Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats

Detalhes bibliográficos
Autor(a) principal: Claudino, Mario A.
Data de Publicação: 2011
Outros Autores: Delbin, Maria A. [UNESP], Franco-Penteado, Carla F., Priviero, Fernanda B. [UNESP], De Nucci, Gilberto, Antunes, Edson, Zanesco, Angelina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.lfs.2010.11.018
http://hdl.handle.net/11449/72300
Resumo: Aims: The effect of exercise training (ET) on vascular responsiveness in diabetes mellitus has been largely well studied. However, limited studies have investigated the effects of ET on functional responses of the corpus cavernosum (CC) in diabetic animals. Therefore, the aim of this study was to investigate whether prior ET prevents the impairment of erectile function in streptozotocin-induced diabetic rats. Main methods: Rats were exercised for four weeks prior to the induction of diabetes, and then again for another 4 weeks thereafter. Concentration-response curves to acetylcholine, sodium nitroprusside, Y-27632, BAY 412272 and phenylephrine (PE) were obtained in CC. The excitatory and inhibitory effects of electrical-field stimulation were also evaluated. Key findings: Plasma SOD levels were markedly decreased in the sedentary diabetic group (D-SD) as compared to control sedentary animals (C-SD), approximately 53% (P < 0.05) and this reduction was restored in trained diabetic animals. Physical training restored the impairment of endothelium-dependent and -independent relaxation responses seen in the D-SD group. The potency values for Y-27632 in the CC were significantly reduced in the D-SD group, which was reversed by physical training. The impairment of electrical-field stimulation (EFS)-induced relaxation seen in the D-SD group was restored by physical training. On the other hand, both EFS-induced contractions and concentration-response curves to PE in cavernosal strips were not modified by either diabetes or physical training. Significance: Practice of regular physical exercise may be an important approach in preventing erectile dysfunction associated with diabetes mellitus by re-establishment of the balance between NO production and its inactivation. © 2010 Elsevier Inc. All rights reserved.
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spelling Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic ratsCorpus cavernosumDiabetesPhysical trainingSuperoxide dismutase4 (1 aminoethyl) n (4 pyridyl)cyclohexanecarboxamide4 amino 5 cyclopropyl 2 [1 (2 fluorobenzyl) 1h pyrazolo[3,4 b]pyridin 3 yl]pyrimidineacetylcholinenitric oxidenitroprusside sodiumphenylephrinesuperoxide dismutaseanimal experimentanimal modelanimal tissueblood vessel reactivitycontrolled studycorpus cavernosumdiabetes mellituselectrostimulationerectile dysfunctionexercisemalenitrergic nervenonhumanratsmooth muscle relaxationstreptozocin diabetesvascular endotheliumAnimalsCells, CulturedDiabetes Mellitus, ExperimentalErectile DysfunctionMaleMuscle ContractionMuscle, SmoothPenile ErectionPhysical Conditioning, AnimalRatsAnimaliaRattusAims: The effect of exercise training (ET) on vascular responsiveness in diabetes mellitus has been largely well studied. However, limited studies have investigated the effects of ET on functional responses of the corpus cavernosum (CC) in diabetic animals. Therefore, the aim of this study was to investigate whether prior ET prevents the impairment of erectile function in streptozotocin-induced diabetic rats. Main methods: Rats were exercised for four weeks prior to the induction of diabetes, and then again for another 4 weeks thereafter. Concentration-response curves to acetylcholine, sodium nitroprusside, Y-27632, BAY 412272 and phenylephrine (PE) were obtained in CC. The excitatory and inhibitory effects of electrical-field stimulation were also evaluated. Key findings: Plasma SOD levels were markedly decreased in the sedentary diabetic group (D-SD) as compared to control sedentary