroprusside.The contractile responses elicited by the alpha(1)-adrenoceptor agonist phenylephrine were significantly greater in the HFD group compared with the SD group.Similarly, the electrical-field stimulation (2-8 Hz)-induced adrenergic contractions were markedly greater in HFD mice. The pEC(50) for endothelin-1 was about 6.9-fold higher in the HFD compared with SD group.The basal cGMP content was 47% lower in HFD strips compared with SD group. There were no morphological alterations in erectile tissue of HFD group compared with SD mice.CONCLUSIONObesity associated with HFD favours ED as result of impaired endothelial and nitrergic cavernosal relaxations along with increased contractile responses to adrenergic stimulation and endothelin-1 receptor activation.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ Campinas UNICAMP, Fac Med Sci, Dept Pharmacol & Internal Med, São Paulo, BrazilUniv São Paulo State UNESP, Dept Phys Educ, São Paulo, BrazilMed Coll Georgia, Dept Pharmacol & Toxicol, Augusta, GA 30912 USAUniv São Paulo State UNESP, Dept Phys Educ, São Paulo, BrazilWiley-BlackwellUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Med Coll GeorgiaToque, Haroldo A.da Silva, Fabio H.Calixto, Marina C.Lintomen, LeticiaSchenka, Andre A.Saad, Mario J.Zanesco, Angelina [UNESP]Antunes, Edson2013-09-30T18:49:20Z2014-05-20T13:58:46Z2013-09-30T18:49:20Z2014-05-20T13:58:46Z2011-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1628-1634http://dx.doi.org/10.1111/j.1464-410X.2010.09704.xBju International. Malden: Wiley-blackwell, v. 107, n. 10, p. 1628-1634, 2011.1464-4096http://hdl.handle.net/11449/2088410.1111/j.1464-410X.2010.09704.xWOS:0002898991000164472007237545596Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBju International4.6882,094info:eu-repo/semantics/openAccess2021-10-22T19:32:46Zoai:repositorio.unesp.br:11449/20884Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-22T19:32:46Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
title High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
spellingShingle High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
Toque, Haroldo A.
obesity
male impotence
nitric oxide
endothelin-1
noradrenaline
cyclic GMP
title_short High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
title_full High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
title_fullStr High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
title_full_unstemmed High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
title_sort High-fat diet associated with obesity induces impairment of mouse corpus cavernosum responses
author Toque, Haroldo A.
author_facet Toque, Haroldo A.
da Silva, Fabio H.
Calixto, Marina C.
Lintomen, Leticia
Schenka, Andre A.
Saad, Mario J.
Zanesco, Angelina [UNESP]
Antunes, Edson
author_role author
author2 da Silva, Fabio H.
Calixto, Marina C.
Lintomen, Leticia
Schenka, Andre A.
Saad, Mario J.
Zanesco, Angelina [UNESP]
Antunes, Edson
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (Unesp)
Med Coll Georgia
dc.contributor.author.fl_str_mv Toque, Haroldo A.
da Silva, Fabio H.
Calixto, Marina C.
Lintomen, Leticia
Schenka, Andre A.
Saad, Mario J.
Zanesco, Angelina [UNESP]
Antunes, Edson
dc.subject.por.fl_str_mv obesity
male impotence
nitric oxide
endothelin-1
noradrenaline
cyclic GMP
topic obesity
male impotence
nitric oxide
endothelin-1
noradrenaline
cyclic GMP
description What's known on the subject? and What does the study add?Erectile dysfunction (ED) is defined as the persistent inability to achieve and/or maintain an erection sufficient for satisfactory sexual performance. ED has been found in patients with cardiovascular and endocrine-metabolic diseases. Overweight, obesity and weight gain have been shown to be independent risk factors for the development of ED. Clinical studies show that ED should be considered an early clinical manifestation of risk factors for cardiovascular events, including acute myocardial infarction. However, the mechanisms that explains ED associated with obesity are yet to be fully elucidated.Using a mice model of high-fat diet associated with obesity, we have demonstrated that ED is the result of impaired endothelial and nitrergic cavernosal relaxations along with increased contractile responses, favouring penile detumescence.OBJECTIVEObesity induced by high-fat diet (HFD) is one of the most important risk factor for the development of erectile dysfunction (ED) in man. This study aimed to characterize the ED resulting from obesity associated with HFD in mice.MATERIALS and METHODSC57BL/6 mice fed for 10 weeks with either HFD to induce obesity or a standard-chow diet (SD) were used. Corpus cavernosum was surgically dissected free, and strips were mounted in 10-mL organ baths containing Krebs solution.Functional responses to endothelium-dependent and -independent agents, as well as to electrical-field stimulation were measured in the cavernosal tissue. Levels of cGMP in erectile tissue were detected by enzyme immunoassay assay.RESULTSThe potency (pEC(50)) and maximal response (E(max)) to acetylcholine were significantly lower in the HFD group compared with the SD group. A marked decrease in the non-adrenergic non-cholinergic (nitrergic) cavernosal relaxations in the HFD group was also detected. There were no significant differences between the SD and HFD groups for the cavernosal relaxations in response to sodium nitroprusside.The contractile responses elicited by the alpha(1)-adrenoceptor agonist phenylephrine were significantly greater in the HFD group compared with the SD group.Similarly, the electrical-field stimulation (2-8 Hz)-induced adrenergic contractions were markedly greater in HFD mice. The pEC(50) for endothelin-1 was about 6.9-fold higher in the HFD compared with SD group.The basal cGMP content was 47% lower in HFD strips compared with SD group. There were no morphological alterations in erectile tissue of HFD group compared with SD mice.CONCLUSIONObesity associated with HFD favours ED as result of impaired endothelial and nitrergic cavernosal relaxations along with increased contractile responses to adrenergic stimulation and endothelin-1 receptor activation.
publishDate 2011
dc.date.none.fl_str_mv 2011-05-01
2013-09-30T18:49:20Z
2013-09-30T18:49:20Z
2014-05-20T13:58:46Z
2014-05-20T13:58:46Z
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/10.1111/j.1464-410X.2010.09704.x
Bju International. Malden: Wiley-blackwell, v. 107, n. 10, p. 1628-1634, 2011.
1464-4096
http://hdl.handle.net/11449/20884
10.1111/j.1464-410X.2010.09704.x
WOS:000289899100016
4472007237545596
url http://dx.doi.org/10.1111/j.1464-410X.2010.09704.x
http://hdl.handle.net/11449/20884
identifier_str_mv Bju International. Malden: Wiley-blackwell, v. 107, n. 10, p. 1628-1634, 2011.
1464-4096
10.1111/j.1464-410X.2010.09704.x
WOS:000289899100016
4472007237545596
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Bju International
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dc.format.none.fl_str_mv 1628-1634
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv Web of Science
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
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repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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