animals (C-SD), approximately 53% (P < 0.05) and this reduction was restored in trained diabetic animals. Physical training restored the impairment of endothelium-dependent and -independent relaxation responses seen in the D-SD group. The potency values for Y-27632 in the CC were significantly reduced in the D-SD group, which was reversed by physical training. The impairment of electrical-field stimulation (EFS)-induced relaxation seen in the D-SD group was restored by physical training. On the other hand, both EFS-induced contractions and concentration-response curves to PE in cavernosal strips were not modified by either diabetes or physical training. Significance: Practice of regular physical exercise may be an important approach in preventing erectile dysfunction associated with diabetes mellitus by re-establishment of the balance between NO production and its inactivation. © 2010 Elsevier Inc. All rights reserved.Department of Pharmacology Faculty of Medical Sciences University of Campinas (UNICAMP), Campinas (SP)Department of Physical Education Institute of Bioscience UNESP, 13506-900 Rio Claro (SP)Hematology and Hemotherapy Center Faculty of Medical Sciences University of Campinas (UNICAMP), PO Box 6111, 13084-971, Campinas (SP)Department of Physical Education Institute of Bioscience UNESP, 13506-900 Rio Claro (SP)Universidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Claudino, Mario A.Delbin, Maria A. [UNESP]Franco-Penteado, Carla F.Priviero, Fernanda B. [UNESP]De Nucci, GilbertoAntunes, EdsonZanesco, Angelina [UNESP]2014-05-27T11:25:27Z2014-05-27T11:25:27Z2011-01-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article272-277application/pdfhttp://dx.doi.org/10.1016/j.lfs.2010.11.018Life Sciences, v. 88, n. 5-6, p. 272-277, 2011.0024-3205http://hdl.handle.net/11449/7230010.1016/j.lfs.2010.11.0182-s2.0-787516470732-s2.0-78751647073.pdf4472007237545596Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengLife Sciences3.2341,071info:eu-repo/semantics/openAccess2023-10-04T06:09:23Zoai:repositorio.unesp.br:11449/72300Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-05-23T11:30:21.722303Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
title Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
spellingShingle Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
Claudino, Mario A.
Corpus cavernosum
Diabetes
Physical training
Superoxide dismutase
4 (1 aminoethyl) n (4 pyridyl)cyclohexanecarboxamide
4 amino 5 cyclopropyl 2 [1 (2 fluorobenzyl) 1h pyrazolo[3,4 b]pyridin 3 yl]pyrimidine
acetylcholine
nitric oxide
nitroprusside sodium
phenylephrine
superoxide dismutase
animal experiment
animal model
animal tissue
blood vessel reactivity
controlled study
corpus cavernosum
diabetes mellitus
electrostimulation
erectile dysfunction
exercise
male
nitrergic nerve
nonhuman
rat
smooth muscle relaxation
streptozocin diabetes
vascular endothelium
Animals
Cells, Cultured
Diabetes Mellitus, Experimental
Erectile Dysfunction
Male
Muscle Contraction
Muscle, Smooth
Penile Erection
Physical Conditioning, Animal
Rats
Animalia
Rattus
title_short Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
title_full Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
title_fullStr Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
title_full_unstemmed Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
title_sort Exercise training ameliorates the impairment of endothelial and nitrergic corpus cavernosum responses in diabetic rats
author Claudino, Mario A.
author_facet Claudino, Mario A.
Delbin, Maria A. [UNESP]
Franco-Penteado, Carla F.
Priviero, Fernanda B. [UNESP]
De Nucci, Gilberto
Antunes, Edson
Zanesco, Angelina [UNESP]
author_role author
author2 Delbin, Maria A. [UNESP]
Franco-Penteado, Carla F.
Priviero, Fernanda B. [UNESP]
De Nucci, Gilberto
Antunes, Edson
Zanesco, Angelina [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Claudino, Mario A.
Delbin, Maria A. [UNESP]
Franco-Penteado, Carla F.
Priviero, Fernanda B. [UNESP]
De Nucci, Gilberto
Antunes, Edson
Zanesco, Angelina [UNESP]
dc.subject.por.fl_str_mv Corpus cavernosum
Diabetes
Physical training
Superoxide dismutase
4 (1 aminoethyl) n (4 pyridyl)cyclohexanecarboxamide
4 amino 5 cyclopropyl 2 [1 (2 fluorobenzyl) 1h pyrazolo[3,4 b]pyridin 3 yl]pyrimidine
acetylcholine
nitric oxide
nitroprusside sodium
phenylephrine
superoxide dismutase
animal experiment
animal model
animal tissue
blood vessel reactivity
controlled study
corpus cavernosum
diabetes mellitus
electrostimulation
erectile dysfunction
exercise
male
nitrergic nerve
nonhuman
rat
smooth muscle relaxation
streptozocin diabetes
vascular endothelium
Animals
Cells, Cultured
Diabetes Mellitus, Experimental
Erectile Dysfunction
Male
Muscle Contraction
Muscle, Smooth
Penile Erection
Physical Conditioning, Animal
Rats
Animalia
Rattus
topic Corpus cavernosum
Diabetes
Physical training
Superoxide dismutase
4 (1 aminoethyl) n (4 pyridyl)cyclohexanecarboxamide
4 amino 5 cyclopropyl 2 [1 (2 fluorobenzyl) 1h pyrazolo[3,4 b]pyridin 3 yl]pyrimidine
acetylcholine
nitric oxide
nitroprusside sodium
phenylephrine
superoxide dismutase
animal experiment
animal model
animal tissue
blood vessel reactivity
controlled study
corpus cavernosum
diabetes mellitus
electrostimulation
erectile dysfunction
exercise
male
nitrergic nerve
nonhuman
rat
smooth muscle relaxation
streptozocin diabetes
vascular endothelium
Animals
Cells, Cultured
Diabetes Mellitus, Experimental
Erectile Dysfunction
Male
Muscle Contraction
Muscle, Smooth
Penile Erection
Physical Conditioning, Animal
Rats
Animalia
Rattus
description Aims: The effect of exercise training (ET) on vascular responsiveness in diabetes mellitus has been largely well studied. However, limited studies have investigated the effects of ET on functional responses of the corpus cavernosum (CC) in diabetic animals. Therefore, the aim of this study was to investigate whether prior ET prevents the impairment of erectile function in streptozotocin-induced diabetic rats. Main methods: Rats were exercised for four weeks prior to the induction of diabetes, and then again for another 4 weeks thereafter. Concentration-response curves to acetylcholine, sodium nitroprusside, Y-27632, BAY 412272 and phenylephrine (PE) were obtained in CC. The excitatory and inhibitory effects of electrical-field stimulation were also evaluated. Key findings: Plasma SOD levels were markedly decreased in the sedentary diabetic group (D-SD) as compared to control sedentary animals (C-SD), approximately 53% (P < 0.05) and this reduction was restored in trained diabetic animals. Physical training restored the impairment of endothelium-dependent and -independent relaxation responses seen in the D-SD group. The potency values for Y-27632 in the CC were significantly reduced in the D-SD group, which was reversed by physical training. The impairment of electrical-field stimulation (EFS)-induced relaxation seen in the D-SD group was restored by physical training. On the other hand, both EFS-induced contractions and concentration-response curves to PE in cavernosal strips were not modified by either diabetes or physical training. Significance: Practice of regular physical exercise may be an important approach in preventing erectile dysfunction associated with diabetes mellitus by re-establishment of the balance between NO production and its inactivation. © 2010 Elsevier Inc. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-31
2014-05-27T11:25:27Z
2014-05-27T11:25:27Z
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/10.1016/j.lfs.2010.11.018
Life Sciences, v. 88, n. 5-6, p. 272-277, 2011.
0024-3205
http://hdl.handle.net/11449/72300
10.1016/j.lfs.2010.11.018
2-s2.0-78751647073
2-s2.0-78751647073.pdf
4472007237545596
url http://dx.doi.org/10.1016/j.lfs.2010.11.018
http://hdl.handle.net/11449/72300
identifier_str_mv Life Sciences, v. 88, n. 5-6, p. 272-277, 2011.
0024-3205
10.1016/j.lfs.2010.11.018
2-s2.0-78751647073
2-s2.0-78751647073.pdf
4472007237545596
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Life Sciences
3.234
1,071
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 272-277
application/pdf
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
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